Fengrui Zhang , Yujun Di , Jinjun Li , Yan Shi , Liping Zhang , Chunyan Wang , Xianghuo He , Yongzhong Liu , Dafang Wan , Keke Huo , Jianren Gu
{"title":"通过与JAB1相互作用调控AP-1的人Aph2基因的克隆与表征","authors":"Fengrui Zhang , Yujun Di , Jinjun Li , Yan Shi , Liping Zhang , Chunyan Wang , Xianghuo He , Yongzhong Liu , Dafang Wan , Keke Huo , Jianren Gu","doi":"10.1016/j.bbaexp.2006.10.002","DOIUrl":null,"url":null,"abstract":"<div><p>A human <em>Aph2</em> gene (<em>hAph2</em>) was identified and cloned from a human placenta cDNA library. Bioinformatics analysis revealed hAPH2 protein shares 96% identity with mouse APH2 and contains a zf-DHHC domain (148–210aa), which is always involved in protein–protein or protein–DNA interaction. Differential expression patterns of <em>hAph2</em> mRNA were observed in normal human tissues. Yeast two-hybrid screening found another hAPH2-interacting protein JAB1. The zf-DHHC domain of hAPH2 and the C-terminal of JAB1 were confirmed to be critical for the interaction. Fused with GFP and expressed in COS-7, NIH/3T3 and SMMC-7721 cell lines, hAPH2 showed predominant distribution in the cytoplasm and co-localized with JAB1 around the nucleus. Furthermore, overexpression of hAPH2 could increase apoptosis of COS-7 cells and negatively regulate JAB1-induced activation of AP-1 in a concentration dependent manner. The expression level of c-jun was also down-regulated by overexpression of hAPH2 in COS-7 cells. These data showed some basic characterization and function of <em>hAph2</em> (hAPH2), dependent or independent with JAB1.</p></div>","PeriodicalId":100161,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression","volume":"1759 11","pages":"Pages 514-525"},"PeriodicalIF":0.0000,"publicationDate":"2006-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bbaexp.2006.10.002","citationCount":"11","resultStr":"{\"title\":\"Molecular cloning and characterization of human Aph2 gene, involved in AP-1 regulation by interaction with JAB1\",\"authors\":\"Fengrui Zhang , Yujun Di , Jinjun Li , Yan Shi , Liping Zhang , Chunyan Wang , Xianghuo He , Yongzhong Liu , Dafang Wan , Keke Huo , Jianren Gu\",\"doi\":\"10.1016/j.bbaexp.2006.10.002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A human <em>Aph2</em> gene (<em>hAph2</em>) was identified and cloned from a human placenta cDNA library. Bioinformatics analysis revealed hAPH2 protein shares 96% identity with mouse APH2 and contains a zf-DHHC domain (148–210aa), which is always involved in protein–protein or protein–DNA interaction. Differential expression patterns of <em>hAph2</em> mRNA were observed in normal human tissues. Yeast two-hybrid screening found another hAPH2-interacting protein JAB1. The zf-DHHC domain of hAPH2 and the C-terminal of JAB1 were confirmed to be critical for the interaction. Fused with GFP and expressed in COS-7, NIH/3T3 and SMMC-7721 cell lines, hAPH2 showed predominant distribution in the cytoplasm and co-localized with JAB1 around the nucleus. Furthermore, overexpression of hAPH2 could increase apoptosis of COS-7 cells and negatively regulate JAB1-induced activation of AP-1 in a concentration dependent manner. The expression level of c-jun was also down-regulated by overexpression of hAPH2 in COS-7 cells. These data showed some basic characterization and function of <em>hAph2</em> (hAPH2), dependent or independent with JAB1.</p></div>\",\"PeriodicalId\":100161,\"journal\":{\"name\":\"Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression\",\"volume\":\"1759 11\",\"pages\":\"Pages 514-525\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.bbaexp.2006.10.002\",\"citationCount\":\"11\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0167478106001837\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167478106001837","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Molecular cloning and characterization of human Aph2 gene, involved in AP-1 regulation by interaction with JAB1
A human Aph2 gene (hAph2) was identified and cloned from a human placenta cDNA library. Bioinformatics analysis revealed hAPH2 protein shares 96% identity with mouse APH2 and contains a zf-DHHC domain (148–210aa), which is always involved in protein–protein or protein–DNA interaction. Differential expression patterns of hAph2 mRNA were observed in normal human tissues. Yeast two-hybrid screening found another hAPH2-interacting protein JAB1. The zf-DHHC domain of hAPH2 and the C-terminal of JAB1 were confirmed to be critical for the interaction. Fused with GFP and expressed in COS-7, NIH/3T3 and SMMC-7721 cell lines, hAPH2 showed predominant distribution in the cytoplasm and co-localized with JAB1 around the nucleus. Furthermore, overexpression of hAPH2 could increase apoptosis of COS-7 cells and negatively regulate JAB1-induced activation of AP-1 in a concentration dependent manner. The expression level of c-jun was also down-regulated by overexpression of hAPH2 in COS-7 cells. These data showed some basic characterization and function of hAph2 (hAPH2), dependent or independent with JAB1.