Determinants of species- and placenta-specific expression of p100 GAP

This study was based on the hypothesis that both primary sequence and methylation status of the GTPase activating protein (GAP) gene limits expression of p100 GAP to primate placenta. Due to alternate splicing, a 65-bp insert appears between the first and second coding exons of p100 GAP mRNA, and tr...

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Veröffentlicht in:Placenta (Eastbourne) 1998-03, Vol.19 (2), p.225-230
Hauptverfasser: Liao, L., Trouba, K.J., Vorce, R.L.
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container_title Placenta (Eastbourne)
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creator Liao, L.
Trouba, K.J.
Vorce, R.L.
description This study was based on the hypothesis that both primary sequence and methylation status of the GTPase activating protein (GAP) gene limits expression of p100 GAP to primate placenta. Due to alternate splicing, a 65-bp insert appears between the first and second coding exons of p100 GAP mRNA, and translation of p100 GAP initiates within this insert. Examination of the sequence surrounding the 65-bp insert revealed that the monkey GAP gene contained both the 3′ splice donor site and the internal start codon, whereas the mouse GAP gene contained neither. To address p100 GAP tissue specificity, the methylation status of the GAP gene was examined. Site-specific demethylation was found to correlate with synthesis of p100 GAP, suggesting that methylation regulates the expression of different GAP isoforms. The results of this study provide a mechanistic basis for the observation that p100 GAP is synthesized only in primate placenta and suggest that its expression is regulated, in part, by gene methylation.
doi_str_mv 10.1016/S0143-4004(98)90012-1
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Fetal membranes</subject><subject>GTP Phosphohydrolases - genetics</subject><subject>GTP Phosphohydrolases - metabolism</subject><subject>GTPase-Activating Proteins</subject><subject>Haplorhini</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Placenta - enzymology</subject><subject>Polymerase Chain Reaction</subject><subject>Pregnancy</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Species Specificity</subject><subject>Tumor Cells, Cultured - enzymology</subject><issn>0143-4004</issn><issn>1532-3102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkN9LwzAQgIMoOqd_gtAHEX2o3iVpbZ5kzDkFQUF9DllyhUjX1qQT_e9tt7FXuYeDu-9-8DF2hnCNgPnNG6AUqQSQl6q4UgDIU9xjI8wETwUC32ejHXLEjmP8BAAlkR-yQ5XJAhWM2OyeOgpLX5u6i0lTJrEl6ymmiald0lbGUt2ZdF0tvU3opw0Uo2_qAW4RIJlPXk_YQWmqSKfbPGYfD7P36WP6_DJ_mk6eUysK1fWfLGQm8gIgv6V8geTIojICFBq5UCUvrCsBeIZWkMsckSpK56SzsqfyTIzZxWZvG5qvFcVOL320VFWmpmYV9a3qA7jowWwD2tDEGKjUbfBLE341gh706bU-PbjRqtBrfRr7ubPtgdViSW43tfXV98-3fROtqcpgauvjDuMcOMBw_m6DUS_j21PQsZdaW3I-kO20a_w_j_wBGnyKXA</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>Liao, L.</creator><creator>Trouba, K.J.</creator><creator>Vorce, R.L.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</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>19980301</creationdate><title>Determinants of species- and placenta-specific expression of p100 GAP</title><author>Liao, L. ; Trouba, K.J. ; Vorce, R.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-40b453680067e6b1edec19a3091a4b9f28cdf00251c3ed5dee98fdd4dc49a3653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>DNA - analysis</topic><topic>DNA Methylation</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Female</topic><topic>Fetal membranes</topic><topic>Fibroblasts - enzymology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects. Development. Fetal membranes</topic><topic>GTP Phosphohydrolases - genetics</topic><topic>GTP Phosphohydrolases - metabolism</topic><topic>GTPase-Activating Proteins</topic><topic>Haplorhini</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Placenta - enzymology</topic><topic>Polymerase Chain Reaction</topic><topic>Pregnancy</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Species Specificity</topic><topic>Tumor Cells, Cultured - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liao, L.</creatorcontrib><creatorcontrib>Trouba, K.J.</creatorcontrib><creatorcontrib>Vorce, R.L.</creatorcontrib><collection>Pascal-Francis</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>Placenta (Eastbourne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liao, L.</au><au>Trouba, K.J.</au><au>Vorce, R.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Determinants of species- and placenta-specific expression of p100 GAP</atitle><jtitle>Placenta (Eastbourne)</jtitle><addtitle>Placenta</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>19</volume><issue>2</issue><spage>225</spage><epage>230</epage><pages>225-230</pages><issn>0143-4004</issn><eissn>1532-3102</eissn><coden>PLACDF</coden><abstract>This study was based on the hypothesis that both primary sequence and methylation status of the GTPase activating protein (GAP) gene limits expression of p100 GAP to primate placenta. Due to alternate splicing, a 65-bp insert appears between the first and second coding exons of p100 GAP mRNA, and translation of p100 GAP initiates within this insert. Examination of the sequence surrounding the 65-bp insert revealed that the monkey GAP gene contained both the 3′ splice donor site and the internal start codon, whereas the mouse GAP gene contained neither. To address p100 GAP tissue specificity, the methylation status of the GAP gene was examined. Site-specific demethylation was found to correlate with synthesis of p100 GAP, suggesting that methylation regulates the expression of different GAP isoforms. The results of this study provide a mechanistic basis for the observation that p100 GAP is synthesized only in primate placenta and suggest that its expression is regulated, in part, by gene methylation.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>9548190</pmid><doi>10.1016/S0143-4004(98)90012-1</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Adult
Animals
Base Sequence
Biological and medical sciences
DNA - analysis
DNA Methylation
Embryology: invertebrates and vertebrates. Teratology
Female
Fetal membranes
Fibroblasts - enzymology
Fundamental and applied biological sciences. Psychology
General aspects. Development. Fetal membranes
GTP Phosphohydrolases - genetics
GTP Phosphohydrolases - metabolism
GTPase-Activating Proteins
Haplorhini
Humans
Male
Mice
Molecular Sequence Data
Placenta - enzymology
Polymerase Chain Reaction
Pregnancy
Proteins - genetics
Proteins - metabolism
Rats
Rats, Sprague-Dawley
Sequence Homology, Nucleic Acid
Species Specificity
Tumor Cells, Cultured - enzymology
title Determinants of species- and placenta-specific expression of p100 GAP
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