Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks
The normal adult human mammary gland is a continuous bilayered epithelial system. Bipotent and myoepithelial progenitors are prominent and unique components of the outer (basal) layer. The inner (luminal) layer includes both luminal-restricted progenitors and a phenotypically separable fraction that...
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creator | Pellacani, Davide Bilenky, Misha Kannan, Nagarajan Heravi-Moussavi, Alireza Knapp, David J.H.F. Gakkhar, Sitanshu Moksa, Michelle Carles, Annaick Moore, Richard Mungall, Andrew J. Marra, Marco A. Jones, Steven J.M. Aparicio, Samuel Hirst, Martin Eaves, Connie J. |
description | The normal adult human mammary gland is a continuous bilayered epithelial system. Bipotent and myoepithelial progenitors are prominent and unique components of the outer (basal) layer. The inner (luminal) layer includes both luminal-restricted progenitors and a phenotypically separable fraction that lacks progenitor activity. We now report an epigenomic comparison of these three subsets with one another, with their associated stromal cells, and with three immortalized, non-tumorigenic human mammary cell lines. Each genome-wide analysis contains profiles for six histone marks, methylated DNA, and RNA transcripts. Analysis of these datasets shows that each cell type has unique features, primarily within genomic regulatory regions, and that the cell lines group together. Analyses of the promoter and enhancer profiles place the luminal progenitors in between the basal cells and the non-progenitor luminal subset. Integrative analysis reveals networks of subset-specific transcription factors.
[Display omitted]
•Epigenomes of four normal human breast cell fractions and three cell lines are reported•Luminal progenitor and mature luminal cell epigenomes differ greatly•Enhancers define luminal progenitors as intermediate between basal and luminal cells•Transcription factor binding sites in active enhancers point to distinct regulators
Pellacani et al. present comprehensive histone and DNA modification profiles for four cell types in normal human breast tissue and three immortalized human mammary epithelial cell lines. Analysis of activated enhancers place luminal progenitors in between bipotent progenitor-containing basal cells and nonproliferative luminal cells. Explore consortium data at the Cell Press IHEC webportal at http://www.cell.com/consortium/IHEC. |
doi_str_mv | 10.1016/j.celrep.2016.10.058 |
format | Article |
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[Display omitted]
•Epigenomes of four normal human breast cell fractions and three cell lines are reported•Luminal progenitor and mature luminal cell epigenomes differ greatly•Enhancers define luminal progenitors as intermediate between basal and luminal cells•Transcription factor binding sites in active enhancers point to distinct regulators
Pellacani et al. present comprehensive histone and DNA modification profiles for four cell types in normal human breast tissue and three immortalized human mammary epithelial cell lines. Analysis of activated enhancers place luminal progenitors in between bipotent progenitor-containing basal cells and nonproliferative luminal cells. Explore consortium data at the Cell Press IHEC webportal at http://www.cell.com/consortium/IHEC.</description><identifier>ISSN: 2211-1247</identifier><identifier>EISSN: 2211-1247</identifier><identifier>DOI: 10.1016/j.celrep.2016.10.058</identifier><identifier>PMID: 27851968</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Breast - metabolism ; Cell Separation ; chromatin ; Chromatin - metabolism ; enhancer ; Enhancer Elements, Genetic - genetics ; Epigenesis, Genetic ; epigenomic ; Epithelial Cells - cytology ; Epithelial Cells - metabolism ; Female ; Gene Regulatory Networks ; Humans ; mammary cells ; normal human breast ; Phenotype ; profiling ; Promoter Regions, Genetic ; regulatory network ; Reproducibility of Results ; stem cells ; transcription factors ; Transcription Factors - metabolism ; transcriptome</subject><ispartof>Cell reports (Cambridge), 2016-11, Vol.17 (8), p.2060-2074</ispartof><rights>2016 The Author(s)</rights><rights>Copyright © 2016 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-ff8b4a46281bb16ad61e035716581edd44364217442133adca60d9c800d3cfbf3</citedby><cites>FETCH-LOGICAL-c474t-ff8b4a46281bb16ad61e035716581edd44364217442133adca60d9c800d3cfbf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27851968$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pellacani, Davide</creatorcontrib><creatorcontrib>Bilenky, Misha</creatorcontrib><creatorcontrib>Kannan, Nagarajan</creatorcontrib><creatorcontrib>Heravi-Moussavi, Alireza</creatorcontrib><creatorcontrib>Knapp, David J.H.F.</creatorcontrib><creatorcontrib>Gakkhar, Sitanshu</creatorcontrib><creatorcontrib>Moksa, Michelle</creatorcontrib><creatorcontrib>Carles, Annaick</creatorcontrib><creatorcontrib>Moore, Richard</creatorcontrib><creatorcontrib>Mungall, Andrew J.</creatorcontrib><creatorcontrib>Marra, Marco A.</creatorcontrib><creatorcontrib>Jones, Steven J.M.</creatorcontrib><creatorcontrib>Aparicio, Samuel</creatorcontrib><creatorcontrib>Hirst, Martin</creatorcontrib><creatorcontrib>Eaves, Connie J.</creatorcontrib><title>Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks</title><title>Cell reports (Cambridge)</title><addtitle>Cell Rep</addtitle><description>The normal adult human mammary gland is a continuous bilayered epithelial system. Bipotent and myoepithelial progenitors are prominent and unique components of the outer (basal) layer. The inner (luminal) layer includes both luminal-restricted progenitors and a phenotypically separable fraction that lacks progenitor activity. We now report an epigenomic comparison of these three subsets with one another, with their associated stromal cells, and with three immortalized, non-tumorigenic human mammary cell lines. Each genome-wide analysis contains profiles for six histone marks, methylated DNA, and RNA transcripts. Analysis of these datasets shows that each cell type has unique features, primarily within genomic regulatory regions, and that the cell lines group together. Analyses of the promoter and enhancer profiles place the luminal progenitors in between the basal cells and the non-progenitor luminal subset. Integrative analysis reveals networks of subset-specific transcription factors.
