Induction of heat shock protein transcripts and B2 transcripts by various stresses in Chinese hamster cells

We have investigated the induction of known hsp (heat shock protein) RNA and other heat shock (HS) inducible transcripts in Chinese hamster cells by various stresses including DNA damaging agents. cDNA clones coding for at least 14 different HS-inducible transcripts were isolated. By DNA sequence an...

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Veröffentlicht in:Experimental cell research 1989-05, Vol.182 (1), p.61-74
Hauptverfasser: Fornace, Albert J., Alamo, Isaac, Hollander, M.Christine, Lamoreaux, Etienne
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creator Fornace, Albert J.
Alamo, Isaac
Hollander, M.Christine
Lamoreaux, Etienne
description We have investigated the induction of known hsp (heat shock protein) RNA and other heat shock (HS) inducible transcripts in Chinese hamster cells by various stresses including DNA damaging agents. cDNA clones coding for at least 14 different HS-inducible transcripts were isolated. By DNA sequence analysis and homology with cDNA clones of other species, some of these cDNA clones were identified as coding for hsp27, hsp89α, hsp89β, two different hsp70s, ubiquitin, and the HS-inducible RNA polymerase III transcript B2. In addition, hsp-related cDNA clones, hsp60 and four with hsp70 homology, were isolated which coded for transcripts which were not induced by HS or other stresses in two different Chinese hamster cell lines. After HS or treatment with the HS-mimetic agent ethanol, there was coordinate induction of all 14 transcripts. With severe HS treatments which produced substantial cytotoxicity, the increase in all transcripts except B2 RNA was delayed and, in some cases, suppressed. The only DNA damaging agent, which induced many HS-inducible transcripts, was high-dose methylmethane sulfonate (MMS). However, induction by MMS was not coordinate for all transcripts as it was for HS, and B2 RNA was not induced. hsp27 RNA induction differed from the others in several respects including induction by irradiation and other agents which produce high levels of DNA damage repaired by nucleotide excision repair. The implications of these findings in cellular events such as cytotoxicity, thermotolerance, and regulation of stress responses will be discussed.
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However, induction by MMS was not coordinate for all transcripts as it was for HS, and B2 RNA was not induced. hsp27 RNA induction differed from the others in several respects including induction by irradiation and other agents which produce high levels of DNA damage repaired by nucleotide excision repair. The implications of these findings in cellular events such as cytotoxicity, thermotolerance, and regulation of stress responses will be discussed.</description><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/0014-4827(89)90279-6</identifier><identifier>PMID: 2541007</identifier><identifier>CODEN: ECREAL</identifier><language>eng</language><publisher>Orlando, FL: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Blotting, Northern ; Cell Cycle ; Cell Line ; Cell Nucleus - physiology ; Cloning, Molecular ; Cricetinae ; DNA - genetics ; DNA Damage ; Fundamental and applied biological sciences. 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By DNA sequence analysis and homology with cDNA clones of other species, some of these cDNA clones were identified as coding for hsp27, hsp89α, hsp89β, two different hsp70s, ubiquitin, and the HS-inducible RNA polymerase III transcript B2. In addition, hsp-related cDNA clones, hsp60 and four with hsp70 homology, were isolated which coded for transcripts which were not induced by HS or other stresses in two different Chinese hamster cell lines. After HS or treatment with the HS-mimetic agent ethanol, there was coordinate induction of all 14 transcripts. With severe HS treatments which produced substantial cytotoxicity, the increase in all transcripts except B2 RNA was delayed and, in some cases, suppressed. The only DNA damaging agent, which induced many HS-inducible transcripts, was high-dose methylmethane sulfonate (MMS). However, induction by MMS was not coordinate for all transcripts as it was for HS, and B2 RNA was not induced. hsp27 RNA induction differed from the others in several respects including induction by irradiation and other agents which produce high levels of DNA damage repaired by nucleotide excision repair. The implications of these findings in cellular events such as cytotoxicity, thermotolerance, and regulation of stress responses will be discussed.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Cell Cycle</subject><subject>Cell Line</subject><subject>Cell Nucleus - physiology</subject><subject>Cloning, Molecular</subject><subject>Cricetinae</subject><subject>DNA - genetics</subject><subject>DNA Damage</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation</subject><subject>Heat-Shock Proteins - genetics</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>Stress, Physiological - physiopathology</subject><subject>Time Factors</subject><subject>Transcription, Genetic</subject><subject>Transcription. Transcription factor. Splicing. 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Psychology</topic><topic>Gene Expression Regulation</topic><topic>Heat-Shock Proteins - genetics</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>Stress, Physiological - physiopathology</topic><topic>Time Factors</topic><topic>Transcription, Genetic</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><topic>Ubiquitins - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fornace, Albert J.</creatorcontrib><creatorcontrib>Alamo, Isaac</creatorcontrib><creatorcontrib>Hollander, M.Christine</creatorcontrib><creatorcontrib>Lamoreaux, Etienne</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>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fornace, Albert J.</au><au>Alamo, Isaac</au><au>Hollander, M.Christine</au><au>Lamoreaux, Etienne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of heat shock protein transcripts and B2 transcripts by various stresses in Chinese hamster cells</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>1989-05-01</date><risdate>1989</risdate><volume>182</volume><issue>1</issue><spage>61</spage><epage>74</epage><pages>61-74</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><coden>ECREAL</coden><abstract>We have investigated the induction of known hsp (heat shock protein) RNA and other heat shock (HS) inducible transcripts in Chinese hamster cells by various stresses including DNA damaging agents. cDNA clones coding for at least 14 different HS-inducible transcripts were isolated. By DNA sequence analysis and homology with cDNA clones of other species, some of these cDNA clones were identified as coding for hsp27, hsp89α, hsp89β, two different hsp70s, ubiquitin, and the HS-inducible RNA polymerase III transcript B2. In addition, hsp-related cDNA clones, hsp60 and four with hsp70 homology, were isolated which coded for transcripts which were not induced by HS or other stresses in two different Chinese hamster cell lines. After HS or treatment with the HS-mimetic agent ethanol, there was coordinate induction of all 14 transcripts. With severe HS treatments which produced substantial cytotoxicity, the increase in all transcripts except B2 RNA was delayed and, in some cases, suppressed. The only DNA damaging agent, which induced many HS-inducible transcripts, was high-dose methylmethane sulfonate (MMS). However, induction by MMS was not coordinate for all transcripts as it was for HS, and B2 RNA was not induced. hsp27 RNA induction differed from the others in several respects including induction by irradiation and other agents which produce high levels of DNA damage repaired by nucleotide excision repair. The implications of these findings in cellular events such as cytotoxicity, thermotolerance, and regulation of stress responses will be discussed.</abstract><cop>Orlando, FL</cop><pub>Elsevier Inc</pub><pmid>2541007</pmid><doi>10.1016/0014-4827(89)90279-6</doi><tpages>14</tpages></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Biological and medical sciences
Blotting, Northern
Cell Cycle
Cell Line
Cell Nucleus - physiology
Cloning, Molecular
Cricetinae
DNA - genetics
DNA Damage
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation
Heat-Shock Proteins - genetics
Molecular and cellular biology
Molecular genetics
Repetitive Sequences, Nucleic Acid
Stress, Physiological - physiopathology
Time Factors
Transcription, Genetic
Transcription. Transcription factor. Splicing. Rna processing
Ubiquitins - genetics
title Induction of heat shock protein transcripts and B2 transcripts by various stresses in Chinese hamster cells
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