AP-1-Mediated Expression of Brain-Specific Class IVa β-Tubulin in P19Embryonal Carcinoma Cells

Journal of Veterinary Medical Science

Emi KINOSHITA¹  Kazuhiko ARAHARA¹  Yuka MARUYAMA¹  Katsuhiko ARAI¹ 

[1] Department of Tissue Physiology, Tokyo University of Agriculture and Technology, Fuchu, Tokyo 183-8509, Japan

关键词: embryonal carcinoma cell;    neuronal differentiation;    promoter analysis;    retinoic acid;    tubulin isotype;   

DOI  :  10.1292/jvms.14-0343

学科分类：兽医学

来源: Japanese Society of Veterinary Science

【 摘 要 】

References(36)Cited-By(1)Supplementary materials(1)Expression of brain-specificphenotypes increased in all trans retinoic acid (ATRA)-induced neuraldifferentiation of mouse P19 embryonal carcinoma cells. Among these phenotypes, expressionof class IVa β-tubulin isotype (TUBB4a) was particularly enhanced in neuraldifferentiation. Transient transfection assays employing a reporter construct found thatATRA-mediated regulatory region of the TUBB4a gene lay in the region from �?83 nt to +137nt relative to the +1 transcription start site. Site-directed mutagenesis in the AP-1binding site at �?29/�?17 suggested that the AP-1 binding site was a critical region forATRA-mediated TUBB4a expression. Chromatin immunoprecipitation experiments suggestedparticipation of JunD and activating transcription factor-2 (ATF2) in TUBB4a expression.Additionally, exogenous induction of the dominant-negative (dn) type of JunD canceledATRA-induced upregulation of TUBB4a, and the dn type of ATF2 suppressed even the basalactivity. Further immunoblot study revealed an ATRA-mediated increase in JunD protein,while a significant amount of ATF2 protein was constantly produced. These results suggestthat differentiation-mediated activation of JunD results in enhanced TUBB4aexpression.

【 授权许可】

Unknown