Identification of Genes Differentially Regulated by Interferon α , β , or γ Using Oligonucleotide Arrays
The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-α , -β , or -γ treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with pro...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1998-12, Vol.95 (26), p.15623-15628 |
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description | The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-α , -β , or -γ treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with probe sets corresponding to more than 6,800 human genes. Among these were transcripts for known IFN-stimulated genes (ISGs), the expression of which were consistent with previous studies in which the particular ISG was characterized as responsive to either Type I (α , β ) or Type II (γ ) IFNs, or both. Importantly, many novel IFN-stimulated genes were identified that were diverse in their known biological functions. For instance, several novel ISGs were identified that are implicated in apoptosis (including RAP46/Bag-1, phospholipid scramblase, and hypoxia inducible factor-1α ). Furthermore, several IFN-repressed genes also were identified. These results demonstrate the usefulness of oligonucleotide arrays in monitoring mammalian gene expression on a broad and unprecedented scale. In particular, these findings provide insights into the basic mechanisms of IFN actions and ultimately may contribute to better therapeutic uses for IFNs. |
doi_str_mv | 10.1073/pnas.95.26.15623 |
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G. Williams ; Silverman, Robert H.</creator><creatorcontrib>Der, Sandy D. ; Zhou, Aimin ; Bryan R. G. Williams ; Silverman, Robert H.</creatorcontrib><description>The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-α , -β , or -γ treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with probe sets corresponding to more than 6,800 human genes. Among these were transcripts for known IFN-stimulated genes (ISGs), the expression of which were consistent with previous studies in which the particular ISG was characterized as responsive to either Type I (α , β ) or Type II (γ ) IFNs, or both. Importantly, many novel IFN-stimulated genes were identified that were diverse in their known biological functions. For instance, several novel ISGs were identified that are implicated in apoptosis (including RAP46/Bag-1, phospholipid scramblase, and hypoxia inducible factor-1α ). Furthermore, several IFN-repressed genes also were identified. These results demonstrate the usefulness of oligonucleotide arrays in monitoring mammalian gene expression on a broad and unprecedented scale. In particular, these findings provide insights into the basic mechanisms of IFN actions and ultimately may contribute to better therapeutic uses for IFNs.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.95.26.15623</identifier><identifier>PMID: 9861020</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Apoptosis ; Biological Sciences ; Carrier Proteins - genetics ; Cell lines ; Cellular biology ; Complementary DNA ; Complementary RNA ; Datasets ; DNA-Binding Proteins - genetics ; Enzymes - immunology ; Fibrosarcoma ; Gene expression regulation ; Gene Expression Regulation, Neoplastic - drug effects ; Gene Expression Regulation, Neoplastic - immunology ; Genes ; Humans ; Hypoxia-Inducible Factor 1 ; Hypoxia-Inducible Factor 1, alpha Subunit ; Interferon ; Interferon-alpha - pharmacology ; Interferon-alpha - physiology ; Interferon-beta - pharmacology ; Interferon-beta - physiology ; Interferon-gamma - pharmacology ; Interferon-gamma - physiology ; Membrane Proteins - genetics ; Messenger RNA ; Nuclear Proteins - genetics ; Oligonucleotide Probes ; Oligonucleotides ; Phospholipid Transfer Proteins ; Proteins - genetics ; RNA ; RNA, Messenger - genetics ; Transcription Factors ; Transcription, Genetic ; Tumor Cells, Cultured</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1998-12, Vol.95 (26), p.15623-15628</ispartof><rights>Copyright 1993-1998 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Dec 22, 1998</rights><rights>Copyright © 1998, The National Academy of Sciences 1998</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-92ebcd785faae77622b3837473d30c42a0526d2d40e13ab87179f781693242d23</citedby><cites>FETCH-LOGICAL-c523t-92ebcd785faae77622b3837473d30c42a0526d2d40e13ab87179f781693242d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/95/26.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/46429$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/46429$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9861020$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Der, Sandy D.</creatorcontrib><creatorcontrib>Zhou, Aimin</creatorcontrib><creatorcontrib>Bryan R. G. Williams</creatorcontrib><creatorcontrib>Silverman, Robert H.</creatorcontrib><title>Identification of Genes Differentially Regulated by Interferon α , β , or γ Using Oligonucleotide Arrays</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-α , -β , or -γ treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with probe sets corresponding to more than 6,800 human genes. Among these were transcripts for known IFN-stimulated genes (ISGs), the expression of which were consistent with previous studies in which the particular ISG was characterized as responsive to either Type I (α , β ) or Type II (γ ) IFNs, or both. Importantly, many novel IFN-stimulated genes were identified that were diverse in their known biological functions. For instance, several novel ISGs were identified that are implicated in apoptosis (including RAP46/Bag-1, phospholipid scramblase, and hypoxia inducible factor-1α ). Furthermore, several IFN-repressed genes also were identified. These results demonstrate the usefulness of oligonucleotide arrays in monitoring mammalian gene expression on a broad and unprecedented scale. In particular, these findings provide insights into the basic mechanisms of IFN actions and ultimately may contribute to better therapeutic uses for IFNs.