- Open Access
4sUDRB-seq: measuring genomewide transcriptional elongation rates and initiation frequencies within cells
- Gilad Fuchs†1Email author,
- Yoav Voichek†2,
- Sima Benjamin3,
- Shlomit Gilad3,
- Ido Amit4 and
- Moshe Oren1Email author
© Fuchs et al.; licensee BioMed Central Ltd. 2014
- Received: 10 February 2014
- Accepted: 9 May 2014
- Published: 9 May 2014
Although transcriptional elongation by RNA polymerase II is coupled with many RNA-related processes, genomewide elongation rates remain unknown. We describe a method, called 4sUDRB-seq, based on reversible inhibition of transcription elongation coupled with tagging newly transcribed RNA with 4-thiouridine and high throughput sequencing to measure simultaneously with high confidence genome-wide transcription elongation rates in cells. We find that most genes are transcribed at about 3.5 Kb/min, with elongation rates varying between 2 Kb/min and 6 Kb/min. 4sUDRB-seq can facilitate genomewide exploration of the involvement of specific elongation factors in transcription and the contribution of deregulated transcription elongation to various pathologies.
- Transcription Start Site
- Elongation Rate
- Biological Repeat
- Initiation Frequency
- OPA1 Gene
Gene transcription is a multistep process consisting of recruitment of RNA polymerase II (Pol II) to promoters, transcription initiation, elongation, and termination. In addition to producing RNA polymers based on the DNA template, the Pol II holoenzyme also regulates numerous RNA processing events, including 5′ cap formation, splicing, polyadenylation, and RNA transport [1–7].
While historically most studies focused on understanding how promoter binding and transcription initiation are regulated, recent studies have shown that additional stages of the transcription process are also tightly regulated and are critical for gene activation. These studies have demonstrated that binding of Pol II to gene promoters is not sufficient for productive transcription. Instead, in the majority of genes Pol II is partly ‘paused’ 20 to 60 nt from the transcription start site (TSS), and several regulated steps are needed in order for Pol II to depart from the TSS and transcribe the rest of the gene [8–15].
The rate of Pol II movement through gene bodies has also been linked to various aspects of co-transcriptional RNA processing. For example, changes in transcription elongation rates can affect the outcome of the splicing machinery [7, 16, 17], and slow elongation by Pol II was shown to enhance the inclusion of specific weak exons ; in support of this notion, Pol II was found to accumulate at exons [18–20]. Likewise, the rate of elongation by Pol II has been linked to regulation of alternative polyadenylation ; indeed, Pol II accumulates at polyadenylation sites .
The importance of steps subsequent to transcriptional initiation is also underscored by the impact of misregulation of these steps on cellular and organismal viability. For example, many of the MLL gene translocation partners, thought to drive aggressive acute leukemia, are part of the super elongation complex (SEC). Leukemia-associated MLL fusion proteins relocalize the SEC to MLL target genes, bypassing normal transcriptional control and causing aberrant expression of those genes . Similarly, excessive c-Myc was suggested to augment gene expression by increasing the release of paused Pol II and thus facilitating active elongation, thereby alleviating rate-limiting constraints on tumor cell growth and proliferation . Furthermore, viruses utilize or modify transcription elongation-related processes to their benefit. For example, the influenza A NS1 protein comprises a histone-like sequence that can target the PAF1 elongation complex, enabling selective modulation of host cell gene expression and contributing to suppression of the antiviral response . In addition, during active HIV-1 infection, viral transactivator of transcription (Tat) recruits the SEC to the HIV-1 long terminal repeat (LTR) to activate expression of the provirus in host cells [25–27]. Thus, better elucidation of the regulation of transcriptional elongation could contribute to the understanding of molecular mechanisms of disease, and even suggest novel therapeutic approaches.
Despite the documented links between elongation rates and numerous RNA-related functions, the actual elongation rates within cells remain under debate, with reported values ranging from 1 kilobase per minute (Kb/min) to 6 Kb/min . In most cases, elongation rates of only a few genes at a time were measured; one study, utilizing Global Run-On sequencing (GRO-seq), was able to determine the rates for approximately 166 long genes upregulated in response to short treatment with physiological, non-toxic inducers . Since the elongation rates of individual genes can be altered in a stimulus-dependent manner , it is important to measure the elongation rates of non-stimulated genes in order to derive more general understanding of the relationship between basal transcription elongation rates and steady state RNA processing and gene expression. Moreover, assessment of a large number of genes may provide more definitive information on the factors that affect transcription elongation rates. Here we describe a method that enables to easily measure simultaneously, in a single experiment, the steady state elongation rates of thousands of genes within live cells.
