{"title":"成年黑腹果蝇觅食基因的表达。","authors":"Aaron M Allen, Marla B Sokolowski","doi":"10.1080/01677063.2021.1941946","DOIUrl":null,"url":null,"abstract":"<p><p>The <i>foraging</i> gene in <i>Drosophila melanogaster</i>, which encodes a cGMP-dependent protein kinase, is a highly conserved, complex gene with multiple pleiotropic behavioral and physiological functions in both the larval and adult fly. Adult <i>foraging</i> expression is less well characterized than in the larva. We characterized <i>foraging</i> expression in the brain, gastric system, and reproductive systems using a <i>T2A-Gal4</i> gene-trap allele. In the brain, <i>foraging</i> expression appears to be restricted to multiple sub-types of glia. This glial-specific cellular localization of <i>foraging</i> was supported by single-cell transcriptomic atlases of the adult brain. <i>foraging</i> is extensively expressed in most cell types in the gastric and reproductive systems. We then mapped multiple <i>cis</i>-regulatory elements responsible for parts of the observed expression patterns by a nested cloned promoter-<i>Gal4</i> analysis. The mapped <i>cis</i>-regulatory elements were consistently modular when comparing the larval and adult expression patterns. These new data using the <i>T2A-Gal4</i> gene-trap and cloned <i>foraging</i> promoter fusion <i>GAL4</i>'s are discussed with respect to previous work using an anti-FOR antibody, which we show here to be non-specific. Future studies of <i>foraging</i>'s function will consider roles for glial subtypes and peripheral tissues (gastric and reproductive systems) in <i>foraging</i>'s pleiotropic behavioral and physiological effects.</p>","PeriodicalId":16491,"journal":{"name":"Journal of neurogenetics","volume":" ","pages":"192-212"},"PeriodicalIF":1.8000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846931/pdf/","citationCount":"7","resultStr":"{\"title\":\"Expression of the <i>foraging</i> gene in adult <i>Drosophila melanogaster</i>.\",\"authors\":\"Aaron M Allen, Marla B Sokolowski\",\"doi\":\"10.1080/01677063.2021.1941946\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The <i>foraging</i> gene in <i>Drosophila melanogaster</i>, which encodes a cGMP-dependent protein kinase, is a highly conserved, complex gene with multiple pleiotropic behavioral and physiological functions in both the larval and adult fly. Adult <i>foraging</i> expression is less well characterized than in the larva. We characterized <i>foraging</i> expression in the brain, gastric system, and reproductive systems using a <i>T2A-Gal4</i> gene-trap allele. In the brain, <i>foraging</i> expression appears to be restricted to multiple sub-types of glia. This glial-specific cellular localization of <i>foraging</i> was supported by single-cell transcriptomic atlases of the adult brain. <i>foraging</i> is extensively expressed in most cell types in the gastric and reproductive systems. We then mapped multiple <i>cis</i>-regulatory elements responsible for parts of the observed expression patterns by a nested cloned promoter-<i>Gal4</i> analysis. The mapped <i>cis</i>-regulatory elements were consistently modular when comparing the larval and adult expression patterns. These new data using the <i>T2A-Gal4</i> gene-trap and cloned <i>foraging</i> promoter fusion <i>GAL4</i>'s are discussed with respect to previous work using an anti-FOR antibody, which we show here to be non-specific. Future studies of <i>foraging</i>'s function will consider roles for glial subtypes and peripheral tissues (gastric and reproductive systems) in <i>foraging</i>'s pleiotropic behavioral and physiological effects.</p>\",\"PeriodicalId\":16491,\"journal\":{\"name\":\"Journal of neurogenetics\",\"volume\":\" \",\"pages\":\"192-212\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2021-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846931/pdf/\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of neurogenetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/01677063.2021.1941946\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2021/8/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of neurogenetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/01677063.2021.1941946","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2021/8/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Expression of the foraging gene in adult Drosophila melanogaster.
The foraging gene in Drosophila melanogaster, which encodes a cGMP-dependent protein kinase, is a highly conserved, complex gene with multiple pleiotropic behavioral and physiological functions in both the larval and adult fly. Adult foraging expression is less well characterized than in the larva. We characterized foraging expression in the brain, gastric system, and reproductive systems using a T2A-Gal4 gene-trap allele. In the brain, foraging expression appears to be restricted to multiple sub-types of glia. This glial-specific cellular localization of foraging was supported by single-cell transcriptomic atlases of the adult brain. foraging is extensively expressed in most cell types in the gastric and reproductive systems. We then mapped multiple cis-regulatory elements responsible for parts of the observed expression patterns by a nested cloned promoter-Gal4 analysis. The mapped cis-regulatory elements were consistently modular when comparing the larval and adult expression patterns. These new data using the T2A-Gal4 gene-trap and cloned foraging promoter fusion GAL4's are discussed with respect to previous work using an anti-FOR antibody, which we show here to be non-specific. Future studies of foraging's function will consider roles for glial subtypes and peripheral tissues (gastric and reproductive systems) in foraging's pleiotropic behavioral and physiological effects.
期刊介绍:
The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms