A small RNA makes a Bic difference
Genome Biology volume 8, Article number: 221 (2007)
The first highly specific knockouts of a microRNA, miR155, in mice result in multiple defects in adaptive immunity, and also show the feasibility of investigating at least some microRNAs by gene knockout.
MicroRNAs (miRNAs) are endogenous, small noncoding RNAs that are critical for setting the precise tempo of gene expression for numerous cellular processes in virtually every eukaryotic organism. A common theme in miRNA function across multicellular organisms is that they affect developmental transitions and cell-specific functions. There are more than 500 miRNAs in humans and 450 miRs in mice . Computational methods predict that miRNAs could post-transcriptionally regulate more than one third of all protein-coding genes [2, 3], implying that they regulate enormous genetic regulatory circuits. The importance of miRNA-mediated regulation of gene networks is highlighted in mice lacking the enzyme Dicer. Knocking out this enzyme, which is essential for the production of mature, functional 21-23-nucleotide miRNAs from long precursor transcripts, proves lethal in the embryo . The Dicer knockout underscores the importance of miRNAs in development, but it does not help illuminate the regulatory circuits affected by individual miRNAs. The highly specific gene knockouts of an immunologically important miRNA reported recently by Rodriguez et al.  and Thai et al. , who have independently produced knockout mice for miR155, begin to shed light on the complex molecular circuitry of individual miRNAs. Here we review some of their findings and some of the reasons for their success.
Advantages of miR155as a target for gene knockout
From a genomic perspective, miR155 was an appealing choice. Many miRNAs have multiple copies in the genome, or share seed-region homology with other miRNAs. The seed region, nucleotides 2 to 8 relative to the 5' end of the miRNA, is a critical determinant of miRNA targeting of mRNAs. Perfectly complementary base-pairing in the seed region is the most important determinant of miRNA repression of target mRNA translation, and miRNAs with identical seed regions are predicted to have overlapping regulatory roles. Thus, a full phenotypic analysis would require the knockout of multiple genomic loci. To make matters even more complicated, increased base-pairing in the 3' end of a miRNA with its target mRNA can partially compensate for translational repression for miRNAs with nucleotide mismatches in the seed region of the miRNA . The miR155 gene is present in only one copy, and miR155 does not share significant sequence with other reported miRNAs. Therefore, a single knockout will eliminate a distinct subtype of regulation.
Another attractive property of miR155 for gene knockout is its gene architecture. Most miRNA genes resemble typical protein-coding genes, although miRNAs derived from RNA polymerase III promoters were described recently . Most miRNA genes contain a TATA box in the core promoter and cell-specific transcriptional regulatory elements affecting miRNA expression. Some miRNAs, however, are processed from transcripts with a second function, either from introns in a protein-coding gene, or as a multicistronic unit containing multiple miRNAs. Interestingly, miRNAs from a common cluster are not necessarily processed to the same degree [9, 10], suggesting post-transcriptional control of miRNA expression. These multifunctional transcripts complicate the specific targeting of an individual miRNA. In contrast, miR155 is contained in an exon of a noncoding RNA gene called Bic, which does not contain other miRNAs, and which does not have any other conserved RNA sequence. Thus, miR155 can be easily targeted for disruption without interfering with the expression of a protein-coding gene or a second transcriptionally linked miRNA.
miR155 was also an attractive target from a functional perspective. MicroRNAs and RNA-based gene regulation are known to have roles in immune-system function (reviewed in [11, 12]), and miR155 is uniquely expressed in activated cells of the immune system [13–15]. In addition, this miRNA is highly expressed in Hodgkin's lymphoma and in diffuse large B cell lymphomas  and ectopic overexpression of miR155 indicates that it is an oncogene . Despite its immune-restricted expression, neither the miR155-null mice of Rodriguez et al.  nor those of Thai et al.  demonstrated major defects in hematopoiesis. Unlike previous experiments using dominant expression [18–20] or dominant repression  of miRNAs expressed in the immune system, the miR155-null mice did not demonstrate lineage biasing of normal hematopoiesis. In contrast, ectopic expression of another miRNA, miR181, increased the ratio of circulating B cells to T cells, although without the loss of one lineage entirely in favor of another lineage. These results suggest that miRNAs act as modulators rather than switches. Although no significant developmental defects were seen, both groups [5, 6] observed that the miR155 null mice had serious defects in immune function, a phenotype consistent with the expression of miR155 primarily in activated lymphoid and myeloid cells.
