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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genomics (San Diego, Calif.) Calif.), 2001-01, Vol.71 (2), p.256-259
Hauptverfasser: Saunders, Laura R., Jurecic, Vesna, Barber, Glen N.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 259
container_issue 2
container_start_page 256
container_title Genomics (San Diego, Calif.)
container_volume 71
creator Saunders, Laura R.
Jurecic, Vesna
Barber, Glen N.
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70604967</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0888754300964231</els_id><sourcerecordid>70604967</sourcerecordid><originalsourceid>FETCH-LOGICAL-c465t-863d90ff02cf3e737b9f06b97633deed0e430f60155ae170311aea05a064e22c3</originalsourceid><addsrcrecordid>eNqFkU1vEzEQhi0EoqFw5YgsIXHbMF7v-uMYpS1Fqgoq4Ww53jE17NrB3gD99zhKBCfEyRr5mdHM-xDyksGSAYi3XzCmZQsAS9G1_BFZMFC6UaITj8kClFKN7Dt-Rp6V8rVSmqv2KTljjAmmWliQX5t7pBoaauNAGYPm24Wl1_vJRnp7tbqjH3OaMcRCVxnpJttYRjvjQH1OE938TPQieI8Z4xzsOD7QT7sxuPo_3d2uCr2MLg21SpGu72tHKmlCyvSO8efkibdjwRen95x8vrrcrK-bmw_v3q9XN43rRD_XS_igwXtonecoudxqD2KrpeB8QBwAOw5eAOt7i0wCZ8yihd6C6LBtHT8nb45zdzl932OZzRSKw3G0EdO-GAkCOi3kf0EmFUiueAWXR9DlVEpGb3Y5TDY_GAbmIMUcpJiDFHOQUhtenSbvtxMOf_GThQq8PgG2ODv6GrML5Q-nNaheVUodKaxx_QiYTXEBY007ZHSzGVL41wa_AYblpKU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>17807383</pqid></control><display><type>article</type><title>The 90- and 110-kDa Human NFAR Proteins Are Translated from Two Differentially Spliced mRNAs Encoded on Chromosome 19p13</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Saunders, Laura R. ; Jurecic, Vesna ; Barber, Glen N.</creator><creatorcontrib>Saunders, Laura R. ; Jurecic, Vesna ; Barber, Glen N.</creatorcontrib><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><identifier>ISSN: 0888-7543</identifier><identifier>EISSN: 1089-8646</identifier><identifier>DOI: 10.1006/geno.2000.6423</identifier><identifier>PMID: 11161820</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>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</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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=990858$$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>
fulltext fulltext
identifier ISSN: 0888-7543
ispartof Genomics (San Diego, Calif.), 2001-01, Vol.71 (2), p.256-259
issn 0888-7543
1089-8646
language eng
recordid cdi_proquest_miscellaneous_70604967
source MEDLINE; Access via ScienceDirect (Elsevier)
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T05%3A47%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%2090-%20and%20110-kDa%20Human%20NFAR%20Proteins%20Are%20Translated%20from%20Two%20Differentially%20Spliced%20mRNAs%20Encoded%20on%20Chromosome%2019p13&rft.jtitle=Genomics%20(San%20Diego,%20Calif.)&rft.au=Saunders,%20Laura%20R.&rft.date=2001-01-15&rft.volume=71&rft.issue=2&rft.spage=256&rft.epage=259&rft.pages=256-259&rft.issn=0888-7543&rft.eissn=1089-8646&rft_id=info:doi/10.1006/geno.2000.6423&rft_dat=%3Cproquest_cross%3E70604967%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=17807383&rft_id=info:pmid/11161820&rft_els_id=S0888754300964231&rfr_iscdi=true