Aberrant regulation of imprinted gene expression in Gtl2 mice

The imprinted region on mouse distal chromosome 12 covers about 1 Mb and contains at least three paternally expressed genes (Pegs: Peg9/Dlk1, Peg11/Rtl1, and Dio3) and four maternally expressed genes (Megs: Meg3/Gtl2, antiPeg11/antiRlt1, Meg8/Rian, and Meg9/Mirg). Gtl2lacZ (Gene trap locus 2) mice h...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cytogenetic and genome research 2006-03, Vol.113 (1-4), p.223-229
Hauptverfasser: Sekita, Y, Wagatsuma, H, Irie, M, Kobayashi, S, Kohda, T, Matsuda, J, Yokoyama, M, Ogura, A, Schuster-Gossler, K, Gossler, A, Ishino, F, Kaneko-Ishino, T
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 229
container_issue 1-4
container_start_page 223
container_title Cytogenetic and genome research
container_volume 113
creator Sekita, Y
Wagatsuma, H
Irie, M
Kobayashi, S
Kohda, T
Matsuda, J
Yokoyama, M
Ogura, A
Schuster-Gossler, K
Gossler, A
Ishino, F
Kaneko-Ishino, T
description The imprinted region on mouse distal chromosome 12 covers about 1 Mb and contains at least three paternally expressed genes (Pegs: Peg9/Dlk1, Peg11/Rtl1, and Dio3) and four maternally expressed genes (Megs: Meg3/Gtl2, antiPeg11/antiRlt1, Meg8/Rian, and Meg9/Mirg). Gtl2lacZ (Gene trap locus 2) mice have a transgene (TG) insertion 2.3 kb upstream from the Meg3/Gtl2 promoter and show about 40% growth retardation when the TG-inserted allele is paternally derived. Quantitative RT-PCR experiments showed that the expression levels of Pegs in this region were reduced below 50%. These results are consistent with the observed phenotype in Gtl2lacZ mice, because at least two Pegs(Peg9/Dlk1 and Dio3) have growth-promoting effects. The aberrant induction of Megs from silent paternal alleles was also observed in association with changes in the DNA methylation level of a differentially methylated region (DMR) located around Meg3/Gtl2 exon 1. Interestingly, a 60∼80% reduction in all Megs was observed when the TG was maternally derived, although the pups showed no apparent growth or morphological abnormalities. Therefore, the paternal or maternal inheritance of the TG results in the down-regulation in cis of either Pegs or Megs, respectively, suggesting that the TG insertion influences the mechanism regulating the entire imprinted region. Copyright © 2006 S. Karger AG, Basel
doi_str_mv 10.1159/000090836
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_21273944</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>21273944</sourcerecordid><originalsourceid>FETCH-LOGICAL-p244t-dc429eeed22f60e75fe412f945b680b872fe956df7467838b0e8b0d7bc44a2fc3</originalsourceid><addsrcrecordid>eNqFkE9LxDAQxYMouK4e_AbBg7dqMp00ycHDsugqLHhR8Fb6Z7J06aY1ScGPb0Xx4MWB4T14PwbeMHYpxY2Uyt6KeawweXHEFhIBM6Ps2_GvN_KUncW4F0IaVMWC3a1qCqHyiQfaTX2VusHzwfHuMIbOJ2r5jjxx-hgDxfgVdp5vUg_80DV0zk5c1Ue6-NEle324f1k_ZtvnzdN6tc1GQExZ2yBYImoBXCFIK0cowVlUdWFEbTQ4sqponcZCm9zUguZtdd0gVuCafMmuv--OYXifKKby0MWG-r7yNEyxBAk6t4j_g8JKmP80g1d_wP0wBT-XKAEQQGol8k8TY2Nf</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>224221750</pqid></control><display><type>article</type><title>Aberrant regulation of imprinted gene expression in Gtl2 mice</title><source>Karger Journals</source><source>Alma/SFX Local Collection</source><creator>Sekita, Y ; Wagatsuma, H ; Irie, M ; Kobayashi, S ; Kohda, T ; Matsuda, J ; Yokoyama, M ; Ogura, A ; Schuster-Gossler, K ; Gossler, A ; Ishino, F ; Kaneko-Ishino, T</creator><creatorcontrib>Sekita, Y ; Wagatsuma, H ; Irie, M ; Kobayashi, S ; Kohda, T ; Matsuda, J ; Yokoyama, M ; Ogura, A ; Schuster-Gossler, K ; Gossler, A ; Ishino, F ; Kaneko-Ishino, T</creatorcontrib><description>The imprinted region on mouse distal chromosome 12 covers about 1 Mb and contains at least three paternally expressed genes (Pegs: Peg9/Dlk1, Peg11/Rtl1, and Dio3) and four maternally expressed genes (Megs: Meg3/Gtl2, antiPeg11/antiRlt1, Meg8/Rian, and Meg9/Mirg). Gtl2lacZ (Gene trap locus 2) mice have a transgene (TG) insertion 2.3 kb upstream from the Meg3/Gtl2 promoter and show about 40% growth retardation when the TG-inserted allele is paternally derived. Quantitative