miR155-null mice display defects in adaptive and innate immunity
In their knockout mice, Rodriguez et al.  deleted the miR155-containing portion of exon 2 of the Bic gene. Multiple aspects of protective immunity were seriously compromised in these mice. Most dramatically, vaccination of miR155-null mice with live attenuated vaccine against Salmonella typhimurium failed to protect them against challenge with virulent Salmonella. Rodriguez et al. found defects in all aspects of adaptive immunity. B cells from miR155-null mice secreted lower levels of IgM and had fewer class-switched antibodies after immunization compared with normal mice. Dendritic cells from the miR155-null mice did not present antigen efficiently and activate T cells. T cells from these mice activated in vitro displayed an increased predilection to differentiate into the Th2 T-cell lineage, as indicated by Th2-type cytokine production. mRNA expression profiling indicated that predicted targets of miR155 were upregulated in the miR155-null, activated T cells. Rodriguez et al.  suggest that production of the transcription factor c-Maf is targeted by miR155 during T-cell activation, and that dysregulation of c-Maf may be responsible for the altered T-cell cytokine production in the miR155-null mice. In addition to the deficiency in adaptive immunity, the authors also observed autoimmune phenotypes in the lungs of miR155-null mice. The increased airway remodeling and leukocyte invasion suggested that miR155 plays a role in regulating the response of the immune system to self-antigens.
Thai et al.  engineered two transgenic mouse strains. In the miR155 knockout mouse, they replaced exon 2 of Bic with a LacZ reporter gene, which allowed them easily to detect which cells activated gene expression from this locus. Thai et al.  also engineered a mouse that conditionally coexpressed miR155 and the enhanced green fluorescent protein (GFP) in mature B cells. These two mice were used in combination to examine the effect of miR155 on adaptive B-cell responses to antigen in germinal centers (GC). Germinal centers are microscopically visible areas that form in immune tissues such as lymph nodes in response to antigenic challenge. They consist of interacting dendritic cells, T cells and B cells and serve as foci for B-cell switching to produce different classes of antibodies, affinity maturation (the production of antibodies with progressively higher affinity for the antigen) and the generation of memory cells. In their miR155-null mice, Thai et al.  observed fewer and smaller germinal centers in response to antigenic challenge compared with control mice. Consistent with these observations, miR155-null mice were deficient in the production of class-switched and affinity-matured antibody. In contrast, mice ectopically expressing miR155 produced more and larger germinal centers, and marginally more class-switched antibody. Thai et al.  attribute the changes in germinal center formation to deficiencies in the production of the germinal center-promoting chemokines lymphotoxin-α and tumor necrosis factor by miR155-null B cells. In addition, they also observed the Th2-biased T-cell chemokine production found by Rodriguez et al .
These two studies [5, 6] provide considerable insights into the role of miR155 in adaptive immunity. Perhaps more importantly, they show that a subset of miRNAs is amenable to analysis through genetic manipulation. But, despite these advances in interfering with miRNA-based regulation of immune activation, further analysis of miR155-null mice is required. Multiple interacting genetic networks in multiple immune cell types are regulated by miR155. For example, deletion of miR155 affects both the ability of a dendritic cell to activate T cells and the subsequent response of the T cells to activation. To decipher the genetic networks in their proper cellular context, hematopoietic lineage-specific knockouts of miR155 would be useful. In addition, such crosses could help to order the genes in a miRNA-regulated network, as complementation crosses have done in other eukaryotes. Alternatively, adoptive transfer of specific cell lineages between miR155-null and wild-type mice could illuminate the roles of miR155 in specific cell types.
Approximately one-third of all miRs demonstrate the properties of miR155. These miRs are not contained within a protein-coding transcript and are expressed from single copy genes without redundant family members [1, 21]. To elucidate the functional roles of the remaining miRs through homologous recombination of its gene or genes, new techniques are required, such as targeting very small genomic regions that contain multi-cistronic genes whose expression depends upon RNA secondary structure. Another technical advance that would facilitate phenotyping redundant miR families is rapid engineering of knockout mice altered at multiple redundant miR gene loci. Such gene inactivation through homologous recombination of several miR loci may help decipher the genetic regulatory networks governed through redundant miR activities.
