Physical mapping and genomic structure of the human TNFR2 gene

The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is the principal mediator of the effects of TNF on cellular immunity, and it may cooperate with TNFR1 in the killing of non...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genomics 1996-07, Vol.35 (1), p.94-100
Hauptverfasser: BELTINGER, C. P, WHITE, P. S, MARIS, J. M, SULMAN, E. P, JENSEN, S. J, LEPASLIER, D, STALLARD, B. J, GOEDDEL, D. V, DE SAUVAGE, F. J, BRODEUR, G. M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 100
container_issue 1
container_start_page 94
container_title Genomics
container_volume 35
creator BELTINGER, C. P
WHITE, P. S
MARIS, J. M
SULMAN, E. P
JENSEN, S. J
LEPASLIER, D
STALLARD, B. J
GOEDDEL, D. V
DE SAUVAGE, F. J
BRODEUR, G. M
description The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is the principal mediator of the effects of TNF on cellular immunity, and it may cooperate with TNFR1 in the killing of nonlymphoid cells. Therefore, we undertook an analysis of the genomic structure and precise physical mapping of this gene. The TNFR2 gene is contained on 10 exons that span 26 kb. Most of the functional domains of TNFR2 are encoded by separate exons, and each of the repeats of the extracellular cysteine-rich domain is interrupted by an intron. The genomic structure reveals a close relationship to TNFR1, another member of the TNFR superfamily. Based on electrophoretic analysis of yeast artificial chromosomes, TNFR2 maps within 400 kb of the genetic marker D1S434. In addition, we have identified a new polymorphic dinucleotide repeat within intron 4 of TNFR2. The genetic sequence information and exon-intron boundaries we have determined will facilitate mutational analysis of this gene to determine its potential role in neuroblastoma, as well as in other cancers with characteristic deletions or rearrangements of 1p36.
doi_str_mv 10.1006/geno.1996.0327
format Article
fullrecord <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_proquest_miscellaneous_78173732</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15668846</sourcerecordid><originalsourceid>FETCH-LOGICAL-o292t-28ff8190e6943cbdb9bfe0942155e61892231e5f2d01ae45cd04235398aca7c43</originalsourceid><addsrcrecordid>eNqF0M1LwzAYBvAgypzTqzchgnjrzFfT5CLIcCoMFZnnkqZv10qb1iY97L-3w-LV03t4fjy8PAhdUrKkhMi7Hbh2SbWWS8JZcoTmlCgdKSnkMZoTpVSUxIKfojPvvwghmis2QzMlJaVEz9H9e7n3lTU1bkzXVW6HjcvxobSpLPahH2wYesBtgUMJuBwa4_D2df3BDgjO0Ulhag8X012gz_XjdvUcbd6eXlYPm6hlmoWIqaJQVBOQWnCb5ZnOCiBaMBrHIKnSjHEKccFyQg2I2OZEMB5zrYw1iRV8ga5_e1sfqtTbKoAtbesc2JAKKQnjo7n9NV3ffg_gQ9pU3kJdGwft4NNE0YQnnP0LaSylUkKO8GqCQ9ZAnnZ91Zh-n07rjfnNlBs_Tlj0xtnK_zFOJU_Gx34AvrR7xA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15668846</pqid></control><display><type>article</type><title>Physical mapping and genomic structure of the human TNFR2 gene</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>BELTINGER, C. P ; WHITE, P. S ; MARIS, J. M ; SULMAN, E. P ; JENSEN, S. J ; LEPASLIER, D ; STALLARD, B. J ; GOEDDEL, D. V ; DE SAUVAGE, F. J ; BRODEUR, G. M</creator><creatorcontrib>BELTINGER, C. P ; WHITE, P. S ; MARIS, J. M ; SULMAN, E. P ; JENSEN, S. J ; LEPASLIER, D ; STALLARD, B. J ; GOEDDEL, D. V ; DE SAUVAGE, F. J ; BRODEUR, G. M</creatorcontrib><description>The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is the principal mediator of the effects of TNF on cellular immunity, and it may cooperate with TNFR1 in the killing of nonlymphoid cells. Therefore, we undertook an analysis of the genomic structure and precise physical mapping of this gene. The TNFR2 gene is contained on 10 exons that span 26 kb. Most of the functional domains of TNFR2 are encoded by separate exons, and each of the repeats of the extracellular cysteine-rich domain is interrupted by an intron. The genomic structure reveals a close relationship to TNFR1, another member of the TNFR superfamily. Based on electrophoretic analysis of yeast artificial chromosomes, TNFR2 maps within 400 kb of the genetic marker D1S434. In addition, we have identified a new polymorphic dinucleotide repeat within intron 4 of TNFR2. The genetic sequence information and exon-intron boundaries we have determined will facilitate mutational analysis of this gene to determine its potential role in neuroblastoma, as well as in other cancers with characteristic deletions or rearrangements of 1p36.