Epigenetic Protection of Vertebrate Lymphoid Progenitor Cells by Dnmt1
DNA methylation is a universal epigenetic mechanism involved in regulation of gene expression and genome stability. The DNA maintenance methylase DNMT1 ensures that DNA methylation patterns are faithfully transmitted to daughter cells during cell division. Because loss of DNMT1 is lethal, a pan-orga...
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creator | Iwanami, Norimasa Takeshita, Kohei Lawir, Divine-Fondzenyuy Suetake, Isao Tajima, Shoji Sikora, Katarzyna Trancoso, Inês ÓMeara, Connor Siamishi, Iliana Takahama, Yousuke Furutani-Seiki, Makoto Kondoh, Hisato Yonezawa, Yasushige Schorpp, Michael Boehm, Thomas |
description | DNA methylation is a universal epigenetic mechanism involved in regulation of gene expression and genome stability. The DNA maintenance methylase DNMT1 ensures that DNA methylation patterns are faithfully transmitted to daughter cells during cell division. Because loss of DNMT1 is lethal, a pan-organismic analysis of DNMT1 function is lacking. We identified new recessive dnmt1 alleles in medaka and zebrafish and, guided by the structures of mutant proteins, generated a recessive variant of mouse Dnmt1. Each of the three missense mutations studied here distorts the catalytic pocket and reduces enzymatic activity. Because all three DNMT1 mutant animals are viable, it was possible to examine their phenotypes throughout life. The consequences of genome-wide hypomethylation of DNA of somatic tissues in the Dnmt1 mutants are surprisingly mild but consistently affect the development of the lymphoid lineage. Our findings indicate that developing lymphocytes in vertebrates are sensitive to perturbations of DNA maintenance methylation.
[Display omitted]
•Genetic screens identified recessive viable missense alleles of dnmt1 in teleosts•A viable mouse Dnmt1 mutant generated by structure-guided precision mutagenesis•Missense mutations distort the catalytic pocket and reduce enzymatic activity•DNA hypomethylation consistently affects development of the lymphoid lineage
Molecular Genetics; Phenotyping; Transcriptomics |
doi_str_mv | 10.1016/j.isci.2020.101260 |
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[Display omitted]
•Genetic screens identified recessive viable missense alleles of dnmt1 in teleosts•A viable mouse Dnmt1 mutant generated by structure-guided precision mutagenesis•Missense mutations distort the catalytic pocket and reduce enzymatic activity•DNA hypomethylation consistently affects development of the lymphoid lineage
Molecular Genetics; Phenotyping; Transcriptomics</description><identifier>ISSN: 2589-0042</identifier><identifier>EISSN: 2589-0042</identifier><identifier>DOI: 10.1016/j.isci.2020.101260</identifier><identifier>PMID: 32585597</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Molecular Genetics ; Phenotyping ; Transcriptomics</subject><ispartof>iScience, 2020-07, Vol.23 (7), p.101260-101260, Article 101260</ispartof><rights>2020 The Author(s)</rights><rights>Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.</rights><rights>2020 The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c587t-bd8d52969a353009374a0fd5ecd9afc91acb29148f0acb95e3fd3351fcfd8d6f3</citedby><cites>FETCH-LOGICAL-c587t-bd8d52969a353009374a0fd5ecd9afc91acb29148f0acb95e3fd3351fcfd8d6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322073/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322073/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32585597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Iwanami, Norimasa</creatorcontrib><creatorcontrib>Takeshita, Kohei</creatorcontrib><creatorcontrib>Lawir, Divine-Fondzenyuy</creatorcontrib><creatorcontrib>Suetake, Isao</creatorcontrib><creatorcontrib>Tajima, Shoji</creatorcontrib><creatorcontrib>Sikora, Katarzyna</creatorcontrib><creatorcontrib>Trancoso, Inês</creatorcontrib><creatorcontrib>ÓMeara, Connor</creatorcontrib><creatorcontrib>Siamishi, Iliana</creatorcontrib><creatorcontrib>Takahama, Yousuke</creatorcontrib><creatorcontrib>Furutani-Seiki, Makoto</creatorcontrib><creatorcontrib>Kondoh, Hisato</creatorcontrib><creatorcontrib>Yonezawa, Yasushige</creatorcontrib><creatorcontrib>Schorpp, Michael</creatorcontrib><creatorcontrib>Boehm, Thomas</creatorcontrib><title>Epigenetic