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bric à brac (bab), a central player in the gene regulatory network that mediates thermal plasticity of pigmentation in Drosophila melanogaster
Drosophila body pigmentation has emerged as a major Evo-Devo model. Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation vari...
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Published in: | PLoS genetics 2018-08, Vol.14 (8), p.e1007573-e1007573 |
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description | Drosophila body pigmentation has emerged as a major Evo-Devo model. Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation varies with genotype in natural populations and is sensitive to temperature during development. We demonstrate that the bric à brac (bab) genes, that are differentially expressed between the two lines and whose expression levels vary with temperature, participate in the pigmentation difference between the Dark and Pale lines. The two lines differ in a bab regulatory sequence, the dimorphic element (called here bDE). Both bDE alleles are temperature-sensitive, but the activity of the bDE allele from the Dark line is lower than that of the bDE allele from the Pale line. Our results suggest that this difference could partly be due to differential regulation by AbdB. bab has been previously reported to be a repressor of abdominal pigmentation. We show here that one of its targets in this process is the pigmentation gene tan (t), regulated via the tan abdominal enhancer (t_MSE). Furthermore, t expression is strongly modulated by temperature in the two lines. Thus, temperature sensitivity of t expression is at least partly a consequence of bab thermal transcriptional plasticity. We therefore propose that a gene regulatory network integrating both genetic variation and temperature sensitivity modulates female abdominal pigmentation. Interestingly, both bDE and t_MSE were previously shown to have been recurrently involved in abdominal pigmentation evolution in drosophilids. We propose that the environmental sensitivity of these enhancers has turned them into evolutionary hotspots. |
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Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation varies with genotype in natural populations and is sensitive to temperature during development. We demonstrate that the bric à brac (bab) genes, that are differentially expressed between the two lines and whose expression levels vary with temperature, participate in the pigmentation difference between the Dark and Pale lines. The two lines differ in a bab regulatory sequence, the dimorphic element (called here bDE). Both bDE alleles are temperature-sensitive, but the activity of the bDE allele from the Dark line is lower than that of the bDE allele from the Pale line. Our results suggest that this difference could partly be due to differential regulation by AbdB. bab has been previously reported to be a repressor of abdominal pigmentation. We show here that one of its targets in this process is the pigmentation gene tan (t), regulated via the tan abdominal enhancer (t_MSE). Furthermore, t expression is strongly modulated by temperature in the two lines. Thus, temperature sensitivity of t expression is at least partly a consequence of bab thermal transcriptional plasticity. We therefore propose that a gene regulatory network integrating both genetic variation and temperature sensitivity modulates female abdominal pigmentation. Interestingly, both bDE and t_MSE were previously shown to have been recurrently involved in abdominal pigmentation evolution in drosophilids. We propose that the environmental sensitivity of these enhancers has turned them into evolutionary hotspots.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1007573</identifier><identifier>PMID: 30067846</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abdomen ; Alleles ; Animals ; Assimilation ; Base Sequence ; Binding Sites ; Biology and Life Sciences ; Chromosomal Proteins, Non-Histone - genetics ; Chromosomal Proteins, Non-Histone - physiology ; Developmental biology ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - physiology ; Drosophila melanogaster ; Drosophila melanogaster - genetics ; Drosophila Proteins - genetics ; Drosophila Proteins - physiology ; Enhancers ; Environmental factors ; Epigenetics ; Evolution & development ; Evolution, Molecular ; Female ; Females ; Gene Expression Regulation ; Gene Regulatory Networks ; Genes ; Genetic analysis ; Genetic diversity ; Genetic Variation ; Genomes ; Genomics ; Genotypes ; Genotyping Techniques ; Homeostasis ; Hypotheses ; Insects ; Life Sciences ; Medicine and Health Sciences ; Morphology ; Mutation ; Nutrition research ; Pigmentation ; Pigmentation - genetics ; Plasticity ; Ponds ; Regulatory sequences ; Research and Analysis Methods ; Sequence Analysis, DNA ; Studies ; Temperature ; Temperature effects ; Transcription ; Transcription Factors - genetics ; Transcription Factors - physiology</subject><ispartof>PLoS genetics, 2018-08, Vol.14 (8), p.e1007573-e1007573</ispartof><rights>2018 De Castro et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation varies with genotype in natural populations and is sensitive to temperature during development. We demonstrate that the bric à brac (bab) genes, that are differentially expressed between the two lines and whose expression levels vary with temperature, participate in the pigmentation difference between the Dark and Pale lines. The two lines differ in a bab regulatory sequence, the dimorphic element (called here bDE). Both bDE alleles are temperature-sensitive, but the activity of the bDE allele from the Dark line is lower than that of the bDE allele from the Pale line. Our results suggest that this difference could partly be due to differential regulation by AbdB. bab has been previously reported to be a repressor of abdominal pigmentation. We show here that one of its targets in this process is the pigmentation gene tan (t), regulated via the tan abdominal enhancer (t_MSE). Furthermore, t expression is strongly modulated by temperature in the two lines. Thus, temperature sensitivity of t expression is at least partly a consequence of bab thermal transcriptional plasticity. We therefore propose that a gene regulatory network integrating both genetic variation and temperature sensitivity modulates female abdominal pigmentation. Interestingly, both bDE and t_MSE were previously shown to have been recurrently involved in abdominal pigmentation evolution in drosophilids. We propose that the environmental sensitivity of these enhancers has turned them into evolutionary hotspots.</description><subject>Abdomen</subject><subject>Alleles</subject><subject>Animals</subject><subject>Assimilation</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Biology and Life Sciences</subject><subject>Chromosomal Proteins, Non-Histone - genetics</subject><subject>Chromosomal Proteins, Non-Histone - physiology</subject><subject>Developmental biology</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - physiology</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - physiology</subject><subject>Enhancers</subject><subject>Environmental factors</subject><subject>Epigenetics</subject><subject>Evolution & development</subject><subject>Evolution, Molecular</subject><subject>Female</subject><subject>Females</subject><subject>Gene Expression Regulation</subject><subject>Gene Regulatory Networks</subject><subject>Genes</subject><subject>Genetic analysis</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Genotypes</subject><subject>Genotyping Techniques</subject><subject>Homeostasis</subject><subject>Hypotheses</subject><subject>Insects</subject><subject>Life Sciences</subject><subject>Medicine and Health Sciences</subject><subject>Morphology</subject><subject>Mutation</subject><subject>Nutrition research</subject><subject>Pigmentation</subject><subject>Pigmentation - genetics</subject><subject>Plasticity</subject><subject>Ponds</subject><subject>Regulatory sequences</subject><subject>Research and Analysis Methods</subject><subject>Sequence Analysis, DNA</subject><subject>Studies</subject><subject>Temperature</subject><subject>Temperature effects</subject><subject>Transcription</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - physiology</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUt1uFCEYnRiNratvYJTEmzZxV2CAmbkxaepPmzTxRq8JMB-zrLPDCGzNPoWv4Lv4YjLutGkbb4B8nHM-vsMpipcEr0hZkXcbvwuD6ldjB8OKYFzxqnxUHBPOy2XFMHt853xUPItxg3HJ66Z6WhyVGIuqZuK4-KWDM-jPb6SDMuhEK336FilkYEhB9Wjs1R4CcgNKa0C5E6AA3a5XyYc9GiD99OF7vlMJbaF1KkGckGF74MbkjEt75C0aXbfNoio5P0x6H4KPfly7XmVmrwbfZTSE58UTq_oIL-Z9UXz79PHr-cXy6svny_Ozq6XhAqclK0lb86YSBEDXlOqSCFMyRetasVZXYExrQYtGABXGCgNWCWtbTSwzHNtyUbw-6I69j3L2MkpKORaCYcoz4vKAaL3ayDG4rQp76ZWT_wo-dFKFPF8P0tCmyu_BIKhm1GqthbbAGeXAAQzLWu_nbjudfZrdvSd6_2Zwa9n5aylw3TA-CZweBNYPaBdnV3KqYVJXIi_XJGNP5mbB_9hBTHLrooE-mwx-l2fENcVNiXNeFsWbB9D_O8EOKJP_LAawty8gWE5ZvGHJKYtyzmKmvbo79C3pJnzlXz8l4Lk</recordid><startdate>201808</startdate><enddate>201808</enddate><creator>De Castro, Sandra</creator><creator>Peronnet, Frédérique</creator><creator>Gilles, Jean-François</creator><creator>Mouchel-Vielh, Emmanuèle</creator><creator>Gibert, Jean-Michel</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1579-0266</orcidid><orcidid>https://orcid.org/0000-0003-1354-240X</orcidid><orcidid>https://orcid.org/0000-0001-9428-5243</orcidid></search><sort><creationdate>201808</creationdate><title>bric à brac (bab), a central player in the gene regulatory network that mediates thermal plasticity of pigmentation in Drosophila melanogaster</title><author>De Castro, Sandra ; Peronnet, Frédérique ; Gilles, Jean-François ; Mouchel-Vielh, Emmanuèle ; Gibert, Jean-Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-431d859761eeb822b316c34a288a4db7eccdfeb696e26cf6cefa6ffdb1f4c50f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Abdomen</topic><topic>Alleles</topic><topic>Animals</topic><topic>Assimilation</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Biology