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Most Caenorhabditis elegans microRNAs Are Individually Not Essential for Development or Viability
Open accessAbstract
MicroRNAs (miRNAs), a large class of short noncoding RNAs found in many plants and animals, often act to post-transcriptionally inhibit gene expression. We report the generation of deletion mutations in 87 miRNA genes in Caenorhabditis elegans, expanding the number of mutated miRNA genes to 95, or 83% of known C. elegans miRNAs. We find that the majority of miRNAs are not essential for the viability or development of C. elegans, and mutations in most miRNA genes do not result in grossly abnormal phenotypes. These observations are consistent with the hypothesis that there is significant functional redundancy among miRNAs or among gene pathways regulated by miRNAs. This study represents the first comprehensive genetic analysis of miRNA function in any organism and provides a unique, permanent resource for the systematic study of miRNAs.
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“which may help to explain the robustness of miRNA regulatory networks and their resilience to mutations of individual miRNAs in knockout experiments (Miska et al., 2007).”
From Scalable and deep profiling of mRNA targets for individual microRNAs with chimeric eCLIP (2022) · cites this paper as Miska et al., 2007
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Cites
Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714
THE GENETICS OF CAENORHABDITIS ELEGANS
Brenner, S. (1974) · Genetics · doi:10.1093/genetics/77.1.71 · Cited by 15,161
The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14
Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948 · cited 2×
“We performed a broad phenotypic study of all available miRNA loss-of-function mutants, including mutants that had been reported earlier [2,4,20,52].”
BackgroundMethodSelf-citationLewis, B. P., Burge, C. B., & Bartel, D. P. (2005) · Cell · doi:10.1016/j.cell.2004.12.035 · Cited by 11,855 · cited 1×
“]. Because many messages have been under selective pressure to preserve pairing to a 6mer in the 5′ region of the miRNA known as the miRNA seed (nucleotides 2–7), targets of metazoan miRNAs can be predicted above the background of false-positives by searching for conserved matches to the seed region [”
BackgroundSelf-citationThe nuclear RNase III Drosha initiates microRNA processing
Lee, Y., Ahn, C., Han, J., Choi, H., Kim, J., Yim, J., Lee, J., Provost, P., Rådmark, O., Kim, S., et al. (2003) · Nature · doi:10.1038/nature01957 · Cited by 5,294 · cited 1×
“In animals, miRNAs are transcribed as long RNA precursors (pri-miRNAs), which are processed in the nucleus by the RNase III enzyme complex Drosha-Pasha/DGCR8 to form the approximately 70-base pre-miRNAs [21–25] or are derived directly from introns [26,27].”
BackgroundPrediction of Mammalian MicroRNA Targets
Lewis, B. P., Shih, I.-H., Jones-Rhoades, M. W., Bartel, D. P., & Burge, C. B. (2003) · Cell · doi:10.1016/s0092-8674(03)01018-3 · Cited by 5,199 · cited 1×
“Because many messages have been under selective pressure to preserve pairing to a 6mer in the 59 region of the miRNA known as the miRNA seed (nucleotides 2–7), targets of metazoan miRNAs can be predicted above the background of false-positives by searching for conserved matches to the seed region [41–45].”
BackgroundSelf-citationThe 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans
Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R., & Ruvkun, G. (2000) · Nature · doi:10.1038/35002607 · Cited by 4,989
Self-citationIdentification of Novel Genes Coding for Small Expressed RNAs
Lagos-Quintana, M., Rauhut, R., Lendeckel, W., & Tuschl, T. (2001) · Science · doi:10.1126/science.1064921 · Cited by 4,956 · cited 1×
“miRNAs have been identified in organisms as diverse as roundworms, flies, fish, frogs, mammals, flowering plants, mosses, and even viruses, using genetics, molecular cloning, and predictions from bioinformatics [7–16].”
BackgroundMicroarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
Lim, L. P., Lau, N. C., Garrett-Engele, P., Grimson, A., Schelter, J. M., Castle, J., Bartel, D. P., Linsley, P. S., & Johnson, J. M. (2005) · Nature · doi:10.1038/nature03315 · Cited by 4,755
Self-citationSelf-assembly of mesoscopically ordered chromatic polydiacetylene/silica nanocomposites
Lu, Y.-F., Yang, Y., Sellinger, A., Lu, M.-C., Huang, J.-M., Fan, H., Haddad, R., López, G. P., Burns, A. R., Sasaki, D., et al. (2001) · Nature · doi:10.1038/35073544 · Cited by 4,708 · cited 2×
“We performed a broad phenotypic study of all available miRNA loss-of-function mutants, including mutants that had been reported earlier [2,4,20,52].”
