- Open Access
H2A ubiquitination is essential for Polycomb Repressive Complex 1-mediated gene regulation in Marchantia polymorpha
Genome Biology volume 22, Article number: 253 (2021)
Polycomb repressive complex 1 (PRC1) and PRC2 are chromatin regulators maintaining transcriptional repression. The deposition of H3 lysine 27 tri-methylation (H3K27me3) by PRC2 is known to be required for transcriptional repression, whereas the contribution of H2A ubiquitination (H2Aub) in the Polycomb repressive system remains unclear in plants.
We directly test the requirement of H2Aub for gene regulation in Marchantia polymorpha by generating point mutations in H2A that prevent ubiquitination by PRC1. These mutants show reduced H3K27me3 levels on the same target sites as mutants defective in PRC1 subunits MpBMI1 and the homolog MpBMI1L, revealing that PRC1-catalyzed H2Aub is essential for Polycomb system function. Furthermore, by comparing transcriptome data between mutants in MpH2A and MpBMI1/1L, we demonstrate that H2Aub contributes to the PRC1-mediated transcriptional level of genes and transposable elements.
Together, our data demonstrates that H2Aub plays a direct role in H3K27me3 deposition and is required for PRC1-mediated transcriptional changes in both genes and transposable elements in Marchantia.
Polycomb group (PcG) proteins are evolutionarily conserved epigenetic regulators which maintain transcriptional gene repression in essential cellular and developmental processes in eukaryotes [1,2,3,4]. PcG proteins typically belong to one of the two functionally distinct multi-protein complexes: Polycomb Repressive Complex 1 (PRC1) and PRC2. PRC1 promotes chromatin compaction and catalyzes mono-ubiquitination on histone 2A (H2Aub) mainly at lysine 119 in mammals, lysine 118 in Drosophila, and lysine 121 in Arabidopsis [4,5,6,7,8], whereas PRC2 tri-methylates histone 3 at lysine 27 (H3K27me3) [9,10,11,12]. The catalytic core of the mammalian PRC1 is composed of the E3 ubiquitin ligases RING1A or RING1B and one of six Polycomb RING finger (PCGF) proteins [13,14,15], while in Drosophila it consists of RING1 (encoded by the Sce gene) and one of two PCGF proteins: Psc or Su(z)2 [16,17,18]. The Arabidopsis PRC1 core includes AtRING1A or AtRING1B and one of the three AtBMI1s (homologs of PCGF4) [6, 19,20,21].
Previous studies on the Polycomb repressive system in Drosophila and mammals first proposed a PRC2-initiated hierarchical model where PRC2 establishes H3K27me3, which is then recognized by chromodomain-containing subunits of the canonical PRC1 (cPRC1). Nevertheless, later studies found this classical hierarchical model not sufficient to explain the Polycomb repressive system [13, 22, 23]. Instead, it was found that non-canonical PRC1 (ncPRC1) lacking chromodomain-containing subunits can recruit PRC2 and establish stable Polycomb repressive domains [24,25,26,27]. This data points that the PRC1 catalytic function is required for PRC2 recruitment, which was supported by recent work showing that in mouse embryonic stem cells (ESCs), loss of RING1B catalytic activity largely phenocopies the complete removal of the RING1B protein [28, 29]. Nevertheless, whether this is a generally applicable concept remains to be established. In Drosophila, H2AK118ub seems not required for repression of Polycomb target genes during the early stages of embryo development and PRC2 binding to chromatin requires PRC1 but not H2Aub [30, 31]. Similarly, during neuronal fate restriction in mouse, PRC1 repression was shown to function independently of ubiquitination . This data suggests that there are developmental context-specific differences in the functional requirement of the catalytic activity of PRC1.
PRC1-catalyzed H2Aub has been intensively studied in Arabidopsis thaliana. H2Aub level, H3K27me3 incorporation and chromatin accessibility were shown to be affected by the depletion of components of PRC1 in Arabidopsis [33,34,35]. Nevertheless, it remains unclear thus far whether H2Aub is required for H3K27me3 targeting. PRC1 is composed of multiple proteins that engage in interactions with PRC2 components. Thus, AtRING and AtBMI1 in PRC1 can interact with LHP1, which co-purifies with PRC2 in Arabidopsis [19, 20, 36], suggesting that PRC1 rather than H2Aub promotes H3K27me3 by interacting and recruiting PRC2 to chromatin. H2Aub is associated with permissively accessible chromatin and the average transcription levels of only-H2Aub marked genes are higher than that of H2Aub/H3K27me3 and only-H3K27me3 marked genes in Arabidopsis [33, 35]. Consistently, removal of H2Aub is required for stable repression of Polycomb target genes . Considering these studies proposing an activating role of H2Aub together with the fact that H2Aub is not required for Polycomb-mediated repression in Drosophila and neuronal fate restriction of mouse, it remains to be investigated whether H2Aub is indeed essential for PRC1-mediated gene repression. Thus, to directly test the functional role of H2Aub, we generated H2Aub mutants by replacing the endogenous H2A by H2A variants with mutated lysines in the liverwort Marchantia polymorpha.
Marchantia shares many signaling pathways with Arabidopsis and other seed plants . Together with its low genetic redundancy and possibilities to easily generate mutants, Marchantia is an ideal plant model to study the evolutionarily conserved Polycomb system. There is only a single gene encoding canonical H2A in Marchantia, compared to four genes in Arabidopsis . We generated lysine to arginine substitutions in H2A on residues K115/116/119 and demonstrate that all three lysines are ubiquitinated in vivo and likely have redundant functions. We furthermore show that H2Aub mediates H3K27me3 incorporation in both genes and transposable elements (TEs) in Marchantia and reveal that H2Aub is essential for both PRC1-mediated transcriptional activation and silencing.
H2Aub mediates H3K27me3 deposition on Polycomb target sites in genes and TEs
In mutants of PRC1 components, decreased H2Aub correlates with reduced H3K27me3 in Arabidopsis [33, 35]. To elucidate the functional requirement of H2Aub to induce H3K27me3 incorporation, we generated H2Aub depleted lines by introducing point mutations in the potential ubiquitination sites of canonical MpH2A (Additional file 1: Figure S1a). We co-transformed the point mutated H2A variants and a CRISPR construct designed to knock out the endogenous H2A (Additional file 1: Figure S1b, c). Lysine 120 (K120) and K121 of Arabidopsis H2A were shown to be ubiquitinated by AtBMI1 in vitro [6, 20], corresponding to K115 and K116 in MpH2A (Fig. 1a). In Drosophila, mutations of four close lysine sites (K117, K118, K121 and K122) are required to abolish total H2Aub . We therefore generated Mph2a;H2AK115R/K116R and Mph2a;H2AK119R mutants (jointly referred to as h2a_ub mutants) by substituting the C-terminal lysine residues K115 and K116 or K119 of MpH2A with arginine. We failed to obtain Mph2a mutants expressing H2A variants with all three point mutations, indicating that the three lysine sites of MpH2A are functionally redundant. The global H2Aub level was strongly decreased in lines of Mph2a;H2AK115R/K116R and Mph2a;H2AK119R mutants compared to wild type (WT) (Fig. 1b). Nevertheless, there was a remaining H2Aub signal in both mutant lines, indicating that all lysine residues can be ubiquitinated in vivo and likely act redundantly. The most obvious defects of h2a_ub mutants were downward curled edges of the thallus that grew into the growth media and decreased gemmae dormancy compared to WT (Fig. 1c–h).
