Genomic imprinting of Mash2 , a mouse gene required for trophoblast development
The mouse gene Mash2 encodes a transcription factor required for development of trophoblast progenitors. Mash2 − homozygous mutant embryos die at 10 days post–coitum from placental failure. Here we show that Mash2 is genomically imprinted. First, Mash2+/− embryos inheriting a wild–type allele from t...
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Veröffentlicht in: | Nature genetics 1995-03, Vol.9 (3), p.235-242 |
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creator | Anderson, David J Nagy, András Caspary, Tamara Tilghman, Shirley M Copeland, Neal G Gilbert, Debra J Guillemot, François Rossant, Janet Jenkins, Nancy A Joyner, Alexandra L |
description | The mouse gene
Mash2
encodes a transcription factor required for development of trophoblast progenitors.
Mash2
− homozygous mutant embryos die at 10 days post–coitum from placental failure. Here we show that
Mash2
is genomically imprinted. First,
Mash2+/−
embryos inheriting a wild–type allele from their father die at the same stage as −/− embryos, with a similar placental phenotype. Second, the
Mash2
paternal allele is initially expressed by groups of trophoblast cells at 6.5 and 7.5 days post–coitum, but appears almost completely repressed by 8.5 days post–coitum. Finally, we have genetically and physically mapped
Mash2
to the distal region of chromosome 7, within a cluster of imprinted genes, including
insulin–2
,
insulin–like growth factor–2
and
H19
. |
doi_str_mv | 10.1038/ng0395-235 |
format | Article |
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Mash2
encodes a transcription factor required for development of trophoblast progenitors.
Mash2
− homozygous mutant embryos die at 10 days post–coitum from placental failure. Here we show that
Mash2
is genomically imprinted. First,
Mash2+/−
embryos inheriting a wild–type allele from their father die at the same stage as −/− embryos, with a similar placental phenotype. Second, the
Mash2
paternal allele is initially expressed by groups of trophoblast cells at 6.5 and 7.5 days post–coitum, but appears almost completely repressed by 8.5 days post–coitum. Finally, we have genetically and physically mapped
Mash2
to the distal region of chromosome 7, within a cluster of imprinted genes, including
insulin–2
,
insulin–like growth factor–2
and
H19
.</description><identifier>ISSN: 1061-4036</identifier><identifier>EISSN: 1546-1718</identifier><identifier>DOI: 10.1038/ng0395-235</identifier><identifier>PMID: 7773285</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Agriculture ; Alleles ; Animal Genetics and Genomics ; Animals ; Base Sequence ; Basic Helix-Loop-Helix Transcription Factors ; Biochemistry, Molecular Biology ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Chromosome Mapping ; Crosses, Genetic ; DNA Primers - genetics ; DNA-Binding Proteins - genetics ; Female ; Gene Expression Regulation, Developmental ; Gene Function ; Genetic Linkage ; Genomic Imprinting ; Gestational Age ; Heterozygote ; Homozygote ; Human Genetics ; Life Sciences ; Male ; Mice ; Molecular Sequence Data ; Mutation ; Pregnancy ; Transcription Factors ; Trophoblasts - metabolism</subject><ispartof>Nature genetics, 1995-03, Vol.9 (3), p.235-242</ispartof><rights>Springer Nature America, Inc. 1995</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-427ea10021102317974c333a68c5b0e08e7c4c826683aefe40aa674f562fcd183</citedby><cites>FETCH-LOGICAL-c474t-427ea10021102317974c333a68c5b0e08e7c4c826683aefe40aa674f562fcd183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/ng0395-235$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/ng0395-235$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,778,782,883,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7773285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03951344$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, David J</creatorcontrib><creatorcontrib>Nagy, András</creatorcontrib><creatorcontrib>Caspary, Tamara</creatorcontrib><creatorcontrib>Tilghman, Shirley M</creatorcontrib><creatorcontrib>Copeland, Neal G</creatorcontrib><creatorcontrib>Gilbert, Debra J</creatorcontrib><creatorcontrib>Guillemot, François</creatorcontrib><creatorcontrib>Rossant, Janet</creatorcontrib><creatorcontrib>Jenkins, Nancy A</creatorcontrib><creatorcontrib>Joyner, Alexandra L</creatorcontrib><title>Genomic imprinting of Mash2 , a mouse gene required for trophoblast development</title><title>Nature genetics</title><addtitle>Nat Genet</addtitle><addtitle>Nat Genet</addtitle><description>The mouse gene
Mash2
encodes a transcription factor required for development of trophoblast progenitors.