BackgroundMethod
Research works printed but not linked: 3
- RubyJGStarkAJohnstonWKellisMBartelDP 2007 Biogenesis, expression, and target predictions for an expanded set of microRNA genes in Drosophila. Genome Res In press. · DOI
- WoodWB and the Community of C. elegans Researchers 1988 The nematode Caenorhabditis elegans Cold Spring Harbor, New York Cold Spring Harbor Press
- FixsenWD 1985 The genetic control of hypodermal cell lineages during nematode development [Ph.D.]. Cambridge Massachusetts Institute of Technology
Cited by
Sorted by citations
MicroRNAs: Target Recognition and Regulatory Functions
Bartel, D. P. (2009) · Cell · doi:10.1016/j.cell.2009.01.002 · Cited by 20,068
“Of the 95 C. elegans miRNA genes tested, only a few have grossly abnormal phenotypes when individually knocked out (Miska et al., 2007).”
Self-citationBartel, D. P. (2018) · Cell · doi:10.1016/j.cell.2018.03.006 · Cited by 3,751
“…Importance of miRNAs Systematic generation and analysis of miRNA knockouts in C. elegans created the initial impression that most metazoan miRNAs—even most miRNAs that are broadly conserved— have only subtle or redundant biological functions (Miska et al., 2007; Alvarez-Saavedra and Horvitz, 2010).”
BackgroundInfluentialSelf-citationOrigin, Biogenesis, and Activity of Plant MicroRNAs
Voinnet, O. (2009) · Cell · doi:10.1016/j.cell.2009.01.046 · Cited by 2,251
“elegans coupled with in-depth screens for altered morphology, growth, development, and behavior identified only four gene knockouts with detectable phenotypes (Miska et al., 2007).”
MicroRNAs in Stress Signaling and Human Disease
Mendell, J. T., & Olson, E. N. (2012) · Cell · doi:10.1016/j.cell.2012.02.005 · Cited by 1,673
“and Human Disease”
BackgroundRoles for MicroRNAs in Conferring Robustness to Biological Processes
Ebert, M. S., & Sharp, P. A. (2012) · Cell · doi:10.1016/j.cell.2012.04.005 · Cited by 1,564
“In worms, most individual miRNA mutants show no gross phenotype (Miska et al., 2007); the same is true for several of the mouse knockouts generated to date, including miR-21, miR-210, miR-214, miR-206, and miR-143 (E. Olson, personal communication).”
Small non-coding RNAs in animal development
Stefani, G., & Slack, F. J. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2347 · Cited by 1,387
“elegans strains that carry mutations of multiple miRNA-encoding loci suggest that this is indeed the case in certain instance”
BackgroundMicroRNA control of signal transduction
Inui, M., Martello, G., & Piccolo, S. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2868 · Cited by 1,272
Diversifying microRNA sequence and function
Ameres, S. L., & Zamore, P. D. (2013) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3611 · Cited by 1,175
Lujambio, A., & Lowe, S. W. (2012) · Nature · doi:10.1038/nature10888 · Cited by 1,084
Gene regulation by transcription factors and microRNAs
Hobert, O. (2008) · Science · doi:10.1126/science.1151651 · Cited by 913
MicroRNA functions in stress responses
Leung, A. K. L., & Sharp, P. A. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.027 · Cited by 865
“Perhaps somewhat surprisingly, systematic inactivation of individual miRNA in flies and worms has revealed that many miRNAs are dispensable for development or viability under standard laboratory conditions (Bushati and Cohen, 2007; Leaman et al., 2005; Miska et al., 2007).”
Mogilyansky, E., & Rigoutsos, I. (2013) · Cell Death & Differentiation · doi:10.1038/cdd.2013.125 · Cited by 889
“In the worm, let-7 is a component of the heterochronic pathway; it is expressed at a late stage of larva development, regulates the transition from larva to adult(5) and is embryonic lethal.(140) In the fruit fly, let-7-knockout flies are externally normal but exhibit behavioral defects and juvenile features in their…”
Biological principles of microRNA-mediated regulation: shared themes amid diversity
Flynt, A. S., & Lai, E. C. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2455 · Cited by 793
Evolution of microRNA diversity and regulation in animals
Berezikov, E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg3079 · Cited by 712
“This canalizing function of miRNAs can explain why a loss of an miRNA often does not result in a visible phenotyp”
BackgroundSilencing of microRNA families by seed-targeting tiny LNAs
Obad, S., dos Santos, C. O., Petri, A., Heidenblad, M., Broom, O. J., Ruse, C. I., Fu, C., Lindow, M., Stenvang, J., Straarup, E. M., et al. (2011) · Nature Genetics · doi:10.1038/ng.786 · Cited by 644
Non-coding RNAs as regulators of embryogenesis
Pauli, A., Rinn, J. L., & Schier, A. F. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2904 · Cited by 637
“elegans show that single and even double and triple mutants do not result in easily recognizable phenotype”
BackgroundMicroRNA therapeutics for cardiovascular disease: opportunities and obstacles
van Rooij, E., & Olson, E. N. (2012) · Nature Reviews Drug Discovery · doi:10.1038/nrd3864 · Cited by 631
Identification and consequences of miRNA–target interactions — beyond repression of gene expression
Hausser, J., & Zavolan, M. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3765 · Cited by 633
Inhibition of microRNA function by antimiR oligonucleotides
Stenvang, J., Petri, A., Lindow, M., Obad, S., & Kauppinen, S. (2012) · Silence · doi:10.1186/1758-907x-3-1 · Cited by 570
“elegans and Drosophila, and has also been reported for many individual miRNAs in the mouse [8,10,65-71].”