Protection of Vertebrate Lymphoid Progenitor Cells by Dnmt1</title><title>iScience</title><addtitle>iScience</addtitle><description>DNA methylation is a universal epigenetic mechanism involved in regulation of gene expression and genome stability. The DNA maintenance methylase DNMT1 ensures that DNA methylation patterns are faithfully transmitted to daughter cells during cell division. Because loss of DNMT1 is lethal, a pan-organismic analysis of DNMT1 function is lacking. We identified new recessive dnmt1 alleles in medaka and zebrafish and, guided by the structures of mutant proteins, generated a recessive variant of mouse Dnmt1. Each of the three missense mutations studied here distorts the catalytic pocket and reduces enzymatic activity. Because all three DNMT1 mutant animals are viable, it was possible to examine their phenotypes throughout life. The consequences of genome-wide hypomethylation of DNA of somatic tissues in the Dnmt1 mutants are surprisingly mild but consistently affect the development of the lymphoid lineage. Our findings indicate that developing lymphocytes in vertebrates are sensitive to perturbations of DNA maintenance methylation.
[Display omitted]
•Genetic screens identified recessive viable missense alleles of dnmt1 in teleosts•A viable mouse Dnmt1 mutant generated by structure-guided precision mutagenesis•Missense mutations distort the catalytic pocket and reduce enzymatic activity•DNA hypomethylation consistently affects development of the lymphoid lineage
Molecular Genetics; Phenotyping; Transcriptomics</description><subject>Molecular Genetics</subject><subject>Phenotyping</subject><subject>Transcriptomics</subject><issn>2589-0042</issn><issn>2589-0042</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kU1r3DAQhkVpSUKaP5BD8bGX3erDsi0ohbJN2sBCc0h7FbI02mixra2kDey_72ychuTSk4aZd57RzEvIJaNLRlnzabsM2YYlp_wxwRv6hpxx2akFpTV_-yI-JRc5bylFJeW1ak7IqcCilKo9I9dXu7CBCUqw1W2KBWwJcaqir35DKtAnU6BaH8bdfQzuqEBxKDFVKxiGXPWH6ts0FvaevPNmyHDx9J6TX9dXd6sfi_XP7zerr-uFlV1bFr3rnOSqUUZIQakSbW2odxKsU8ZbxYztuWJ15ylGSoLwTgjJvPXY2XhxTm5mrotmq3cpjCYddDRBPyZi2miTcJcBtHJW9dYrykDWIFwn2l4Iz0zT8p4xhqwvM2u370dwFqaSzPAK-royhXu9iQ-6FZzTViDg4xMgxT97yEWP6AnexUwQ91nzmnUM12QtSvkstSnmnMA_j2FUH_3UW330Ux_91LOf2PTh5QefW_65h4LPswDw5A8BkkYETBZcSGgk3iT8j_8XyNqx4w</recordid><startdate>20200724</startdate><enddate>20200724</enddate><creator>Iwanami, Norimasa</creator><creator>Takeshita, Kohei</creator><creator>Lawir, Divine-Fondzenyuy</creator><creator>Suetake, Isao</creator><creator>Tajima, Shoji</creator><creator>Sikora, Katarzyna</creator><creator>Trancoso, Inês</creator><creator>ÓMeara, Connor</creator><creator>Siamishi, Iliana</creator><creator>Takahama, Yousuke</creator><creator>Furutani-Seiki, Makoto</creator><creator>Kondoh, Hisato</creator><creator>Yonezawa, Yasushige</creator><creator>Schorpp, Michael</creator><creator>Boehm, Thomas</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20200724</creationdate><title>Epigenetic Protection of Vertebrate Lymphoid Progenitor Cells by Dnmt1</title><author>Iwanami, Norimasa ; Takeshita, Kohei ; Lawir, Divine-Fondzenyuy ; Suetake, Isao ; Tajima, Shoji ; Sikora, Katarzyna ; Trancoso, Inês ; ÓMeara, Connor ; Siamishi, Iliana ; Takahama, Yousuke ; Furutani-Seiki, Makoto ; Kondoh, Hisato ; Yonezawa, Yasushige ; Schorpp, Michael ; Boehm, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c587t-bd8d52969a353009374a0fd5ecd9afc91acb29148f0acb95e3fd3351fcfd8d6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Molecular Genetics</topic><topic>Phenotyping</topic><topic>Transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Iwanami, Norimasa</creatorcontrib><creatorcontrib>Takeshita, Kohei</creatorcontrib><creatorcontrib>Lawir, Divine-Fondzenyuy</creatorcontrib><creatorcontrib>Suetake, Isao</creatorcontrib><creatorcontrib>Tajima, Shoji</creatorcontrib><creatorcontrib>Sikora, Katarzyna</creatorcontrib><creatorcontrib>Trancoso, Inês</creatorcontrib><creatorcontrib>ÓMeara, Connor</creatorcontrib><creatorcontrib>Siamishi, Iliana</creatorcontrib><creatorcontrib>Takahama, Yousuke</creatorcontrib><creatorcontrib>Furutani-Seiki, Makoto</creatorcontrib><creatorcontrib>Kondoh, Hisato</creatorcontrib><creatorcontrib>Yonezawa, Yasushige</creatorcontrib><creatorcontrib>Schorpp, Michael</creatorcontrib><creatorcontrib>Boehm, Thomas</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>iScience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Iwanami, Norimasa</au><au>Takeshita, Kohei</au><au>Lawir, Divine-Fondzenyuy</au><au>Suetake, Isao</au><au>Tajima, Shoji</au><au>Sikora, Katarzyna</au><au>Trancoso, Inês</au><au>ÓMeara, Connor</au><au>Siamishi, Iliana</au><au>Takahama, Yousuke</au><au>Furutani-Seiki, Makoto</au><au>Kondoh, Hisato</au><au>Yonezawa, Yasushige</au><au>Schorpp, Michael</au><au>Boehm, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Epigenetic Protection of Vertebrate Lymphoid Progenitor Cells by Dnmt1</atitle><jtitle>iScience</jtitle><addtitle>iScience</addtitle><date>2020-07-24</date><risdate>2020</risdate><volume>23</volume><issue>7</issue><spage>101260</spage><epage>101260</epage><pages>101260-101260</pages><artnum>101260</artnum><issn>2589-0042</issn><eissn>2589-0042</eissn><abstract>DNA methylation is a universal epigenetic mechanism involved in regulation of gene expression and genome stability. The DNA maintenance methylase DNMT1 ensures that DNA methylation patterns are faithfully transmitted to daughter cells during cell division. Because loss of DNMT1 is lethal, a pan-organismic analysis of DNMT1 function is lacking. We identified new recessive dnmt1 alleles in medaka and zebrafish and, guided by the structures of mutant proteins, generated a recessive variant of mouse Dnmt1. Each of the three missense mutations studied here distorts the catalytic pocket and reduces enzymatic activity. Because all three DNMT1 mutant animals are viable, it was possible to examine their phenotypes throughout life. The consequences of genome-wide hypomethylation of DNA of somatic tissues in the Dnmt1 mutants are surprisingly mild but consistently affect the development of the lymphoid lineage. Our findings indicate that developing lymphocytes in vertebrates are sensitive to perturbations of DNA maintenance methylation.
[Display omitted]
•Genetic screens identified recessive viable missense alleles of dnmt1 in teleosts•A viable mouse Dnmt1 mutant generated by structure-guided precision mutagenesis•Missense mutations distort the catalytic pocket and reduce enzymatic activity•DNA hypomethylation consistently affects development of the lymphoid lineage
Molecular Genetics; Phenotyping; Transcriptomics</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32585597</pmid><doi>10.1016/j.isci.2020.101260</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Molecular Genetics Phenotyping Transcriptomics |
title | Epigenetic Protection of Vertebrate Lymphoid Progenitor Cells by Dnmt1 |
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