PHF3 expression is frequently reduced in glioma
Glioblastoma is the most frequent brain tumor and accounts for approximately 50–60% of all astrocytic tumors. Many chromosome alterations have been described in glioblastoma, but only for a few alterations were the genes identified and linked to genetic pathways in glioblastoma development. To contr...
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creator | Fischer, U. Struss, A.-K. Hemmer, D. Michel, A. Henn, W. Steudel, W.-I. Meese, E. |
description | Glioblastoma is the most frequent brain tumor and accounts for approximately 50–60% of all astrocytic tumors. Many chromosome alterations have been described in glioblastoma, but only for a few alterations were the genes identified and linked to genetic pathways in glioblastoma development. To contribute to the identification of novel genes involved in glioblastoma development we used a combined immunological and molecular screening approach. Here we report the identification and expression analysis of a novel gene from human chromosome 6q12 that is considered to be the third member of a family of PHD finger containing genes and is termed PHF3. PHF3 is ubiquitously expressed in normal tissues including brain, but its expression is significantly reduced or lost in glioblastoma, glioblastoma cell lines, anaplastic astrocytomas and astrocytomas. The PHF3 protein sequence contains several protein motifs frequently found in transcription factors. One of those motifs is a PHD finger, also termed LAP motif and known to bind large portions of DNA. Another region of the protein revealed a high homology to the transcription factor TFIIS, especially to a region that is necessary for the Polymerase II binding properties of TFIIS. Combining these results, PHF3 is a novel member of a large class of regulatory proteins containing a LAP motif, and loss of its expression in glioblastoma may contribute to glioma development. |
doi_str_mv | 10.1159/000048804 |
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Many chromosome alterations have been described in glioblastoma, but only for a few alterations were the genes identified and linked to genetic pathways in glioblastoma development. To contribute to the identification of novel genes involved in glioblastoma development we used a combined immunological and molecular screening approach. Here we report the identification and expression analysis of a novel gene from human chromosome 6q12 that is considered to be the third member of a family of PHD finger containing genes and is termed PHF3. PHF3 is ubiquitously expressed in normal tissues including brain, but its expression is significantly reduced or lost in glioblastoma, glioblastoma cell lines, anaplastic astrocytomas and astrocytomas. The PHF3 protein sequence contains several protein motifs frequently found in transcription factors. One of those motifs is a PHD finger, also termed LAP motif and known to bind large portions of DNA. Another region of the protein revealed a high homology to the transcription factor TFIIS, especially to a region that is necessary for the Polymerase II binding properties of TFIIS. Combining these results, PHF3 is a novel member of a large class of regulatory proteins containing a LAP motif, and loss of its expression in glioblastoma may contribute to glioma development. </description><identifier>ISSN: 1424-8581</identifier><identifier>ISSN: 0301-0171</identifier><identifier>EISSN: 1424-859X</identifier><identifier>DOI: 10.1159/000048804</identifier><identifier>PMID: 11856869</identifier><identifier>CODEN: CGCGBR</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Adult ; Aged ; Amino Acid Motifs ; Amino Acid Sequence ; Base Sequence ; Biological and medical sciences ; Brain - metabolism ; chromosome 6 ; Chromosomes, Human, Pair 6 - genetics ; Classical genetics, quantitative genetics, hybrids ; Cloning, Molecular ; Down-Regulation ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Gene Mapping, Cloning and Sequencing ; Genetics of eukaryotes. Biological and molecular evolution ; Glioblastoma - genetics ; Glioblastoma - pathology ; Human ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Medical sciences ; Middle Aged ; Molecular Sequence Data ; Neurology ; PHF3 gene ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; RNA, Neoplasm - genetics ; RNA, Neoplasm - metabolism ; Transcription Factors - chemistry ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Tumors of the nervous system. Phacomatoses</subject><ispartof>Cytogenetic and genome research, 2001-01, Vol.94 (3-4), p.131-136</ispartof><rights>2002 S. Karger AG, Basel</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 S. Karger AG, Basel</rights><rights>Copyright S. Karger AG 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-a9294fda7f37529c8f988f8abbb67e157397de13824f9419b4e706382af11c4b3</citedby><cites>FETCH-LOGICAL-c416t-a9294fda7f37529c8f988f8abbb67e157397de13824f9419b4e706382af11c4b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,2425,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13530112$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11856869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fischer, U.</creatorcontrib><creatorcontrib>Struss, A.-K.</creatorcontrib><creatorcontrib>Hemmer, D.</creatorcontrib><creatorcontrib>Michel, A.</creatorcontrib><creatorcontrib>Henn, W.</creatorcontrib><creatorcontrib>Steudel, W.-I.</creatorcontrib><creatorcontrib>Meese, E.