BackgroundMicroRNA Regulatory Networks in Cardiovascular Development
Liu, N., & Olson, E. N. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.03.010 · Cited by 497
The biological functions of miRNAs: lessons from in vivo studies
Vidigal, J. A., & Ventura, A. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.11.004 · Cited by 507
A MicroRNA Imparts Robustness against Environmental Fluctuation during Development
Li, X., Cassidy, J. J., Reinke, C. A., Fischboeck, S., & Carthew, R. W. (2009) · Cell · doi:10.1016/j.cell.2009.01.058 · Cited by 431
“It also explains why miRNAs frequently appear dispensable under uniform laboratory conditions (Bushati and Cohen, 2007; Leaman et al., 2005; Miska et al., 2007).”
Amaral, P., & Mattick, J. S. (2008) · Mammalian Genome · doi:10.1007/s00335-008-9136-7 · Cited by 491
“Furthermore, these analyses may also be complicated by functional redundancy of important regulatory molecules, even for conserved miRNAs with roles in development, which individually are mostly not essential for C. elegans viability (Miska et al. 2007).”
Das, P. P., Bagijn, M. P., Goldstein, L. D., Woolford, J. R., Lehrbach, N. J., Sapetschnig, A., Buhecha, H. R., Gilchrist, M. J., Howe, K., Stark, R., et al. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.06.003 · Cited by 424
“New deletion alleles for prg-1 and prg-2 were generated as described previously (Miska et al., 2007) and are listed in Table 3.”
InfluentialSelf-citationVirus-Encoded microRNAs: An Overview and a Look to the Future
Kincaid, R. P., & Sullivan, C. S. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1003018 · Cited by 400
“Additionally, gene knockout studies in animals demonstrate that numerous miRNAs are not essential for viability [30,31].”
BackgroundMicroRNA control of protein expression noise
Schmiedel, J. M., Klemm, S. L., Zheng, Y., Sahay, A., Blüthgen, N., Marks, D. S., & van Oudenaarden, A. (2015) · Science · doi:10.1126/science.aaa1738 · Cited by 395
Todesco, M., Rubio‐Somoza, I., Paz‐Ares, J., & Weigel, D. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001031 · Cited by 403
“One fifth of these lines have obvious morphological defects, which is in the same range as the approximately 10% of miRNA knockouts that caused phenotypic abnormalities or lethality in Caenorhabditis elegans [31].”
BackgroundMicroRNAs and their roles in aging
Smith-Vikos, T., & Slack, F. J. (2012) · Journal of Cell Science · doi:10.1242/jcs.099200 · Cited by 333
“Jo ur na l o f C el l S ci en ce these miRNAs do not affect the developmental progression of C. elegans (Miska et al., 2007). mir-71, -238 and -246 mutants display a significantly shorter lifespan than those of wild-type animals, and overexpressing miR-71 or miR-246 increases lifespan, indicating…”
BackgroundAdult-specific functions of animal microRNAs
Sun, K., & Lai, E. C. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3471 · Cited by 335
Large-Scale Screening for Targeted Knockouts in the Caenorhabditis elegans Genome
The C. elegans Deletion Mutant Consortium (2012) · G3 Genes Genomes Genetics · doi:10.1534/g3.112.003830 · Cited by 381
“Just over 40% of these genes have been deleted, and most do not display an overt phenotype (Miska et al. 2007).”
BackgroundMethodMicroRNAs: From Mechanism to Organism
Dexheimer, P. J., & Cochella, L. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00409 · Cited by 405
Portrait of the PI3K/AKT pathway in colorectal cancer
Danielsen, S. A., Eide, P. W., Nesbakken, A., Guren, T. K., Leithe, E., & Lothe, R. A. (2014) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2014.09.008 · Cited by 336
Many Families of C. elegans MicroRNAs Are Not Essential for Development or Viability
Alvarez-Saavedra, E., & Horvitz, H. R. (2010) · Current Biology · doi:10.1016/j.cub.2009.12.051 · Cited by 295
“let-7 family animals were scored after passage through dauer to suppress the early adult lethality [1].”
BackgroundMethodInfluentialSelf-citationMicroRNAs Both Promote and Antagonize Longevity in C. elegans
de Lencastre, A., Pincus, Z., Zhou, K. I., Kato, M., Lee, S. S., & Slack, F. J. (2010) · Current Biology · doi:10.1016/j.cub.2010.11.015 · Cited by 292
“However, none of these mutants exhibited any physiological or behavioral abnormalities during growth and development [25, 26]; Figure S4 and Table S4).”
