Sperm-storage defects and live birth in Drosophila females lacking spermathecal secretory cells
Male Drosophila flies secrete seminal-fluid proteins that mediate proper sperm storage and fertilization, and that induce changes in female behavior. Females also produce reproductive-tract secretions, yet their contributions to postmating physiology are poorly understood. Large secretory cells line...
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description | Male Drosophila flies secrete seminal-fluid proteins that mediate proper sperm storage and fertilization, and that induce changes in female behavior. Females also produce reproductive-tract secretions, yet their contributions to postmating physiology are poorly understood. Large secretory cells line the female's spermathecae, a pair of sperm-storage organs. We identified the regulatory regions controlling transcription of two genes exclusively expressed in these spermathecal secretory cells (SSC): Spermathecal endopeptidase 1 (Send1), which is expressed in both unmated and mated females, and Spermathecal endopeptidase 2 (Send2), which is induced by mating. We used these regulatory sequences to perform precise genetic ablations of the SSC at distinct time points relative to mating. We show that the SSC are required for recruiting sperm to the spermathecae, but not for retaining sperm there. The SSC also act at a distance in the reproductive tract, in that their ablation: (1) reduces sperm motility in the female's other sperm-storage organ, the seminal receptacle; and (2) causes ovoviviparity--the retention and internal development of fertilized eggs. These results establish the reproductive functions of the SSC, shed light on the evolution of live birth, and open new avenues for studying and manipulating female fertility in insects. |
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Females also produce reproductive-tract secretions, yet their contributions to postmating physiology are poorly understood. Large secretory cells line the female's spermathecae, a pair of sperm-storage organs. We identified the regulatory regions controlling transcription of two genes exclusively expressed in these spermathecal secretory cells (SSC): Spermathecal endopeptidase 1 (Send1), which is expressed in both unmated and mated females, and Spermathecal endopeptidase 2 (Send2), which is induced by mating. We used these regulatory sequences to perform precise genetic ablations of the SSC at distinct time points relative to mating. We show that the SSC are required for recruiting sperm to the spermathecae, but not for retaining sperm there. The SSC also act at a distance in the reproductive tract, in that their ablation: (1) reduces sperm motility in the female's other sperm-storage organ, the seminal receptacle; and (2) causes ovoviviparity--the retention and internal development of fertilized eggs. These results establish the reproductive functions of the SSC, shed light on the evolution of live birth, and open new avenues for studying and manipulating female fertility in insects.</description><identifier>ISSN: 1545-7885</identifier><identifier>ISSN: 1544-9173</identifier><identifier>EISSN: 1545-7885</identifier><identifier>DOI: 10.1371/journal.pbio.1001192</identifier><identifier>PMID: 22087073</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Anatomy & physiology ; Animal reproduction ; Animals ; Biology ; Drosophila ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Embryos ; Evolution ; Experiments ; Female ; Females ; Fertilization (Biology) ; Genetic aspects ; Insects ; Male ; Microscopy ; Motility ; Physiological aspects ; Proteins ; Reproduction - genetics ; Reproduction - physiology ; Sperm ; Sperm Motility - genetics ; Sperm Motility - physiology ; Spermatozoa ; Spermatozoa - metabolism ; Spermatozoa - physiology</subject><ispartof>PLoS biology, 2011-11, Vol.9 (11), p.e1001192-e1001192</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Schnakenberg 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: Schnakenberg SL, Matias WR, Siegal ML (2011) Sperm-Storage Defects and Live Birth in Drosophila Females Lacking Spermathecal Secretory Cells. 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Females also produce reproductive-tract secretions, yet their contributions to postmating physiology are poorly understood. Large secretory cells line the female's spermathecae, a pair of sperm-storage organs. We identified the regulatory regions controlling transcription of two genes exclusively expressed in these spermathecal secretory cells (SSC): Spermathecal endopeptidase 1 (Send1), which is expressed in both unmated and mated females, and Spermathecal endopeptidase 2 (Send2), which is induced by mating. We used these regulatory sequences to perform precise genetic ablations of the SSC at distinct time points relative to mating. We show that the SSC are required for recruiting sperm to the spermathecae, but not for retaining sperm there. The SSC also act at a distance in the reproductive tract, in that their ablation: (1) reduces sperm motility in the female's other sperm-storage organ, the seminal receptacle; and (2) causes ovoviviparity--the retention and internal development of fertilized eggs. These results establish the reproductive functions of the SSC, shed light on the evolution of live birth, and open new avenues for studying and manipulating female fertility in insects.