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The Ubx Polycomb response element bypasses an unpaired Fab-8 insulator via cis transvection in Drosophila

Chromatin insulators or boundary elements protect genes from regulatory activities from neighboring genes or chromatin domains. In the Drosophila Abdominal-B (Abd-B) locus, the deletion of such elements, such as Frontabdominal-7 (Fab-7) or Fab-8 led to dominant gain of function phenotypes, presumabl...

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Published in:PloS one 2018-06, Vol.13 (6), p.e0199353-e0199353
Main Authors: Lu, Danfeng, Li, Zhuoran, Li, Lingling, Yang, Liping, Chen, Guijun, Yang, Deying, Zhang, Yue, Singh, Vikrant, Smith, Sheryl, Xiao, Yu, Wang, Erlin, Ye, Yunshuang, Zhang, Wei, Zhou, Lei, Rong, Yikang, Zhou, Jumin
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cited_by cdi_FETCH-LOGICAL-c692t-a26d242363d6badefa3854a674ab3cee4927fdc24f8e58bf215e2e612282ed53
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container_end_page e0199353
container_issue 6
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creator Lu, Danfeng
Li, Zhuoran
Li, Lingling
Yang, Liping
Chen, Guijun
Yang, Deying
Zhang, Yue
Singh, Vikrant
Smith, Sheryl
Xiao, Yu
Wang, Erlin
Ye, Yunshuang
Zhang, Wei
Zhou, Lei
Rong, Yikang
Zhou, Jumin
description Chromatin insulators or boundary elements protect genes from regulatory activities from neighboring genes or chromatin domains. In the Drosophila Abdominal-B (Abd-B) locus, the deletion of such elements, such as Frontabdominal-7 (Fab-7) or Fab-8 led to dominant gain of function phenotypes, presumably due to the loss of chromatin barriers. Homologous chromosomes are paired in Drosophila, creating a number of pairing dependent phenomena including transvection, and whether transvection may affect the function of Polycomb response elements (PREs) and thus contribute to the phenotypes are not known. Here, we studied the chromatin barrier activity of Fab-8 and how it is affected by the zygosity of the transgene, and found that Fab-8 is able to block the silencing effect of the Ubx PRE on the DsRed reporter gene in a CTCF binding sites dependent manner. However, the blocking also depends on the zygosity of the transgene in that the barrier activity is present when the transgene is homozygous, but absent when the transgene is heterozygous. To analyze this effect, we performed chromatin immunoprecipitation and quantitative PCR (ChIP-qPCR) experiments on homozygous transgenic embryos, and found that H3K27me3 and H3K9me3 marks are restricted by Fab-8, but they spread beyond Fab-8 into the DsRed gene when the two CTCF binding sites within Fab-8 were mutated. Consistent with this, the mutation reduced H3K4me3 and RNA Pol II binding to the DsRed gene, and consequently, DsRed expression. Importantly, in heterozygous embryos, Fab-8 is unable to prevent the spread of H3K27me3 and H3K9me3 marks from crossing Fab-8 into DsRed, suggesting an insulator bypass. These results suggest that in the Abd-B locus, deletion of the insulator in one copy of the chromosome could lead to the loss of insulator activity on the homologous chromosome, and in other loci where chromosomal deletion created hemizygous regions of the genome, the chromatin barrier could be compromised. This study highlights a role of homologous chromosome pairing in the regulation of gene expression in the Drosophila genome.