BackgroundThe interplay between transcription factors and microRNAs in genome‐scale regulatory networks
Martinez, N. J., & Walhout, A. J. M. (2009) · BioEssays · doi:10.1002/bies.200800212 · Cited by 278
“elegans can tolerate removal of most individual miRNAs without obvious developmental defects.((40)) The lack of clear miRNA hubs and the fact that most of them are not essential for viability both agree with the hypothesis that miRNAs do not function as master regulators, but rather predominantly function to fine tune…”
BackgroundPeterson, K. J., Dietrich, M. R., & McPeek, M. A. (2009) · BioEssays · doi:10.1002/bies.200900033 · Cited by 252
“These preliminary considerations suggest that if the primary function served by miRNA gene regulation is to stabilize gene expression levels, miRNA knockouts may not have strongly deleterious phenotypes in individuals,((45)) as recently realized in a large-scale knockout study.((78)) Although we are in very early days…”
BackgroundMicroRNA let-7 regulates 3T3-L1 adipogenesis.
Sun, T.-W., Fu, M., Bookout, A., Kliewer, S., & Mangelsdorf, D. (2009) · Molecular Endocrinology · doi:10.1210/me.2008-0298 · Cited by 277
MicroRNAs shape the neuronal landscape
McNeill, E., & Van Vactor, D. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.005 · Cited by 274
Martinez, N. J., Ow, M. C., Barrasa, M. I., Hammell, M., Sequerra, R., Doucette-Stamm, L., Roth, F. P., Ambros, V., & Walhout, A. J. M. (2008) · Genes & Development · doi:10.1101/gad.1678608 · Cited by 242
Self-citationImpact of microRNA regulation on variation in human gene expressionPreprint
Lü, J., & Clark, A. G. (2012) · Genome Research · doi:10.1101/gr.132514.111 · Cited by 258
“…with disease, cancer, or phenotypic abnormalities (Bartel 2004, 2009; He and Hannon 2004; Sokol and Ambros 2005; Calin and Croce 2006; Esquela-Kerscher and Slack 2006; Li et al. 2006; Ghildiyal and Zamore 2009), yet miRNA knockouts often result in only subtle phenotypic effects (Miska et al. 2007).”
Kalla, R., Ventham, N. T., Kennedy, N. A., Quintana, J. F., Nimmo, E. R., Buck, A. H., & Satsangi, J. (2014) · Gut · doi:10.1136/gutjnl-2014-307891 · Cited by 281
Genome-scale spatiotemporal analysis of Caenorhabditis elegans microRNA promoter activityPreprint
Martinez, N. J., Ow, M. C., Reece-Hoyes, J. S., Barrasa, M. I., Ambros, V., & Walhout, A. J. M. (2008) · Genome Research · doi:10.1101/gr.083055.108 · Cited by 218
Self-citationKato, M., Paranjape, T., Ullrich, R., Nallur, S. V., Gillespie, E., Keane, K., Esquela‐Kerscher, A., Weidhaas, J. B., & Slack, F. J. (2009) · Oncogene · doi:10.1038/onc.2009.106 · Cited by 240
“This is the first demonstration that mir-34 plays a role in the response to radiation in vivo and is the first known phenotype associated with mir-34 deletion mutants in C. elegans (Miska et al., 2007) or in any animals.”
Background5′ isomiR variation is of functional and evolutionary importance
Tan, G. C., Chan, E., Molnar, A., Sarkar, R., Alexieva, D., Isa, I. M., Robinson, S., Zhang, S., Ellis, P., Langford, C. F., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku656 · Cited by 255
“It has proven difficult to determine the importance of isomiRs both because of the limited tools that are available for modulating the levels of specific isomiRs (16) and because of the overlapping and redundant nature of most miRNA genes (24).”
BackgroundAnalysis of microRNA knockouts in mice
Park, C. Y., Choi, Y. S., & McManus, M. T. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq367 · Cited by 218
“In worms, ,10% of systematic miRNA deletions cause embryonic death or grossly abnormal phenotypes (90).”
BackgroundAn Essential Mesenchymal Function for miR-143/145 in Intestinal Epithelial Regeneration
Chivukula, R. R., Shi, G., Acharya, A., Mills, E. W., Zeitels, L. R., Anandam, J., Abdelnaby, A. A., Balch, G. C., Mansour, J. C., Yopp, A. C., et al. (2014) · Cell · doi:10.1016/j.cell.2014.03.055 · Cited by 213
miR-34/449 miRNAs are required for motile ciliogenesis by repressing CP110
Song, R., Walentek, P., Sponer, N., Klimke, A., Lee, J. S., Dixon, G., Harland, R., Wan, Y., Lishko, P., Lize, M., et al. (2014) · Nature · doi:10.1038/nature13413 · Cited by 228
Boulias, K., & Horvitz, H. R. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.02.014 · Cited by 184
Self-citationMicroRNA Predictors of Longevity in Caenorhabditis elegans
Pincus, Z., Smith-Vikos, T., & Slack, F. J. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002306 · Cited by 193
“Beyond differences in lifespan and stress-resistance [36], mir-71 mutant animals appear phenotypically wild-type [46].”