</description><subject>Apoptosis</subject><subject>Biological Sciences</subject><subject>Carrier Proteins - genetics</subject><subject>Cell lines</subject><subject>Cellular biology</subject><subject>Complementary DNA</subject><subject>Complementary RNA</subject><subject>Datasets</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Enzymes - immunology</subject><subject>Fibrosarcoma</subject><subject>Gene expression regulation</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Gene Expression Regulation, Neoplastic - immunology</subject><subject>Genes</subject><subject>Humans</subject><subject>Hypoxia-Inducible Factor 1</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit</subject><subject>Interferon</subject><subject>Interferon-alpha - pharmacology</subject><subject>Interferon-alpha - physiology</subject><subject>Interferon-beta - pharmacology</subject><subject>Interferon-beta - physiology</subject><subject>Interferon-gamma - pharmacology</subject><subject>Interferon-gamma - physiology</subject><subject>Membrane Proteins - genetics</subject><subject>Messenger RNA</subject><subject>Nuclear Proteins - genetics</subject><subject>Oligonucleotide Probes</subject><subject>Oligonucleotides</subject><subject>Phospholipid Transfer Proteins</subject><subject>Proteins - genetics</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>Transcription Factors</subject><subject>Transcription, Genetic</subject><subject>Tumor Cells, Cultured</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU-LEzEYh4Moa3f1LoIY9iAenPrmz0wm4GVZdS0sLIh7DpmZTE1Nk5rMiP1Y6vfoZzJjS3E9eEkOz_NL3pcfQk8IzAkI9nrjdZrLck6rOSkryu6hGQFJiopLuI9mAFQUNaf8ITpNaQUAsqzhBJ3IuiJAYYa-LDrjB9vbVg82eBx6fGW8Sfit7XsTJ6ad2-KPZjk6PZgON1u88IOJmWZ_9wO_wruf-QgR737h22T9Et84uwx-bJ0Jg-0MvohRb9Mj9KDXLpnHh_sM3b5_9-nyQ3F9c7W4vLgu2pKyoZDUNG0n6rLX2ghRUdqwmgkuWMeg5VRDSauOdhwMYbqpBRGyFzWpJKOcdpSdoTf7dzdjszZdm5eI2qlNtGsdtypoq-4Sbz-rZfimaA2S5_iLQzyGr6NJg1rb1BrntDdhTIoIwksqp3_O_xFXYYw-r6YoEM5LAJYl2EttDClF0x_nIKCmDtXUoZKlopX602GOPPt7_mPgUFrmzw98Sh7pnRde_t9Q_ejcYL4PWX26V1dpCPHo8opTyX4DHmK7fQ</recordid><startdate>19981222</startdate><enddate>19981222</enddate><creator>Der, Sandy D.</creator><creator>Zhou, Aimin</creator><creator>Bryan R. 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G. Williams</au><au>Silverman, Robert H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Genes Differentially Regulated by Interferon α , β , or γ Using Oligonucleotide Arrays</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1998-12-22</date><risdate>1998</risdate><volume>95</volume><issue>26</issue><spage>15623</spage><epage>15628</epage><pages>15623-15628</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The pleiotropic activities of interferons (IFNs) are mediated primarily through the transcriptional regulation of many downstream effector genes. The mRNA profiles from IFN-α , -β , or -γ treatments of the human fibrosarcoma cell line, HT1080, were determined by using oligonucleotide arrays with probe sets corresponding to more than 6,800 human genes. Among these were transcripts for known IFN-stimulated genes (ISGs), the expression of which were consistent with previous studies in which the particular ISG was characterized as responsive to either Type I (α , β ) or Type II (γ ) IFNs, or both. Importantly, many novel IFN-stimulated genes were identified that were diverse in their known biological functions. For instance, several novel ISGs were identified that are implicated in apoptosis (including RAP46/Bag-1, phospholipid scramblase, and hypoxia inducible factor-1α ). Furthermore, several IFN-repressed genes also were identified. These results demonstrate the usefulness of oligonucleotide arrays in monitoring mammalian gene expression on a broad and unprecedented scale. In particular, these findings provide insights into the basic mechanisms of IFN actions and ultimately may contribute to better therapeutic uses for IFNs.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9861020</pmid><doi>10.1073/pnas.95.26.15623</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Biological Sciences Carrier Proteins - genetics Cell lines Cellular biology Complementary DNA Complementary RNA Datasets DNA-Binding Proteins - genetics Enzymes - immunology Fibrosarcoma Gene expression regulation Gene Expression Regulation, Neoplastic - drug effects Gene Expression Regulation, Neoplastic - immunology Genes Humans Hypoxia-Inducible Factor 1 Hypoxia-Inducible Factor 1, alpha Subunit Interferon Interferon-alpha - pharmacology Interferon-alpha - physiology Interferon-beta - pharmacology Interferon-beta - physiology Interferon-gamma - pharmacology Interferon-gamma - physiology Membrane Proteins - genetics Messenger RNA Nuclear Proteins - genetics Oligonucleotide Probes Oligonucleotides Phospholipid Transfer Proteins Proteins - genetics RNA RNA, Messenger - genetics Transcription Factors Transcription, Genetic Tumor Cells, Cultured |
title | Identification of Genes Differentially Regulated by Interferon α , β , or γ Using Oligonucleotide Arrays |
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