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Evolution of microRNA genes by inverted duplication of target gene sequences in Arabidopsis thaliana

Allen, Edwards, Xie, Zhixin, Gustafson, Adam M, Sung, Gi-Ho, Spatafora, Joseph W, Carrington, James C·2004·Nature Genetics

Abstract

MicroRNAs (miRNAs) in plants and animals function as post-transcriptional regulators of target genes, many of which are involved in multicellular development. miRNAs guide effector complexes to target mRNAs through base-pair complementarity, facilitating site-specific cleavage or translational repression. Biogenesis of miRNAs involves nucleolytic processing of a precursor transcript with extensive foldback structure. Here, we provide evidence that genes encoding miRNAs in plants originated by inverted duplication of target gene sequences. Several recently evolved genes encoding miRNAs in Arabidopsis thaliana and other small RNA-generating loci possess the hallmarks of inverted duplication events that formed the arms on each side of their respective foldback precursors. We propose a model for miRNA evolution that suggests a mechanism for de novo generation of new miRNA genes with unique target specificities.

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  1. Bartel, D. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116, 281–297 (2004). · DOI
  2. Ketting, R.F. et al. Dicer functions in RNA interference and in synthesis of small RNA involved in developmental timing in C. elegans. Genes Dev. 15, 2654–2659 (2001). · DOI · Paper page
  3. Hutvagner, G. et al. A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science 293, 834–838 (2001). · DOI · Paper page
  4. Lee, Y. et al. The nuclear RNase III Drosha initiates microRNA processing. Nature 425, 415–419 (2003). · DOI
  5. Park, W., Li, J., Song, R., Messing, J. & Chen, X. CARPEL FACTORY, a Dicer homolog, and HEN1, a novel protein, act in microRNA metabolism in Arabidopsis thaliana . Curr. Biol. 12, 1484–1495 (2002). · DOI
  6. Kurihara, Y. & Watanabe, Y. Arabidopsis micro-RNA biogenesis through Dicer-like 1 protein functions. Proc. Natl. Acad. Sci. USA 101, 12753–12758 (2004). · DOI
  7. Reinhart, B.J., Weinstein, E.G., Rhoades, M.W., Bartel, B. & Bartel, D.P. MicroRNAs in plants. Genes Dev. 16, 1616–1626 (2002). · DOI
  8. Finnegan, E.J. & Matzke, M.A. The small RNA world. J. Cell Sci. 116, 4689–4693 (2003). · DOI
  9. Floyd, S.K. & Bowman, J.L. Gene regulation: ancient microRNA target sequences in plants. Nature 428, 485–486 (2004). · DOI
  10. Pasquinelli, A.E. et al. Conservation of the sequence and temporal expression of let-7 heterochronic regulatory RNA. Nature 408, 86–89 (2000). · DOI
  11. Meyerowitz, E.M. Plants compared to animals: the broadest comparative study of development. Science 295, 1482–1485 (2002). · DOI
  12. Poethig, R.S. Life with 25,000 genes. Genome Res. 11, 313–316 (2001). · DOI
  13. Jones-Rhoades, M.W. & Bartel, D.P. Computational identification of plant microRNAs and their targets, including a stress-induced miRNA. Mol. Cell 14, 787–799 (2004). · DOI
  14. Griffiths-Jones, S., Bateman, A., Marshall, M., Khanna, A. & Eddy, S.R. Rfam: an RNA family database. Nucleic Acids Res. 31, 439–441 (2003). · DOI
  15. Palatnik, J.F. et al. Control of leaf morphogenesis by microRNAs. Nature 425, 257–263 (2003). · DOI
  16. Aukerman, M.J. & Sakai, H. Regulation of flowering time and floral organ identity by a microRNA and its APETALA2-like target genes. Plant Cell 15, 2730–2741 (2003). · DOI
  17. Chen, X. A microRNA as a translational repressor of APETALA2 in Arabidopsis flower development. Science 303, 2022–2025 (2004). · DOI
  18. Mallory, A.C., Dugas, D.V., Bartel, D.P. & Bartel, B. MicroRNA regulation of NAC-domain targets is required for proper formation and separation of adjacent embryonic, vegetative, and floral organs. Curr. Biol. 14, 1035–106 (2004). · DOI
  19. Achard, P., Herr, A., Baulcombe, D.C. & Harberd, N.P. Modulation of floral development by a gibberellin-regulated microRNA. Development 131, 3357–3365 (2004). · DOI
  20. Laufs, P., Peaucelle, A., Morin, H. & Traas, J. MicroRNA regulation of the CUC genes is required for boundary size control in Arabidopsis meristems. Development 131, 4311–4322 (2004). · DOI · Paper page
  21. Sunkar, R. & Zhu, J.K. Novel and stress-regulated microRNAs and other small RNAs from Arabidopsis . Plant Cell 16, 2001–2019 (2004). · DOI