BackgroundMolecular architecture of a miRNA-regulated 3′ UTR
Didiano, D., & Hobert, O. (2008) · RNA · doi:10.1261/rna.1082708 · Cited by 187
“First, we assayed the regulation of the wild-type cog-1 39 UTR sensor in mir265 null mutants (Miska et al. 2007) and found no effect on sensor gene expression (Fig.”
MethodMicroRNAs in placental health and disease
Mouillet, J.-F., Ouyang, Y., Coyne, C. B., & Sadovsky, Y. (2015) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2015.05.057 · Cited by 195
MicroRNAs and neurodegeneration: role and impact
Abe, M., & Bonini, N. M. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.08.013 · Cited by 190
“elegans have provided crucial insights into miRNA function; not all miRNAs that change with age lead to modulated lifespan upon altered activity [90], and many miRNAs are not required for development or viability [91, 92].”
BackgroundMicroRNA-mediated control of macrophages and its implications for cancer
Squadrito, M. L., Etzrodt, M., Palma, M. D., & Pittet, M. J. (2013) · Trends in Immunology · doi:10.1016/j.it.2013.02.003 · Cited by 190
A Resource for the Conditional Ablation of microRNAs in the Mouse
Park, C. Y., Jeker, L. T., Carver-Moore, K., Oh, A., Liu, H. J., Cameron, R., Richards, H. W., Li, Z., Adler, D., Yoshinaga, Y., et al. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.02.008 · Cited by 177
“elegans, where less than 10% of miRNAs give rise to embryonic developmental or grossly abnormal phenotypes but which may appear in sensitized backgrounds or under stress (Alvarez-Saavedra and Horvitz, 2010; Brenner et al., 2010; Miska et al., 2007).”
BackgroundIbáñez‐Ventoso, C., Vora, M., & Driscoll, M. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002818 · Cited by 189
“Initial studies support that evaluation of functional redundancies will be an important factor in this analysis [39,40,42,48] and that conserved regulatory functions may shed light on disease mechanisms [6,42].”
InfluentialmiR-219 Cooperates with miR-338 in Myelination and Promotes Myelin Repair in the CNS
Wang, H., Moyano, A. L., Ma, Z., Deng, Y., Lin, Y., Zhao, C., Zhang, L., Jiang, M., He, X., Ma, Z., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.03.001 · Cited by 174
“Remarkably, although loss-of-function mutation of most individual miRNAs yields no overt developmental defects in multiple organisms (Miska et al., 2007), the essential role of miR-219 in myelination indicates that miR-219 plays a central role in rather than just fine-tuning myelinogenesis.”
Wang, J., Czech, B., Crunk, A. E., Wallace, A. D., Mitreva, M., Hannon, G. J., & Davis, R. E. (2011) · Genome Research · doi:10.1101/gr.121426.111 · Cited by 169
“…miRNAs or miRNA seed families in C. elegans leads to developmental phenotypes including death of embryos or early larvae and defects in locomotion, body size, egg laying, and dauer larvae formation (Miska et al. 2007; Alvarez- Saavedra and Horvitz 2010; Brenner et al. 2010; Shaw et al. 2010).”
Regulation of immune responses and tolerance: the micro RNA perspective
Chen, C., Schaffert, S. A., Fragoso, R., & Loh, C. (2013) · Immunological Reviews · doi:10.1111/imr.12060 · Cited by 167
Physiological roles of long noncoding RNAs: insight from knockout mice
Li, L., & Chang, H. Y. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.06.003 · Cited by 167
“Future studies may reveal a phenotype in organ homeostasis over time or under stress and pathological conditions, as was revealed for many microRNA knockouts [54, 55].”
BackgroundMiRNAs confer phenotypic robustness to gene networks by suppressing biological noise
Siciliano, V., Garzilli, I., Fracassi, C., Criscuolo, S., Ventre, S., & di Bernardo, D. (2013) · Nature Communications · doi:10.1038/ncomms3364 · Cited by 166
“S7 and Supplementary Table S2): (1) unregulated transcription, that is, the mRNA is transcribed from a constitutive promoter30; (2) regulated transcription where the protein activates its own transcription (that is, the PFL motif); (3) a NFL mediated by the miRNA inducing degradation of the target mRNA (that is, a NFL…”
BackgroundKato, M., de Lencastre, A., Pincus, Z., & Slack, F. J. (2009) · Genome biology · doi:10.1186/gb-2009-10-5-r54 · Cited by 138
“Some sets of miRNA map to specific chromosomal clusters, as in the case of miR-35 to miR-41, which have redundant functions in embryonic development [42] and are abundantly expressed in the embryonic stage (Figures 3b and 7).”
BackgroundEvolution under canalization and the dual roles of microRNAs—A hypothesisPreprint
Wu, C., Shen, Y., & Tang, T. (2009) · Genome Research · doi:10.1101/gr.084640.108 · Cited by 167
Liu, X., Huang, J. Q., Wang, Y., Khanna, K., Xie, Z., Owen, H. A., & Zhao, D. (2010) · The Plant Journal · doi:10.1111/j.1365-313x.2010.04164.x · Cited by 168
“able phenotypes have been identified in MIRs in plants and other organisms (Miska et al., 2007; Voinnet, 2009).”
