Birth and expression evolution of mammalian microRNA genes

  1. Henrik Kaessmann1,2,7
  1. 1Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland;
  2. 2SIB Swiss Institute of Bioinformatics, 1015 Lausanne, Switzerland;
  3. 3Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Chinese Academy of Sciences, 200031 Shanghai, China
    • Present addresses: 4GenoSplice technology, 75010 Paris, France;

    • 5 Harvard Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA;

    • 6 Broad Institute, Cambridge, Massachusetts 02142, USA.

    Abstract

    MicroRNAs (miRNAs) are major post-transcriptional regulators of gene expression, yet their origins and functional evolution in mammals remain little understood due to the lack of appropriate comparative data. Using RNA sequencing, we have generated extensive and comparable miRNA data for five organs in six species that represent all main mammalian lineages and birds (the evolutionary outgroup) with the aim to unravel the evolution of mammalian miRNAs. Our analyses reveal an overall expansion of miRNA repertoires in mammals, with threefold accelerated birth rates of miRNA families in placentals and marsupials, facilitated by the de novo emergence of miRNAs in host gene introns. Generally, our analyses suggest a high rate of miRNA family turnover in mammals with many newly emerged miRNA families being lost soon after their formation. Selectively preserved mammalian miRNA families gradually evolved higher expression levels, as well as altered mature sequences and target gene repertoires, and were apparently mainly recruited to exert regulatory functions in nervous tissues. However, miRNAs that originated on the X chromosome evolved high expression levels and potentially diverse functions during spermatogenesis, including meiosis, through selectively driven duplication-divergence processes. Overall, our study thus provides detailed insights into the birth and evolution of mammalian miRNA genes and the associated selective forces.

    Footnotes

    • 7 Corresponding authors

      E-mail Julien.Meunier{at}unil.ch

      E-mail Henrik.Kaessmann{at}unil.ch

    • [Supplemental material is available for this article.]

    • Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.140269.112.

      Freely available online through the Genome Research Open Access option.

    • Received March 7, 2012.
    • Accepted September 14, 2012.

    This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported License), as described at http://creativecommons.org/licenses/by-nc/3.0/.

    | Table of Contents
    OPEN ACCESS ARTICLE

    Preprint Server