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      Testis single-cell RNA-seq reveals the dynamics of de novo gene transcription and germline mutational bias in Drosophila

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          Abstract

          The testis is a peculiar tissue in many respects. It shows patterns of rapid gene evolution and provides a hotspot for the origination of genetic novelties such as de novo genes, duplications and mutations. To investigate the expression patterns of genetic novelties across cell types, we performed single-cell RNA-sequencing of adult Drosophila testis. We found that new genes were expressed in various cell types, the patterns of which may be influenced by their mode of origination. In particular, lineage-specific de novo genes are commonly expressed in early spermatocytes, while young duplicated genes are often bimodally expressed. Analysis of germline substitutions suggests that spermatogenesis is a highly reparative process, with the mutational load of germ cells decreasing as spermatogenesis progresses. By elucidating the distribution of genetic novelties across spermatogenesis, this study provides a deeper understanding of how the testis maintains its core reproductive function while being a hotbed of evolutionary innovation.

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            Models of speciation by sexual selection on polygenic traits

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              Origins, evolution, and phenotypic impact of new genes.

              Ever since the pre-molecular era, the birth of new genes with novel functions has been considered to be a major contributor to adaptive evolutionary innovation. Here, I review the origin and evolution of new genes and their functions in eukaryotes, an area of research that has made rapid progress in the past decade thanks to the genomics revolution. Indeed, recent work has provided initial whole-genome views of the different types of new genes for a large number of different organisms. The array of mechanisms underlying the origin of new genes is compelling, extending way beyond the traditionally well-studied source of gene duplication. Thus, it was shown that novel genes also regularly arose from messenger RNAs of ancestral genes, protein-coding genes metamorphosed into new RNA genes, genomic parasites were co-opted as new genes, and that both protein and RNA genes were composed from scratch (i.e., from previously nonfunctional sequences). These mechanisms then also contributed to the formation of numerous novel chimeric gene structures. Detailed functional investigations uncovered different evolutionary pathways that led to the emergence of novel functions from these newly minted sequences and, with respect to animals, attributed a potentially important role to one specific tissue--the testis--in the process of gene birth. Remarkably, these studies also demonstrated that novel genes of the various types significantly impacted the evolution of cellular, physiological, morphological, behavioral, and reproductive phenotypic traits. Consequently, it is now firmly established that new genes have indeed been major contributors to the origin of adaptive evolutionary novelties.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                16 August 2019
                2019
                : 8
                : e47138
                Affiliations
                [1]deptLaboratory of Evolutionary Genetics and Genomics The Rockefeller University New YorkUnited States
                Université Laval Canada
                University of Michigan United States
                Université Laval Canada
                Cardiff University United Kingdom
                Author information
                https://orcid.org/0000-0003-2973-6946
                https://orcid.org/0000-0002-6411-5339
                https://orcid.org/0000-0001-9617-2752
                https://orcid.org/0000-0001-6776-1996
                Article
                47138
                10.7554/eLife.47138
                6697446
                31418408
                3029729f-c31a-46fd-8b3e-4753fab60056
                © 2019, Witt et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 25 March 2019
                : 06 July 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100013961, Robertson Foundation;
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100011331, Monique Weill-Caulier Trust;
                Award ID: Monique Weill-Caulier Career Scientist Award
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000879, Alfred P. Sloan Foundation;
                Award ID: Research Fellowship
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Evolutionary Biology
                Genetics and Genomics
                Custom metadata
                Single-cell RNA-sequencing and germline substitutions provide novel insights into how testis is a hotspot for evolutionary innovation of genes, expression, and mutation at the single-cell level.

                Life sciences
                de novo gene,mutational load,single-cell sequencing,expression dynamics,drosophila,spermatogenesis,d. melanogaster

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