Differential gene expression between young and senescent, quiescent WI-38 cells
To investigate age-related changes in gene expression in WI-38 cells, we isolated RNA from young and senescent, quiescent cultures and made subtracted cDNA libraries. Density-arrested cells were incubated in serum-free MCDB-104 for 3 days. RNA was then isolated and subtracted cDNA libraries were mad...
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Veröffentlicht in: | Mechanisms of ageing and development 1992-09, Vol.65 (2), p.239-255 |
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description | To investigate age-related changes in gene expression in WI-38 cells, we isolated RNA from young and senescent, quiescent cultures and made subtracted cDNA libraries. Density-arrested cells were incubated in serum-free MCDB-104 for 3 days. RNA was then isolated and subtracted cDNA libraries were made in the phagemid vector pCDM8. Both by picking clones at random from these subtracted libraries and by differential hybridization screening with subtracted cDNA probes from young and senescent cells, we have identified a total of 11 genes for which RNA is expressed differentially in these quiescent young and senescent WI-38 cultures. Two genes, EPC-1 and EPC-A2, with elevated RNA levels in young cells, have sequences which have not previously been identified. Two of the genes with elevated RNA expression in the senescent cells are the mitochodnria-coded genes for NADH dehydrogenase subunit 4 and for cytochrome
b. We also identified seven other genes with elevated RNA levels in senescent cells. Three of these, LPC-1, LPC-14 and LPC-24, have been partially sequenced and have not previously been identified. These studies show that density-arrested, serum-deprived, quiescent young and senescent cells express a number of genes differentially. These differences are not growth-dependent, but are age-dependent. Our studies also show that the methods employed here, which include careful regulation of the cell cultures and subtraction of the libraries, result in libraries from which differentially expressed genes can be identified, either by random selection or by differential hybridization screening with subtracted probes. |
doi_str_mv | 10.1016/0047-6374(92)90039-G |
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b. We also identified seven other genes with elevated RNA levels in senescent cells. Three of these, LPC-1, LPC-14 and LPC-24, have been partially sequenced and have not previously been identified. These studies show that density-arrested, serum-deprived, quiescent young and senescent cells express a number of genes differentially. These differences are not growth-dependent, but are age-dependent. Our studies also show that the methods employed here, which include careful regulation of the cell cultures and subtraction of the libraries, result in libraries from which differentially expressed genes can be identified, either by random selection or by differential hybridization screening with subtracted probes.</description><identifier>ISSN: 0047-6374</identifier><identifier>EISSN: 1872-6216</identifier><identifier>DOI: 10.1016/0047-6374(92)90039-G</identifier><identifier>PMID: 1279330</identifier><identifier>CODEN: MAGDA3</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Aging - genetics ; Biological and medical sciences ; Cell Line ; Culture Media, Serum-Free ; Cytochrome b Group - genetics ; Fundamental and applied biological sciences. Psychology ; Gene Expression - genetics ; Gene Library ; Mitochondria - metabolism ; Molecular and cellular biology ; Molecular genetics ; NADH Dehydrogenase - genetics ; Nucleic Acid Hybridization - methods ; RNA</subject><ispartof>Mechanisms of ageing and development, 1992-09, Vol.65 (2), p.239-255</ispartof><rights>1992</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-c5d0e2ee7854b2f39a90f95721394bd958534391969ecfa6cb220aaeaf1d36733</citedby><cites>FETCH-LOGICAL-c415t-c5d0e2ee7854b2f39a90f95721394bd958534391969ecfa6cb220aaeaf1d36733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/004763749290039G$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4421035$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1279330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Doggett, David L.</creatorcontrib><creatorcontrib>Rotenberg, Mitch O.</creatorcontrib><creatorcontrib>Pignolo, Robert J.</creatorcontrib><creatorcontrib>Phillips, Paul D.</creatorcontrib><creatorcontrib>Cristofalo, Vincent J.</creatorcontrib><title>Differential gene expression between young and senescent, quiescent WI-38 cells</title><title>Mechanisms of ageing and development</title><addtitle>Mech Ageing Dev</addtitle><description>To investigate age-related changes in gene expression in WI-38 cells, we isolated RNA from young and senescent, quiescent cultures and made subtracted cDNA libraries. Density-arrested cells were incubated in serum-free MCDB-104 for 3 days. RNA was then isolated and subtracted cDNA libraries were made in the phagemid vector pCDM8. Both by picking clones at random from these subtracted libraries and by differential hybridization screening with subtracted cDNA probes from young and senescent cells, we have identified a total of 11 genes for which RNA is expressed differentially in these quiescent young and senescent WI-38 cultures. Two genes, EPC-1 and EPC-A2, with elevated RNA levels in young cells, have sequences which have not previously been identified. Two of the genes with elevated RNA expression in the senescent cells are the mitochodnria-coded genes for NADH dehydrogenase subunit 4 and for cytochrome