Adaptation of the DRB assay for measuring elongation rates in short time scales by RNA sequencing
In order to obtain genomewide information on elongation rates, this protocol had to be adapted to RNA-seq. Nascent RNA constitutes only a very small fraction of the total RNA within cells; therefore, it is necessary to enrich it prior to sequencing. In principle, such enrichment is achievable by GRO-seq, which is becoming increasingly popular [29, 31–33]. However, GRO-seq requires prior isolation of nuclei, which takes a relatively long time; this might introduce biases in short time scale measurements. We therefore added to the protocol a step of labeling nascent RNA in vivo with 4-thiouridine (4sU), which can be incorporated into intact cells [34, 35], followed by specific purification of 4sU-containing RNA.
To test whether short 4sU labeling can indeed enrich for nascent RNA, HeLa cells were treated with 4sU for 8 min. 4sU-tagged RNA was biotinylated in vitro, purified on streptavidin beads and subjected to qRT-PCR analysis. Pre-mRNA/mature RNA ratios were calculated for OPA1 and TTC17 both in the 4sU-enriched fraction and in the total (non-enriched) RNA. Similar to a previous report , the short 4sU labeling yielded an approximately 20- to 35-fold enrichment of nascent RNA of these genes relative to the total RNA population (Figure 1B).
We next set out to determine the rate of movement of RNA Pol II on individual genes. To that end, we monitored the changes in nascent RNA abundance throughout those genes at different time points after resumption of RNA synthesis following DRB removal. HeLa cells were treated with DRB for 3 hours and harvested either 4 or 8 min following DRB removal. In both cases, the cells were pulsed with 4sU for the last 8 min before being harvested (Additional file 1). Cells were harvested in QIAzol lysis buffer directly on the culture dish. Next, 4sU-tagged nascent RNA from each sample was biotinylated and collected on streptavidin beads. This experimental procedure was performed separately in two biological repeats for the 4 min samples and four biological repeats for the 8 min samples. Finally, the RNA was subjected to deep sequencing (see Materials and Methods). The entire protocol, schematically illustrated in Figure 1C, was termed 4sUDRB-seq.
Genomewide analysis of transcription elongation rates by 4sUDRB-seq
The density of reads decreases gradually towards the advancing front of the transcription wave (Figure 2B, C). Hence, the exact border of the advancing transcription wave is not sharp and is hard to define. Furthermore, DRB does not enforce a complete transcription arrest, as evident by the presence of scattered low abundance reads throughout gene bodies (Figure 2B, C). Therefore, we developed an algorithm that determines the front border of the elongation wave for each gene at a given time point, taking into consideration the above observations. To avoid biases due to sequence properties, the pre-DRB release pattern was used for correction. Only genes with a primary transcript longer than 25 Kb were considered.
In some cases, the algorithm identified a clear front boundary for a particular gene in some of the experiments, but failed to do so in one or more of the other experiments (data not shown). Consequently, we calculated elongation rates only for genes that yielded distinct boundaries in at least two independent repeats of a given time point. To assess the reliability of our measurements, the confidence level of the elongation rate for each gene was calculated (Materials and Methods). As seen in Additional file 3, for most of the genes the confidence level was better than ± 0.5 Kb/min. For subsequent analysis, only genes with confidence levels better than ± 0.5 Kb/min were considered (Additional file 3). In addition, the estimated delay time, namely the time it takes transcription to reinitiate effectively following DRB removal, was also calculated; this was defined as the time interval missing in order for the distance between the TSS and the 4 min boundary to be equal to the distance between the 4 and 8 min boundaries, given the calculated elongation rate. This calculation is based on the assumption that the elongation rate is uniform throughout the gene. However, it remains formally possible that the rate is slower at the beginning of the gene, in which case the calculated delay times may represent overestimates.
Overall, we could measure with high confidence the elongation rates of 1,577 genes. The full list of elongation rates generated by this analysis is presented in Additional file 4. Examples of elongation rate measurements for several representative genes are shown in Figure 3B. As also seen in Figure 3C, while most genes are transcribed at a rate of approximately 3.5 Kb/min, actual transcription elongation rates vary between 2 Kb/min and 6 Kb/min. Overall, these rates are in the same range as those determined previously for a small number of specific genes [28, 30].
