Functional dissection of the neural substrates for sexual behaviors in Drosophila melanogaster
The male-specific Fruitless proteins (FruM) act to establish the potential for male courtship behavior in Drosophila melanogaster and are expressed in small groups of neurons throughout the nervous system. We screened ∼1000 GAL4 lines, using assays for general courtship, male-male interactions, and...
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creator | Meissner, Geoffrey W Manoli, Devanand S Chavez, Jose F Knapp, Jon-Michael Lin, Tasha L Stevens, Robin J Mellert, David J Tran, David H Baker, Bruce S |
description | The male-specific Fruitless proteins (FruM) act to establish the potential for male courtship behavior in Drosophila melanogaster and are expressed in small groups of neurons throughout the nervous system. We screened ∼1000 GAL4 lines, using assays for general courtship, male-male interactions, and male fertility to determine the phenotypes resulting from the GAL4-driven inhibition of FruM expression in subsets of these neurons. A battery of secondary assays showed that the phenotypic classes of GAL4 lines could be divided into subgroups on the basis of additional neurobiological and behavioral criteria. For example, in some lines, restoration of FruM expression in cholinergic neurons restores fertility or reduces male-male courtship. Persistent chains of males courting each other in some lines results from males courting both sexes indiscriminately, whereas in other lines this phenotype results from apparent habituation deficits. Inhibition of ectopic FruM expression in females, in populations of neurons where FruM is necessary for male fertility, can rescue female infertility. To identify the neurons responsible for some of the observed behavioral alterations, we determined the overlap between the identified GAL4 lines and endogenous FruM expression in lines with fertility defects. The GAL4 lines causing fertility defects generally had widespread overlap with FruM expression in many regions of the nervous system, suggesting likely redundant FruM-expressing neuronal pathways capable of conferring male fertility. From associations between the screened behaviors, we propose a functional model for courtship initiation. |
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We screened ∼1000 GAL4 lines, using assays for general courtship, male-male interactions, and male fertility to determine the phenotypes resulting from the GAL4-driven inhibition of FruM expression in subsets of these neurons. A battery of secondary assays showed that the phenotypic classes of GAL4 lines could be divided into subgroups on the basis of additional neurobiological and behavioral criteria. For example, in some lines, restoration of FruM expression in cholinergic neurons restores fertility or reduces male-male courtship. Persistent chains of males courting each other in some lines results from males courting both sexes indiscriminately, whereas in other lines this phenotype results from apparent habituation deficits. Inhibition of ectopic FruM expression in females, in populations of neurons where FruM is necessary for male fertility, can rescue female infertility. To identify the neurons responsible for some of the observed behavioral alterations, we determined the overlap between the identified GAL4 lines and endogenous FruM expression in lines with fertility defects. The GAL4 lines causing fertility defects generally had widespread overlap with FruM expression in many regions of the nervous system, suggesting likely redundant FruM-expressing neuronal pathways capable of conferring male fertility. From associations between the screened behaviors, we propose a functional model for courtship initiation.</description><identifier>ISSN: 1943-2631</identifier><identifier>ISSN: 0016-6731</identifier><identifier>EISSN: 1943-2631</identifier><identifier>DOI: 10.1534/genetics.111.129940</identifier><identifier>PMID: 21705753</identifier><identifier>CODEN: GENTAE</identifier><language>eng</language><publisher>United States: Genetics Society of America</publisher><subject>Animal reproduction ; Animals ; Cholinergic Neurons - metabolism ; Courtship ; Drosophila melanogaster - genetics ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Female ; Females ; Fertility - genetics ; Gene Expression Regulation ; High-Throughput Screening Assays ; Investigations ; Male ; Males ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Nervous system ; Phenotype ; Sexual Behavior, Animal ; Studies ; Transcription Factors - genetics ; Transcription Factors - metabolism</subject><ispartof>Genetics (Austin), 2011-09, Vol.189 (1), p.195-211</ispartof><rights>Copyright Genetics Society of America Sep 2011</rights><rights>Copyright © 2011 by the Genetics Society of America 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-308589942b972848b8eeddde5e4ebb90943fc236be0a00b478a444aeb7ebc9553</citedby><cites>FETCH-LOGICAL-c431t-308589942b972848b8eeddde5e4ebb90943fc236be0a00b478a444aeb7ebc9553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21705753$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meissner, Geoffrey W</creatorcontrib><creatorcontrib>Manoli, Devanand S</creatorcontrib><creatorcontrib>Chavez, Jose F</creatorcontrib><creatorcontrib>Knapp, Jon-Michael</creatorcontrib><creatorcontrib>Lin, Tasha L</creatorcontrib><creatorcontrib>Stevens, Robin J</creatorcontrib><creatorcontrib>Mellert, David J</creatorcontrib><creatorcontrib>Tran, David H</creatorcontrib><creatorcontrib>Baker, Bruce S</creatorcontrib><title>Functional dissection of the neural substrates for sexual behaviors in Drosophila melanogaster</title><title>Genetics (Austin)</title><addtitle>Genetics</addtitle><description>The male-specific Fruitless proteins (FruM) act to establish the potential for male courtship behavior in Drosophila melanogaster and are expressed in small groups of neurons throughout the nervous system. We screened ∼1000 GAL4 lines, using assays for general courtship, male-male interactions, and male fertility to determine the phenotypes resulting from the GAL4-driven inhibition of FruM expression in subsets of these neurons. A battery of secondary assays showed that the phenotypic classes