</description><identifier>ISSN: 0888-7543</identifier><identifier>EISSN: 1089-8646</identifier><identifier>DOI: 10.1006/geno.1996.0327</identifier><identifier>PMID: 8661109</identifier><language>eng</language><publisher>San Diego, CA: Elsevier</publisher><subject>Amino Acid Sequence ; ANIMAL CELLS ; Antigens, CD - genetics ; Base Sequence ; Biological and medical sciences ; BIOLOGICAL MARKERS ; BIOLOGY AND MEDICINE, BASIC STUDIES ; CHROMOSOMAL ABERRATIONS ; Chromosomes, Human, Pair 1 - genetics ; Dinucleotide Repeats ; DNA SEQUENCING ; ELECTROPHORESIS ; Exons - genetics ; Fundamental and applied biological sciences. Psychology ; GENE MUTATIONS ; GENES ; Genes. Genome ; GENETIC MAPPING ; HEREDITARY DISEASES ; HUMAN CHROMOSOME 1 ; Humans ; IN-SITU HYBRIDIZATION ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; NECROSIS ; NEOPLASMS ; Neoplasms - genetics ; Neuroblastoma - genetics ; NUCLEOTIDES ; PATIENTS ; POLYMERASE CHAIN REACTION ; Receptors, Tumor Necrosis Factor - genetics ; Receptors, Tumor Necrosis Factor, Type II ; Sequence Alignment ; Sequence Homology, Amino Acid ; SPLICING ; STRUCTURE-ACTIVITY RELATIONSHIPS</subject><ispartof>Genomics, 1996-07, Vol.35 (1), p.94-100</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3163723$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8661109$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/466023$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>BELTINGER, C. P</creatorcontrib><creatorcontrib>WHITE, P. S</creatorcontrib><creatorcontrib>MARIS, J. M</creatorcontrib><creatorcontrib>SULMAN, E. P</creatorcontrib><creatorcontrib>JENSEN, S. J</creatorcontrib><creatorcontrib>LEPASLIER, D</creatorcontrib><creatorcontrib>STALLARD, B. J</creatorcontrib><creatorcontrib>GOEDDEL, D. V</creatorcontrib><creatorcontrib>DE SAUVAGE, F. J</creatorcontrib><creatorcontrib>BRODEUR, G. M</creatorcontrib><title>Physical mapping and genomic structure of the human TNFR2 gene</title><title>Genomics</title><addtitle>Genomics</addtitle><description>The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is the principal mediator of the effects of TNF on cellular immunity, and it may cooperate with TNFR1 in the killing of nonlymphoid cells. Therefore, we undertook an analysis of the genomic structure and precise physical mapping of this gene. The TNFR2 gene is contained on 10 exons that span 26 kb. Most of the functional domains of TNFR2 are encoded by separate exons, and each of the repeats of the extracellular cysteine-rich domain is interrupted by an intron. The genomic structure reveals a close relationship to TNFR1, another member of the TNFR superfamily. Based on electrophoretic analysis of yeast artificial chromosomes, TNFR2 maps within 400 kb of the genetic marker D1S434. In addition, we have identified a new polymorphic dinucleotide repeat within intron 4 of TNFR2. The genetic sequence information and exon-intron boundaries we have determined will facilitate mutational analysis of this gene to determine its potential role in neuroblastoma, as well as in other cancers with characteristic deletions or rearrangements of 1p36.