To validate the rates deduced by 4sUDRB-seq, two genes with different calculated elongation rates (RBM33 = 4.53 Kb/min, CLCN3 = 2 Kb/min) were examined at higher temporal resolution, starting at 2 min after DRB release. Pre-mRNA was quantified by qRT-PCR with intron-derived primers. Reassuringly, the elongation rates determined by qRT-PCR (RBM33 = 5 Kb/min, CLCN3 = 2.7 Kb/min) were in reasonably good agreement with the rates determined by 4sUDRB-seq (Additional file 5A); the small differences might be due to the lower spatial resolution of qRT-PCR as compared to RNA-seq. Similar results were observed by measuring the elongation rates of those genes with different sets of primers (Additional file 5B).
Histone post-translational modifications (PTMs) were suggested to alter transcriptional elongation rates [36–38]. Hence, we asked whether the variance in elongation rates correlates with differences in a particular PTM. Interestingly 48% of genes in the upper quartile of genes with the highest elongation rate were found to be enriched in H3K79me2 within their gene body, compared to only 19% of genes from the slowest elongation rate quartile (Fisher’s exact test, P = 5.5e-18; data not shown). In contrast, no significant enrichment was observed for H3K36me3 (Fisher’s exact test, P = 0.99). Further analysis of genes that have H3K79me2 or H3K36me3 in their gene body confirmed that H3K79me2 is significantly higher in the fast elongation rate quartile (t-test, P = 1e-7), while H3K36me3 is relatively similar in both quartiles (t-test, P = 0.57) (Figure 3D). Since the average expression level was similar in both quartiles (t-test, P = 0.43, data not shown), the difference in H3K79me2 cannot simply be due to differences in expression. Further experiments will be required in order to determine whether H3K79me2 accelerates elongation or the high levels of this PTM are merely a consequence of the faster elongation. The fact that we did not detect a correlation between H3K36me3 and elongation rates is surprising, since such correlation was recently observed in response to a specific stimulus . This might suggest that elongation during induced transcription utilizes a different set of histone PTMs than those associated with constitutive basal transcription.
Calculation of genomewide relative transcription initiation frequencies by 4sUDRB-seq
We report here that, by combining the reversible inhibitor DRB and 4sU tagging, transcription elongation rates and relative initiation frequencies within intact cells can be relatively easily measured on a genomewide scale. This method can be utilized in order to compare elongation rates between different regions within genes, different tissues, or different biological contexts such as differentiation and transformation. Moreover, by coupling 4sUDRB-seq with depletion of specific transcription-regulatory factors, one should be able to discriminate between factors that impact gene expression by modulating transcription initiation frequencies and those that affect the elongation step.
Note: while this manuscript was under revision, an essentially similar method was described by Veloso et al..
Cell culture and treatments
Human cervical carcinoma HeLa cells were grown in DMEM with 10% bovine serum supplemented with antibiotics and maintained at 37°C. 5,6-dichlorobenzimidazole 1-β-d-ribofuranoside (DRB) was purchased from Sigma (D1916), and used at a final concentration of 100μM. 4-thiouridine (4sU) was purchased from Sigma (T4509) and used at a final concentration of 1mM. In two of the NT, 0 and 8 min samples, cells were transfected with non-targeting siRNA (Dharmacon) 48 h before addition of DRB, employing the Dharmafect 1 reagent according to the manufacturer’s instructions.
RNA purification and quantitative RT-PCR
For quantitative reverse transcriptase PCR (qRT-PCR) analysis, total RNA was extracted with the miRNeasy kit (Qiagen). Two microgram of each RNA sample was reverse transcribed with Moloney murine leukemia virus reverse transcriptase (Promega, Madison, WI, USA) and random hexamer primers (Applied Biosystems). Real-time PCR was done in a StepOne real-time PCR instrument (Applied Biosystems, Foster City, CA, USA) with Syber Green PCR supermix (Invitrogen).