Mash2
− homozygous mutant embryos die at 10 days post–coitum from placental failure. Here we show that
Mash2
is genomically imprinted. First,
Mash2+/−
embryos inheriting a wild–type allele from their father die at the same stage as −/− embryos, with a similar placental phenotype. Second, the
Mash2
paternal allele is initially expressed by groups of trophoblast cells at 6.5 and 7.5 days post–coitum, but appears almost completely repressed by 8.5 days post–coitum. Finally, we have genetically and physically mapped
Mash2
to the distal region of chromosome 7, within a cluster of imprinted genes, including
insulin–2
,
insulin–like growth factor–2
and
H19
.</description><subject>Agriculture</subject><subject>Alleles</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Basic Helix-Loop-Helix Transcription Factors</subject><subject>Biochemistry, Molecular Biology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Chromosome Mapping</subject><subject>Crosses, Genetic</subject><subject>DNA Primers - genetics</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Female</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Function</subject><subject>Genetic Linkage</subject><subject>Genomic Imprinting</subject><subject>Gestational Age</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Human Genetics</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Pregnancy</subject><subject>Transcription Factors</subject><subject>Trophoblasts - metabolism</subject><issn>1061-4036</issn><issn>1546-1718</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkkFL7DAUhYMo6lM37oWsBH1Wc5s0ySxFfCqMuNF1yGRuZyptMiat4L83Q4dx88BVQu7H4dxzQsgpsGtgXN_4BeOTqih5tUMOoRKyAAV6N9-ZhEIwLg_In5TeGQMhmN4n-0opXurqkLw8oA9d42jTrWLj-8YvaKjps03Lkl5RS7swJKQL9EgjfgxNxDmtQ6R9DKtlmLU29XSOn9iGVYe-PyZ7tW0TnmzOI_L27_717rGYvjw83d1OCyeU6AtRKrTAWAnASg5qooTjnFupXTVjyDQqJ5wupdTcYo2CWSuVqCtZ1m4Omh-Ri1F3aVuTnXc2fplgG_N4OzXrt3UiwIX4hMyej-wqho8BU2-6JjlsW-sxb2dyFgAV17-CIFW2q0QGL0fQxZBSxHprAZhZV2LGSkyuJMNnG9Vh1uF8i246yPO_4zytG1hgNO9hiD6n9381OtLe9kPErdrPH-Df4zOc3Q</recordid><startdate>19950301</startdate><enddate>19950301</enddate><creator>Anderson, David J</creator><creator>Nagy, András</creator><creator>Caspary, Tamara</creator><creator>Tilghman, Shirley M</creator><creator>Copeland, Neal G</creator><creator>Gilbert, Debra J</creator><creator>Guillemot, François</creator><creator>Rossant, Janet</creator><creator>Jenkins, Nancy A</creator><creator>Joyner, Alexandra L</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>19950301</creationdate><title>Genomic imprinting of Mash2 , a mouse gene required for trophoblast development</title><author>Anderson, David J ; Nagy, András ; Caspary, Tamara ; Tilghman, Shirley M ; Copeland, Neal G ; Gilbert, Debra J ; Guillemot, François ; Rossant, Janet ; Jenkins, Nancy A ; Joyner, Alexandra L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-427ea10021102317974c333a68c5b0e08e7c4c826683aefe40aa674f562fcd183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Agriculture</topic><topic>Alleles</topic><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Basic Helix-Loop-Helix Transcription Factors</topic><topic>Biochemistry, Molecular Biology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Chromosome Mapping</topic><topic>Crosses, Genetic</topic><topic>DNA Primers - genetics</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Female</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gene Function</topic><topic>Genetic Linkage</topic><topic>Genomic Imprinting</topic><topic>Gestational Age</topic><topic>Heterozygote</topic><topic>Homozygote</topic><topic>Human Genetics</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Mutation</topic><topic>Pregnancy</topic><topic>Transcription Factors</topic><topic>Trophoblasts - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, David J</creatorcontrib><creatorcontrib>Nagy, András</creatorcontrib><creatorcontrib>Caspary, Tamara</creatorcontrib><creatorcontrib>Tilghman, Shirley M</creatorcontrib><creatorcontrib>Copeland, Neal G</creatorcontrib><creatorcontrib>Gilbert, Debra J</creatorcontrib><creatorcontrib>Guillemot, François</creatorcontrib><creatorcontrib>Rossant, Janet</creatorcontrib><creatorcontrib>Jenkins, Nancy A</creatorcontrib><creatorcontrib>Joyner, Alexandra L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Nature genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, David J</au><au>Nagy, András</au><au>Caspary, Tamara</au><au>Tilghman, Shirley M</au><au>Copeland, Neal G</au><au>Gilbert, Debra J</au><au>Guillemot, François</au><au>Rossant, Janet</au><au>Jenkins, Nancy A</au><au>Joyner, Alexandra L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genomic imprinting of Mash2 , a mouse gene required for trophoblast development</atitle><jtitle>Nature genetics</jtitle><stitle>Nat Genet</stitle><addtitle>Nat Genet</addtitle><date>1995-03-01</date><risdate>1995</risdate><volume>9</volume><issue>3</issue><spage>235</spage><epage>242</epage><pages>235-242</pages><issn>1061-4036</issn><eissn>1546-1718</eissn><abstract>The mouse gene
Mash2
encodes a transcription factor required for development of trophoblast progenitors.
Mash2
− homozygous mutant embryos die at 10 days post–coitum from placental failure. Here we show that
Mash2
is genomically imprinted. First,
Mash2+/−
embryos inheriting a wild–type allele from their father die at the same stage as −/− embryos, with a similar placental phenotype. Second, the
Mash2
paternal allele is initially expressed by groups of trophoblast cells at 6.5 and 7.5 days post–coitum, but appears almost completely repressed by 8.5 days post–coitum. Finally, we have genetically and physically mapped
Mash2
to the distal region of chromosome 7, within a cluster of imprinted genes, including
insulin–2
,
insulin–like growth factor–2
and
H19
.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>7773285</pmid><doi>10.1038/ng0395-235</doi><tpages>8</tpages></addata></record> |
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subjects | Agriculture Alleles Animal Genetics and Genomics Animals Base Sequence Basic Helix-Loop-Helix Transcription Factors Biochemistry, Molecular Biology Biomedical and Life Sciences Biomedicine Cancer Research Chromosome Mapping Crosses, Genetic DNA Primers - genetics DNA-Binding Proteins - genetics Female Gene Expression Regulation, Developmental Gene Function Genetic Linkage Genomic Imprinting Gestational Age Heterozygote Homozygote Human Genetics Life Sciences Male Mice Molecular Sequence Data Mutation Pregnancy Transcription Factors Trophoblasts - metabolism |
title | Genomic imprinting of Mash2 , a mouse gene required for trophoblast development |
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