To understand the connection between H2Aub and H3K27me3 in the Polycomb repressive system, we generated ChIP-seq data for H3, H2Aub, and H3K27me3 in WT, Mph2a;H2AK115R/K116R #1, and Mph2a;H2AK119R #1 mutants. To validate our ChIP-seq data, we compared the H3K27me3 peaks in our WT with previously published data . The majority of peaks overlapped between both datasets (Additional file 1: Figure S2), supporting the quality of our data. We found that genes with decreased H2Aub in the Mph2a;H2AK115R/K116R mutant had also decreased H2Aub and H3K27me3 levels in the Mph2a;H2AK119R mutant, but to a lesser extent (Fig. 1i, Additional file 1: Figure S3a, c). Decreased levels of H2Aub and H3K27me3 occurred over the whole length of genes, including the 1 kb upstream and downstream regions (Additional file 1: Figure S3a). Conversely, genes with reduced H2Aub level in the Mph2a;H2AK119R mutant were less affected in the Mph2a;H2AK115R/K116R mutant (Fig. 1j, Additional file 1: Figure S3b, d), supporting the notion that all three lysine residues of MpH2A are targeted by ubiquitination and H3K27me3 deposition is affected upon H2Aub depletion. In those H2Aub marked genes that did not undergo changes of H2Aub in either h2a_ub mutant, also the level of H3K27me3 level did not obviously change (Fig. 1k). We further analyzed H3K27me3 on genes marked by both H2Aub and H3K27me3 (H2Aub/H3K27me3, overlapped genes in Fig. 1l) and found H3K27me3 levels to be decreased in both h2a_ub mutants compared to WT (Fig.1m, Additional file 1: Figure S3e). Due to compensated ubiquitination of K115/K116 and K119 in H2A, decreased H2Aub was only observed in the promoter region of H2Aub/H3K27me3 gene (Additional file 1: Figure S3f). Reduced H3K27me3 in the gene body of H2Aub/H3K27me3 genes implies that the ubiquitination on K115/K116 and K119 in H2A is not completely functionally redundant. H3K27me3 was also decreased on only-H3K27me3 marked genes (n=583), correlating with mildly increased levels of H2Aub on the 1 kb promoter and highly increased levels of H2Aub on the gene body of only-H3K27me3 genes in h2a_ub mutants (Additional file 1: Figure S3g, h). Gain of H2Aub is associated with the recruitment of REF6 that mediates H3K27me3 demethylation in Arabidopsis , providing an explanation for the loss of H3K27me3 on only-H3K27me3 genes.
In Marchantia, 60% of H3K27me3 peaks are present in intergenic regions ; however, the location of H2Aub peaks remains to be explored. Out of 6575 H2Aub peaks identified in WT, about 20% mapped to intergenic regions, while most of the H2Aub peaks were located in gene body or promoter regions (Additional file 1: Figure S4). We found H2Aub and H3K27me3 peaks to be enriched on TEs (Fig. 1n), especially the H3K27me3-only peaks. TEs covered by H2Aub and H3K27me3 had also decreased H3K27me3 levels in both h2a_ub mutants (Fig. 1o), revealing that H2Aub is required to recruit H3K27me3 to TE regions in plants. To understand whether H3K27me3 is affected genome-wide in h2a_ub mutants, we tested H3K27me3 levels on all genes and all TEs. H3K27me3 was globally decreased on genes but not on TEs (Additional file 1: Figure S5), consistent with H2Aub mainly targeting genic region.
H2Aub contributes to transcriptional repression and activation
Although many transcriptionally active genes are marked with H2Aub and H2Aub is associated with a permissive chromatin state in Arabidopsis [33,34,35], it is unknown whether H2Aub is required for gene activation. We noted that in h2a_ub mutants there were more downregulated than upregulated genes (Fig. 2a, b), suggesting that H2Aub has an activating role for gene expression in Marchantia. Both upregulated and downregulated genes in h2a_ub mutants were enriched for genes with H2Aub and H3K27me3 marks (Fig. 2c). The only-H2Aub marked genes had a higher number of highly transcriptional active genes compared to H2Aub/H3K27me3 and only-H3K27me3 genes (Fig. 2d). We tested the H2Aub level on upregulated and downregulated genes in h2a_ub mutants and found that H2Aub levels were decreased in the promoter regions but not in the gene body region of both gene categories (Fig. 2e–h and Additional file 1: Figure S6a-d). Since the accessibility of promoter regions is essential for transcription factor binding, we propose that decreased H2Aub in promoter regions contributes to gene repression as well as activation. We also found more downregulated than upregulated TEs in h2a_ub mutants (Fig. 2i, j), indicating a role of H2Aub in TE activation. H2Aub and H3K27me3 marked TEs were enriched among deregulated TEs (Fig. 2k). The only-H2Aub and H2Aub/H3K27me3 marked TEs were more frequently highly transcriptionally active than the only-H3K27me3 marked TEs (Fig. 2l), pointing that H2Aub has the potential to activate TE expression and that removal of H2Aub is required for stable repression. We found significantly decreased H2Aub levels only on downregulated TEs, while upregulated TEs had very low levels of H2Aub (Fig. 2m–p, Additional file 1: Figure S6i, j), supporting the notion that H2Aub has an activating role towards TE transcription. Downregulated TEs had also decreased levels of H3K27me3 (Additional file 1: Figure S6k, l), suggesting that loss of H3K27me3 is not sufficient for TE activation.