RT-PCR experiments showed that the expression levels of Pegs in this region were reduced below 50%. These results are consistent with the observed phenotype in Gtl2lacZ mice, because at least two Pegs(Peg9/Dlk1 and Dio3) have growth-promoting effects. The aberrant induction of Megs from silent paternal alleles was also observed in association with changes in the DNA methylation level of a differentially methylated region (DMR) located around Meg3/Gtl2 exon 1. Interestingly, a 60∼80% reduction in all Megs was observed when the TG was maternally derived, although the pups showed no apparent growth or morphological abnormalities. Therefore, the paternal or maternal inheritance of the TG results in the down-regulation in cis of either Pegs or Megs, respectively, suggesting that the TG insertion influences the mechanism regulating the entire imprinted region. Copyright © 2006 S. Karger AG, Basel</description><identifier>ISSN: 1424-8581</identifier><identifier>EISSN: 1424-859X</identifier><identifier>DOI: 10.1159/000090836</identifier><language>eng</language><publisher>Basel: S. Karger AG</publisher><ispartof>Cytogenetic and genome research, 2006-03, Vol.113 (1-4), p.223-229</ispartof><rights>Copyright (c) 2006 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Sekita, Y</creatorcontrib><creatorcontrib>Wagatsuma, H</creatorcontrib><creatorcontrib>Irie, M</creatorcontrib><creatorcontrib>Kobayashi, S</creatorcontrib><creatorcontrib>Kohda, T</creatorcontrib><creatorcontrib>Matsuda, J</creatorcontrib><creatorcontrib>Yokoyama, M</creatorcontrib><creatorcontrib>Ogura, A</creatorcontrib><creatorcontrib>Schuster-Gossler, K</creatorcontrib><creatorcontrib>Gossler, A</creatorcontrib><creatorcontrib>Ishino, F</creatorcontrib><creatorcontrib>Kaneko-Ishino, T</creatorcontrib><title>Aberrant regulation of imprinted gene expression in Gtl2 mice</title><title>Cytogenetic and genome research</title><description>The imprinted region on mouse distal chromosome 12 covers about 1 Mb and contains at least three paternally expressed genes (Pegs: Peg9/Dlk1, Peg11/Rtl1, and Dio3) and four maternally expressed genes (Megs: Meg3/Gtl2, antiPeg11/antiRlt1, Meg8/Rian, and Meg9/Mirg). Gtl2lacZ (Gene trap locus 2) mice have a transgene (TG) insertion 2.3 kb upstream from the Meg3/Gtl2 promoter and show about 40% growth retardation when the TG-inserted allele is paternally derived. Quantitative RT-PCR experiments showed that the expression levels of Pegs in this region were reduced below 50%. These results are consistent with the observed phenotype in Gtl2lacZ mice, because at least two Pegs(Peg9/Dlk1 and Dio3) have growth-promoting effects. The aberrant induction of Megs from silent paternal alleles was also observed in association with changes in the DNA methylation level of a differentially methylated region (DMR) located around Meg3/Gtl2 exon 1. Interestingly, a 60∼80% reduction in all Megs was observed when the TG was maternally derived, although the pups showed no apparent growth or morphological abnormalities. Therefore, the paternal or maternal inheritance of the TG results in the down-regulation in cis of either Pegs or Megs, respectively, suggesting that the TG insertion influences the mechanism regulating the entire imprinted region. Copyright © 2006 S. Karger AG, Basel</description><issn>1424-8581</issn><issn>1424-859X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFkE9LxDAQxYMouK4e_AbBg7dqMp00ycHDsugqLHhR8Fb6Z7J06aY1ScGPb0Xx4MWB4T14PwbeMHYpxY2Uyt6KeawweXHEFhIBM6Ps2_GvN_KUncW4F0IaVMWC3a1qCqHyiQfaTX2VusHzwfHuMIbOJ2r5jjxx-hgDxfgVdp5vUg_80DV0zk5c1Ue6-NEle324f1k_ZtvnzdN6tc1GQExZ2yBYImoBXCFIK0cowVlUdWFEbTQ4sqponcZCm9zUguZtdd0gVuCafMmuv--OYXifKKby0MWG-r7yNEyxBAk6t4j_g8JKmP80g1d_wP0wBT-XKAEQQGol8k8TY2Nf</recordid><startdate>200603</startdate><enddate>200603</enddate><creator>Sekita, Y</creator><creator>Wagatsuma, H</creator><creator>Irie, M</creator><creator>Kobayashi, S</creator><creator>Kohda, T</creator><creator>Matsuda, J</creator><creator>Yokoyama, M</creator><creator>Ogura, A</creator><creator>Schuster-Gossler, K</creator><creator>Gossler, A</creator><creator>Ishino, F</creator><creator>Kaneko-Ishino, T</creator><general>S. Karger