doi_str_mv 10.1371/journal.pone.0199353
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In the Drosophila Abdominal-B (Abd-B) locus, the deletion of such elements, such as Frontabdominal-7 (Fab-7) or Fab-8 led to dominant gain of function phenotypes, presumably due to the loss of chromatin barriers. Homologous chromosomes are paired in Drosophila, creating a number of pairing dependent phenomena including transvection, and whether transvection may affect the function of Polycomb response elements (PREs) and thus contribute to the phenotypes are not known. Here, we studied the chromatin barrier activity of Fab-8 and how it is affected by the zygosity of the transgene, and found that Fab-8 is able to block the silencing effect of the Ubx PRE on the DsRed reporter gene in a CTCF binding sites dependent manner. However, the blocking also depends on the zygosity of the transgene in that the barrier activity is present when the transgene is homozygous, but absent when the transgene is heterozygous. To analyze this effect, we performed chromatin immunoprecipitation and quantitative PCR (ChIP-qPCR) experiments on homozygous transgenic embryos, and found that H3K27me3 and H3K9me3 marks are restricted by Fab-8, but they spread beyond Fab-8 into the DsRed gene when the two CTCF binding sites within Fab-8 were mutated. Consistent with this, the mutation reduced H3K4me3 and RNA Pol II binding to the DsRed gene, and consequently, DsRed expression. Importantly, in heterozygous embryos, Fab-8 is unable to prevent the spread of H3K27me3 and H3K9me3 marks from crossing Fab-8 into DsRed, suggesting an insulator bypass. These results suggest that in the Abd-B locus, deletion of the insulator in one copy of the chromosome could lead to the loss of insulator activity on the homologous chromosome, and in other loci where chromosomal deletion created hemizygous regions of the genome, the chromatin barrier could be compromised. This study highlights a role of homologous chromosome pairing in the regulation of gene expression in the Drosophila genome.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0199353</identifier><identifier>PMID: 29928011</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Animals, Genetically Modified ; Binding sites ; Biology and Life Sciences ; Blocking ; Boundaries ; Boundary element method ; CCCTC-Binding Factor - metabolism ; Chromatin ; Chromatin - metabolism ; Chromosome deletion ; Chromosomes ; Chromosomes, Insect - genetics ; DNA-directed RNA polymerase ; Drosophila ; Drosophila melanogaster ; Drosophila melanogaster - embryology ; Drosophila melanogaster - genetics ; Drosophila Proteins - metabolism ; Embryo, Nonmammalian - metabolism ; Embryos ; Epigenetic inheritance ; Gene deletion ; Gene expression ; Genes ; Genes, Reporter ; Genetic aspects ; Genomes ; Heterozygote ; Histones - metabolism ; Homeodomain Proteins - metabolism ; Homology ; Homozygote ; Immunoprecipitation ; Insects ; Insulator Elements - genetics ; Insulators ; Laboratories ; Life sciences ; Loci ; Lysine - metabolism ; Methylation ; Models, Biological ; Mutation ; Peptides ; Phenotype ; Phenotypes ; Physical Sciences ; Polycomb group proteins ; Polymerase chain reaction ; Promoter Regions, Genetic - genetics ; Proteins ; Regulatory sequences ; Reporter gene ; Research and Analysis Methods ; Response Elements - genetics ; Ribonucleic acid ; RNA ; RNA polymerase ; RNA polymerase II ; RNA Polymerase II - metabolism ; Transcription Factors - metabolism ; Transgenes ; Transgenic ; Zoology ; Zygosity</subject><ispartof>PloS one, 2018-06, Vol.13 (6), p.e0199353-e0199353</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Lu 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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In the Drosophila Abdominal-B (Abd-B) locus, the deletion of such elements, such as Frontabdominal-7 (Fab-7) or Fab-8 led to dominant gain of function phenotypes, presumably due to the loss of chromatin barriers. Homologous chromosomes are paired in Drosophila, creating a number of pairing dependent phenomena including transvection, and whether transvection may affect the function of Polycomb response elements (PREs) and thus contribute to the phenotypes are not known. Here, we studied the chromatin barrier activity of Fab-8 and how it is affected by the zygosity of the transgene, and found that Fab-8 is able to block the silencing