</description><subject>Amino Acid Sequence</subject><subject>ANIMAL CELLS</subject><subject>Antigens, CD - genetics</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>BIOLOGICAL MARKERS</subject><subject>BIOLOGY AND MEDICINE, BASIC STUDIES</subject><subject>CHROMOSOMAL ABERRATIONS</subject><subject>Chromosomes, Human, Pair 1 - genetics</subject><subject>Dinucleotide Repeats</subject><subject>DNA SEQUENCING</subject><subject>ELECTROPHORESIS</subject><subject>Exons - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE MUTATIONS</subject><subject>GENES</subject><subject>Genes. Genome</subject><subject>GENETIC MAPPING</subject><subject>HEREDITARY DISEASES</subject><subject>HUMAN CHROMOSOME 1</subject><subject>Humans</subject><subject>IN-SITU HYBRIDIZATION</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>NECROSIS</subject><subject>NEOPLASMS</subject><subject>Neoplasms - genetics</subject><subject>Neuroblastoma - genetics</subject><subject>NUCLEOTIDES</subject><subject>PATIENTS</subject><subject>POLYMERASE CHAIN REACTION</subject><subject>Receptors, Tumor Necrosis Factor - genetics</subject><subject>Receptors, Tumor Necrosis Factor, Type II</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>SPLICING</subject><subject>STRUCTURE-ACTIVITY RELATIONSHIPS</subject><issn>0888-7543</issn><issn>1089-8646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0M1LwzAYBvAgypzTqzchgnjrzFfT5CLIcCoMFZnnkqZv10qb1iY97L-3w-LV03t4fjy8PAhdUrKkhMi7Hbh2SbWWS8JZcoTmlCgdKSnkMZoTpVSUxIKfojPvvwghmis2QzMlJaVEz9H9e7n3lTU1bkzXVW6HjcvxobSpLPahH2wYesBtgUMJuBwa4_D2df3BDgjO0Ulhag8X012gz_XjdvUcbd6eXlYPm6hlmoWIqaJQVBOQWnCb5ZnOCiBaMBrHIKnSjHEKccFyQg2I2OZEMB5zrYw1iRV8ga5_e1sfqtTbKoAtbesc2JAKKQnjo7n9NV3ffg_gQ9pU3kJdGwft4NNE0YQnnP0LaSylUkKO8GqCQ9ZAnnZ91Zh-n07rjfnNlBs_Tlj0xtnK_zFOJU_Gx34AvrR7xA</recordid><startdate>19960701</startdate><enddate>19960701</enddate><creator>BELTINGER, C. P</creator><creator>WHITE, P. S</creator><creator>MARIS, J. M</creator><creator>SULMAN, E. P</creator><creator>JENSEN, S. J</creator><creator>LEPASLIER, D</creator><creator>STALLARD, B. J</creator><creator>GOEDDEL, D. V</creator><creator>DE SAUVAGE, F. J</creator><creator>BRODEUR, G. M</creator><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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>19960701</creationdate><title>Physical mapping and genomic structure of the human TNFR2 gene</title><author>BELTINGER, C. P ; WHITE, P. S ; MARIS, J. M ; SULMAN, E. P ; JENSEN, S. J ; LEPASLIER, D ; STALLARD, B. J ; GOEDDEL, D. V ; DE SAUVAGE, F. J ; BRODEUR, G. M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-o292t-28ff8190e6943cbdb9bfe0942155e61892231e5f2d01ae45cd04235398aca7c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Amino Acid Sequence</topic><topic>ANIMAL CELLS</topic><topic>Antigens, CD - genetics</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>BIOLOGICAL MARKERS</topic><topic>BIOLOGY AND MEDICINE, BASIC STUDIES</topic><topic>CHROMOSOMAL ABERRATIONS</topic><topic>Chromosomes, Human, Pair 1 - genetics</topic><topic>Dinucleotide Repeats</topic><topic>DNA SEQUENCING</topic><topic>ELECTROPHORESIS</topic><topic>Exons - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GENE MUTATIONS</topic><topic>GENES</topic><topic>Genes. Genome</topic><topic>GENETIC MAPPING</topic><topic>HEREDITARY DISEASES</topic><topic>HUMAN CHROMOSOME 1</topic><topic>Humans</topic><topic>IN-SITU HYBRIDIZATION</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>NECROSIS</topic><topic>NEOPLASMS</topic><topic>Neoplasms - genetics</topic><topic>Neuroblastoma - genetics</topic><topic>NUCLEOTIDES</topic><topic>PATIENTS</topic><topic>POLYMERASE CHAIN REACTION</topic><topic>Receptors, Tumor Necrosis Factor - genetics</topic><topic>Receptors, Tumor Necrosis Factor, Type II</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>SPLICING</topic><topic>STRUCTURE-ACTIVITY RELATIONSHIPS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BELTINGER, C. P</creatorcontrib><creatorcontrib>WHITE, P. S</creatorcontrib><creatorcontrib>MARIS, J. M</creatorcontrib><creatorcontrib>SULMAN, E. P</creatorcontrib><creatorcontrib>JENSEN, S. J</creatorcontrib><creatorcontrib>LEPASLIER, D</creatorcontrib><creatorcontrib>STALLARD, B. J</creatorcontrib><creatorcontrib>GOEDDEL, D. V</creatorcontrib><creatorcontrib>DE