MpBMI1/1L regulate morphological development of Marchantia and are involved in gene repression and activation
In Arabidopsis, AtBMI1s have been shown to be involved in H2A ubiquitination [6, 20, 21, 33]. To explore the extent to which MpBMI1/1L function relies on H2Aub, we generated MpBMI1 knock out mutants by CRISPR/Cas9 in Marchantia. Using the AtBMI1A protein sequence as a query in a protein blast, we identified two genes (Mp7g12670 and Mp6g09730 in the MpTak1 v5.1 annotation) encoding AtBMI1 homologs in Marchantia. MpBMI1, encoded by Mp7g12670, contains an N-terminal RING finger domain and a C-terminal ubiquitin-like (RAWUL) domain , while Mp6g09730 encodes for a protein named MpBMI1-LIKE (MpBMI1L) that only has a C-terminal RAWUL domain. The RAWUL domain is involved in protein-protein interaction and oligomerization of BMI1, which is essential for H2Aub activity of PRC1 in mammals [41,42,43,44]. We generated Mpbmi1/1l double knockout mutants by CRISPR/Cas9 and obtained combinations of double mutants with different mutations at the Cas9 target sites (mutant information shown in Additional file 1: Figures S7 and S8). Combinations of strong mutant alleles for both genes Mpbmi1-1/Mpbmi1l-1 (named Mpbmi1/1l#1, Additional file 1: Figure S7a) and Mpbmi1-2/Mpbmi1l-2 (named Mpbmi1/1l #2, Additional file 1: Figure S7b) caused strongly reduced growth rates and substantial size-reduction of gemma cups that contained only few and smaller gemmae compared to WT (Fig. 3a–c, f–h). The slightly more severe size reduction in Mpbmi1/1l #1 compared to Mpbmi1/1l #2 is likely due to the different extent of deletions and insertions caused by CRISPR/Cas9 in these two lines (Additional file 1: Figure S7). We also obtained one double mutant with a strong Mpbmi1-3 allele and a weak Mpbmi1l-3 allele (named Mpbmi1/1l #3, Additional file 1: Figure S8a) and one Mpbmi1l-4 single mutant (Additional file 1: Figure S8b), which showed weakly reduced growth rates compared to WT (Fig. 3d, e). The fact that Mpbmi1/1l mutants had a more severe phenotype than h2a_ub mutants is consistent with the proposed redundant function of ubiquitination on K115/K116 and K119 in H2A. Western blot analysis revealed a global decrease of H2Aub in Mpbmi1/1l #1, Mpbmi1/1l #2, and Mpbmi1/1l #3 double mutants compared to WT (Fig. 3i), with a more pronounced reduction in the Mpbmi1/1l #1 mutant combination. We therefore used Mpbmi1/1l #1 in subsequent analyses. The residual H2Aub signal in the Mpbmi1/1l mutants possibly reflects remaining functional activity of MpBMI1/1L generated in the mutants. Alternatively, MpRING proteins have low functional activity in the absence of MpBMI1/1L. We found 2085 genes being upregulated and 1023 genes being downregulated in the Mpbmi1/1l mutants (Fig. 3j), suggesting that MpBMI1/1L mainly function as repressors, but also possibly as activators. We analyzed H2Aub levels on the deregulated genes in the Mpbmi1/1l mutants and found H2Aub to be significantly decreased on both upregulated genes and downregulated genes (Fig. 3k, Additional file 1: Figure S9a, b), implying that H2Aub is required for MpBMI1/1L-mediated gene silencing and activation. H3K27me3 level only decreased on upregulated but not on downregulated genes (Fig. 3l, Additional file 1: Figure S9c-f), indicating that PRC1-mediated gene silencing is dependent on H3K27me3. Accordingly, H2Aub marked genes were enriched in both upregulated and downregulated genes in Mpbmi1/1l mutants (Fig. 3m). There was also a large number of up- and downregulated TEs in Mpbmi1/1l mutants (Fig. 3n) that were enriched for H2Aub and H3K27me3 (Fig. 3o).
Ubiquitination of H2AK115/K116 and H2AK119 is required for PRC1-mediated gene and TE expression
To test whether impaired H2A ubiquitination and loss of PRC1 function has similar consequences, we compared transcriptome data of the Mph2a;H2AK115R/K116R and Mph2a;H2AK119R mutants with that of the Mpbmi1/1l mutants. Both h2a_ub mutants shared a significant number of upregulated genes (p = 2.36e−165) and we also found a significant overlap of upregulated genes between the Mpbmi1/1l mutants and h2a_ub mutants (Fig. 4a) as well as between all mutants (Fig. 4a, p = 3.37e−101). Similarly, a significant number of downregulated genes overlapped between two h2a_ub mutants and Mpbmi1/1l mutants (Fig. 4b). Genes commonly upregulated in Mpbmi1/1l and Mph2a;H2AK115R/K116R or Mph2a;H2AK119R mutants were more strongly upregulated in Mpbmi1/1l than in h2a_ub mutants (Fig. 4c, d), supporting the idea that mono-ubiquitination on H2AK115/K116 and H2AK119 is functionally redundant and mediated by MpBMI1/1L. Commonly downregulated genes in h2a_ub and Mpbmi1/1l mutants were expressed at similar low levels in h2a_ub and Mpbmi1/1l mutants (Fig. 4e, f), supporting the idea that H2Aub is required for PRC1-mediated gene activation. Consistent with the transcriptional state, H2Aub level was decreased in the promoter region of commonly upregulated genes in h2a_ub mutants and more strongly decreased with spanning into gene body in Mpbmi1/1l mutants (Fig. 4g, h, Additional file 1: Figure S10a, b), supporting the idea that PRC1-mediated H2Aub is required for gene repression. H2Aub was also significantly decreased in the promoter and gene body regions of downregulated genes in Mpbmi1/1l mutants (Fig. 4i, j, Additional file 1: Figure S10c, d), supporting an activating role of H2Aub. We noticed a trend of reduced H2Aub in the promoter region of downregulated genes in h2a_ub mutants, but the difference was not significant. This data suggests that in h2a_ub mutants, the ubiquitination of the non-mutated lysine residues H2AK115/K116 or H2AK119 is compensated, but is not functionally redundant for activating gene expression. Correlating with the H2Aub level, H3K27me3 was mildly decreased on the upregulated genes in h2a_ub mutants and strongly decreased in Mpbmi1/1l mutants (Fig. 4k, l, Additional file 1: Figure S10e, f). H3K27me3 was also decreased on the downregulated genes in h2a_ub mutants but not in Mpbmi1/1l mutants (Fig. 4m, n, Additional file 1: Figure S10g, h), indicating that PRC1-mediated gene activation is independent of H3K27me3. GO enrichment analyses of upregulated genes overlapping between Mpbmi1/1l and Mph2a;H2AK115R/K116R mutants (Fig. 5a) or Mpbmi1/1l and Mph2a;H2AK119R mutants (Fig. 5b) both showed that response pathways were over-represented. Among downregulated genes overlapped between Mpbmi1/1l and h2a_ub mutants, we also found a significant enrichment for response pathway-related GOs (Fig. 5c, d), which were nevertheless largely distinct from the enriched GO terms of upregulated genes.
Our data suggests that H2Aub is required for TE activation (Fig. 2o, p). Further supporting this idea, we also identified 700 downregulated TEs in Mpbmi1/1l mutants (Fig. 3n), of which a significant number overlapped with downregulated TEs in h2a_ub mutants (Fig. 5e). Like for genes, transcript levels of downregulated TEs were decreased to a similar level in h2a_ub and Mpbmi1/1l mutants (Fig 5f, g) and H2Aub levels were decreased even more strongly in Mph2a;H2AK115R/K116R and Mph2a;H2AK119R compared to Mpbmi1/1l mutants (Fig. 5h, i, and Additional file 1: Figure S11), suggesting that ubiquitination on H2AK115/K116 and H2AK119 is not functionally redundant for TE activation.