[Display omitted]
•Epigenomes of four normal human breast cell fractions and three cell lines are reported•Luminal progenitor and mature luminal cell epigenomes differ greatly•Enhancers define luminal progenitors as intermediate between basal and luminal cells•Transcription factor binding sites in active enhancers point to distinct regulators
Pellacani et al. present comprehensive histone and DNA modification profiles for four cell types in normal human breast tissue and three immortalized human mammary epithelial cell lines. Analysis of activated enhancers place luminal progenitors in between bipotent progenitor-containing basal cells and nonproliferative luminal cells. Explore consortium data at the Cell Press IHEC webportal at http://www.cell.com/consortium/IHEC.</description><subject>Adult</subject><subject>Breast - metabolism</subject><subject>Cell Separation</subject><subject>chromatin</subject><subject>Chromatin - metabolism</subject><subject>enhancer</subject><subject>Enhancer Elements, Genetic - genetics</subject><subject>Epigenesis, Genetic</subject><subject>epigenomic</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - metabolism</subject><subject>Female</subject><subject>Gene Regulatory Networks</subject><subject>Humans</subject><subject>mammary cells</subject><subject>normal human breast</subject><subject>Phenotype</subject><subject>profiling</subject><subject>Promoter Regions, Genetic</subject><subject>regulatory network</subject><subject>Reproducibility of Results</subject><subject>stem cells</subject><subject>transcription factors</subject><subject>Transcription Factors - metabolism</subject><subject>transcriptome</subject><issn>2211-1247</issn><issn>2211-1247</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc9u3CAQxlHVKImSvEEUcczFW8bG2HuJtFrtNpXSVMqfM8Iwbtja4AK7UR6g711Wm1Y9lQPMjH4zI76PkEtgM2AgPm1mGoeA06zMWS7NWN1-IKdlCVBAyZuP_8Qn5CLGDctHMIA5PyYnZdPWMBftKfm1cGp4izZS39N7H0Y10NvtqBz9qsZRhTe6mux3dH7ESB9wh2qIdInDUDxOqG1vNV3oZHdIV-5FOY2BPiaVMqycoYsYvbY5NfQpKBd1sFOy3tG10skHeo_p1Ycf8Zwc9XkwXry_Z-R5vXpa3hZ33z5_WS7uCs0bnoq-bzuuuChb6DoQyghAVtUNiLoFNIbzSvASGp6vqlJGK8HMXLeMmUr3XV-dkevD3Cn4n1uMSY42ZiUH5dBvo4SWA1R12bCM8gOqg48xYC-nYPeCSGBy74HcyIMHcu_Bvpo9yG1X7xu23Yjmb9MfxTNwcwAw_3NnMcioLWbhjA2okzTe_n_DbxyimuU</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Pellacani, Davide</creator><creator>Bilenky, Misha</creator><creator>Kannan, Nagarajan</creator><creator>Heravi-Moussavi, Alireza</creator><creator>Knapp, David J.H.F.</creator><creator>Gakkhar, Sitanshu</creator><creator>Moksa, Michelle</creator><creator>Carles, Annaick</creator><creator>Moore, Richard</creator><creator>Mungall, Andrew J.</creator><creator>Marra, Marco A.</creator><creator>Jones, Steven J.M.</creator><creator>Aparicio, Samuel</creator><creator>Hirst, Martin</creator><creator>Eaves, Connie J.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>20161115</creationdate><title>Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks</title><author>Pellacani, Davide ; Bilenky, Misha ; Kannan, Nagarajan ; Heravi-Moussavi, Alireza ; Knapp, David J.H.F. ; Gakkhar, Sitanshu ; Moksa, Michelle ; Carles, Annaick ; Moore, Richard ; Mungall, Andrew J. ; Marra, Marco A. ; Jones, Steven J.M. ; Aparicio, Samuel ; Hirst, Martin ; Eaves, Connie J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-ff8b4a46281bb16ad61e035716581edd44364217442133adca60d9c800d3cfbf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Breast - metabolism</topic><topic>Cell Separation</topic><topic>chromatin</topic><topic>Chromatin - metabolism</topic><topic>enhancer</topic><topic>Enhancer Elements, Genetic - genetics</topic><topic>Epigenesis, Genetic</topic><topic>epigenomic</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - metabolism</topic><topic>Female</topic><topic>Gene Regulatory Networks</topic><topic>Humans</topic><topic>mammary cells</topic><topic>normal human breast</topic><topic>Phenotype</topic><topic>profiling</topic><topic>Promoter Regions, Genetic</topic><topic>regulatory network</topic><topic>Reproducibility of Results</topic><topic>stem cells</topic><topic>transcription factors</topic><topic>Transcription Factors - metabolism</topic><topic>transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pellacani, Davide</creatorcontrib><creatorcontrib>Bilenky, Misha</creatorcontrib><creatorcontrib>Kannan, Nagarajan</creatorcontrib><creatorcontrib>Heravi-Moussavi, Alireza</creatorcontrib><creatorcontrib>Knapp, David J.H.F.