SAUVAGE, F. J</creatorcontrib><creatorcontrib>BRODEUR, G. M</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BELTINGER, C. P</au><au>WHITE, P. S</au><au>MARIS, J. M</au><au>SULMAN, E. P</au><au>JENSEN, S. J</au><au>LEPASLIER, D</au><au>STALLARD, B. J</au><au>GOEDDEL, D. V</au><au>DE SAUVAGE, F. J</au><au>BRODEUR, G. M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical mapping and genomic structure of the human TNFR2 gene</atitle><jtitle>Genomics</jtitle><addtitle>Genomics</addtitle><date>1996-07-01</date><risdate>1996</risdate><volume>35</volume><issue>1</issue><spage>94</spage><epage>100</epage><pages>94-100</pages><issn>0888-7543</issn><eissn>1089-8646</eissn><abstract>The tumor necrosis factor receptor 2 (TNFR2) gene localizes to 1p36. 2, a genomic region characteristically deleted in neuroblastomas and other malignancies. In addition, TNFR2 is the principal mediator of the effects of TNF on cellular immunity, and it may cooperate with TNFR1 in the killing of nonlymphoid cells. Therefore, we undertook an analysis of the genomic structure and precise physical mapping of this gene. The TNFR2 gene is contained on 10 exons that span 26 kb. Most of the functional domains of TNFR2 are encoded by separate exons, and each of the repeats of the extracellular cysteine-rich domain is interrupted by an intron. The genomic structure reveals a close relationship to TNFR1, another member of the TNFR superfamily. Based on electrophoretic analysis of yeast artificial chromosomes, TNFR2 maps within 400 kb of the genetic marker D1S434. In addition, we have identified a new polymorphic dinucleotide repeat within intron 4 of TNFR2. The genetic sequence information and exon-intron boundaries we have determined will facilitate mutational analysis of this gene to determine its potential role in neuroblastoma, as well as in other cancers with characteristic deletions or rearrangements of 1p36.</abstract><cop>San Diego, CA</cop><pub>Elsevier</pub><pmid>8661109</pmid><doi>10.1006/geno.1996.0327</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0888-7543
ispartof Genomics, 1996-07, Vol.35 (1), p.94-100
issn 0888-7543
1089-8646
language eng
recordid cdi_proquest_miscellaneous_78173732
source MEDLINE; Elsevier ScienceDirect Journals
subjects Amino Acid Sequence
ANIMAL CELLS
Antigens, CD - genetics
Base Sequence
Biological and medical sciences
BIOLOGICAL MARKERS
BIOLOGY AND MEDICINE, BASIC STUDIES
CHROMOSOMAL ABERRATIONS
Chromosomes, Human, Pair 1 - genetics
Dinucleotide Repeats
DNA SEQUENCING
ELECTROPHORESIS
Exons - genetics
Fundamental and applied biological sciences. Psychology
GENE MUTATIONS
GENES
Genes. Genome
GENETIC MAPPING
HEREDITARY DISEASES
HUMAN CHROMOSOME 1
Humans
IN-SITU HYBRIDIZATION
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
NECROSIS
NEOPLASMS
Neoplasms - genetics
Neuroblastoma - genetics
NUCLEOTIDES
PATIENTS
POLYMERASE CHAIN REACTION
Receptors, Tumor Necrosis Factor - genetics
Receptors, Tumor Necrosis Factor, Type II
Sequence Alignment
Sequence Homology, Amino Acid
SPLICING
STRUCTURE-ACTIVITY RELATIONSHIPS
title Physical mapping and genomic structure of the human TNFR2 gene
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T06%3A49%3A45IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Physical%20mapping%20and%20genomic%20structure%20of%20the%20human%20TNFR2%20gene&rft.jtitle=Genomics&rft.au=BELTINGER,%20C.%20P&rft.date=1996-07-01&rft.volume=35&rft.issue=1&rft.spage=94&rft.epage=100&rft.pages=94-100&rft.issn=0888-7543&rft.eissn=1089-8646&rft_id=info:doi/10.1006/geno.1996.0327&rft_dat=%3Cproquest_osti_%3E15668846%3C/proquest_osti_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=15668846&rft_id=info:pmid/8661109&rfr_iscdi=true