</creatorcontrib><title>PHF3 expression is frequently reduced in glioma</title><title>Cytogenetic and genome research</title><addtitle>Cytogenet Genome Res</addtitle><description>Glioblastoma is the most frequent brain tumor and accounts for approximately 50–60% of all astrocytic tumors. Many chromosome alterations have been described in glioblastoma, but only for a few alterations were the genes identified and linked to genetic pathways in glioblastoma development. To contribute to the identification of novel genes involved in glioblastoma development we used a combined immunological and molecular screening approach. Here we report the identification and expression analysis of a novel gene from human chromosome 6q12 that is considered to be the third member of a family of PHD finger containing genes and is termed PHF3. PHF3 is ubiquitously expressed in normal tissues including brain, but its expression is significantly reduced or lost in glioblastoma, glioblastoma cell lines, anaplastic astrocytomas and astrocytomas. The PHF3 protein sequence contains several protein motifs frequently found in transcription factors. One of those motifs is a PHD finger, also termed LAP motif and known to bind large portions of DNA. Another region of the protein revealed a high homology to the transcription factor TFIIS, especially to a region that is necessary for the Polymerase II binding properties of TFIIS. Combining these results, PHF3 is a novel member of a large class of regulatory proteins containing a LAP motif, and loss of its expression in glioblastoma may contribute to glioma development. </description><subject>Adult</subject><subject>Aged</subject><subject>Amino Acid Motifs</subject><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Brain - metabolism</subject><subject>chromosome 6</subject><subject>Chromosomes, Human, Pair 6 - genetics</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Cloning, Molecular</subject><subject>Down-Regulation</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene Mapping, Cloning and Sequencing</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Glioblastoma - genetics</subject><subject>Glioblastoma - pathology</subject><subject>Human</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Molecular Sequence Data</subject><subject>Neurology</subject><subject>PHF3 gene</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>RNA, Neoplasm - genetics</subject><subject>RNA, Neoplasm - metabolism</subject><subject>Transcription Factors - chemistry</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Tumors of the nervous system. 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Psychology</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene Mapping, Cloning and Sequencing</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Glioblastoma - genetics</topic><topic>Glioblastoma - pathology</topic><topic>Human</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Molecular Sequence Data</topic><topic>Neurology</topic><topic>PHF3 gene</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>RNA, Neoplasm - genetics</topic><topic>RNA, Neoplasm - metabolism</topic><topic>Transcription Factors - chemistry</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Tumors of the nervous system. 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Many chromosome alterations have been described in glioblastoma, but only for a few alterations were the genes identified and linked to genetic pathways in glioblastoma development. To contribute to the identification of novel genes involved in glioblastoma development we used a combined immunological and molecular screening approach. Here we report the identification and expression analysis of a novel gene from human chromosome 6q12 that is considered to be the third member of a family of PHD finger containing genes and is termed PHF3. PHF3 is ubiquitously expressed in normal tissues including brain, but its expression is significantly reduced or lost in glioblastoma, glioblastoma cell lines, anaplastic astrocytomas and astrocytomas. The PHF3 protein sequence contains several protein motifs frequently found in transcription factors. One of those motifs is a PHD finger, also termed LAP motif and known to bind large portions of DNA. Another region of the protein revealed a high homology to the transcription factor TFIIS, especially to a region that is necessary for the Polymerase II binding properties of TFIIS. Combining these results, PHF3 is a novel member of a large class of regulatory proteins containing a LAP motif, and loss of its expression in glioblastoma may contribute to glioma development. </abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>11856869</pmid><doi>10.1159/000048804</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Amino Acid Motifs Amino Acid Sequence Base Sequence Biological and medical sciences Brain - metabolism chromosome 6 Chromosomes, Human, Pair 6 - genetics Classical genetics, quantitative genetics, hybrids Cloning, Molecular Down-Regulation Female Fundamental and applied biological sciences. Psychology Gene Expression Profiling Gene Expression Regulation, Neoplastic Gene Mapping, Cloning and Sequencing Genetics of eukaryotes. Biological and molecular evolution Glioblastoma - genetics Glioblastoma - pathology Human Humans In Situ Hybridization, Fluorescence Male Medical sciences Middle Aged Molecular Sequence Data Neurology PHF3 gene RNA, Messenger - genetics RNA, Messenger - metabolism RNA, Neoplasm - genetics RNA, Neoplasm - metabolism Transcription Factors - chemistry Transcription Factors - genetics Transcription Factors - metabolism Tumors of the nervous system. Phacomatoses |
title | PHF3 expression is frequently reduced in glioma |
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