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      A sex-ratio Meiotic Drive System in Drosophila simulans. I: An Autosomal Suppressor

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          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Sex ratio distortion ( sex-ratio for short) has been reported in numerous species such as Drosophila, where distortion can readily be detected in experimental crosses, but the molecular mechanisms remain elusive. Here we characterize an autosomal sex-ratio suppressor from D. simulans that we designate as not much yang ( nmy, polytene chromosome position 87F3). Nmy suppresses an X-linked sex-ratio distorter, contains a pair of near-perfect inverted repeats of 345 bp, and evidently originated through retrotransposition from the distorter itself. The suppression is likely mediated by sequence homology between the suppressor and distorter. The strength of sex-ratio is greatly enhanced by lower temperature. This temperature sensitivity was used to assign the sex-ratio etiology to the maturation process of the Y-bearing sperm, a hypothesis corroborated by both light microscope observations and ultrastructural studies. It has long been suggested that an X-linked sex-ratio distorter can evolve by exploiting loopholes in the meiotic machinery for its own transmission advantage, which may be offset by other changes in the genome that control the selfish distorter. Data obtained in this study help to understand this evolutionary mechanism in molecular detail and provide insight regarding its evolutionary impact on genomic architecture and speciation.

          Author Summary

          Genetic conflicts among genes happen when their modes of transmission differ. Genes in the heterogametic (XY) sex can be grouped as X-linked, Y-linked, autosomal, or cytoplasmic. Sex ratio in the progeny greatly affects the transmission advantage of each of the four types of genes, with the optimal sex ratio for each type being respectively 100%, 0%, 50%, and 100% of females. Sex ratio can often be biased from the normal 50% by genes that distort the sex ratio toward their own optimal transmission. Here we report genetic and molecular characterization of an autosomal gene that functions as a suppressor of an X-linked sex-ratio distorter. Male mutants give rise to female-biased progeny. The cause of the distortion was assigned to a failure of the Y-bearing sperm to mature. The DNA sequence of the suppressor gives clues to understanding the sex-ratio meiotic drive at the molecular level. More generally, the genetic conflict over sex ratio may be important in determining the evolutionary dynamics and the architecture of eukaryotic genomes.

          Abstract

          Autosomal genes defend faithful Mendelian segregation by suppressing sex-ratio distorters on the X chromosome. The molecular mechanisms of this kind of genomic policing have begun to be elucidated.

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          Most cited references99

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          Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: a mechanism for non-LTR retrotransposition.

          R2 is a non-LTR retrotransposable element that inserts at a specific site in the 28S rRNA genes of most insects. We have expressed the open reading frame of the R2 element from Bombyx mori, R2Bm, in E. coli and shown that it encodes both sequence-specific endonuclease and reverse transcriptase activities. The R2 protein makes a specific nick in one of the DNA strands at the insertion site and uses the 3' hydroxyl group exposed by this nick to prime reverse transcription of its RNA transcript. After reverse transcription, cleavage of the second DNA strand occurs. A similar mechanism of insertion may be used by other non-LTR retrotransposable elements as well as short interspersed nucleotide elements.
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            Human LINE retrotransposons generate processed pseudogenes.

            Long interspersed elements (LINEs) are endogenous mobile genetic elements that have dispersed and accumulated in the genomes of higher eukaryotes via germline transposition, with up to 100,000 copies in mammalian genomes. In humans, LINEs are the major source of insertional mutagenesis, being involved in both germinal and somatic mutant phenotypes. Here we show that the human LINE retrotransposons, which transpose through the reverse transcription of their own transcript, can also mobilize transcribed DNA not associated with a LINE sequence by a process involving the diversion of the LINE enzymatic machinery by the corresponding mRNA transcripts. This results in the 'retroposition' of the transcribed gene and the formation of new copies that disclose features characteristic of the widespread and naturally occurring processed pseudogenes: loss of intron and promoter, acquisition of a poly(A) 3' end and presence of target-site duplications of varying length. We further show-by introducing deletions within either coding sequence of the human LINE-that both ORFs are necessary for the formation of the processed pseudogenes, and that retroviral-like elements are not able to produce similar structures in the same assay. Our results strengthen the unique versatility of LINEs as genome modellers.
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              Extraordinary sex ratios. A sex-ratio theory for sex linkage and inbreeding has new implications in cytogenetics and entomology.

              W Hamilton (1967)
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                PLoS Biol
                pbio
                plbi
                plosbiol
                PLoS Biology
                Public Library of Science (San Francisco, USA )
                1544-9173
                1545-7885
                November 2007
                6 November 2007
                : 5
                : 11
                : e292
                Affiliations
                [1 ] Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts, United States of America
                [2 ] Department of Biology, Emory University, Atlanta, Georgia, United States of America
                [3 ] Department of Biology, University of Rochester, Rochester, New York, United States of America
                Cornell University, United States of America
                Author notes
                * To whom correspondence should be addressed. E-mail: ytao3@ 123456emory.edu
                Article
                07-PLBI-RA-0951R3 plbi-05-11-09
                10.1371/journal.pbio.0050292
                2062475
                17988172
                bc00a6dc-3cff-4c67-a8e9-54c22c47652d
                Copyright: © 2007 Tao et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 12 April 2007
                : 17 September 2007
                Page count
                Pages: 16
                Categories
                Research Article
                Developmental Biology
                Evolutionary Biology
                Genetics and Genomics
                Molecular Biology
                Custom metadata
                Tao Y, Masly JP, Araripe L, Ke Y, Hartl DL (2007) A s ex-ratio meiotic drive system in Drosophila simulans. I: An autosomal suppressor. PLoS Biol 5(11): e292. doi: 10.1371/journal.pbio.0050292

                Life sciences
                Life sciences

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