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A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster

Comparative genomics has enabled the identification of genes that potentially evolved de novo from non-coding sequences. Many such genes are expressed in male reproductive tissues, but their functions remain poorly understood. To address this, we conducted a functional genetic screen of over 40 puta...

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Autores principales: Rivard, Emily L., Ludwig, Andrew G., Patel, Prajal H., Grandchamp, Anna, Arnold, Sarah E., Berger, Alina, Scott, Emilie M., Kelly, Brendan J., Mascha, Grace C., Bornberg-Bauer, Erich, Findlay, Geoffrey D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445463/
https://www.ncbi.nlm.nih.gov/pubmed/34478447
http://dx.doi.org/10.1371/journal.pgen.1009787
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author Rivard, Emily L.
Ludwig, Andrew G.
Patel, Prajal H.
Grandchamp, Anna
Arnold, Sarah E.
Berger, Alina
Scott, Emilie M.
Kelly, Brendan J.
Mascha, Grace C.
Bornberg-Bauer, Erich
Findlay, Geoffrey D.
author_facet Rivard, Emily L.
Ludwig, Andrew G.
Patel, Prajal H.
Grandchamp, Anna
Arnold, Sarah E.
Berger, Alina
Scott, Emilie M.
Kelly, Brendan J.
Mascha, Grace C.
Bornberg-Bauer, Erich
Findlay, Geoffrey D.
author_sort Rivard, Emily L.
collection PubMed
description Comparative genomics has enabled the identification of genes that potentially evolved de novo from non-coding sequences. Many such genes are expressed in male reproductive tissues, but their functions remain poorly understood. To address this, we conducted a functional genetic screen of over 40 putative de novo genes with testis-enriched expression in Drosophila melanogaster and identified one gene, atlas, required for male fertility. Detailed genetic and cytological analyses showed that atlas is required for proper chromatin condensation during the final stages of spermatogenesis. Atlas protein is expressed in spermatid nuclei and facilitates the transition from histone- to protamine-based chromatin packaging. Complementary evolutionary analyses revealed the complex evolutionary history of atlas. The protein-coding portion of the gene likely arose at the base of the Drosophila genus on the X chromosome but was unlikely to be essential, as it was then lost in several independent lineages. Within the last ~15 million years, however, the gene moved to an autosome, where it fused with a conserved non-coding RNA and evolved a non-redundant role in male fertility. Altogether, this study provides insight into the integration of novel genes into biological processes, the links between genomic innovation and functional evolution, and the genetic control of a fundamental developmental process, gametogenesis.
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spelling pubmed-84454632021-09-17 A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster Rivard, Emily L. Ludwig, Andrew G. Patel, Prajal H. Grandchamp, Anna Arnold, Sarah E. Berger, Alina Scott, Emilie M. Kelly, Brendan J. Mascha, Grace C. Bornberg-Bauer, Erich Findlay, Geoffrey D. PLoS Genet Research Article Comparative genomics has enabled the identification of genes that potentially evolved de novo from non-coding sequences. Many such genes are expressed in male reproductive tissues, but their functions remain poorly understood. To address this, we conducted a functional genetic screen of over 40 putative de novo genes with testis-enriched expression in Drosophila melanogaster and identified one gene, atlas, required for male fertility. Detailed genetic and cytological analyses showed that atlas is required for proper chromatin condensation during the final stages of spermatogenesis. Atlas protein is expressed in spermatid nuclei and facilitates the transition from histone- to protamine-based chromatin packaging. Complementary evolutionary analyses revealed the complex evolutionary history of atlas. The protein-coding portion of the gene likely arose at the base of the Drosophila genus on the X chromosome but was unlikely to be essential, as it was then lost in several independent lineages. Within the last ~15 million years, however, the gene moved to an autosome, where it fused with a conserved non-coding RNA and evolved a non-redundant role in male fertility. Altogether, this study provides insight into the integration of novel genes into biological processes, the links between genomic innovation and functional evolution, and the genetic control of a fundamental developmental process, gametogenesis. Public Library of Science 2021-09-03 /pmc/articles/PMC8445463/ /pubmed/34478447 http://dx.doi.org/10.1371/journal.pgen.1009787 Text en © 2021 Rivard et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rivard, Emily L.
Ludwig, Andrew G.
Patel, Prajal H.
Grandchamp, Anna
Arnold, Sarah E.
Berger, Alina
Scott, Emilie M.
Kelly, Brendan J.
Mascha, Grace C.
Bornberg-Bauer, Erich
Findlay, Geoffrey D.
A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title_full A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title_fullStr A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title_full_unstemmed A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title_short A putative de novo evolved gene required for spermatid chromatin condensation in Drosophila melanogaster
title_sort putative de novo evolved gene required for spermatid chromatin condensation in drosophila melanogaster
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445463/
https://www.ncbi.nlm.nih.gov/pubmed/34478447
http://dx.doi.org/10.1371/journal.pgen.1009787
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