Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes
Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell developm...
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description | Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell development. However, PRC2 independent function is suggested for Drosophila Jumonji (dJmj). To clarify the function of dJmj during cell differentiation, we used Drosophila adult intestinal stem cell system that allows to follow stem cell behaviors in vivo. Overexpression of dJmj in intestinal stem cells/enteroblasts (ISCs/EBs) induces cell-autonomous ISC proliferation followed by differentiation, that is controlled by the Notch and EGFR pathway. In contrast, overexpression of dJmj in enterocytes (ECs) resulted in activation of the JNK pathway in ECs followed by the induction of apoptosis. Activated JNK increased the level of Yorkie in ECs and induced the reduction of Upd proteins and EGFR ligands, which activated the JAK/STAT and EGFR pathway in both ISCs and EBs to promote ISC proliferation. The Notch signaling pathway appears to be highly activated to support the differentiation of EBs to ECs. Thus, the combination of these signaling pathways caused by ECs-specific dJmj-overexpression induced non-cell-autonomous ISC proliferation and differentiation. Surprisingly, these effects did not relate to H3K27me3 status, likely represented PRC2 activity, in cells that overexpressed dJmj. Instead of this, the disappearance of H3K27me3 in ISC/EB-specific overexpressed dJmj suggested a possible PRC2-independent role of dJmj in regulating chromatin structure.
•ISC/EB-specific dJmj-overexpression induced the cell-autonomous ISC over-proliferation.•EC-specific dJmj-overexpression triggered apoptosis in ECs followed by non-cell-autonomous ISC over-proliferation.•Effects caused by dJmj-overexpression do not relate to H3K27me3 status.•PRC2-independent role of dJmj in regulating chromatin structure during differentiation process is suggested. |
doi_str_mv | 10.1016/j.cellsig.2017.10.017 |
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•ISC/EB-specific dJmj-overexpression induced the cell-autonomous ISC over-proliferation.•EC-specific dJmj-overexpression triggered apoptosis in ECs followed by non-cell-autonomous ISC over-proliferation.•Effects caused by dJmj-overexpression do not relate to H3K27me3 status.•PRC2-independent role of dJmj in regulating chromatin structure during differentiation process is suggested.</description><identifier>ISSN: 0898-6568</identifier><identifier>EISSN: 1873-3913</identifier><identifier>DOI: 10.1016/j.cellsig.2017.10.017</identifier><identifier>PMID: 29102770</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Apoptosis - genetics ; Cell Differentiation ; Cell over-proliferation ; Cell Proliferation ; Chromatin - chemistry ; Chromatin - metabolism ; Drosophila intestinal stem cell ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; EGFR ; Enterocytes - cytology ; Enterocytes - metabolism ; ErbB Receptors - genetics ; ErbB Receptors - metabolism ; Gene Expression Regulation, Developmental ; Histone-Lysine N-Methyltransferase - genetics ; Histone-Lysine N-Methyltransferase - metabolism ; Histones - genetics ; Histones - metabolism ; Intestinal Mucosa - metabolism ; Intestines - cytology ; Intestines - growth & development ; JAK/STAT ; JNK ; Jumonji/Jarid2 ; MAP Kinase Signaling System ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Receptors, Invertebrate Peptide - genetics ; Receptors, Invertebrate Peptide - metabolism ; Receptors, Notch - genetics ; Receptors, Notch - metabolism ; STAT Transcription Factors - genetics ; STAT Transcription Factors - metabolism ; Stem Cells - cytology ; Stem Cells - metabolism ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Transcription Factors - genetics ; Transcription Factors - metabolism</subject><ispartof>Cellular signalling, 2018-01, Vol.42, p.194-210</ispartof><rights>2017 Elsevier Inc.</rights><rights>Copyright © 2017 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-cc1539921ca6078f4c35d2056b6a8e17cc20a782f380b29f85ee5238042bf0a93</citedby><cites>FETCH-LOGICAL-c431t-cc1539921ca6078f4c35d2056b6a8e17cc20a782f380b29f85ee5238042bf0a93</cites><orcidid>0000-0002-4445-013X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cellsig.2017.10.017$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29102770$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suong, Dang Ngoc Anh</creatorcontrib><creatorcontrib>Shimaji, Kouhei</creatorcontrib><creatorcontrib>Pyo, Jung-Hoon</creatorcontrib><creatorcontrib>Park, Joung-Sun</creatorcontrib><creatorcontrib>Yoshida, Hideki</creatorcontrib><creatorcontrib>Yoo, Mi-Ae</creatorcontrib><creatorcontrib>Yamaguchi, Masamitsu</creatorcontrib><title>Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes</title><title>Cellular signalling</title><addtitle>Cell Signal</addtitle><description>Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell development. However, PRC2 independent function is suggested for Drosophila Jumonji (dJmj). To clarify the function of dJmj during cell differentiation, we used Drosophila adult intestinal stem cell system that allows to follow stem cell behaviors in vivo. Overexpression of dJmj in intestinal stem cells/enteroblasts (ISCs/EBs) induces cell-autonomous ISC proliferation followed by differentiation, that is controlled by the Notch and EGFR pathway. In contrast, overexpression of dJmj in enterocytes (ECs) resulted in activation of the JNK pathway in ECs followed by the induction of apoptosis. Activated JNK increased the level of Yorkie in ECs and induced the reduction of Upd proteins and EGFR ligands, which activated the JAK/STAT and EGFR pathway in both ISCs and EBs to promote ISC proliferation. The Notch signaling pathway appears to be highly activated to support the differentiation of EBs to ECs. Thus, the combination of these signaling pathways caused by ECs-specific dJmj-overexpression induced non-cell-autonomous ISC proliferation and differentiation. Surprisingly, these effects did not relate to H3K27me3 status, likely represented PRC2 activity, in cells that overexpressed dJmj. Instead of this, the disappearance of H3K27me3 in ISC/EB-specific overexpressed dJmj suggested a possible PRC2-independent role of dJmj in regulating chromatin structure.
