The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13
The NFAR gene (nuclear factor associated with dsRNA) encodes a putative transcription-associated factor that we have shown is a substrate for the interferon-inducible, dsRNA-dependent protein kinase, PKR. However, our protein expression analysis has revealed that NFAR exists as two major protein spe...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2001-01, Vol.71 (2), p.256-259 |
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description | The NFAR gene (nuclear factor associated with dsRNA) encodes a putative transcription-associated factor that we have shown is a substrate for the interferon-inducible, dsRNA-dependent protein kinase, PKR. However, our protein expression analysis has revealed that NFAR exists as two major protein species of 90 kDa (NFAR-1) and 110 kDa (NFAR-2) in the cell. To resolve the genetic identity of NFAR-1 and -2, we carried out sequence analysis of genomic and cDNA NFAR clones and determined that the coding region of this gene spans 16.2 kb and comprises 21 exons. Our data indicate that NFAR-1 and -2 arise from a single gene on chromosome 19p13 and are generated through alternative splicing events. NFAR-1 (HGMW-approved symbol ILF3) was found to comprise 1 extra exon, 18, that contains several stop codons to ensure termination of the protein at amino acid 702. In contrast, NFAR-2 lacks this exon, though it comprises an additional 3 coding exons (exons 19, 20, and 21) located at the carboxyl region to generate an extended product of 894 amino acids. Our studies, the first to elucidate the gene structure and chromosomal assignment of NFAR, establish the genetic basis for future NFAR research in humans. |
doi_str_mv | 10.1006/geno.2000.6423 |
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However, our protein expression analysis has revealed that NFAR exists as two major protein species of 90 kDa (NFAR-1) and 110 kDa (NFAR-2) in the cell. To resolve the genetic identity of NFAR-1 and -2, we carried out sequence analysis of genomic and cDNA NFAR clones and determined that the coding region of this gene spans 16.2 kb and comprises 21 exons. Our data indicate that NFAR-1 and -2 arise from a single gene on chromosome 19p13 and are generated through alternative splicing events. NFAR-1 (HGMW-approved symbol ILF3) was found to comprise 1 extra exon, 18, that contains several stop codons to ensure termination of the protein at amino acid 702. In contrast, NFAR-2 lacks this exon, though it comprises an additional 3 coding exons (exons 19, 20, and 21) located at the carboxyl region to generate an extended product of 894 amino acids. 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Genome ; Humans ; Molecular and cellular biology ; Molecular genetics ; Molecular Sequence Data ; Molecular Weight ; NFAR gene ; Nuclear Factor 90 Proteins ; Nuclear Proteins - genetics ; Phosphoproteins ; Protein Isoforms - genetics ; RNA, Double-Stranded - metabolism ; RNA-Binding Proteins - genetics ; Sequence Analysis, DNA</subject><ispartof>Genomics (San Diego, Calif.), 2001-01, Vol.71 (2), p.256-259</ispartof><rights>2001 Academic Press</rights><rights>2001 INIST-CNRS</rights><rights>Copyright 2001 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-863d90ff02cf3e737b9f06b97633deed0e430f60155ae170311aea05a064e22c3</citedby><cites>FETCH-LOGICAL-c465t-863d90ff02cf3e737b9f06b97633deed0e430f60155ae170311aea05a064e22c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/geno.2000.6423$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=990858$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11161820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saunders, Laura R.</creatorcontrib><creatorcontrib>Jurecic, Vesna</creatorcontrib><creatorcontrib>Barber, Glen N.</creatorcontrib><title>The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13</title><title>Genomics (San Diego, Calif.)</title><addtitle>Genomics</addtitle><description>The NFAR gene (nuclear factor associated with dsRNA) encodes a putative transcription-associated factor that we have shown is a substrate for the interferon-inducible, dsRNA-dependent protein kinase, PKR. However, our protein expression analysis has revealed that NFAR exists as two major protein species of 90 kDa (NFAR-1) and 110 kDa (NFAR-2) in the cell. To resolve the genetic identity of NFAR-1 and -2, we carried out sequence analysis of genomic and cDNA NFAR clones and determined that the coding region of this gene spans 16.2 kb and comprises 21 exons. Our data indicate that NFAR-1 and -2 arise from a single gene on chromosome 19p13 and are generated through alternative splicing events. NFAR-1 (HGMW-approved symbol ILF3) was found to comprise 1 extra exon, 18, that contains several stop codons to ensure termination of the protein at amino acid 702. In contrast, NFAR-2 lacks this exon, though it comprises an additional 3 coding exons (exons 19, 20, and 21) located at the carboxyl region to generate an extended product of 894 amino acids. Our studies, the first to elucidate the gene structure and chromosomal assignment of NFAR, establish the genetic basis for future NFAR research in humans.