and Life Sciences</topic><topic>Chromosomal Proteins, Non-Histone - genetics</topic><topic>Chromosomal Proteins, Non-Histone - physiology</topic><topic>Developmental biology</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - physiology</topic><topic>Drosophila melanogaster</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - physiology</topic><topic>Enhancers</topic><topic>Environmental factors</topic><topic>Epigenetics</topic><topic>Evolution & development</topic><topic>Evolution, Molecular</topic><topic>Female</topic><topic>Females</topic><topic>Gene Expression Regulation</topic><topic>Gene Regulatory Networks</topic><topic>Genes</topic><topic>Genetic analysis</topic><topic>Genetic diversity</topic><topic>Genetic Variation</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Genotypes</topic><topic>Genotyping Techniques</topic><topic>Homeostasis</topic><topic>Hypotheses</topic><topic>Insects</topic><topic>Life Sciences</topic><topic>Medicine and Health Sciences</topic><topic>Morphology</topic><topic>Mutation</topic><topic>Nutrition research</topic><topic>Pigmentation</topic><topic>Pigmentation - genetics</topic><topic>Plasticity</topic><topic>Ponds</topic><topic>Regulatory sequences</topic><topic>Research and Analysis Methods</topic><topic>Sequence Analysis, DNA</topic><topic>Studies</topic><topic>Temperature</topic><topic>Temperature effects</topic><topic>Transcription</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Castro, Sandra</creatorcontrib><creatorcontrib>Peronnet, Frédérique</creatorcontrib><creatorcontrib>Gilles, Jean-François</creatorcontrib><creatorcontrib>Mouchel-Vielh, Emmanuèle</creatorcontrib><creatorcontrib>Gibert, Jean-Michel</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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors 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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest 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>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>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content (ProQuest)</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>Genetics Abstracts</collection><collection>MEDLINE - 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Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation varies with genotype in natural populations and is sensitive to temperature during development. We demonstrate that the bric à brac (bab) genes, that are differentially expressed between the two lines and whose expression levels vary with temperature, participate in the pigmentation difference between the Dark and Pale lines. The two lines differ in a bab regulatory sequence, the dimorphic element (called here bDE). Both bDE alleles are temperature-sensitive, but the activity of the bDE allele from the Dark line is lower than that of the bDE allele from the Pale line. Our results suggest that this difference could partly be due to differential regulation by AbdB. bab has been previously reported to be a repressor of abdominal pigmentation. We show here that one of its targets in this process is the pigmentation gene tan (t), regulated via the tan abdominal enhancer (t_MSE). Furthermore, t expression is strongly modulated by temperature in the two lines. Thus, temperature sensitivity of t expression is at least partly a consequence of bab thermal transcriptional plasticity. We therefore propose that a gene regulatory network integrating both genetic variation and temperature sensitivity modulates female abdominal pigmentation. Interestingly, both bDE and t_MSE were previously shown to have been recurrently involved in abdominal pigmentation evolution in drosophilids. 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subjects | Abdomen Alleles Animals Assimilation Base Sequence Binding Sites Biology and Life Sciences Chromosomal Proteins, Non-Histone - genetics Chromosomal Proteins, Non-Histone - physiology Developmental biology DNA-Binding Proteins - genetics DNA-Binding Proteins - physiology Drosophila melanogaster Drosophila melanogaster - genetics Drosophila Proteins - genetics Drosophila Proteins - physiology Enhancers Environmental factors Epigenetics Evolution & development Evolution, Molecular Female Females Gene Expression Regulation Gene Regulatory Networks Genes Genetic analysis Genetic diversity Genetic Variation Genomes Genomics Genotypes Genotyping Techniques Homeostasis Hypotheses Insects Life Sciences Medicine and Health Sciences Morphology Mutation Nutrition research Pigmentation Pigmentation - genetics Plasticity Ponds Regulatory sequences Research and Analysis Methods Sequence Analysis, DNA Studies Temperature Temperature effects Transcription Transcription Factors - genetics Transcription Factors - physiology |
title | bric à brac (bab), a central player in the gene regulatory network that mediates thermal plasticity of pigmentation in Drosophila melanogaster |
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