  22. Xie, Z., Kasschau, K.D. & Carrington, J.C. Negative feedback regulation of Dicer-Like1 in Arabidopsis by microRNA-guided mRNA degradation. Curr. Biol. 13, 784–789 (2003). · DOI
  23. Vaucheret, H., Vazquez, F., Crete, P. & Bartel, D.P. The action of ARGONAUTE1 in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development. Genes Dev. 18, 1187–117 (2004). · DOI
  24. Teichmann, S.A. & Babu, M.M. Gene regulatory network growth by duplication. Nat. Genet. 36, 492–496 (2004). · DOI
  25. Rhoades, M.W. et al. Prediction of plant microRNA targets. Cell 110, 513–520 (2002). · DOI
  26. Vazquez, F., Gasciolli, V., Crete, P. & Vaucheret, H. The nuclear dsRNA binding protein HYL1 is required for microRNA accumulation and plant development, but not posttranscriptional transgene silencing. Curr. Biol. 14, 346–351 (2004). · DOI
  27. Dunoyer, P., Lecellier, C.H., Parizotto, E.A., Himber, C. & Voinnet, O. Probing the microRNA and small interfering RNA pathways with virus-encoded suppressors of RNA silencing. Plant Cell 16, 1235–1250 (2004). · DOI
  28. Llave, C., Kasschau, K.D., Rector, M.A. & Carrington, J.C. Endogenous and silencing-associated small RNAs in plants. Plant Cell 14, 1605–1619 (2002). · DOI
  29. Papp, I. et al. Evidence for nuclear processing of plant micro RNA and short interfering RNA precursors. Plant Physiol. 132, 1382–1390 (2003). · DOI
  30. Xie, Z. et al. Genetic and functional diversification of small RNA pathways in plants. PLoS Biol. 2, E104 (2004). · DOI
  31. Peragine, A., Yoshikawa, M., Wu, G., Albrecht, H.L. & Poethig, R.S. SGS3 and SGS2/SDE1/RDR6 are required for juvenile development and the production of trans-acting siRNAs in Arabidopsis . Genes Dev. 18, 2368–2379 (2004). · DOI
  32. Vazquez, F. et al. Endogenous trans-acting siRNAs regulate the accumulation of Arabidopsis mRNAs. Mol. Cell 16, 69–79 (2004). · DOI
  33. Schauer, S.E., Jacobsen, S.E., Meinke, D.W. & Ray, A. DICER-LIKE1: blind men and elephants in Arabidopsis development. Trends Plant Sci. 7, 487–491 (2002). · DOI
  34. Holder, M. & Lewis, P.O. Phylogeny estimation: traditional and Bayesian approaches. Nat. Rev. Genet. 4, 275–284 (2003). · DOI
  35. Mallory, A.C. et al. MicroRNA control of PHABULOSA in leaf development: importance of pairing to the microRNA 5′ region. EMBO J. 23, 3356–3364 (2004). · DOI
  36. Kasschau, K.D. et al. P1/HC-Pro, a viral suppressor of RNA silencing, interferes with Arabidopsis development and miRNA unction. Dev. Cell 4, 205–217 (2003). · DOI · Paper page
  37. Bartel, B. & Bartel, D.P. MicroRNAs: at the root of plant development? Plant Physiol. 132, 709–717 (2003). · DOI
  38. Llave, C., Xie, Z., Kasschau, K.D. & Carrington, J.C. Cleavage of Scarecrow-like mRNA targets directed by a class of Arabidopsis miRNA. Science 297, 2053–2056 (2002). · DOI · Paper page
  39. Herbert, A. The four Rs of RNA-directed evolution. Nat. Genet. 36, 19–25 (2004). · DOI
  40. Bartel, D.P. & Chen, C.Z. Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs. Nat. Rev. Genet. 5, 396–400 (2004). · DOI
  41. Hurles, M. Gene duplication: the genomic trade in spare parts. PLoS Biol. 2, E206 (2004). · DOI
  42. Rice, P., Longden, I. & Bleasby, A. EMBOSS: the European Molecular Biology Open Software Suite. Trends Genet. 16, 276–277 (2000). · DOI · Paper page
  43. Hofacker, I.L. Vienna RNA secondary structure server. Nucleic Acids Res. 31, 3429–3431 (2003). · DOI
  44. Lin, J.-T. Alternatives to Hamaker's approximations to the cumulative normal distribution and its inverse. Statistician 37, 413–414 (1988). · DOI
  45. Notredame, C., Higgins, D.G. & Heringa, J. T-Coffee: A novel method for fast and accurate multiple sequence alignment. J. Mol. Biol. 302, 205–217 (2000). · DOI
  46. Huelsenbeck, J.P. & Ronquist, F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17, 754–755 (2001). · DOI · Paper page
  47. Posada, D. & Crandall, K.A. MODELTEST: testing the model of DNA substitution. Bioinformatics 14, 817–818 (1998). · DOI · Paper page
  48. Swofford, D PAUP*: Phylogenetic analysis using parsimony (*and other methods) 4.0b10 edn. (Sinauer, Sunderland, Massachusetts, 2002).

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Metadata

Authors
Allen, E., Xie, Z., Gustafson, A. M., Sung, G.-H., Spatafora, J. W., & Carrington, J. C.
Venue
Nature Genetics
Published
2004-11-21
Volume
36
Issue
12
Pages
1282-1290
ISSN
  • 1061-4036
  • 1546-1718
Cited by
520
References
2
Language
en

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