AG</general><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>S0X</scope></search><sort><creationdate>200603</creationdate><title>Aberrant regulation of imprinted gene expression in Gtl2 mice</title><author>Sekita, Y ; Wagatsuma, H ; Irie, M ; Kobayashi, S ; Kohda, T ; Matsuda, J ; Yokoyama, M ; Ogura, A ; Schuster-Gossler, K ; Gossler, A ; Ishino, F ; Kaneko-Ishino, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p244t-dc429eeed22f60e75fe412f945b680b872fe956df7467838b0e8b0d7bc44a2fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sekita, Y</creatorcontrib><creatorcontrib>Wagatsuma, H</creatorcontrib><creatorcontrib>Irie, M</creatorcontrib><creatorcontrib>Kobayashi, S</creatorcontrib><creatorcontrib>Kohda, T</creatorcontrib><creatorcontrib>Matsuda, J</creatorcontrib><creatorcontrib>Yokoyama, M</creatorcontrib><creatorcontrib>Ogura, A</creatorcontrib><creatorcontrib>Schuster-Gossler, K</creatorcontrib><creatorcontrib>Gossler, A</creatorcontrib><creatorcontrib>Ishino, F</creatorcontrib><creatorcontrib>Kaneko-Ishino, T</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><jtitle>Cytogenetic and genome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sekita, Y</au><au>Wagatsuma, H</au><au>Irie, M</au><au>Kobayashi, S</au><au>Kohda, T</au><au>Matsuda, J</au><au>Yokoyama, M</au><au>Ogura, A</au><au>Schuster-Gossler, K</au><au>Gossler, A</au><au>Ishino, F</au><au>Kaneko-Ishino, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aberrant regulation of imprinted gene expression in Gtl2 mice</atitle><jtitle>Cytogenetic and genome research</jtitle><date>2006-03</date><risdate>2006</risdate><volume>113</volume><issue>1-4</issue><spage>223</spage><epage>229</epage><pages>223-229</pages><issn>1424-8581</issn><eissn>1424-859X</eissn><abstract>The imprinted region on mouse distal chromosome 12 covers about 1 Mb and contains at least three paternally expressed genes (Pegs: Peg9/Dlk1, Peg11/Rtl1, and Dio3) and four maternally expressed genes (Megs: Meg3/Gtl2, antiPeg11/antiRlt1, Meg8/Rian, and Meg9/Mirg). Gtl2lacZ (Gene trap locus 2) mice have a transgene (TG) insertion 2.3 kb upstream from the Meg3/Gtl2 promoter and show about 40% growth retardation when the TG-inserted allele is paternally derived. Quantitative RT-PCR experiments showed that the expression levels of Pegs in this region were reduced below 50%. These results are consistent with the observed phenotype in Gtl2lacZ mice, because at least two Pegs(Peg9/Dlk1 and Dio3) have growth-promoting effects. The aberrant induction of Megs from silent paternal alleles was also observed in association with changes in the DNA methylation level of a differentially methylated region (DMR) located around Meg3/Gtl2 exon 1. Interestingly, a 60∼80% reduction in all Megs was observed when the TG was maternally derived, although the pups showed no apparent growth or morphological abnormalities. Therefore, the paternal or maternal inheritance of the TG results in the down-regulation in cis of either Pegs or Megs, respectively, suggesting that the TG insertion influences the mechanism regulating the entire imprinted region. Copyright © 2006 S. Karger AG, Basel</abstract><cop>Basel</cop><pub>S. Karger AG</pub><doi>10.1159/000090836</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1424-8581
ispartof Cytogenetic and genome research, 2006-03, Vol.113 (1-4), p.223-229
issn 1424-8581
1424-859X
language eng
recordid cdi_proquest_miscellaneous_21273944
source Karger Journals; Alma/SFX Local Collection
title Aberrant regulation of imprinted gene expression in Gtl2 mice
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T12%3A19%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Aberrant%20regulation%20of%20imprinted%20gene%20expression%20in%20Gtl2%20mice&rft.jtitle=Cytogenetic%20and%20genome%20research&rft.au=Sekita,%20Y&rft.date=2006-03&rft.volume=113&rft.issue=1-4&rft.spage=223&rft.epage=229&rft.pages=223-229&rft.issn=1424-8581&rft.eissn=1424-859X&rft_id=info:doi/10.1159/000090836&rft_dat=%3Cproquest%3E21273944%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=224221750&rft_id=info:pmid/&rfr_iscdi=true