Another intriguing possibility is that previous knockout mice may have inadvertently altered intronic miRNA gene expression. To investigate this possibility, we searched known mouse knockout databases against known databases of annotated miRNA genes. Examples of knockouts of protein-coding genes containing intronic miRNA include the calcitonin receptor gene CalcR  and the α-myosin heavy chain gene α-MHC . The CalcR knockout did not delete intronic miR489 and the αMHC knockout did not delete intronic miR208. Deletion of portions of the CalcR gene may have affected miR489 expression and the deletion of portions of the αMHC gene may have affected miR208 expression by disrupting miRNA processing from their host protein coding transcripts. Consistent with this possibility, ablation of the αMHC gene leads to dose-dependent phenotypes. Homozygous αMHC knockout mice are embryonic lethal whereas heterozygous αMHC knockout mice display severe impairment of contractility and alterations in sarcomere structure. The same issue of Science that contains the reports of the intronic miR155 knockout mice [5, 6] also contains a report of the intronic miR208 knockout mouse . The miR208 knockout led to partially overlapping phenotypes with the heterozygous αMHC mice, especially alterations in contractility and sarcomere structure, portending the possibility that some phenotypes observed in αMHC heterozygous mice may be due to altered expression of intronic miRNAs. It is thus important to consider the existence and potential roles of intragenic miRNAs when making transgenic mice. As the numbers of identified miRNAs and knockout mice increases, it becomes increasingly probable that knockout mice may inadvertently affect miRNA gene expression. In these cases, phenotypes must be carefully analyzed for effects due to loss of miRNA function relative to loss of the host gene function.
It is likely that other miRNA knockout mice are under construction. However, it may be some time before the next mouse with a deletion of a single miRNA gene is described. MicroRNA knockouts may yield only subtle phenotypes, possibly due to multiple related miRNAs with sequence similarity, especially in the seed region. The general notion in the miRNA field is that the effect of any one miRNA on any one gene may be small in degree. Indeed, it is likely that miRNAs gain their power from cooperative activity in gene silencing. Either multiple miRNAs act upon one gene or one miRNA acts upon multiple genes in a particular pathway to effect large changes in gene networks. As our knowledge of epigenetic control of gene expression continues to expand, the miR155 knockout mice made by Rodriguez et al.  and Thai et al.  are an important step in deciphering the multiple genetic networks regulated by miRNA function.
Griffiths-Jones S: The microRNA Registry. Nucleic Acids Res. 2004, 32: D109-D111. 10.1093/nar/gkh023.
Xie X, Lu J, Kulbokas EJ, Golub TR, Mootha V, Lindblad-Toh K, Lander ES, Kellis M: Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals. Nature. 2005, 434: 338-345. 10.1038/nature03441.
Lewis BP, Burge CB, Bartel DP: Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell. 2005, 120: 15-20. 10.1016/j.cell.2004.12.035.
Bernstein E, Kim SY, Carmell MA, Murchison EP, Alcorn H, Li MZ, Mills AA, Elledge SJ, Anderson KV, Hannon GJ: Dicer is essential for mouse development. Nat Genet. 2003, 35: 215-217. 10.1038/ng1253.
Rodriguez A, Vigorito E, Clare S, Warren MV, Couttet P, Soond DR, van Dongen S, Grocock RJ, Das PP, Miska EA, et al: Requirement of bic/microRNA-155 for normal immune function. Science. 2007, 316: 608-611. 10.1126/science.1139253.
Thai TH, Calado DP, Casola S, Ansel KM, Xiao C, Xue Y, Murphy A, Frendewey D, Valenzuela D, Kutok JL, et al: Regulation of the germinal center response by microRNA-155. Science. 2007, 316: 604-608. 10.1126/science.1141229.
Doench JG, Sharp PA: Specificity of microRNA target selection in translational repression. Genes Dev. 2004, 18: 504-511. 10.1101/gad.1184404.
Borchert GM, Lanier W, Davidson BL: RNA polymerase III transcribes human microRNAs. Nat Struct Mol Biol. 2006, 13: 1097-1101. 10.1038/nsmb1167.
He L, Thomson JM, Hemann MT, Hernando-Monge E, Mu D, Goodson S, Powers S, Cordon-Cardo C, Lowe SW, Hannon GJ, et al: A microRNA polycistron as a potential human oncogene. Nature. 2005, 435: 828-833. 10.1038/nature03552.