BackgroundSystematic Study of Drosophila MicroRNA Functions Using a Collection of Targeted Knockout Mutations
Chen, Y., Song, S., Weng, R., Verma, P., Kugler, J., Buescher, M., Rouam, S. L., & Cohen, S. M. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.029 · Cited by 152
“Studies with this collection suggested that the majority of miRNA mutants had no detectable phenotypes when mutated individually (Miska et al., 2007).”
BackgroundResultInfluentialMicroRNA transcriptome in the newborn mouse ovaries determined by massive parallel sequencing.
Ahn, H., Morin, R. D., Zhao, H., Harris, R. A., Coarfa, C., Chen, Z.-J., Milosavljevic, A., Marra, M., & Rajkovic, A. (2010) · Molecular human reproduction · doi:10.1093/molehr/gaq017 · Cited by 149
MicroRNA-205 controls neonatal expansion of skin stem cells by modulating the PI(3)K pathway
Wang, D., Zhang, Z., O’Loughlin, E., Wang, L., Fan, X., Lai, E. C., & Yi, R. (2013) · Nature Cell Biology · doi:10.1038/ncb2827 · Cited by 145
“However, genetic KO models in either C. elegans or mouse have implicated very few individual miRNAs as indispensable for animal development 14, 15, 42 .”
A framework for understanding the roles of miRNAs in animal development
Alberti, C., & Cochella, L. (2017) · Development · doi:10.1242/dev.146613 · Cited by 160
“…the most ancient animal miRNA, mir-100 (Grimson et al., 2008); let-7 is also highly conserved and plays broad and essential roles in many contexts (Mondol and Pasquinelli, 2012); and the mir-430/302/290 family also seems to have maintained a core position in development during vertebrate…”
BackgroundmiR-23∼27∼24 clusters control effector T cell differentiation and function
Cho, S., Wu, C.-J., Yasuda, T., Cruz, L. O., Khan, A. A., Lin, L.-L., Nguyen, D. T., Miller, M., Lee, H.-M., Kuo, M., et al. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20150990 · Cited by 137
“However, because many miRNAs can be deleted without resulting in any apparent phenotype, there is also a growing consensus that most miRNAs do not play an indispensable role in dictating the outcomes of biological responses (Miska et al., 2007).”
BackgroundBrenner, J. L., Jasiewicz, K. L., Fahley, A. F., Kemp, B. J., & Abbott, A. L. (2010) · Current Biology · doi:10.1016/j.cub.2010.05.062 · Cited by 123
“elegans, the majority of individual miRNAs are not required for viability or for development, as most loss of function miRNA mutants display no obvious developmental abnormalities [1].”
Self-citationShore, D. E., Carr, C. E., & Ruvkun, G. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002792 · Cited by 124
“elegans are not individually essential for viability under standard laboratory conditions, the possibility that they fulfill conditional functions such as stress response is particularly appealing [77].”
Backgroundde Kouchkovsky, D. A., Esensten, J. H., Rosenthal, W. L., Morar, M. M., Bluestone, J. A., & Jeker, L. T. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1203567 · Cited by 122
“In fact, most individual miRNAs (52) and even many miRNA families altogether (53) are dispensable under homeostatic conditions, indicating that a certain degree of fluctuation or imprecision of gene expression is well tolerated.”
BackgroundMicroRNA miR-30 family regulates non-attachment growth of breast cancer cells
Ouzounova, M., Vuong, T., Ancey, P., Ferrand, M., Durand, G., Calvez‐Kelm, F. L., Croce, C. M., Matar, C., Herceg, Z., & Hernández‐Vargas, H. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-139 · Cited by 122
The roles of microRNAs in mouse development
DeVeale, B., Swindlehurst-Chan, J., & Blelloch, R. (2021) · Nature Reviews Genetics · doi:10.1038/s41576-020-00309-5 · Cited by 121
microRNAs in parasites and parasite infection
Zheng, Y., Cai, X., & Bradley, J. E. (2013) · RNA Biology · doi:10.4161/rna.23716 · Cited by 128
“Although a study in which 95 miRNA genes were mutated in Caenorhabiditis elegans, no abnormal phenotypes were observed, indicating major miRNAs are not vital for the development or viability.(7) Increasing evidence supports the idea that miRNAs participate in complex regulatory networks and the abnormality of some miR…”
BackgroundMiRNA-34 intrinsically links p53 tumor suppressor and Wnt signaling
Cha, Y. H., Kim, N. H., Park, C., Lee, I., Kim, H. S., & Yook, J. I. (2012) · Cell Cycle · doi:10.4161/cc.19618 · Cited by 114
miRNAs at the interface of cellular stress and disease
Emde, A., & Hornstein, E. (2014) · The EMBO Journal · doi:10.15252/embj.201488142 · Cited by 117
“However, genetic knockout of specific miRNAs renders the mutant animals incapable of coping with stress (Miska et al , 2007; Alvarez-Saavedra & Horvitz, 2010).”
