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Published January 2011 | public
Journal Article

microRNA complements in deuterostomes: origin and evolution of microRNAs

Abstract

Although numerous studies have emphasized the role of microRNAs (miRNAs) in the control of many different cellular processes, they might also exert a profound effect on the macroevolution of animal body plans. It has been hypothesized that, because miRNAs increase genic precision and are continuously being added to metazoan genomes through geologic time, miRNAs might be instrumental for canalization of development and morphological evolution. Nonetheless, an outstanding question remains: how are new miRNAs constantly evolving? To address this question, we assessed the miRNA complements of four deuterostome species, chosen because of their sequenced genomes and well-resolved phylogeny. Our comparative analysis shows that each of these four species is characterized by a unique repertoire of miRNAs, with few instances of miRNA loss. Moreover, we find that almost half of the miRNAs identified in this study are located in intronic regions of protein coding genes, suggesting that new miRNAs might arise from intronic regions in a process we term intronic exaptation. We also show that miRNAs often occur within cotranscribed clusters, and describe the biological function of one of these conserved clusters, the miR-1/miR-133 cluster. Taken together, our work shows that miRNAs can easily emerge within already transcribed regions of DNA, whether it be introns or preexisting clusters of miRNAs and/or miRNAs and protein coding genes, and because of their regulatory roles, these novel players change the structure of gene regulatory networks, with potential macroevolutionary results.

Additional Information

© 2011 Wiley. Article first published online: 6 Jan 2011. The authors are indebted to John M. Lawrence at the University of South Florida in Tampa, USA, and to Vincent Laudet at the Ecole Normale Supérieure de Lyon, France, for providing laboratory space. We are grateful to Christophe Tiffoche for useful comments and to Sophie Pantalacci and two anonymous reviewers for critical reading of the manuscript. This research was supported by funds from ANR (ANR-07-BLAN-0038 and ANR-09-BLAN-0262-02) and CNRS (to Michael Schubert), and by CRESCENDO, a European Union Integrated Project of FP6 (to Michael Schubert). R. Andrew Cameron was supported by NIH R01 HD056016A. Kevin J. Peterson was supported by funds from the National Science Foundation and by NASA-Ames.

Additional details

Created:
August 19, 2023
Modified:
October 23, 2023