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      Germ Cell Lineage Homeostasis in Drosophila Requires the Vasa RNA Helicase

      research-article
      , 1
      Genetics
      Genetics Society of America
      vasa, Vasa helicase, Chk2, piRNA pathway, germline, oogenesis

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          Abstract

          The conserved RNA helicase Vasa is required for germ cell development in many organisms. In Drosophila melanogaster loss of PIWI-interacting RNA pathway components, including Vasa, causes Chk2-dependent oogenesis arrest. However, whether the arrest is due to Chk2 signaling at a specific stage and whether continuous Chk2 signaling is required for the arrest is unknown. Here, we show that absence of Vasa during the germarial stages causes Chk2-dependent oogenesis arrest. Additionally, we report the age-dependent decline of the ovariole number both in flies lacking Vasa expression only in the germarium and in loss-of-function vasa mutant flies. We show that Chk2 activation exclusively in the germarium is sufficient to interrupt oogenesis and to reduce ovariole number in aging flies. Once induced in the germarium, Chk2-mediated arrest of germ cell development cannot be overcome by restoration of Vasa or by downregulation of Chk2 in the arrested egg chambers. These findings, together with the identity of Vasa-associated proteins identified in this study, demonstrate an essential role of the helicase in the germ cell lineage maintenance and indicate a function of Vasa in germline stem cell homeostasis.

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          Most cited references55

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          A slicer-mediated mechanism for repeat-associated siRNA 5' end formation in Drosophila.

          In Drosophila, repeat-associated small interfering RNAs (rasiRNAs) are produced in the germ line by a Dicer-independent pathway and function through the PIWI subfamily of Argonautes to ensure silencing of retrotransposons. We sequenced small RNAs associated with the PIWI subfamily member AGO3. Although other members of PIWI, Aubergine (Aub) and Piwi, associated with rasiRNAs derived mainly from the antisense strand of retrotransposons, AGO3-associated rasiRNAs arose mainly from the sense strand. Aub- and Piwi-associated rasiRNAs showed a strong preference for uracil at their 5' ends, and AGO3-associated rasiRNAs showed a strong preference for adenine at nucleotide 10. Comparisons between AGO3- and Aub-associated rasiRNAs revealed pairs of rasiRNAs showing complementarities in their first 10 nucleotides. Aub and AGO3 exhibited Slicer activity in vitro. These data support a model in which formation of a 5' terminus within rasiRNA precursors is guided by rasiRNAs originating from transcripts of the other strand in concert with the Slicer activity of PIWI.
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            Specialized piRNA pathways act in germline and somatic tissues of the Drosophila ovary.

            In Drosophila gonads, Piwi proteins and associated piRNAs collaborate with additional factors to form a small RNA-based immune system that silences mobile elements. Here, we analyzed nine Drosophila piRNA pathway mutants for their impacts on both small RNA populations and the subcellular localization patterns of Piwi proteins. We find that distinct piRNA pathways with differing components function in ovarian germ and somatic cells. In the soma, Piwi acts singularly with the conserved flamenco piRNA cluster to enforce silencing of retroviral elements that may propagate by infecting neighboring germ cells. In the germline, silencing programs encoded within piRNA clusters are optimized via a slicer-dependent amplification loop to suppress a broad spectrum of elements. The classes of transposons targeted by germline and somatic piRNA clusters, though not the precise elements, are conserved among Drosophilids, demonstrating that the architecture of piRNA clusters has coevolved with the transposons that they are tasked to control.
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              A novel class of evolutionarily conserved genes defined by piwi are essential for stem cell self-renewal.

              Germ-line stem cells (GSCs) serve as the source for gametogenesis in diverse organisms. We cloned and characterized the Drosophila piwi gene and showed that it is required for the asymmetric division of GSCs to produce and maintain a daughter GSC but is not essential for the further differentiation of the committed daughter cell. Genetic mosaic and RNA in situ analyses suggest that piwi expression in adjacent somatic cells regulates GSC division. piwi encodes a highly basic novel protein, well conserved during evolution. We isolated piwi homologs in Caenorhabditis elegans and humans and also identified Arabidopsis piwi-like genes known to be required for meristem cell maintenance. Decreasing C. elegans piwi expression reduces the proliferation of GSC-equivalent cells. Thus, piwi represents a novel class of genes required for GSC division in diverse organisms.
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                Author and article information

                Journal
                Genetics
                Genetics
                genetics
                genetics
                genetics
                Genetics
                Genetics Society of America
                0016-6731
                1943-2631
                November 2019
                4 September 2019
                4 September 2019
                : 213
                : 3
                : 911-922
                Affiliations
                [1]Developmental Biology Unit, European Molecular Biology Laboratory, Heidelberg D-69117, Germany
                Author notes
                [1 ]Corresponding author: Developmental Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, Heidelberg D-69117, Germany. E-mail: ephrussi@ 123456embl.de
                Author information
                http://orcid.org/0000-0002-6288-7167
                http://orcid.org/0000-0002-5061-4620
                Article
                302558
                10.1534/genetics.119.302558
                6827371
                31484689
                9968ff56-1c7a-4dfc-81e6-40c2300a839e
                Copyright © 2019 Durdevic and Ephrussi

                Available freely online through the author-supported open access option.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 24 July 2019
                : 29 August 2019
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 57, Pages: 12
                Categories
                Investigations
                Developmental and Behavioral Genetics

                Genetics
                vasa,vasa helicase,chk2,pirna pathway,germline,oogenesis
                Genetics
                vasa, vasa helicase, chk2, pirna pathway, germline, oogenesis

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