<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li XA</submitter><funding>NCI NIH HHS</funding><pagination>3446-53</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC361074</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(7)</volume><pubmed_abstract>GRP78, a 78-kDa protein localized in the endoplasmic reticulum (ER), has been implicated in protein processing and stress protection. Its promoter contains a 36-bp region which is conserved among GRP genes across species and has the ability to compete for trans-acting factors mediating GRP gene expression. Integration of about 800 tandem copies of this sequence into the genome of a Chinese hamster ovary cell line (DG44) results in transfectants with the following phenotypes: (i) the induction level of GRP78 by the calcium ionophore A23187 and tunicamycin is reduced 4- and 2-fold, respectively, (ii) the induction levels of two other ER luminal protein genes, GRP94 and ERp72, are simultaneously down-regulated, (iii) the growth rate of these cells is half that of transfectants without the amp</pubmed_abstract><journal>Molecular and cellular biology</journal><pubmed_title>Competitive inhibition of a set of endoplasmic reticulum protein genes (GRP78, GRP94, and ERp72) retards cell growth and lowers viability after ionophore treatment.</pubmed_title><pmcid>PMC361074</pmcid><funding_grant_id>R37 CA27607</funding_grant_id><pubmed_authors>Li XA</pubmed_authors><pubmed_authors>Lee AS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Competitive inhibition of a set of endoplasmic reticulum protein genes (GRP78, GRP94, and ERp72) retards cell growth and lowers viability after ionophore treatment.</name><description>GRP78, a 78-kDa protein localized in the endoplasmic reticulum (ER), has been implicated in protein processing and stress protection. Its promoter contains a 36-bp region which is conserved among GRP genes across species and has the ability to compete for trans-acting factors mediating GRP gene expression. Integration of about 800 tandem copies of this sequence into the genome of a Chinese hamster ovary cell line (DG44) results in transfectants with the following phenotypes: (i) the induction level of GRP78 by the calcium ionophore A23187 and tunicamycin is reduced 4- and 2-fold, respectively, (ii) the induction levels of two other ER luminal protein genes, GRP94 and ERp72, are simultaneously down-regulated, (iii) the growth rate of these cells is half that of transfectants without the amp</description><dates><release>1991-01-01T00:00:00Z</release><publication>1991 Jul</publication><modification>2025-04-04T09:47:11.006Z</modification><creation>2019-03-27T00:50:09Z</creation></dates><accession>S-EPMC361074</accession><cross_references><pubmed>2046663</pubmed><doi>10.1128/mcb.11.7.3446-3453.1991</doi></cross_references></HashMap>