Guil S, Caceres JF: The multifunctional RNA-binding protein hnRNP A1 is required for processing of miR-18a. Nat Struct Mol Biol. 2007, 14: 591-596. 10.1038/nsmb1250.
Chowdhury D, Novina CD: RNAi and RNA-based regulation of immune system function. Adv Immunol. 2005, 88: 267-292.
Chowdhury D, Novina CD: Potential roles for short RNAs in lymphocytes. Immunol Cell Biol. 2005, 83: 201-210. 10.1111/j.1440-1711.2005.01333.x.
O'Connell RM, Taganov KD, Boldin MP, Cheng G, Baltimore D: MicroRNA-155 is induced during the macrophage inflammatory response. Proc Natl Acad Sci USA. 2007, 104: 1604-1609. 10.1073/pnas.0610731104.
Haasch D, Chen YW, Reilly RM, Chiou XG, Koterski S, Smith ML, Kroeger P, McWeeny K, Halbert DN, Mollison KW, et al: T-cell activation induces a noncoding RNA transcript sensitive to inhibition by immunosuppressant drugs and encoded by the proto-oncogene, BIC. Cell Immunol. 2002, 217: 78-86. 10.1016/S0008-8749(02)00506-3.
van den Berg A, Kroesen BJ, Kooistra K, de Jong D, Briggs J, Blokzijl T, Jacobs S, Kluiver J, Diepstra A, Maggio E, et al: High expression of B-cell receptor inducible gene BIC in all subtypes of Hodgkin lymphoma. Genes Chromosomes Cancer. 2003, 37: 20-28. 10.1002/gcc.10186.
Kluiver J, Poppema S, de Jong D, Blokzijl T, Harms G, Jacobs S, Kroesen BJ, van den Berg A: BIC and miR-155 are highly expressed in Hodgkin, primary mediastinal and diffuse large B cell lymphomas. J Pathol. 2005, 207: 243-249. 10.1002/path.1825.
Costinean S, Zanesi N, Pekarsky Y, Tili E, Volinia S, Heerema N, Croce CM: Pre-B cell proliferation and lymphoblastic leukemia/high-grade lymphoma in Eμ-miR155 transgenic mice. Proc Natl Acad Sci USA. 2006, 103: 7024-7029. 10.1073/pnas.0602266103.
Zhou B, Wang S, Mayr C, Bartel DP, Lodish HF: miR-150, a microRNA expressed in mature B and T cells, blocks early B cell development when expressed prematurely. Proc Natl Acad Sci USA. 2007, 104: 7080-7085. 10.1073/pnas.0702409104.
Li QJ, Chau J, Ebert PJ, Sylvester G, Min H, Liu G, Braich R, Manoharan M, Soutschek J, Skare P, et al: miR-181a is an intrinsic modulator of T cell sensitivity and selection. Cell. 2007, 129: 147-161. 10.1016/j.cell.2007.03.008.
Chen CZ, Li L, Lodish HF, Bartel DP: MicroRNAs modulate hematopoietic lineage differentiation. Science. 2004, 303: 83-86. 10.1126/science.1091903.
Li SC, Tang P, Lin WC: Intronic microRNA: discovery and biological implications. DNA Cell Biol. 2007, 26: 195-207. 10.1089/dna.2006.0558.
Dacquin R, Davey RA, Laplace C, Levasseur R, Morris HA, Goldring SR, Gebre-Medhin S, Galson DL, Zajac JD, Karsenty G: Amylin inhibits bone resorption while the calcitonin receptor controls bone formation in vivo. J Cell Biol. 2004, 164: 509-514. 10.1083/jcb.200312135.
Jones WK, Grupp IL, Doetschman T, Grupp G, Osinska H, Hewett TE, Boivin G, Gulick J, Ng WA, Robbins J: Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart. J Clin Invest. 1996, 98: 1906-1917.
van Rooij E, Sutherland LB, Qi X, Richardson JA, Hill J, Olson EN: Control of stress-dependent cardiac growth and gene expression by a microRNA. Science. 2007, 316: 575-579. 10.1126/science.1139089.
About this article
Cite this article
Moffett, H.F., Novina, C.D. A small RNA makes a Bic difference. Genome Biol 8, 221 (2007). https://doi.org/10.1186/gb-2007-8-7-221
- Germinal Center
- miRNA Gene
- Seed Region
- miRNA Gene Expression
- Intragenic miRNAs