•ISC/EB-specific dJmj-overexpression induced the cell-autonomous ISC over-proliferation.•EC-specific dJmj-overexpression triggered apoptosis in ECs followed by non-cell-autonomous ISC over-proliferation.•Effects caused by dJmj-overexpression do not relate to H3K27me3 status.•PRC2-independent role of dJmj in regulating chromatin structure during differentiation process is suggested.</description><subject>Animals</subject><subject>Apoptosis - genetics</subject><subject>Cell Differentiation</subject><subject>Cell over-proliferation</subject><subject>Cell Proliferation</subject><subject>Chromatin - chemistry</subject><subject>Chromatin - metabolism</subject><subject>Drosophila intestinal stem cell</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>EGFR</subject><subject>Enterocytes - cytology</subject><subject>Enterocytes - metabolism</subject><subject>ErbB Receptors - genetics</subject><subject>ErbB Receptors - metabolism</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Histone-Lysine N-Methyltransferase - genetics</subject><subject>Histone-Lysine N-Methyltransferase - metabolism</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestines - cytology</subject><subject>Intestines - growth & development</subject><subject>JAK/STAT</subject><subject>JNK</subject><subject>Jumonji/Jarid2</subject><subject>MAP Kinase Signaling System</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclear Proteins - metabolism</subject><subject>Receptors, Invertebrate Peptide - genetics</subject><subject>Receptors, Invertebrate Peptide - metabolism</subject><subject>Receptors, Notch - genetics</subject><subject>Receptors, Notch - metabolism</subject><subject>STAT Transcription Factors - genetics</subject><subject>STAT Transcription Factors - metabolism</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - metabolism</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><issn>0898-6568</issn><issn>1873-3913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwCSAv2ST40STOCqGKpyp1A2vLscfIUR7FTiv69zi0IHasrmd8x3N9ELqkJKWE5jd1qqFpgntPGaFF7KVRjtCUioInvKT8GE2JKEWSZ7mYoLMQakJoRnJ2iiaspIQVBZmiarUFD59rDyG4vsO9xealrbFx1saLbnCqaXZYxUoPAbtugDC4TjU4DNDi7wxYdebvwAAGxwP4Xu-i_RydWNUEuDjoDL093L8unpLl6vF5cbdM9JzTIdGaZrwsGdUqJ4Wwc80zw0iWV7kSQAutGVGFYJYLUrHSigwgY7GYs8oSVfIZut6_u_b9xybGlK0LY0DVQb8JkpY5JZyzCGiGsr1V-z4ED1auvWuV30lK5IhX1vKAV454x3aUOHd1WLGpWjC_Uz88o-F2b4D40a0DL4N20GkwzkeA0vTunxVfqXiPww</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Suong, Dang Ngoc Anh</creator><creator>Shimaji, Kouhei</creator><creator>Pyo, Jung-Hoon</creator><creator>Park, Joung-Sun</creator><creator>Yoshida, Hideki</creator><creator>Yoo, Mi-Ae</creator><creator>Yamaguchi, Masamitsu</creator><general>Elsevier Inc</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>7X8</scope><orcidid>https://orcid.org/0000-0002-4445-013X</orcidid></search><sort><creationdate>201801</creationdate><title>Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes</title><author>Suong, Dang Ngoc Anh ; Shimaji, Kouhei ; Pyo, Jung-Hoon ; Park, Joung-Sun ; Yoshida, Hideki ; Yoo, Mi-Ae ; Yamaguchi, Masamitsu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-cc1539921ca6078f4c35d2056b6a8e17cc20a782f380b29f85ee5238042bf0a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Apoptosis - genetics</topic><topic>Cell Differentiation</topic><topic>Cell over-proliferation</topic><topic>Cell Proliferation</topic><topic>Chromatin - chemistry</topic><topic>Chromatin - metabolism</topic><topic>Drosophila intestinal stem cell</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>EGFR</topic><topic>Enterocytes - cytology</topic><topic>Enterocytes - metabolism</topic><topic>ErbB Receptors - genetics</topic><topic>ErbB Receptors - metabolism</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Histone-Lysine N-Methyltransferase - genetics</topic><topic>Histone-Lysine N-Methyltransferase - metabolism</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestines - cytology</topic><topic>Intestines - growth & development</topic><topic>JAK/STAT</topic><topic>JNK</topic><topic>Jumonji/Jarid2</topic><topic>MAP Kinase Signaling System</topic><topic>Nuclear Proteins - genetics</topic><topic>Nuclear Proteins - metabolism</topic><topic>Receptors, Invertebrate Peptide - genetics</topic><topic>Receptors, Invertebrate Peptide - metabolism</topic><topic>Receptors, Notch - genetics</topic><topic>Receptors, Notch - metabolism</topic><topic>STAT Transcription Factors - genetics</topic><topic>STAT Transcription Factors - metabolism</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - metabolism</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suong, Dang Ngoc Anh</creatorcontrib><creatorcontrib>Shimaji, Kouhei</creatorcontrib><creatorcontrib>Pyo, Jung-Hoon</creatorcontrib><creatorcontrib>Park, Joung-Sun</creatorcontrib><creatorcontrib>Yoshida, Hideki</creatorcontrib><creatorcontrib>Yoo, Mi-Ae</creatorcontrib><creatorcontrib>Yamaguchi, Masamitsu</creatorcontrib><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>Cellular signalling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suong, Dang Ngoc Anh</au><au>Shimaji, Kouhei</au><au>Pyo, Jung-Hoon</au><au>Park, Joung-Sun</au><au>Yoshida, Hideki</au><au>Yoo, Mi-Ae</au><au>Yamaguchi, Masamitsu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes</atitle><jtitle>Cellular signalling</jtitle><addtitle>Cell Signal</addtitle><date>2018-01</date><risdate>2018</risdate><volume>42</volume><spage>194</spage><epage>210</epage><pages>194-210</pages><issn>0898-6568</issn><eissn>1873-3913</eissn><abstract>Jumonji (Jmj)/Jarid2 is a DNA-binding transcriptional repressor mediated via histone methylation. Nevertheless, the well-known function of Jmj is as a scaffold for the recruitment of various complexes including Polycomb repressive complex 2 (PRC2), and required for mouse embryonic stem cell development. However, PRC2 independent function is suggested for Drosophila Jumonji (dJmj). To clarify the function of dJmj during cell differentiation, we used Drosophila adult intestinal stem cell system that allows to follow stem cell behaviors in vivo. Overexpression of dJmj in intestinal stem cells/enteroblasts (ISCs/EBs) induces cell-autonomous ISC proliferation followed by differentiation, that is controlled by the Notch and EGFR pathway. In contrast, overexpression of dJmj in enterocytes (ECs) resulted in activation of the JNK pathway in ECs followed by the induction of apoptosis. Activated JNK increased the level of Yorkie in ECs and induced the reduction of Upd proteins and EGFR ligands, which activated the JAK/STAT and EGFR pathway in both ISCs and EBs to promote ISC proliferation. The Notch signaling pathway appears to be highly activated to support the differentiation of EBs to ECs. Thus, the combination of these signaling pathways caused by ECs-specific dJmj-overexpression induced non-cell-autonomous ISC proliferation and differentiation. Surprisingly, these effects did not relate to H3K27me3 status, likely represented PRC2 activity, in cells that overexpressed dJmj. Instead of this, the disappearance of H3K27me3 in ISC/EB-specific overexpressed dJmj suggested a possible PRC2-independent role of dJmj in regulating chromatin structure.
•ISC/EB-specific dJmj-overexpression induced the cell-autonomous ISC over-proliferation.•EC-specific dJmj-overexpression triggered apoptosis in ECs followed by non-cell-autonomous ISC over-proliferation.•Effects caused by dJmj-overexpression do not relate to H3K27me3 status.•PRC2-independent role of dJmj in regulating chromatin structure during differentiation process is suggested.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>29102770</pmid><doi>10.1016/j.cellsig.2017.10.017</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-4445-013X</orcidid></addata></record> |
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subjects | Animals Apoptosis - genetics Cell Differentiation Cell over-proliferation Cell Proliferation Chromatin - chemistry Chromatin - metabolism Drosophila intestinal stem cell Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism EGFR Enterocytes - cytology Enterocytes - metabolism ErbB Receptors - genetics ErbB Receptors - metabolism Gene Expression Regulation, Developmental Histone-Lysine N-Methyltransferase - genetics Histone-Lysine N-Methyltransferase - metabolism Histones - genetics Histones - metabolism Intestinal Mucosa - metabolism Intestines - cytology Intestines - growth & development JAK/STAT JNK Jumonji/Jarid2 MAP Kinase Signaling System Nuclear Proteins - genetics Nuclear Proteins - metabolism Receptors, Invertebrate Peptide - genetics Receptors, Invertebrate Peptide - metabolism Receptors, Notch - genetics Receptors, Notch - metabolism STAT Transcription Factors - genetics STAT Transcription Factors - metabolism Stem Cells - cytology Stem Cells - metabolism Trans-Activators - genetics Trans-Activators - metabolism Transcription Factors - genetics Transcription Factors - metabolism |
title | Overexpression of dJmj differentially affects intestinal stem cells and differentiated enterocytes |
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