Structural relationship of human interferon alpha genes and pseudogenes
We have isolated and characterized DNA segments containing IFN-α-related sequences from human lambda and cosmid clone banks. We describe six linkage groups comprising 18 distinct IFN-α-related loci, and report the nucleotide sequences of nine chromosomal IFN-α genes with intact reading frames, as we...
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Veröffentlicht in: | Journal of molecular biology 1985-09, Vol.185 (2), p.227-260 |
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creator | Henco, K. Brosius, J. Fujisawa, A. Fujisawa, J.-I. Haynes, J.R. Hochstadt, J. Kovacic, T. Pasek, M. Schamböck, A. Schmid, J. Todokoro, K. Wälchli, M. Nagata, S. Weissmann, C. |
description | We have isolated and characterized DNA segments containing
IFN-α-related sequences from human lambda and cosmid clone banks. We describe six linkage groups comprising 18 distinct
IFN-α-related loci, and report the nucleotide sequences of nine chromosomal IFN-α genes with intact reading frames, as well as of five pseudogenes. Taking into account as yet unsequenced genes as well as clones described by others, there are now seven linkage groups and 23 loci, of which 15 correspond to potentially functional genes and six to non-functional genes; two loci remain unsequenced. Eighteen additional sequences are likely to be allelic to the above. The finding that at least two IFN-α genes appear to be natural hybrids of other IFN-α genes, and that two distinct IFN-α loci have completely identical coding sequences, although their flanking regions are different, is evidence for information exchange between the individual genes. |
doi_str_mv | 10.1016/0022-2836(85)90401-2 |
format | Article |
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IFN-α-related sequences from human lambda and cosmid clone banks. We describe six linkage groups comprising 18 distinct
IFN-α-related loci, and report the nucleotide sequences of nine chromosomal IFN-α genes with intact reading frames, as well as of five pseudogenes. Taking into account as yet unsequenced genes as well as clones described by others, there are now seven linkage groups and 23 loci, of which 15 correspond to potentially functional genes and six to non-functional genes; two loci remain unsequenced. Eighteen additional sequences are likely to be allelic to the above. The finding that at least two IFN-α genes appear to be natural hybrids of other IFN-α genes, and that two distinct IFN-α loci have completely identical coding sequences, although their flanking regions are different, is evidence for information exchange between the individual genes.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/0022-2836(85)90401-2</identifier><identifier>PMID: 4057246</identifier><identifier>CODEN: JMOBAK</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Amino Acid Sequence ; Base Sequence ; Biological and medical sciences ; Chromosome Mapping ; Cosmids ; DNA - genetics ; Fundamental and applied biological sciences. Psychology ; Genes ; Genes. Genome ; Genetic Linkage ; Humans ; Interferon Type I - genetics ; Molecular and cellular biology ; Molecular genetics ; Protein Sorting Signals - genetics ; Sequence Homology, Nucleic Acid ; Transcription, Genetic</subject><ispartof>Journal of molecular biology, 1985-09, Vol.185 (2), p.227-260</ispartof><rights>1985</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-543f21819cb6ea8a3dd469d57533b79c7872036f42815d75a1203ddc7d858ae53</citedby><cites>FETCH-LOGICAL-c483t-543f21819cb6ea8a3dd469d57533b79c7872036f42815d75a1203ddc7d858ae53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0022-2836(85)90401-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8510563$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4057246$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Henco, K.</creatorcontrib><creatorcontrib>Brosius, J.</creatorcontrib><creatorcontrib>Fujisawa, A.</creatorcontrib><creatorcontrib>Fujisawa, J.-I.</creatorcontrib><creatorcontrib>Haynes, J.R.</creatorcontrib><creatorcontrib>Hochstadt, J.</creatorcontrib><creatorcontrib>Kovacic, T.</creatorcontrib><creatorcontrib>Pasek, M.</creatorcontrib><creatorcontrib>Schamböck, A.</creatorcontrib><creatorcontrib>Schmid, J.</creatorcontrib><creatorcontrib>Todokoro, K.</creatorcontrib><creatorcontrib>Wälchli, M.</creatorcontrib><creatorcontrib>Nagata, S.</creatorcontrib><creatorcontrib>Weissmann, C.</creatorcontrib><title>Structural relationship of human interferon alpha genes and pseudogenes</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>We have isolated and characterized DNA segments containing
IFN-α-related sequences from human lambda and cosmid clone banks. We describe six linkage groups comprising 18 distinct