</description><subject>Alternative Splicing - genetics</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosome 19</subject><subject>Chromosomes, Human, Pair 19</subject><subject>Codon, Terminator</subject><subject>eIF-2 Kinase</subject><subject>Exons</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes. Genome</subject><subject>Humans</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>Molecular Weight</subject><subject>NFAR gene</subject><subject>Nuclear Factor 90 Proteins</subject><subject>Nuclear Proteins - genetics</subject><subject>Phosphoproteins</subject><subject>Protein Isoforms - genetics</subject><subject>RNA, Double-Stranded - metabolism</subject><subject>RNA-Binding Proteins - genetics</subject><subject>Sequence Analysis, DNA</subject><issn>0888-7543</issn><issn>1089-8646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1vEzEQhi0EoqFw5YgsIXHbMF7v-uMYpS1Fqgoq4Ww53jE17NrB3gD99zhKBCfEyRr5mdHM-xDyksGSAYi3XzCmZQsAS9G1_BFZMFC6UaITj8kClFKN7Dt-Rp6V8rVSmqv2KTljjAmmWliQX5t7pBoaauNAGYPm24Wl1_vJRnp7tbqjH3OaMcRCVxnpJttYRjvjQH1OE938TPQieI8Z4xzsOD7QT7sxuPo_3d2uCr2MLg21SpGu72tHKmlCyvSO8efkibdjwRen95x8vrrcrK-bmw_v3q9XN43rRD_XS_igwXtonecoudxqD2KrpeB8QBwAOw5eAOt7i0wCZ8yihd6C6LBtHT8nb45zdzl932OZzRSKw3G0EdO-GAkCOi3kf0EmFUiueAWXR9DlVEpGb3Y5TDY_GAbmIMUcpJiDFHOQUhtenSbvtxMOf_GThQq8PgG2ODv6GrML5Q-nNaheVUodKaxx_QiYTXEBY007ZHSzGVL41wa_AYblpKU</recordid><startdate>20010115</startdate><enddate>20010115</enddate><creator>Saunders, Laura R.</creator><creator>Jurecic, Vesna</creator><creator>Barber, Glen N.</creator><general>Elsevier Inc</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20010115</creationdate><title>The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13</title><author>Saunders, Laura R. ; Jurecic, Vesna ; Barber, Glen N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-863d90ff02cf3e737b9f06b97633deed0e430f60155ae170311aea05a064e22c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Alternative Splicing - genetics</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosome 19</topic><topic>Chromosomes, Human, Pair 19</topic><topic>Codon, Terminator</topic><topic>eIF-2 Kinase</topic><topic>Exons</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes. Genome</topic><topic>Humans</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>Molecular Weight</topic><topic>NFAR gene</topic><topic>Nuclear Factor 90 Proteins</topic><topic>Nuclear Proteins - genetics</topic><topic>Phosphoproteins</topic><topic>Protein Isoforms - genetics</topic><topic>RNA, Double-Stranded - metabolism</topic><topic>RNA-Binding Proteins - genetics</topic><topic>Sequence Analysis, DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saunders, Laura R.</creatorcontrib><creatorcontrib>Jurecic, Vesna</creatorcontrib><creatorcontrib>Barber, Glen N.</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genomics (San Diego, Calif.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saunders, Laura R.</au><au>Jurecic, Vesna</au><au>Barber, Glen N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13</atitle><jtitle>Genomics (San Diego, Calif.)</jtitle><addtitle>Genomics</addtitle><date>2001-01-15</date><risdate>2001</risdate><volume>71</volume><issue>2</issue><spage>256</spage><epage>259</epage><pages>256-259</pages><issn>0888-7543</issn><eissn>1089-8646</eissn><abstract>The NFAR gene (nuclear factor associated with dsRNA) encodes a putative transcription-associated factor that we have shown is a substrate for the interferon-inducible, dsRNA-dependent protein kinase, PKR. However, our protein expression analysis has revealed that NFAR exists as two major protein species of 90 kDa (NFAR-1) and 110 kDa (NFAR-2) in the cell. To resolve the genetic identity of NFAR-1 and -2, we carried out sequence analysis of genomic and cDNA NFAR clones and determined that the coding region of this gene spans 16.2 kb and comprises 21 exons. Our data indicate that NFAR-1 and -2 arise from a single gene on chromosome 19p13 and are generated through alternative splicing events. NFAR-1 (HGMW-approved symbol ILF3) was found to comprise 1 extra exon, 18, that contains several stop codons to ensure termination of the protein at amino acid 702. In contrast, NFAR-2 lacks this exon, though it comprises an additional 3 coding exons (exons 19, 20, and 21) located at the carboxyl region to generate an extended product of 894 amino acids. Our studies, the first to elucidate the gene structure and chromosomal assignment of NFAR, establish the genetic basis for future NFAR research in humans.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>11161820</pmid><doi>10.1006/geno.2000.6423</doi><tpages>4</tpages></addata></record> |
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subjects | Alternative Splicing - genetics Base Sequence Biological and medical sciences Chromosome 19 Chromosomes, Human, Pair 19 Codon, Terminator eIF-2 Kinase Exons Fundamental and applied biological sciences. Psychology Genes. Genome Humans Molecular and cellular biology Molecular genetics Molecular Sequence Data Molecular Weight NFAR gene Nuclear Factor 90 Proteins Nuclear Proteins - genetics Phosphoproteins Protein Isoforms - genetics RNA, Double-Stranded - metabolism RNA-Binding Proteins - genetics Sequence Analysis, DNA |
title | The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13 |
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