H2Aub and H3K27me3 are affected in genes and TEs by the depletion of MpBMI1/1L
Consistent with the effect caused by AtBMI1 depletion in Arabidopsis , the H2Aub level was significantly decreased on only H2Aub genes as well as H2Aub/H3K27me3 genes in the Mpbmi1/1l mutants compared to WT (Fig. 6a, b, Additional file 1: Figure S12a, b). Also the H3K27me3 level was significantly decreased on H2Aub/H3K27me3 genes, yet not on only-H3K27me3 genes in the Mpbmi1/1l mutants compared to WT (Fig. 6c, d, Additional file 1: Figure S12c, d), implying that PRC1 activity mediates H3K27me3 deposition in Marchantia. The level H2Aub on only-H3K27me3 genes was unchanged in the Mpbmi1/1l mutants compared to WT (Additional file 1: Figure S12e, f), consistent with unchanged levels of H3K27me3. Conversely, genes losing H2Aub showed significantly reduced H3K27me3 levels in the Mpbmi1/1l mutants compared to WT (Fig. 6e). We found that genes losing H2Aub in Mpbmi1/1l mutants had lower H3K27me3 levels compared to H2Aub/H3K27me3 and H3K27me3 only genes (Fig. 6c, d); nevertheless, a significant proportion of genes losing H2Aub in Mpbmi1/1l or h2a_ub mutants are marked by H3K27me3 (Additional file 1: Figure S12g-i). We tested whether genes losing H2Aub in the Mpbmi1/1l mutants belonged to specific pathways. Among the top twenty significantly enriched GO terms, nine GO terms corresponded to multiple response pathways to intrinsic and extrinsic stimuli (Fig. 6f), which occurred in the commonly upregulated and downregulated genes between Mpbmi1/1l and h2a_ub mutants. We tested whether the connection between H2Aub and H3K27me3 was restricted to genes or was also present in TEs. Loss of MpBMI1/1L caused a significant decrease of both H2Aub and H3K27me3 levels on H2Aub/H3K27me3 TEs (Fig. 6g–i), revealing that PRC1-mediated recruitment of PRC2 is not restricted to genic regions.
Understanding the extent to which the function of histone modifying enzymes requires their catalytic activity is an ongoing challenge in the chromatin field. While recent work revealed that the catalytic activity of PRC1 is required in mouse ESCs [28, 29], whether this requirement is evolutionary conserved remains to be demonstrated. We found that PRC1-catalyzed H2Aub contributes to the Polycomb-mediated transcriptional repression in Marchantia, similar to the reported requirements in mouse ESCs [28, 29]. Our study thus supports an evolutionarily conserved Polycomb mechanism in plants and animals.
Loss of MpBMI1/1L activity in Marchantia impaired H3K27me3 deposition on H2Aub and H3K27me3 marked genes, similar to reported findings in Arabidopsis . Nevertheless, it was previously unknown whether the reduction of H3K27me3 in Atbmi1 in Arabidopsis is a consequence of decreased PRC1 catalytic activity or PRC1 non-catalytic activity, since PRC1 and PRC2 were shown to interact [19, 20, 36]. By comparing the H2Aub deficient mutants Mph2a;H2AK115R/K116R and Mph2a;H2AK119R with Mpbmi1/1l mutants, we discovered that reduction of H3K27me3 levels on Polycomb target genes in Mpbmi1/1l mutants also occurred in h2a_ub mutants that evade ubiquitination, demonstrating that H2Aub directly affects H3K27me3 deposition. Previous work showed that PRC1 initiates silencing, followed by PRC2-mediated H3K27me3 that maintains stable repression in Arabidopsis [6, 21, 33, 34]. Our data adds support to this model and extends it by showing that the PRC1-mediated H2Aub is essential for the initial PRC2-mediated repression.
In Marchantia, H3K27me3 is located in heterochromatic regions and marks TEs and repeats , contrasting its mainly genic localization in Arabidopsis . We showed that PRC1-catalyzed H2Aub is required for TE activation in Marchantia, revealing a new role of PRC1 beyond the Polycomb regulatory network. TE activation frequently correlates with loss of DNA methylation in Arabidopsis . Whether H2Aub has antagonizing roles with DNA methylation in Marchantia remains to be explored.
The failure to obtain Mph2a;H2AK115R/K116R/K119R mutants with complete loss of H2Aub strongly suggests that H2Aub has essential functions in Marchantia. Similarly, H2Aub-deficient Drosophila embryos arrest at the end of embryogenesis, indicating that the requirement of H2Aub to regulate essential biological functions is evolutionary conserved . As for H2Aub deficiency, also loss of the RING1 encoding gene Sce causes arrest of embryo development in Drosophila . In contrast, we found that mutants in MpBMI1/1L are viable and similarly, mutants in Arabidopsis BMI encoding genes are also viable . Nevertheless, it is possible that in both systems BMI function is not completely depleted, since the Atbmi1b and Atbmi1c mutant alleles are probably not complete null alleles in Arabidopsis [6, 20] and we found remaining H2Aub present in Mpbmi1/l mutants (Fig. 3i), pointing that the alleles have residual activity. We failed to obtain CRISPR/Cas9 mutants using guide RNAs targeting an N-terminal region in the MpBMI1, suggesting that complete loss of PRC1 function is lethal. Nevertheless, it is also possible that RING proteins can have catalytic activity independently of BMI proteins, as suggested based on in vitro catalytic activity of AtRING1A and AtRING1B proteins in Arabidopsis . Previous work revealed that the H2A variant H2A.Z can be ubiquitinated in Arabidopsis and incorporation of this modification is required for H2A.Z-mediated transcriptional repression . It is possible that MpBMI1/1L also affects ubiquitination of the H2A variant H2A.Z, which could provide an alternative explanation for the more severe phenotype of Mpbmi1/1l mutants compared to h2a_ub. Due to the lack of a suitable antibody, this possibility could not be tested.
Previous work revealed that PRC1-mediated H2Aub is associated with gene responsiveness and that responsive genes require H2Aub to initiate PRC2-mediated repression in Arabidopsis [34, 35]. At the same time, for stable gene repression H2Aub needs to be removed by the H2A deubiquitinases UBP12 and UBP13, likely because the occurrence of H2Aub allows recruitment of the H3K27me3 demethylase REF6 in Arabidopsis . The association of H2Aub with gene activation is also supported by our study; nevertheless, the fact that we found reduced H3K27me3 levels on downregulated genes in h2a_ub mutants suggests that H2Aub also has a direct role for gene activation independent of H3K27me3.
A significant number of downregulated genes overlapped between h2a_ub and Mpbmi1/1l mutants, suggesting that the catalytic activity of PRC1 is required for PRC1-mediated gene activation. It was proposed that the PRC1-catalytic activity may be dispensable for PRC1 function in promoting the expression of active genes in mammalian systems ; however, our data rather suggests that PRC1-catalyzed H2Aub is required for gene activation.