IFN-α-related loci, and report the nucleotide sequences of nine chromosomal IFN-α genes with intact reading frames, as well as of five pseudogenes. Taking into account as yet unsequenced genes as well as clones described by others, there are now seven linkage groups and 23 loci, of which 15 correspond to potentially functional genes and six to non-functional genes; two loci remain unsequenced. Eighteen additional sequences are likely to be allelic to the above. The finding that at least two IFN-α genes appear to be natural hybrids of other IFN-α genes, and that two distinct IFN-α loci have completely identical coding sequences, although their flanking regions are different, is evidence for information exchange between the individual genes.</description><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>Cosmids</subject><subject>DNA - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes</subject><subject>Genes. Genome</subject><subject>Genetic Linkage</subject><subject>Humans</subject><subject>Interferon Type I - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Protein Sorting Signals - genetics</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription, Genetic</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLHEEURgsx6Pj4Bwn0QkQXbepdtzeCSDQBIQvjuqipup2p0FPdVnUH8u_T4wyz1NXl45774BDymdEbRpn-SinnNQehr0BdN1RSVvMDsmAUmhq0gEOy2CPH5KSUP5RSJSQckSNJleFSL8jj85gnP07ZdVXGzo2xT2UVh6pvq9W0dqmKacTcYu5T5bph5arfmLBULoVqKDiF_i2fkU-t6wqe7-opeXn49uv-e_308_HH_d1T7SWIsVZStJwBa_xSowMnQpC6CcooIZam8QYMp0K3kgNTwSjH5hiCNwEUOFTilFxu9w65f52wjHYdi8eucwn7qVijpTCafwwyKSQDEDMot6DPfSkZWzvkuHb5n2XUbkTbjUW7sWhB2TfRls9jX3b7p-Uaw35oZ3buX-z6rnjXtdklH8seA8Wo0pvrt1sMZ2l_I2ZbfMTkMcSMfrShj-__8R-PwJhz</recordid><startdate>19850920</startdate><enddate>19850920</enddate><creator>Henco, K.</creator><creator>Brosius, J.</creator><creator>Fujisawa, A.</creator><creator>Fujisawa, J.-I.</creator><creator>Haynes, J.R.</creator><creator>Hochstadt, J.</creator><creator>Kovacic, T.</creator><creator>Pasek, M.</creator><creator>Schamböck, A.</creator><creator>Schmid, J.</creator><creator>Todokoro, K.</creator><creator>Wälchli, M.</creator><creator>Nagata, S.</creator><creator>Weissmann, C.</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>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19850920</creationdate><title>Structural relationship of human interferon alpha genes and pseudogenes</title><author>Henco, K. ; Brosius, J. ; Fujisawa, A. ; Fujisawa, J.-I. ; Haynes, J.R. ; Hochstadt, J. ; Kovacic, T. ; Pasek, M. ; Schamböck, A. ; Schmid, J. ; Todokoro, K. ; Wälchli, M. ; Nagata, S. ; Weissmann, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-543f21819cb6ea8a3dd469d57533b79c7872036f42815d75a1203ddc7d858ae53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosome Mapping</topic><topic>Cosmids</topic><topic>DNA - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes</topic><topic>Genes. Genome</topic><topic>Genetic Linkage</topic><topic>Humans</topic><topic>Interferon Type I - genetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Protein Sorting Signals - genetics</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Henco, K.</creatorcontrib><creatorcontrib>Brosius, J.</creatorcontrib><creatorcontrib>Fujisawa, A.</creatorcontrib><creatorcontrib>Fujisawa, J.-I.</creatorcontrib><creatorcontrib>Haynes, J.R.</creatorcontrib><creatorcontrib>Hochstadt, J.</creatorcontrib><creatorcontrib>Kovacic, T.</creatorcontrib><creatorcontrib>Pasek, M.</creatorcontrib><creatorcontrib>Schamböck, A.</creatorcontrib><creatorcontrib>Schmid, J.</creatorcontrib><creatorcontrib>Todokoro, K.</creatorcontrib><creatorcontrib>Wälchli, M.</creatorcontrib><creatorcontrib>Nagata, S.</creatorcontrib><creatorcontrib>Weissmann, C.</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>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Henco, K.</au><au>Brosius, J.</au><au>Fujisawa, A.</au><au>Fujisawa, J.-I.</au><au>Haynes, J.R.</au><au>Hochstadt, J.</au><au>Kovacic, T.</au><au>Pasek, M.</au><au>Schamböck, A.</au><au>Schmid, J.</au><au>Todokoro, K.</au><au>Wälchli, M.</au><au>Nagata, S.</au><au>Weissmann, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural relationship of human interferon alpha genes and pseudogenes</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>1985-09-20</date><risdate>1985</risdate><volume>185</volume><issue>2</issue><spage>227</spage><epage>260</epage><pages>227-260</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><coden>JMOBAK</coden><abstract>We have isolated and characterized DNA segments containing
IFN-α-related sequences from human lambda and cosmid clone banks. We describe six linkage groups comprising 18 distinct
IFN-α-related loci, and report the nucleotide sequences of nine chromosomal IFN-α genes with intact reading frames, as well as of five pseudogenes. Taking into account as yet unsequenced genes as well as clones described by others, there are now seven linkage groups and 23 loci, of which 15 correspond to potentially functional genes and six to non-functional genes; two loci remain unsequenced. Eighteen additional sequences are likely to be allelic to the above. The finding that at least two IFN-α genes appear to be natural hybrids of other IFN-α genes, and that two distinct IFN-α loci have completely identical coding sequences, although their flanking regions are different, is evidence for information exchange between the individual genes.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>4057246</pmid><doi>10.1016/0022-2836(85)90401-2</doi><tpages>34</tpages></addata></record> |
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subjects | Amino Acid Sequence Base Sequence Biological and medical sciences Chromosome Mapping Cosmids DNA - genetics Fundamental and applied biological sciences. Psychology Genes Genes. Genome Genetic Linkage Humans Interferon Type I - genetics Molecular and cellular biology Molecular genetics Protein Sorting Signals - genetics Sequence Homology, Nucleic Acid Transcription, Genetic |
title | Structural relationship of human interferon alpha genes and pseudogenes |
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