Biotinylation and purification of 4sU labeled RNA
Biotinylation and purification of 4sU labeled RNA was done as described in , with minor changes. A total of 100 to 180 μg RNA was used for the biotinylation reaction. 4sU-labeled RNA was biotinylated using EZ-Link Biotin-HPDP (Pierce), dissolved in dimethylformamide (DMF) at a concentration of 1 mg/mL and stored at -80°C. Biotinylation was done in labeling buffer (10 mM Tris pH 7.4, 1 mM EDTA) and 0.2 mg/mL Biotin-HPDP for 2 h with rotation at 25°C. Unbound Biotin-HPDP was removed by chloroform/isoamylalcohol (24:1) extraction using MaXtract (high density) tubes (Qiagen). RNA was precipitated at 20,000 g for 20 min at 4°C with a 1:10 volume of 5M NaCl and an equal volume of isopropanol. The pellet was washed with an equal volume of 75% ethanol and precipitated again at 20,000 g for 10 min at 4°C. The pellet was left to dry followed by resuspension in 100 μL RNase-free water. Biotinylated RNA was captured using Dynabeads MyOne Streptavidin T1 beads (Invitrogen). Biotinylated RNA was incubated with 100 μL Dynabeads with rotation for 15 min at 25°C. Beads were magnetically fixed and washed with 1× Dynabeads washing buffer. RNA-4sU was eluted with 100 μL of freshly prepared 100 mM dithiothreitol (DTT), and cleaned on RNeasy MinElute Spin columns (Qiagen).
Preparation and sequencing of 4sU labeled RNA
cDNA libraries were prepared with Illumina TruSeq RNA sample preparation v2 kit according to the manufacturer’s instructions but without the polyA isolation stage. Of note, strand specificity is not achieved with this kit. Random hexamers were used for reverse transcription. Libraries were pooled and sequenced on an Illumina HiSeq 2500 system using the paired-end 50 mode.
All reads were aligned to the human reference genome (hg19, GRCh37) using the bowtie 2 aligner with default parameters (only setting -N 1) . We considered only reads mapped uniquely to the genome and not to chrUn_gl000220 (rRNA) for further analysis. For each experiment we constructed a genome-wide profile of the signal per disjoint 100 bp adjacent bins. The sum of each experiment was normalized to be 106.
All gene annotations were taken from the hg19 RefGene tab. of the UCSC browser.
Boundary detection algorithm
Only genes longer than 25 Kb and with at least 20 intron bins with positive numerical values were included in the boundary detection algorithm. In addition, in cases where a gene has multiple variants, we consider only the longest one.
For each of the filtered genes from the different 4 min or 8 min samples we extracted only the profile data of introns, in order to avoid the confounding effects of reads derived from contaminating mature mRNA. In order to increase the reliability of the signal used for normalization, and to reduce the effects of variability between the 0 min samples due to low read numbers, the profile of the 0 time point was created by averaging four different biological repeats of the 0 min samples. Next, the intron data were smoothed using cubic spline (smoothing parameter - 10-5).
To normalize each gene in each experiment (0, 4, and 8 min) by the background signal, we performed the following procedure. First, for each bin of the gene we estimated the background signal downstream to this bin up to the 3’ end of the gene. This background read distribution was built out of a negative binomial signal. To estimate the average of the background distribution we took the most abundant value. The most abundant value was identified by building a histogram of the data and selecting the bin with the highest count. In cases where we had fewer than 10 values downstream to the last point with positive signals we used the background estimate of the upstream bin.
We next compared the 4 and 8 min normalized profiles to the 0 time point. For each of the 4 and 8 min samples, we chose the first bin downstream the TSS + 2.5 Kb (defined arbitrarily) where the sample’s signal is not higher than the 0 time point at the same position (up to 10%). This bin was defined as the ‘rough estimate’ of the boundary. If the first position (TSS + 2.5 Kb) was identified or no position was identified no boundary was determined.
Refinement using profile derivative
For each gene we took the profile of the introns and as in the ‘rough estimate’, we used cubic spline with the same parameter. Before smoothing the 0 time point bins, we added the value 0.01 to each bin (according to the ‘Rule of Succession’) in order to prevent cases where data are normalized to 0 time points and results in dividing by 0. Then we divided the 4 and 8 min gene profiles by the 0 time point profile and obtained the derivative by subtracting each adjacent bin.
We looked for the local minimums of the derivative using the N.Yoder peak finder (mathworks.com) upstream the ‘rough estimate’ boundary; we considered only derivatives smaller than -0.01. We took the most downstream minimum relative to the ‘rough estimate’ boundary. Next, we identified the most downstream bin relative to the minimum (up to 2 Kb downstream to the ‘rough estimate’) where the derivative was close to 0 (> = -0.002) and defined it as the ‘refined estimate’. If no such bin was found we adhered to the ‘rough’ estimate.