In summary, we show that the ubiquitinated lysines in MpH2A act redundantly and H2Aub directly contributes to the deposition of H3K27me3 in Marchantia, demonstrating the determinant role of PRC1 catalysis in the Polycomb repressive system. Together with previous findings in Arabidopsis and mouse ESCs [28, 29, 33], our study supports an evolutionarily conserved Polycomb mechanism in divergent land plants and animals. Our finding strongly supports a model in which the catalytic activity of PRC1 is required for PRC2-mediated gene repression and at the same time required for PRC2-independent gene activation.
Plant material and growth conditions
Marchantia polymorpha ssp. ruderalis Uppsala accession (Upp) was used as WT and for transformation . Plants were grown on vented petri dishes containing Gamborg’s B5 medium solidified with 1.4% plant agar, pH 5.5, under 16/8 h photoperiod at 22°C with a light intensity of 60–70 umol m−2 s−1. Plate lids were taped to prevent loss of water.
Generation of DNA constructs
Vectors pMpGE_En03, pMpGE010, pMpGWB401, and pMpGWB403 used in this study were previously described [49, 50]. DNA fragments used to generate the guide RNAs against MpBMI1 and MpBMI1L were prepared by annealing two pairs of primers (LH4513/LH4514, LH4517/LH4518, specified in Additional file 2: Table S1). The fragments were inserted into the BsaI site of pMpGE_En03 to yield pMpGE_En03-MpBMI1gRNA02 and pMpGE_En03-MpBMI1LgRNA04, respectively, and then transferred into pMpGE010 and pMpGWB401 using the Gateway LR reaction (Thermo Fisher Scientific) to generate pMpGE010_MpBMI1gRNA and pMpGWB401_MpBMI1LgRNA. Similarly, the two pairs of primers (LH4012/LH4013, LH4303/LH4304) were used to generate pMpGE_En03-MpH2AgRNA2 and pMpGE_En03-MpH2AgRNA3, which were subsequently transferred into pMpGE010 to generate pMpGE010-MpH2AgRNA2 and pMpGE010-MpH2AgRNA3, respectively. H2AK115R/K116R and H2AK119R were amplified by two pairs of primers (LH3848/LH4309 and LH3848/LH3849) and sub-cloned into the pENTR-TOPO vector (Thermo Fisher Scientific) to generate pENTR-H2AK115R/K116R and pENTR-H2AK119R, respectively. The pENTR vectors were transferred into pMpGWB403 by Gateway LR reaction to yield pMpGWB403-H2AK115R/K115R and pMpGWB403-H2AK119R. Primers used are listed in Additional file 2: Table S1.
Generation of transgenic Marchantia polymorpha
The constructs were transformed into spores of Marchantia by Agrobacterium GV3101 as described previously . Spores were grown in liquid Gamborg’s B5 medium with 2% sucrose, 0.1% Casamino acids, and 0.03% L-Glutamine for 10 days under constant light. Agrobacteria containing constructs were grown in liquid LB with antibiotic for 2 days and then pelleted. The pellet was resuspended in the spore growth media with 100 mM acetosyringone and grown for 4 h at 28°C with spinning. Agrobacteria suspension was added to spores together with acetosyringone to a final concentration of 100 mM and the mixture was grown for another 2 days. Sporelings were plated on selection media with 200 mg/ml Timentin. Several independent primary transformants (T1 generation) were analyzed for the presence of the transgene by genomic PCR.
The antibodies used were anti-H3 (07-690, Merck Millipore, Burlington, MA, USA), anti-H2Aub (#8240S, Cell signalling technology, Danvers, MA), and anti-H3K27me3 (07-449, Merck Millipore).
Histone extraction and western blotting
Fifty milligrams of 15-day-old thalli of WT, Mpbmi1/1l, Mph2a;H2AK115R/K116R, and Mph2a;H2AK119R mutants were used for RNA extraction. RNA was extracted using the MagMAX™ Plant RNA Isolation Kit (Thermo Fisher Scientific) in biological triplicates. Libraries were generated using DNA-free RNA with the NEBNext® Ultra™ II RNA Library Prep Kit for Illumina according to manufacturer’s instructions. Sequencing was performed on an Illumina HiSeq2000 in 150-bp pair-end mode at Novogene (Hong Kong).
Transcriptome data analysis
Untrimmed reads were mapped to the Marchantia polymorpha MpTak1 v5.1 reference genome  using STAR (v2.5.3.a ). Read numbers of mapping statistics are reported in Additional file 3: Table S2. Expression counts were generated using the R function summarizeOverlaps from the package HTSeq in union mode on exons from the reference transcriptome MpTak1v5.1_r1. A comparison of RPKM in RNA-seq triplicates showed high reproducibility of data in Additional file 1: Figure S14. Differential expression analyses were performed using the R package DESeq2 (v1.20.0 ). Genes or TEs with an absolute log2 fold change ≥ 1 and FDR ≤ 0.05 were considered as differentially expressed. Differential expressed genes in h2a_ub and Mpbmi1/1l mutants can be found in Additional file 4: Table S3. Differential expressed TEs in h2a_ub and Mpbmi1/1l mutants can be found in Additional file 5: Table S4.
H3, H2Aub1, and H3K27me3 ChIP-seq
For H3, H2Aub, and H3K27me3 ChIP-seq, WT, Mpbmi1/1l, Mph2a;H2AK115R/K116R, and Mph2a;H2AK119R plants were grown for 15 days on B5 medium, and then about 300 mg thalli were harvested. ChIP was performed as described before . In short, vacuum infiltration with formaldehyde was performed for 2 × 10 min. Crosslinking was quenched by adding glycine to a final concentration of 0.125 M under another 5-min vacuum infiltration. Sonication of the chromatin was done for eight 30-s ON, 30-s OFF cycles. Overnight antibody binding was performed directly after sonication, followed by adding washed protein A dynabeads (Thermo Fisher Scientific) to each ChIP aliquot. De-crosslinking and subsequent DNA recovery steps were performed using the Ipure kit v2 (Diagenode, Liège, Belgium). The Ovation Ultralow Sytem V2 (NuGEN, Redwood city, CA, USA) was used for the ChIP-seq library preparation, and 150-bp paired-end sequencing was performed on the HiseqX platform at Novogene (Hong Kong). The ChIP-seq experiments were done using two biological replicates per IP, per genotype.
Quality control and read mapping for ChIP-seq
FastQC (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/) was used to examine read quality of each sample. Low quality ends (phred < 20) and adapter sequences were removed with Trimmomatic (v0.39 ). Reads with low average quality were also discarded (phred < 28). For all experiments, reads were mapped to the M. polymorpha reference genome MpTak1 v5.1 using bowtie2 (v188.8.131.52 ). Details on read numbers can be found in Additional file 6: Table S5. Genome sequence and gene annotation data were downloaded from the Marchantia website (marchantia.info).