Downregulated MicroRNAs in the Differential Diagnosis of Malignant Pleural Mesothelioma
Gee, G. V., Koestler, D., Christensen, B., Sugarbaker, D., Ugolini, D., Ivaldi, G., Resnick, M., Houseman, E., Kelsey, K. T., & Marsit, C. (2010) · International Journal of Cancer · doi:10.1002/ijc.25285 · Cited by 111
“Experiments in simple organisms that show most miRNAs are not essential, and individually often have subtle effects on their downstream targets, provide evidence for the theory of miRNA redundancy.(14,15) Five of 7 of our miRNAs are members of the same gene family (miR-200).”
BackgroundDevelopmental Transitions in C. elegans Larval Stages
Rougvie, A. E., & Moss, E. G. (2013) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-396968-2.00006-3 · Cited by 114
EGF Decreases the Abundance of MicroRNAs That Restrain Oncogenic Transcription Factors
Avraham, R., Sas‐Chen, A., Manor, O., Steinfeld, I., Shalgi, R., Tarcic, G., Moshe, N. B. B., Zeisel, A., Amit, I., Zwang, Y., et al. (2010) · Science Signaling · doi:10.1126/scisignal.2000876 · Cited by 106
“Together, these results confirm attenuation of IEG mRNA abundance by microRNAs and are consistent with studies indicating that promoters of IEGs are poised for activation in resting cells (23, 24). miR-370 miR-188 miR-671 miR-320 miR-198 miR-134 miR-662 miR-575 miR-212 miR-564 miR-638 miR-572 miR-202 miR-452 miR-630 m…”
BackgroundInfluentialMicroRNAs and their roles in mammalian stem cells
Yi, R., & Fuchs, E. V. (2011) · Journal of Cell Science · doi:10.1242/jcs.069104 · Cited by 104
“elegans miRNAs are knocked out individually or in combination as a whole family that shares the same seed sequence, only a few exhibit developmental defects (Alvarez-Saavedra and Horvitz, 2010; Miska et al., 2007).”
BackgroundBarringhaus, K. G., & Zamore, P. D. (2009) · Circulation · doi:10.1161/circulationaha.107.715839 · Cited by 100
microRNAs in cardiac development and regeneration
Porrello, E. R. (2013) · Clinical Science · doi:10.1042/cs20130011 · Cited by 100
MicroRNAs and the Genetic Network in Aging
Inukai, S., & Slack, F. J. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.01.023 · Cited by 100
“elegans strains with mutations for aging-associated miRNAs have been characterized in aging,(41,67) made possible by a large collection of miRNA loss-of-function mutants.(68) When characterized during development, most of these strains did not demonstrate gross abnormalities(68); nevertheless, mutations for some aging…”
A resource of vectors and ES cells for targeted deletion of microRNAs in mice
Prosser, H. M., Koike-Yusa, H., Cooper, J. D., Law, F., & Bradley, A. (2011) · Nature Biotechnology · doi:10.1038/nbt.1929 · Cited by 92
“A genome-wide miRNA knockout resource for the functional analysis of miRNAs currently exists only for the invertebrate Caenorhabditis elegans”
BackgroundClark, A., Goldstein, L. D., Tevlin, M., Tavaré, S., Shaham, S., & Miska, E. A. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq083 · Cited by 95
“As previously described, mir-124 mutants are viable with no gross abnormalities (77).”
BackgroundSelf-citationParchem, R. J., Moore, N., Fish, J. L., Parchem, J. G., Braga, T. T., Shenoy, A., Oldham, M. C., Rubenstein, J. L. R., Schneider, R. A., & Blelloch, R. H. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.06.074 · Cited by 97
Towards computational prediction of microRNA function and activity
Ulitsky, I., Laurent, L. C., & Ron Shamir, A. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq570 · Cited by 87
“Knock-out studies in model organisms have had only limited success in delineating miRNA function, possibly because redundant miRNAs exist at saturating levels in wild-type cells, or because of compensatory effects in downstream signaling pathways (8).”
BackgroundHorwich, M. D., & Zamore, P. D. (2008) · Nature Protocols · doi:10.1038/nprot.2008.145 · Cited by 95
“elegans , loss of most individual miRNA genes caused no obvious phenotyp”
Large-scale sorting of C. elegans embryos reveals the dynamics of small RNA expression
Stoeckius, M., Maaskola, J., Colombo, T., Rahn, H.-P., Friedländer, M. R., Li, N., Chen, W., Piano, F., & Rajewsky, N. (2009) · Nature Methods · doi:10.1038/nmeth.1370 · Cited by 93
“Genetic knockouts and mutations for 95 miRNAs have been publishe”
BackgroundmicroRNA control of cell-cell signaling during development and disease
Hagen, J. W., & Lai, E. C. (2008) · Cell Cycle · doi:10.4161/cc.6447 · Cited by 88
A genome-wide transgenic resource for conditional expression ofDrosophilamicroRNAs
Bejarano, F., Bortolamiol-Bécet, D., Dai, Q., Sun, K., Saj, A., Chou, Y., Raleigh, D. R., Kim, K., Ni, J., Duan, H., et al. (2012) · Development · doi:10.1242/dev.079939 · Cited by 89
“Many miRNAs have subtle if not undetectable loss-of-function phenotypes (Miska et al., 2007; Alvarez-Saavedra and Horvitz, 2010), but it is also the case that many miRNA mutants produce synthetic phenotypes in combination with other genetic insults (Brenner et al.”