Calculating elongation rate and rate confidence interval
In order to calculate the elongation rates, only genes with for which clear elongation boundaries were identified by the algorithm in both of the 4 min samples and in at least three of the four 8 min samples were included. Next, genes in which the average of the 8 min boundaries was lower than that of the 4 min boundaries were excluded. Since we had four biological repeats for the 8 min samples, we used modified Thompson tau outlier method in order to eliminate a maximum of one outlier. Next, the elongation rate was calculated by linearly fitting the averaged 4 and 8 min boundaries as a function of time. The slope of the linear fit was defined as the elongation rate. Next, the 50% confidence interval of the slope was defined as the confidence interval of the elongation rate. Only genes with confidence intervals better than 0.5 Kb/min were retained. The slope was also used to define the delay time, which was defined as being equal to the slope intersection with the time axis. The elongation rate was determined only for genes with delay times between -1 and 4 min.
Processing of ENCODE data
H3K36me3/H3K79me2 data of Hela-S3 were derived from the ENCODE project . Peak calling for H3K36me3 and H3K79me2 was done as follows: for each gene the 20 Kb downstream to the TSS were binned into 100 bp bins, and peak calling was done using N.Yoder peak finder (mathworks.com). Only genes with at least one peak were selected. Next, in order to get an enrichment level for each gene we averaged for each modification the signal for all bins.
RNA-seq data of Hela-S3 were also from the ENCODE project (Caltech RnaSeq Helas3 200SigRep1V4) . Expression per gene was the average for the signal on all exons.
Calculating relative initiation frequency
The intron signal was derived from each 8 min sample, divided by the averaged signal from the 0 min samples plus 1 (as pseudocounts to prevent dividing by 0). This calculation was performed separately for all four biological repeats and outliers were excluded using the modified Thompson Tau outlier method. Relative initiation frequencies were determined by averaging the rates from the biological repeats.
Primers used in this study: OPA1 mRNA F 5′-TTTTTACCTCAGGTTCTCCGGA, OPA1 mRNA R 5′CACGATCTGTTGCTCTAAACGC; OPA1+2 Kb F 5′ ACCATGGATGCCATTGAGTCA, OPA1+2 Kb R 5′TGTGCCATCACCAGGAGACAT; OPA1+10 Kb F 5′TCTGTTCCATGATGAGCTGTGG, OPA1+10 Kb R 5′CCTGGTCCTTCCTGAATCTTTG; TTC17 mRNA F 5′ATCAAAGCCAAGGTGCCCT, TTC17 mRNA R 5′GGACTGATGTCTTTGCTCTCCA; TTC17+1 Kb F 5′ TCAGAGGCGAGACTGCTTTTC, TTC17+1 Kb R 5′GCATTTACAAAACGCAGGCA; TTC17+10 Kb F 5′ TCCAGCCTCAGACACCACTTT, TTC17+10 Kb R 5′ TGGTTTGAAGAACATCCCGAG; RBM33+5 Kb F 5′TTCCACATCTTCCTGGCACA, RBM33+5 Kb R 5′ACACAGGTGAATCATGTGGAAT; RBM33+10 Kb F 5′GAACTCAGCCTCTGTGCTGT, RBM33+10 Kb R 5′ACAATGTGATGAGGGCTGGG; RBM33+14.2 Kb F 5′TCCTCTCTGCCAGTCTGTGA, RBM33+14.2 Kb R 5′GAAGGACTGGCATCTGGCAT; RBM33+20 Kb F 5′CCATGATTTGGAAAAGTGTGACGA, RBM33+20 Kb R 5′TGTGACATGCTAAAAAGTTAGAGAC; CLCN3+4 Kb F 5′ACAGCATCCCTCTTGAGGAAAA, CLCN3+4 Kb R 5′GGCCCTACAGCTTTCAGTAGA; CLCN3+9.3 Kb F 5′ACGTTCTACAATGGCAGACAGA, CLCN3+9.3 Kb R 5′GCTTCGCTGACCCACTTACT; CLCN3+20 Kb F 5′ACAGGAAGGGAGAGCCAAGA, CLCN3+20 Kb R 5′AGCTGCACTCATGAACAGTCA; 18S F 5′CGCCGCTAGAGGTGAAATTCT, 18S R 5′CATTCTTGGCAAATGCTTTCG.
Raw data have been deposited into GEO with accession number: GSE57116.
We thank Michal Rabani, Eitan Yaffe, Ilya Soifer and Dror Hollander for helpful discussions and Minho Chae and W. Lee Kraus for sharing with us the implementation of the Gro-HMM. This work was supported in part by a student-initiated project grant from the Kahn Center for Systems Biology, grant 293438 (RUBICAN) from the European Research Council, the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation, and the Lower Saxony-Israeli Association. MO is incumbent of the Andre Lwoff chair in molecular biology.
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