H2Aub and H3K27me3 aligned .sam files were imported into Homer . Duplicated mappings were removed using Homer. Peak calling was done using Homer with histone style settings and using histone H3 as the background to control for nucleosome occupancy. The same analysis was performed with the published WT H3K27me3 data (SRA: PRJNA553138) in Marchantia . The peak tag counts were generated by Homer. A comparison of normalized peak tag counts (RPKM) by Homer in ChIP-seq replicates showed high reproducibility of data in Additional file 1: Figure S15. Only peaks present in two replicates of ChIP-seq data were considered as real peaks and retained for subsequent analyses. Peaks were correlated with a gene when the peaks were located at any region of this gene or at most 2 kb upstream of its transcription start site. Lists of genes defined by the presence of H2Aub and H3K27me3 are shown in Additional file 7: Table S6. TEs covered by H2Aub and H3K27me3 are listed in Additional file 8: Table S7. The statistical comparison of differential peak tag counts was performed with DEseq2 package in R using the raw tag counts outputs from Homer. Peaks with the adjusted p-value (FDR) < 0.05 were considered as differentially changed peaks. Differential H2Aub peaks in h2a_ub and Mpbmi1/1l mutants can be found in Additional file 9: Table S8. Differential H3K27me3 peaks in h2a_ub and Mpbmi1/1l mutants can be found in Additional file 10: Table S9.
Peak profiles were visualized by the Integrative Genome Viewer (IGV) . Bigwig files were outputted from “bamCoverage” function in deepTools  using Reads Per Kilobase Million (RPKM) as normalization parameter. The Bigwig files were further used in the “computMatrix” function in deepTools with the “scale-regions” as setting parameter to generate H2Aub and H3K27me3 matrix on genes from 3 kb upstream of the transcriptional start to 3 kb downstream of the transcriptional end of genes and on TEs from 3 kb upstream of the start to 3 kb downstream of the end of TEs with a bin size of 50 bp. H2Aub and H3K27me3 levels (RPKM) on genes and TEs in boxplots were calculated as the average RPKM on defined regions for specified group of genes and TEs.
GO analysis was performed on the Arabidopsis homologs of Marchantia genes. The homologs of Marchantia genes in Arabidopsis were retrieved from PLAZA 4.0 DICOT, inferred by the Best-Hits-and-Inparalogs (BHIF) approach (, https://bioinformatics.psb.ugent.be/plaza/versions/plaza_v4_dicots/, Additional file 11: Table S10). GO term enrichment was performed in PLAZA 4.0 DICOT.
Availability of data and materials
The datasets supporting the conclusions of this article are available in the Gene Expression Omnibus (GEO) with the accession number GSE164394 .
Di Croce L, Helin K. Transcriptional regulation by Polycomb group proteins. Nat Struct Mol Biol. Nature Publishing Group. 2013;20(10):1147–55. https://doi.org/10.1038/nsmb.2669.
Schwartz YB, Pirrotta V. A new world of Polycombs: unexpected partnerships and emerging functions. Nat Rev Genet. Nature Publishing Group. 2013;14(12):853–64. https://doi.org/10.1038/nrg3603.
Mozgova I, Hennig L. The Polycomb Group Protein Regulatory Network. Annu Rev Plant Biol. Annual Reviews. 2015;66(1):269–96. https://doi.org/10.1146/annurev-arplant-043014-115627.
Schuettengruber B, Bourbon H-M, Di Croce L, Cavalli G. Genome regulation by Polycomb and Trithorax: 70 years and counting. Cell. 2017;171(1):34–57. https://doi.org/10.1016/j.cell.2017.08.002.
Francis NJ, Kingston RE, Woodcock CL. Chromatin compaction by a Polycomb group protein complex. Science. American Association for the Advancement of Science. 2004;306(5701):1574–7. https://doi.org/10.1126/science.1100576.
Bratzel F, López-Torrejón G, Koch M, Del Pozo JC, Calonje M. Keeping cell identity in Arabidopsis requires PRC1 RING-finger homologs that catalyze H2A monoubiquitination. Curr Biol. 2010;20(20):1853–9. https://doi.org/10.1016/j.cub.2010.09.046.
Eskeland R, Leeb M, Grimes GR, Kress C, Boyle S, Sproul D, et al. Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination. Mol Cell. 2010;38(3):452–64. https://doi.org/10.1016/j.molcel.2010.02.032.
Xiao J, Wagner D. Polycomb repression in the regulation of growth and development in Arabidopsis. Curr Opin Plant Biol. 2015;23:15–24. https://doi.org/10.1016/j.pbi.2014.10.003.
Cao R, Wang L, Wang H, Xia L, Erdjument-Bromage H, Tempst P, et al. Role of histone H3 lysine 27 methylation in Polycomb-group silencing. Science. American Association for the Advancement of Science. 2002;298(5595):1039–43. https://doi.org/10.1126/science.1076997.
Czermin B, Melfi R, McCabe D, Seitz V, Imhof A, Pirrotta V. Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites. Cell. 2002;111(2):185–96. https://doi.org/10.1016/S0092-8674(02)00975-3.
Kuzmichev A, Nishioka K, Erdjument-Bromage H, Tempst P, Reinberg D. Histone methyltransferase activity associated with a human multiprotein complex containing the Enhancer of Zeste protein. Genes Dev. 2002;16(22):2893–905. https://doi.org/10.1101/gad.1035902.
Müller J, Hart CM, Francis NJ, Vargas ML, Sengupta A, Wild B, et al. Histone methyltransferase activity of a Drosophila polycomb group repressor complex. Cell. 2002;111(2):197–208. https://doi.org/10.1016/S0092-8674(02)00976-5.
Gao Z, Zhang J, Bonasio R, Strino F, Sawai A, Parisi F, et al. PCGF homologs, CBX proteins, and RYBP define functionally distinct PRC1 family complexes. Mol Cell. 2012;45(3):344–56. https://doi.org/10.1016/j.molcel.2012.01.002.
Hauri S, Comoglio F, Seimiya M, Gerstung M, Glatter T, Hansen K, et al. A high-density map for navigating the human polycomb complexome. Cell Rep. 2016;17(2):583–95. https://doi.org/10.1016/j.celrep.2016.08.096.
Wang H, Wang L, Erdjument-Bromage H, Vidal M, Tempst P, Jones RS, et al. Role of histone H2A ubiquitination in Polycomb silencing. Nature. Nature Publishing Group. 2004;431:873–8.
Shao Z, Raible F, Mollaaghababa R, Guyon JR, Wu C, Bender W, et al. Stabilization of chromatin structure by PRC1, a polycomb complex. Cell. 1999;98(1):37–46. https://doi.org/10.1016/S0092-8674(00)80604-2.
Francis NJ, Saurin AJ, Shao Z, Kingston RE. Reconstitution of a functional core polycomb repressive complex. Mol Cell. 2001;8(3):545–56. https://doi.org/10.1016/S1097-2765(01)00316-1.
Lo SM, Ahuja NK, Francis NJ. Polycomb group protein suppressor 2 of Zeste is a functional homolog of posterior sex combs. Mol Cell Biol. American Society for Microbiology Journals. 2009;29:515–25.
Xu L, Shen W-H. Polycomb silencing of KNOX genes confines shoot stem cell niches in Arabidopsis. Curr Biol. 2008;18(24):1966–71. https://doi.org/10.1016/j.cub.2008.11.019.