effect of the Ubx PRE on the DsRed reporter gene in a CTCF binding sites dependent manner. However, the blocking also depends on the zygosity of the transgene in that the barrier activity is present when the transgene is homozygous, but absent when the transgene is heterozygous. To analyze this effect, we performed chromatin immunoprecipitation and quantitative PCR (ChIP-qPCR) experiments on homozygous transgenic embryos, and found that H3K27me3 and H3K9me3 marks are restricted by Fab-8, but they spread beyond Fab-8 into the DsRed gene when the two CTCF binding sites within Fab-8 were mutated. Consistent with this, the mutation reduced H3K4me3 and RNA Pol II binding to the DsRed gene, and consequently, DsRed expression. Importantly, in heterozygous embryos, Fab-8 is unable to prevent the spread of H3K27me3 and H3K9me3 marks from crossing Fab-8 into DsRed, suggesting an insulator bypass. These results suggest that in the Abd-B locus, deletion of the insulator in one copy of the chromosome could lead to the loss of insulator activity on the homologous chromosome, and in other loci where chromosomal deletion created hemizygous regions of the genome, the chromatin barrier could be compromised. This study highlights a role of homologous chromosome pairing in the regulation of gene expression in the Drosophila genome.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Binding sites</subject><subject>Biology and Life Sciences</subject><subject>Blocking</subject><subject>Boundaries</subject><subject>Boundary element method</subject><subject>CCCTC-Binding Factor - metabolism</subject><subject>Chromatin</subject><subject>Chromatin - metabolism</subject><subject>Chromosome deletion</subject><subject>Chromosomes</subject><subject>Chromosomes, Insect - genetics</subject><subject>DNA-directed RNA polymerase</subject><subject>Drosophila</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Embryo, Nonmammalian - metabolism</subject><subject>Embryos</subject><subject>Epigenetic inheritance</subject><subject>Gene deletion</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genes, Reporter</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Heterozygote</subject><subject>Histones - 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metabolism</topic><topic>Methylation</topic><topic>Models, Biological</topic><topic>Mutation</topic><topic>Peptides</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Physical Sciences</topic><topic>Polycomb group proteins</topic><topic>Polymerase chain reaction</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Proteins</topic><topic>Regulatory sequences</topic><topic>Reporter gene</topic><topic>Research and Analysis Methods</topic><topic>Response Elements - genetics</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA polymerase</topic><topic>RNA polymerase II</topic><topic>RNA Polymerase II - metabolism</topic><topic>Transcription Factors - metabolism</topic><topic>Transgenes</topic><topic>Transgenic</topic><topic>Zoology</topic><topic>Zygosity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Danfeng</creatorcontrib><creatorcontrib>Li, Zhuoran</creatorcontrib><creatorcontrib>Li, Lingling</creatorcontrib><creatorcontrib>Yang, Liping</creatorcontrib><creatorcontrib>Chen, Guijun</creatorcontrib><creatorcontrib>Yang, Deying</creatorcontrib><creatorcontrib>Zhang, Yue</creatorcontrib><creatorcontrib>Singh, Vikrant</creatorcontrib><creatorcontrib>Smith, Sheryl</creatorcontrib><creatorcontrib>Xiao, Yu</creatorcontrib><creatorcontrib>Wang, Erlin</creatorcontrib><creatorcontrib>Ye, Yunshuang</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Zhou, Lei</creatorcontrib><creatorcontrib>Rong, Yikang</creatorcontrib><creatorcontrib>Zhou, Jumin</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: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological &amp; Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical 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 Technology 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>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</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 &amp; Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Danfeng</au><au>Li, Zhuoran</au><au>Li, Lingling</au><au>Yang, Liping</au><au>Chen, Guijun</au><au>Yang, Deying</au><au>Zhang, Yue</au><au>Singh, Vikrant</au><au>Smith, Sheryl</au><au>Xiao, Yu</au><au>Wang, Erlin</au><au>Ye, Yunshuang</au><au>Zhang, Wei</au><au>Zhou, Lei</au><au>Rong, Yikang</au><au>Zhou, Jumin</au><au>Wutz, Anton</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Ubx