b. We also identified seven other genes with elevated RNA levels in senescent cells. Three of these, LPC-1, LPC-14 and LPC-24, have been partially sequenced and have not previously been identified. These studies show that density-arrested, serum-deprived, quiescent young and senescent cells express a number of genes differentially. These differences are not growth-dependent, but are age-dependent. Our studies also show that the methods employed here, which include careful regulation of the cell cultures and subtraction of the libraries, result in libraries from which differentially expressed genes can be identified, either by random selection or by differential hybridization screening with subtracted probes.</description><subject>Aging - genetics</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Culture Media, Serum-Free</subject><subject>Cytochrome b Group - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - genetics</subject><subject>Gene Library</subject><subject>Mitochondria - metabolism</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>NADH Dehydrogenase - genetics</subject><subject>Nucleic Acid Hybridization - methods</subject><subject>RNA</subject><issn>0047-6374</issn><issn>1872-6216</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMoOl7eQCELEQWrufWSjSBeRmFgNorLkKYnEumkY9Kq8_a2dtCdq3Pg_87h50PokJILSmh2SYjIk4zn4lSyM0kIl8l0A01okbMkYzTbRJNfZAftxvhGCKGCZdtom7Jcck4maH7rrIUAvnW6xq_gAcPXMkCMrvG4hPYTwONV0_lXrH2FY09E0-Pn-L1z44pfHhNeYAN1HffRltV1hIP13EPP93dPNw_JbD59vLmeJUbQtE1MWhFgAHmRipJZLrUkVqY5o1yKspJpkXLBJZWZBGN1ZkrGiNagLa14lnO-h07Gv8vQvHcQW7VwcWigPTRdVD1CKSsGUIygCU2MAaxaBrfQYaUoUYNHNUhSgyQlmfrxqKb92dH6f1cuoPo7GsX1-fE619Ho2gbtjYu_mBCMEp722NWIQe_iw0FQ0TjwBioXwLSqatz_Pb4B76yNzg</recordid><startdate>19920901</startdate><enddate>19920901</enddate><creator>Doggett, David L.</creator><creator>Rotenberg, Mitch O.</creator><creator>Pignolo, Robert J.</creator><creator>Phillips, Paul D.</creator><creator>Cristofalo, Vincent J.</creator><general>Elsevier Ireland Ltd</general><general>Elsevier Science</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>7X8</scope></search><sort><creationdate>19920901</creationdate><title>Differential gene expression between young and senescent, quiescent WI-38 cells</title><author>Doggett, David L. ; Rotenberg, Mitch O. ; Pignolo, Robert J. ; Phillips, Paul D. ; Cristofalo, Vincent J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-c5d0e2ee7854b2f39a90f95721394bd958534391969ecfa6cb220aaeaf1d36733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Aging - genetics</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Culture Media, Serum-Free</topic><topic>Cytochrome b Group - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - genetics</topic><topic>Gene Library</topic><topic>Mitochondria - metabolism</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>NADH Dehydrogenase - genetics</topic><topic>Nucleic Acid Hybridization - methods</topic><topic>RNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doggett, David L.</creatorcontrib><creatorcontrib>Rotenberg, Mitch O.</creatorcontrib><creatorcontrib>Pignolo, Robert J.</creatorcontrib><creatorcontrib>Phillips, Paul D.</creatorcontrib><creatorcontrib>Cristofalo, Vincent J.</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>MEDLINE - Academic</collection><jtitle>Mechanisms of ageing and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doggett, David L.</au><au>Rotenberg, Mitch O.</au><au>Pignolo, Robert J.</au><au>Phillips, Paul D.</au><au>Cristofalo, Vincent J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential gene expression between young and senescent, quiescent WI-38 cells</atitle><jtitle>Mechanisms of ageing and development</jtitle><addtitle>Mech Ageing Dev</addtitle><date>1992-09-01</date><risdate>1992</risdate><volume>65</volume><issue>2</issue><spage>239</spage><epage>255</epage><pages>239-255</pages><issn>0047-6374</issn><eissn>1872-6216</eissn><coden>MAGDA3</coden><abstract>To investigate age-related changes in gene expression in WI-38 cells, we isolated RNA from young and senescent, quiescent cultures and made subtracted cDNA libraries. Density-arrested cells were incubated in serum-free MCDB-104 for 3 days. RNA was then isolated and subtracted cDNA libraries were made in the phagemid vector pCDM8. Both by picking clones at random from these subtracted libraries and by differential hybridization screening with subtracted cDNA probes from young and senescent cells, we have identified a total of 11 genes for which RNA is expressed differentially in these quiescent young and senescent WI-38 cultures. Two genes, EPC-1 and EPC-A2, with elevated RNA levels in young cells, have sequences which have not previously been identified. Two of the genes with elevated RNA expression in the senescent cells are the mitochodnria-coded genes for NADH dehydrogenase subunit 4 and for cytochrome
b. We also identified seven other genes with elevated RNA levels in senescent cells. Three of these, LPC-1, LPC-14 and LPC-24, have been partially sequenced and have not previously been identified. These studies show that density-arrested, serum-deprived, quiescent young and senescent cells express a number of genes differentially. These differences are not growth-dependent, but are age-dependent. Our studies also show that the methods employed here, which include careful regulation of the cell cultures and subtraction of the libraries, result in libraries from which differentially expressed genes can be identified, either by random selection or by differential hybridization screening with subtracted probes.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>1279330</pmid><doi>10.1016/0047-6374(92)90039-G</doi><tpages>17</tpages></addata></record> |
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subjects | Aging - genetics Biological and medical sciences Cell Line Culture Media, Serum-Free Cytochrome b Group - genetics Fundamental and applied biological sciences. Psychology Gene Expression - genetics Gene Library Mitochondria - metabolism Molecular and cellular biology Molecular genetics NADH Dehydrogenase - genetics Nucleic Acid Hybridization - methods RNA |
title | Differential gene expression between young and senescent, quiescent WI-38 cells |
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