Bratzel F, Yang C, Angelova A, López-Torrejón G, Koch M, del Pozo JC, et al. Regulation of the New Arabidopsis Imprinted Gene AtBMI1C Requires the Interplay of Different Epigenetic Mechanisms. Mol Plant. Elsevier. 2012;5(1):260–9. https://doi.org/10.1093/mp/ssr078.
Yang C, Bratzel F, Hohmann N, Koch M, Turck F, Calonje M. VAL- and AtBMI1-mediated H2Aub initiate the switch from embryonic to postgerminative growth in Arabidopsis. Curr Biol. 2013;23(14):1324–9. https://doi.org/10.1016/j.cub.2013.05.050.
Morey L, Aloia L, Cozzuto L, Benitah SA, Di Croce L. RYBP and Cbx7 define specific biological functions of polycomb complexes in mouse embryonic stem cells. Cell Rep. 2013;3(1):60–9. https://doi.org/10.1016/j.celrep.2012.11.026.
Tavares L, Dimitrova E, Oxley D, Webster J, Poot R, Demmers J, et al. RYBP-PRC1 complexes mediate H2A ubiquitylation at polycomb target sites independently of PRC2 and H3K27me3. Cell. 2012;148(4):664–78. https://doi.org/10.1016/j.cell.2011.12.029.
Blackledge NP, Farcas AM, Kondo T, King HW, McGouran JF, Hanssen LLP, et al. Variant PRC1 complex-dependent H2A ubiquitylation drives PRC2 recruitment and polycomb domain formation. Cell. 2014;157(6):1445–59. https://doi.org/10.1016/j.cell.2014.05.004.
Endoh M, Endo TA, Endoh T, Isono K, Sharif J, Ohara O, et al. Histone H2A mono-ubiquitination is a crucial step to mediate PRC1-dependent repression of developmental genes to maintain ES cell identity. PLoS Genet. Public Library of Science. 2012;8:e1002774.
Cooper S, Dienstbier M, Hassan R, Schermelleh L, Sharif J, Blackledge NP, et al. Targeting polycomb to pericentric heterochromatin in embryonic stem cells reveals a role for H2AK119u1 in PRC2 recruitment. Cell Rep. 2014;7(5):1456–70. https://doi.org/10.1016/j.celrep.2014.04.012.
Illingworth RS, Moffat M, Mann AR, Read D, Hunter CJ, Pradeepa MM, et al. The E3 ubiquitin ligase activity of RING1B is not essential for early mouse development. Genes Dev. 2015;29(18):1897–902. https://doi.org/10.1101/gad.268151.115.
Blackledge NP, Fursova NA, Kelley JR, Huseyin MK, Feldmann A, Klose RJ. PRC1 catalytic activity is central to polycomb system function. Mol Cell. 2020;77:857–874.e9.
Tamburri S, Lavarone E, Fernández-Pérez D, Conway E, Zanotti M, Manganaro D, et al. Histone H2AK119 mono-ubiquitination is essential for polycomb-mediated transcriptional repression. Mol Cell. 2020;77:840–856.e5.
Pengelly AR, Kalb R, Finkl K, Müller J. Transcriptional repression by PRC1 in the absence of H2A monoubiquitylation. Genes Dev. Cold Spring Harbor Laboratory Press. 2015;29:1487.
Kahn TG, Dorafshan E, Schultheis D, Zare A, Stenberg P, Reim I, et al. Interdependence of PRC1 and PRC2 for recruitment to polycomb response elements. Nucleic Acids Res. Oxford Academic. 2016;44:10132–49.
Tsuboi M, Kishi Y, Yokozeki W, Koseki H, Hirabayashi Y, Gotoh Y. Ubiquitination-independent repression of PRC1 targets during neuronal fate restriction in the developing mouse neocortex. Dev Cell. 2018;47:758–772.e5.
Zhou Y, Romero-Campero FJ, Gómez-Zambrano Á, Turck F, Calonje M. H2A monoubiquitination in Arabidopsis thaliana is generally independent of LHP1 and PRC2 activity. Genome Biol. 2017;18(1):69. https://doi.org/10.1186/s13059-017-1197-z.
Kralemann LEM, Liu S, Trejo-Arellano MS, Muñoz-Viana R, Köhler C, Hennig L. Removal of H2Aub1 by ubiquitin-specific proteases 12 and 13 is required for stable Polycomb-mediated gene repression in Arabidopsis. Genome Biol. 2020;21(1):144. https://doi.org/10.1186/s13059-020-02062-8.
Yin X, Romero-Campero FJ, de Los Reyes P, Yan P, Yang J, Tian G, et al. H2AK121ub in Arabidopsis associates with a less accessible chromatin state at transcriptional regulation hotspots. Nat Commun. Nature Publishing Group. 2021;12:315.
Derkacheva M, Liu S, Figueiredo DD, Gentry M, Mozgova I, Nanni P, et al. H2A deubiquitinases UBP12/13 are part of the Arabidopsis polycomb group protein system. Nat Plants. Nature Publishing Group. 2016;2:1–10.
Bowman JL, Kohchi T, Yamato KT, Jenkins J, Shu S, Ishizaki K, et al. Insights into land plant evolution garnered from the Marchantia polymorpha genome. Cell. 2017;171:287–304.e15.
Kawashima T, Lorković ZJ, Nishihama R, Ishizaki K, Axelsson E, Yelagandula R, et al. Diversification of histone H2A variants during plant evolution. Trends Plant Sci. 2015;20(7):419–25. https://doi.org/10.1016/j.tplants.2015.04.005.
Montgomery SA, Tanizawa Y, Galik B, Wang N, Ito T, Mochizuki T, et al. Chromatin organization in early land plants reveals an ancestral association between H3K27me3, transposons, and constitutive heterochromatin. Curr Biol. 2020;30:573–588.e7.
Sanchez-Pulido L, Devos D, Sung ZR, Calonje M. RAWUL: A new ubiquitin-like domain in PRC1 Ring finger proteins that unveils putative plant and worm PRC1 orthologs. BMC Genomics. 2008;9(1):308. https://doi.org/10.1186/1471-2164-9-308.
Junco SE, Wang R, Gaipa JC, Taylor AB, Schirf V, Gearhart MD, et al. Structure of the polycomb group protein PCGF1 in complex with BCOR reveals basis for binding selectivity of PCGF homologs. Structure. 2013;21(4):665–71. https://doi.org/10.1016/j.str.2013.02.013.
Gray F, Cho HJ, Shukla S, He S, Harris A, Boytsov B, et al. BMI1 regulates PRC1 architecture and activity through homo- and hetero-oligomerization. Nat Commun. Nature Publishing Group. 2016;7:13343.
Wong SJ, Gearhart MD, Taylor AB, Nanyes DR, Ha DJ, Robinson AK, et al. KDM2B recruitment of the polycomb group ccomplex, PRC1.1, requires cooperation between PCGF1 and BCORL1. Structure. 2016;24(10):1795–801. https://doi.org/10.1016/j.str.2016.07.011.