</creatorcontrib><creatorcontrib>Gakkhar, Sitanshu</creatorcontrib><creatorcontrib>Moksa, Michelle</creatorcontrib><creatorcontrib>Carles, Annaick</creatorcontrib><creatorcontrib>Moore, Richard</creatorcontrib><creatorcontrib>Mungall, Andrew J.</creatorcontrib><creatorcontrib>Marra, Marco A.</creatorcontrib><creatorcontrib>Jones, Steven J.M.</creatorcontrib><creatorcontrib>Aparicio, Samuel</creatorcontrib><creatorcontrib>Hirst, Martin</creatorcontrib><creatorcontrib>Eaves, Connie J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cell reports (Cambridge)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pellacani, Davide</au><au>Bilenky, Misha</au><au>Kannan, Nagarajan</au><au>Heravi-Moussavi, Alireza</au><au>Knapp, David J.H.F.</au><au>Gakkhar, Sitanshu</au><au>Moksa, Michelle</au><au>Carles, Annaick</au><au>Moore, Richard</au><au>Mungall, Andrew J.</au><au>Marra, Marco A.</au><au>Jones, Steven J.M.</au><au>Aparicio, Samuel</au><au>Hirst, Martin</au><au>Eaves, Connie J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks</atitle><jtitle>Cell reports (Cambridge)</jtitle><addtitle>Cell Rep</addtitle><date>2016-11-15</date><risdate>2016</risdate><volume>17</volume><issue>8</issue><spage>2060</spage><epage>2074</epage><pages>2060-2074</pages><issn>2211-1247</issn><eissn>2211-1247</eissn><abstract>The normal adult human mammary gland is a continuous bilayered epithelial system. Bipotent and myoepithelial progenitors are prominent and unique components of the outer (basal) layer. The inner (luminal) layer includes both luminal-restricted progenitors and a phenotypically separable fraction that lacks progenitor activity. We now report an epigenomic comparison of these three subsets with one another, with their associated stromal cells, and with three immortalized, non-tumorigenic human mammary cell lines. Each genome-wide analysis contains profiles for six histone marks, methylated DNA, and RNA transcripts. Analysis of these datasets shows that each cell type has unique features, primarily within genomic regulatory regions, and that the cell lines group together. Analyses of the promoter and enhancer profiles place the luminal progenitors in between the basal cells and the non-progenitor luminal subset. Integrative analysis reveals networks of subset-specific transcription factors.
[Display omitted]
•Epigenomes of four normal human breast cell fractions and three cell lines are reported•Luminal progenitor and mature luminal cell epigenomes differ greatly•Enhancers define luminal progenitors as intermediate between basal and luminal cells•Transcription factor binding sites in active enhancers point to distinct regulators
Pellacani et al. present comprehensive histone and DNA modification profiles for four cell types in normal human breast tissue and three immortalized human mammary epithelial cell lines. Analysis of activated enhancers place luminal progenitors in between bipotent progenitor-containing basal cells and nonproliferative luminal cells. Explore consortium data at the Cell Press IHEC webportal at http://www.cell.com/consortium/IHEC.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27851968</pmid><doi>10.1016/j.celrep.2016.10.058</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Breast - metabolism Cell Separation chromatin Chromatin - metabolism enhancer Enhancer Elements, Genetic - genetics Epigenesis, Genetic epigenomic Epithelial Cells - cytology Epithelial Cells - metabolism Female Gene Regulatory Networks Humans mammary cells normal human breast Phenotype profiling Promoter Regions, Genetic regulatory network Reproducibility of Results stem cells transcription factors Transcription Factors - metabolism transcriptome |
title | Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks |
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