</description><subject>Anatomy & physiology</subject><subject>Animal reproduction</subject><subject>Animals</subject><subject>Biology</subject><subject>Drosophila</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Embryos</subject><subject>Evolution</subject><subject>Experiments</subject><subject>Female</subject><subject>Females</subject><subject>Fertilization (Biology)</subject><subject>Genetic aspects</subject><subject>Insects</subject><subject>Male</subject><subject>Microscopy</subject><subject>Motility</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Reproduction - genetics</subject><subject>Reproduction - physiology</subject><subject>Sperm</subject><subject>Sperm Motility - genetics</subject><subject>Sperm Motility - 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genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Embryos</topic><topic>Evolution</topic><topic>Experiments</topic><topic>Female</topic><topic>Females</topic><topic>Fertilization (Biology)</topic><topic>Genetic aspects</topic><topic>Insects</topic><topic>Male</topic><topic>Microscopy</topic><topic>Motility</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Reproduction - genetics</topic><topic>Reproduction - physiology</topic><topic>Sperm</topic><topic>Sperm Motility - genetics</topic><topic>Sperm Motility - physiology</topic><topic>Spermatozoa</topic><topic>Spermatozoa - metabolism</topic><topic>Spermatozoa - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schnakenberg, Sandra L</creatorcontrib><creatorcontrib>Matias, Wilfredo R</creatorcontrib><creatorcontrib>Siegal, Mark L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><collection>PLoS Biology</collection><jtitle>PLoS biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schnakenberg, Sandra L</au><au>Matias, Wilfredo R</au><au>Siegal, Mark L</au><au>Wolfner, Mariana Federica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sperm-storage defects and live birth in Drosophila females lacking spermathecal secretory cells</atitle><jtitle>PLoS biology</jtitle><addtitle>PLoS Biol</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>9</volume><issue>11</issue><spage>e1001192</spage><epage>e1001192</epage><pages>e1001192-e1001192</pages><issn>1545-7885</issn><issn>1544-9173</issn><eissn>1545-7885</eissn><abstract>Male Drosophila flies secrete seminal-fluid proteins that mediate proper sperm storage and fertilization, and that induce changes in female behavior. Females also produce reproductive-tract secretions, yet their contributions to postmating physiology are poorly understood. Large secretory cells line the female's spermathecae, a pair of sperm-storage organs. We identified the regulatory regions controlling transcription of two genes exclusively expressed in these spermathecal secretory cells (SSC): Spermathecal endopeptidase 1 (Send1), which is expressed in both unmated and mated females, and Spermathecal endopeptidase 2 (Send2), which is induced by mating. We used these regulatory sequences to perform precise genetic ablations of the SSC at distinct time points relative to mating. We show that the SSC are required for recruiting sperm to the spermathecae, but not for retaining sperm there. The SSC also act at a distance in the reproductive tract, in that their ablation: (1) reduces sperm motility in the female's other sperm-storage organ, the seminal receptacle; and (2) causes ovoviviparity--the retention and internal development of fertilized eggs. These results establish the reproductive functions of the SSC, shed light on the evolution of live birth, and open new avenues for studying and manipulating female fertility in insects.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22087073</pmid><doi>10.1371/journal.pbio.1001192</doi><oa>free_for_read</oa></addata></record> |
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subjects | Anatomy & physiology Animal reproduction Animals Biology Drosophila Drosophila Proteins - genetics Drosophila Proteins - metabolism Embryos Evolution Experiments Female Females Fertilization (Biology) Genetic aspects Insects Male Microscopy Motility Physiological aspects Proteins Reproduction - genetics Reproduction - physiology Sperm Sperm Motility - genetics Sperm Motility - physiology Spermatozoa Spermatozoa - metabolism Spermatozoa - physiology |
title | Sperm-storage defects and live birth in Drosophila females lacking spermathecal secretory cells |
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