Chittock EC, Latwiel S, Miller TCR, Müller CW. Molecular architecture of polycomb repressive complexes. Biochem Soc Trans. Portland Press. 2017;45(1):193–205. https://doi.org/10.1042/BST20160173.
Liu S, de Jonge J, Trejo-Arellano MS, Santos-González J, Köhler C, Hennig L. Role of H1 and DNA methylation in selective regulation of transposable elements during heat stress. New Phytol. 2020; Available from: https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.17018;229(4):2238–50.
Gómez-Zambrano Á, Merini W, Calonje M. The repressive role of Arabidopsis H2A.Z in transcriptional regulation depends on AtBMI1 activity. Nat Commun. Nature Publishing Group. 2019;10:2828.
Gao Z, Lee P, Stafford JM, von Schimmelmann M, Schaefer A, Reinberg D. An AUTS2–Polycomb complex activates gene expression in the CNS. Nature. Nature Publishing Group. 2014;516:349–54.
Linde A-M, Eklund DM, Kubota A, Pederson ERA, Holm K, Gyllenstrand N, et al. Early evolution of the land plant circadian clock. New Phytol. 2017;216(2):576–90. https://doi.org/10.1111/nph.14487.
Ishizaki K, Nishihama R, Ueda M, Inoue K, Ishida S, Nishimura Y, et al. Development of gateway binary vector series with four different selection markers for the liverwort Marchantia polymorpha. PLoS One. Public Library of Science. 2015;10:e0138876.
Sugano SS, Nishihama R, Shirakawa M, Takagi J, Matsuda Y, Ishida S, et al. Efficient CRISPR/Cas9-based genome editing and its application to conditional genetic analysis in Marchantia polymorpha. PLoS One. Public Library of Science. 2018;13:e0205117.
Eklund DM, Kanei M, Flores-Sandoval E, Ishizaki K, Nishihama R, Kohchi T, et al. An evolutionarily conserved abscisic acid signaling pathway regulates dormancy in the liverwort Marchantia polymorpha. Curr Biol. 2018;28:3691–3699.e3.
Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. Oxford Academic. 2013;29(1):15–21. https://doi.org/10.1093/bioinformatics/bts635.
Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15(12):550. https://doi.org/10.1186/s13059-014-0550-8.
Villar CBR, Köhler C. Plant chromatin immunoprecipitation. In: Hennig L, Köhler C, editors. Plant Dev Biol Methods Protoc [Internet]. Totowa: Humana Press; 2010. p. 401–11. https://doi.org/10.1007/978-1-60761-765-5_27.
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. Oxford Academic. 2014;30(15):2114–20. https://doi.org/10.1093/bioinformatics/btu170.
Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nat Methods. Nature Publishing Group. 2012;9(4):357–9. https://doi.org/10.1038/nmeth.1923.
Heinz S, Benner C, Spann N, Bertolino E, Lin YC, Laslo P, et al. Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. Mol Cell. 2010;38(4):576–89. https://doi.org/10.1016/j.molcel.2010.05.004.
Thorvaldsdóttir H, Robinson JT, Mesirov JP. Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration. Brief Bioinform. Oxford Academic. 2013;14(2):178–92. https://doi.org/10.1093/bib/bbs017.
Ramírez F, Dündar F, Diehl S, Grüning BA, Manke T. deepTools: a flexible platform for exploring deep-sequencing data. Nucleic Acids Res. Oxford Academic. 2014;42:W187–91.
Van Bel M, Diels T, Vancaester E, Kreft L, Botzki A, Van de Peer Y, et al. PLAZA 4.0: an integrative resource for functional, evolutionary and comparative plant genomics. Nucleic Acids Res. Oxford Academic. 2018;46:D1190–6.
Liu S, Trejo-Arellano MS, Qiu Y, Eklund DM, Köhler C, Hennig L. H2A ubiquitination is essential for Polycomb Repressive Complex 1-mediated gene regulation in Marchantia polymorpha. ChIP-seq and RNA seq data. Gene Expression Omnibus. 2021. https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE164394. Accessed 13 Aug 2021.
The computations of the RNA-seq data were performed on resources provided by SNIC through the Uppsala Multidisciplinary Center for Advanced Computational Science (UPPMAX) under Project SNIC 2017/7-6. We would like to thank Frédéric Berger (GMI) for kindly providing Marchantia H2A antibodies.
The review history is available as Additional file 12.
Peer review information
Wenjing She was the primary editor of this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.
This work was funded by the Swedish Research Council VR (grant no. 2014-05822 to L.H.) and the Swedish Research Council Formas (grant no. 2016-00961 to L.H.) and a grant from the Knut and Alice Wallenberg foundation (grant no. 2012.0087 to L.H.). Open Access funding enabled and organized by Projekt DEAL.
Ethics approval and consent to participate
Consent for publication
The authors declare no conflicts of interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Strategy of generating H2Aub depleted lines. Figure S2. Comparison of H3K27me3 data of this study with previously published data. Figure S3. H2Aub is essential for H3K27me3 incorporation. Figure S4. Distribution of H2Aub and H3K27me3 peaks among functional features of the Marchantia genome. Figure S5. H3K27me3 targeting is generally affected on genes in H2Aub deficient lines. Figure S6. H2Aub is required for gene repression and activation. Figure S7. Characterization of strong double mutant allele combinations in MpBMI1/1L. Figure S8. Characterization of weak double mutant allele combinations in MpBMI1/1L. Figure S9. Deposition of H2Aub is affected on upregulated and downregulated genes by loss of MpBMI1/1L. Figure S10. PRC1-mediated gene repression and activation depends on H2Aub. Figure S11. H2Aub contributes to PRC1-mediated transposable element activation. Figure S12. H2Aub and H3K27me3 deposition are affected by loss of MpBMI1/1L. Figure S13. Western blots of H2A and H2Aub. Figure S14. Scatter plots comparing RNA-seq triplicates. Figure S15. Scatter plots comparing ChIP-seq replicates.
Primers used in the constructs.
Mapping statistics of RNA-seq data.
Genes deregulated in h2a_ub and Mpbmi1/1l mutants.
TEs deregulated in h2a_ub and Mpbmi1/1l mutants.
Mapping statistics of ChIP-seq data.
Three specified group of genes defined by H2Aub and H3K27me3 marks.
TEs marked by H2Aub and H3K27me3.
Differential H2Aub peaks in h2a_ub and Mpbmi1/1l mutants.
Differential H3K27me3 peaks in h2a_ub and Mpbmi1/1l mutants.
Arabidopsis homologs of Marchantia genes.
About this article
Cite this article
Liu, S., Trejo-Arellano, M.S., Qiu, Y. et al. H2A ubiquitination is essential for Polycomb Repressive Complex 1-mediated gene regulation in Marchantia polymorpha. Genome Biol 22, 253 (2021). https://doi.org/10.1186/s13059-021-02476-y
- Gene regulation
- Marchantia polymorpha