Polycomb response element bypasses an unpaired Fab-8 insulator via cis transvection in Drosophila</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-06-21</date><risdate>2018</risdate><volume>13</volume><issue>6</issue><spage>e0199353</spage><epage>e0199353</epage><pages>e0199353-e0199353</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Chromatin insulators or boundary elements protect genes from regulatory activities from neighboring genes or chromatin domains. In the Drosophila Abdominal-B (Abd-B) locus, the deletion of such elements, such as Frontabdominal-7 (Fab-7) or Fab-8 led to dominant gain of function phenotypes, presumably due to the loss of chromatin barriers. Homologous chromosomes are paired in Drosophila, creating a number of pairing dependent phenomena including transvection, and whether transvection may affect the function of Polycomb response elements (PREs) and thus contribute to the phenotypes are not known. Here, we studied the chromatin barrier activity of Fab-8 and how it is affected by the zygosity of the transgene, and found that Fab-8 is able to block the silencing effect of the Ubx PRE on the DsRed reporter gene in a CTCF binding sites dependent manner. However, the blocking also depends on the zygosity of the transgene in that the barrier activity is present when the transgene is homozygous, but absent when the transgene is heterozygous. To analyze this effect, we performed chromatin immunoprecipitation and quantitative PCR (ChIP-qPCR) experiments on homozygous transgenic embryos, and found that H3K27me3 and H3K9me3 marks are restricted by Fab-8, but they spread beyond Fab-8 into the DsRed gene when the two CTCF binding sites within Fab-8 were mutated. Consistent with this, the mutation reduced H3K4me3 and RNA Pol II binding to the DsRed gene, and consequently, DsRed expression. Importantly, in heterozygous embryos, Fab-8 is unable to prevent the spread of H3K27me3 and H3K9me3 marks from crossing Fab-8 into DsRed, suggesting an insulator bypass. These results suggest that in the Abd-B locus, deletion of the insulator in one copy of the chromosome could lead to the loss of insulator activity on the homologous chromosome, and in other loci where chromosomal deletion created hemizygous regions of the genome, the chromatin barrier could be compromised. This study highlights a role of homologous chromosome pairing in the regulation of gene expression in the Drosophila genome.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29928011</pmid><doi>10.1371/journal.pone.0199353</doi><tpages>e0199353</tpages><orcidid>https://orcid.org/0000-0003-1389-1087</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
ispartof PloS one, 2018-06, Vol.13 (6), p.e0199353-e0199353
issn 1932-6203
1932-6203
language eng
recordid cdi_plos_journals_2057887722
source PubMed (Medline); Publicly Available Content Database
subjects Animals
Animals, Genetically Modified
Binding sites
Biology and Life Sciences
Blocking
Boundaries
Boundary element method
CCCTC-Binding Factor - metabolism
Chromatin
Chromatin - metabolism
Chromosome deletion
Chromosomes
Chromosomes, Insect - genetics
DNA-directed RNA polymerase
Drosophila
Drosophila melanogaster
Drosophila melanogaster - embryology
Drosophila melanogaster - genetics
Drosophila Proteins - metabolism
Embryo, Nonmammalian - metabolism
Embryos
Epigenetic inheritance
Gene deletion
Gene expression
Genes
Genes, Reporter
Genetic aspects
Genomes
Heterozygote
Histones - metabolism
Homeodomain Proteins - metabolism
Homology
Homozygote
Immunoprecipitation
Insects
Insulator Elements - genetics
Insulators
Laboratories
Life sciences
Loci
Lysine - metabolism
Methylation
Models, Biological
Mutation
Peptides
Phenotype
Phenotypes
Physical Sciences
Polycomb group proteins
Polymerase chain reaction
Promoter Regions, Genetic - genetics
Proteins
Regulatory sequences
Reporter gene
Research and Analysis Methods
Response Elements - genetics
Ribonucleic acid
RNA
RNA polymerase
RNA polymerase II
RNA Polymerase II - metabolism
Transcription Factors - metabolism
Transgenes
Transgenic
Zoology
Zygosity
title The Ubx Polycomb response element bypasses an unpaired Fab-8 insulator via cis transvection in Drosophila
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