BackgroundInfluentialBiological Robustness and the Role of MicroRNAs
Peláez, N., & Carthew, R. W. (2012) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-387038-4.00009-4 · Cited by 102
“Systematic mutagenesis of many individual miRNA genes (Miska et al., 2007) and paralogous families of miRNA genes (Alvarez-Saavedra and Horvitz, 2010) were performed in the nematode Caenorhabditis elegans.”
Neuronal Responses to Physiological Stress
Kagias, K., Nehammer, C., & Pocock, R. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00222 · Cited by 94
Zhang, X.-C., Zabinsky, R., Teng, Y., Cui, M., & Han, M. (2011) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1105982108 · Cited by 94
“Following the studies by Horvitz and colleagues (7, 8) that showed that single mutations of the vast majority of miRNAs did not reveal obvious developmental or growth defects, our study reinforces the idea that most miRNAs do not regulate specific physiological functions through a robust regulatory interaction between…”
BackgroundResultBabiarz, J., Ravon, M., Sridhar, S., Ravindran, P., Swanson, B., Bitter, H., Weiser, T. W., Chiao, E. T., Certa, U., & Kolaja, K. L. (2011) · Stem Cells and Development · doi:10.1089/scd.2011.0357 · Cited by 92
“For example, deletions of each miRNA gene individually in Caenorhabditis elegans results in few, if any, phenotypic consequences [49].”
BackgroundMicroRNAs in parasitic diseases: Potential for diagnosis and targeting
Manzano-Román, R., & Siles‐Lucas, M. (2012) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2012.10.001 · Cited by 94
Small RNA expression and strain specificity in the rat
Linsen, S. E. V., de Wit, E., de Bruijn, E., & Cuppen, E. P. J. G. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-249 · Cited by 82
“miRNAs may act redundantly [42] or in concert [43,44].”
BackgroundA quantitative targeted proteomics approach to validate predicted microRNA targets in C. elegans
Jovanović, M., Reiter, L., Picotti, P., Lange, V., Bogan, E., Hurschler, B. A., Blenkiron, C., Lehrbach, N. J., Ding, X. C., Weiß, M., et al. (2010) · Nature Methods · doi:10.1038/nmeth.1504 · Cited by 83
Self-citationDeletion of microRNA-80 Activates Dietary Restriction to Extend C. elegans Healthspan and Lifespan
Vora, M., Shah, M. B., Ostafi, S., Onken, B., Xue, J., Ni, J. Z., Gu, S. G., & Driscoll, M. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003737 · Cited by 83
“elegans mir deletion strains [20] for differences in autofluorescent age pigment levels in old animals.”
BackgroundInfluentialWinter, A. D., Weir, W., Hunt, M., Berriman, M., Gilleard, J. S., Devaney, E., & Britton, C. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-4 · Cited by 89
“elegans miRNAs, either individually [23] or by combined mutation of related sequences [24], results in no observable effect on development or viability.”
Background
Metadata
- Authors
- Miska, E. A., Alvarez-Saavedra, E., Abbott, A. L., Lau, N. C., Hellman, A. B., McGonagle, S. M., Bartel, D. P., Ambros, V. R., & Horvitz, H. R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Whitehead Institute for Biomedical Research (US)
- Corresponding author
- Horvitz, H. Robert
- ORCID
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2007-12-14
- Volume
- 3
- Issue
- 12
- Pages
- e215
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC2134938
- OpenAlex
- W2003952411
- Cited by
- 484
- References
- 111
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 17 · 2023: 14 · 2022: 12 · 2021: 15 · 2020: 16 · 2019: 21 · 2018: 24 · 2017: 28 · 2016: 29 · 2015: 33 · 2014: 46 · 2013: 39 · 2012: 60
- FWCI
- 9.91
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- e-Publications@Marquette (Marquette University) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Ellison Medical Foundation
- Wellcome Trust (061641)
- National Institutes of Health (5f32gm065721-03)
- National Institute of General Medical Sciences (GM067031, R01GM067031, 5F32GM065721-02, GM34028, R01GM034028, F32 GM065721)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- microRNA, Caenorhabditis elegans, post-transcriptional regulation
- MeSH terms
- Animals, Mutation, Phenotype, Conserved Sequence, Caenorhabditis elegans, Genes, Helminth, Sequence Deletion, RNA, Helminth, Evolution, Molecular, MicroRNAs
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