of GAL4 lines could be divided into subgroups on the basis of additional neurobiological and behavioral criteria. For example, in some lines, restoration of FruM expression in cholinergic neurons restores fertility or reduces male-male courtship. Persistent chains of males courting each other in some lines results from males courting both sexes indiscriminately, whereas in other lines this phenotype results from apparent habituation deficits. Inhibition of ectopic FruM expression in females, in populations of neurons where FruM is necessary for male fertility, can rescue female infertility. To identify the neurons responsible for some of the observed behavioral alterations, we determined the overlap between the identified GAL4 lines and endogenous FruM expression in lines with fertility defects. The GAL4 lines causing fertility defects generally had widespread overlap with FruM expression in many regions of the nervous system, suggesting likely redundant FruM-expressing neuronal pathways capable of conferring male fertility. From associations between the screened behaviors, we propose a functional model for courtship initiation.</description><subject>Animal reproduction</subject><subject>Animals</subject><subject>Cholinergic Neurons - metabolism</subject><subject>Courtship</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Female</subject><subject>Females</subject><subject>Fertility - genetics</subject><subject>Gene Expression Regulation</subject><subject>High-Throughput Screening Assays</subject><subject>Investigations</subject><subject>Male</subject><subject>Males</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Nervous system</subject><subject>Phenotype</subject><subject>Sexual Behavior, Animal</subject><subject>Studies</subject><subject>Transcription Factors - 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metabolism</topic><topic>Courtship</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Female</topic><topic>Females</topic><topic>Fertility - genetics</topic><topic>Gene Expression Regulation</topic><topic>High-Throughput Screening Assays</topic><topic>Investigations</topic><topic>Male</topic><topic>Males</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Nervous system</topic><topic>Phenotype</topic><topic>Sexual Behavior, Animal</topic><topic>Studies</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meissner, Geoffrey W</creatorcontrib><creatorcontrib>Manoli, Devanand S</creatorcontrib><creatorcontrib>Chavez, Jose F</creatorcontrib><creatorcontrib>Knapp, Jon-Michael</creatorcontrib><creatorcontrib>Lin, Tasha L</creatorcontrib><creatorcontrib>Stevens, Robin J</creatorcontrib><creatorcontrib>Mellert, David J</creatorcontrib><creatorcontrib>Tran, David H</creatorcontrib><creatorcontrib>Baker, Bruce S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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>Research Library (Alumni Edition)</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>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>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genetics (Austin)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meissner, Geoffrey W</au><au>Manoli, Devanand S</au><au>Chavez, Jose F</au><au>Knapp, Jon-Michael</au><au>Lin, Tasha L</au><au>Stevens, Robin J</au><au>Mellert, David J</au><au>Tran, David H</au><au>Baker, Bruce S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional dissection of the neural substrates for sexual behaviors in Drosophila melanogaster</atitle><jtitle>Genetics (Austin)</jtitle><addtitle>Genetics</addtitle><date>2011-09</date><risdate>2011</risdate><volume>189</volume><issue>1</issue><spage>195</spage><epage>211</epage><pages>195-211</pages><issn>1943-2631</issn><issn>0016-6731</issn><eissn>1943-2631</eissn><coden>GENTAE</coden><abstract>The male-specific Fruitless proteins (FruM) act to establish the potential for male courtship behavior in Drosophila melanogaster and are expressed in small groups of neurons throughout the nervous system. We screened ∼1000 GAL4 lines, using assays for general courtship, male-male interactions, and male fertility to determine the phenotypes resulting from the GAL4-driven inhibition of FruM expression in subsets of these neurons. A battery of secondary assays showed that the phenotypic classes of GAL4 lines could be divided into subgroups on the basis of additional neurobiological and behavioral criteria. For example, in some lines, restoration of FruM expression in cholinergic neurons restores fertility or reduces male-male courtship. Persistent chains of males courting each other in some lines results from males courting both sexes indiscriminately, whereas in other lines this phenotype results from apparent habituation deficits. Inhibition of ectopic FruM expression in females, in populations of neurons where FruM is necessary for male fertility, can rescue female infertility. To identify the neurons responsible for some of the observed behavioral alterations, we determined the overlap between the identified GAL4 lines and endogenous FruM expression in lines with fertility defects. The GAL4 lines causing fertility defects generally had widespread overlap with FruM expression in many regions of the nervous system, suggesting likely redundant FruM-expressing neuronal pathways capable of conferring male fertility. From associations between the screened behaviors, we propose a functional model for courtship initiation.</abstract><cop>United States</cop><pub>Genetics Society of America</pub><pmid>21705753</pmid><doi>10.1534/genetics.111.129940</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal reproduction Animals Cholinergic Neurons - metabolism Courtship Drosophila melanogaster - genetics Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Female Females Fertility - genetics Gene Expression Regulation High-Throughput Screening Assays Investigations Male Males Nerve Tissue Proteins - genetics Nerve Tissue Proteins - metabolism Nervous system Phenotype Sexual Behavior, Animal Studies Transcription Factors - genetics Transcription Factors - metabolism |
title | Functional dissection of the neural substrates for sexual behaviors in Drosophila melanogaster |
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