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小鼠核受体转录因子NURR1编码基因的克隆与结构组织

Cloning and structural organization of the gene encoding the murine nuclear receptor transcription factor, NURR1.

作者信息

Saucedo-Cardenas O, Kardon R, Ediger T R, Lydon J P, Conneely O M

机构信息

Baylor College of Medicine, Department of Cell Biology, Houston, TX 77030, USA.

出版信息

Gene. 1997 Mar 10;187(1):135-9. doi: 10.1016/s0378-1119(96)00736-6.

Abstract

NURR1 is an immediate early gene product and a member of the nuclear receptor superfamily of transcription factors. Using the NURR1 cDNA as a probe, we isolated the genomic DNA encoding NURR1 from a mouse 129SvEv genomic library. The NURR1 gene is approximately 6.2 kb long and is organized into 7 exons separated by 6 introns. Structural analysis of the NURR1 reveals that this gene shares a similar structure with that of the nuclear receptor NUR77/NGF1-B. As in NUR77, the promoter region of NURR1 lacks an identifiable TATA box, but is GC-rich. The proximal promoter region also contains an ATF/CREB consensus binding site that may participate in cAMP-mediated induction of this immediate early gene product. Isolation and structural characterization of the NURR1 gene provides information for further developmental and transcriptional regulation studies of this gene.

摘要

NURR1是一种即刻早期基因产物,属于核受体转录因子超家族成员。我们以NURR1互补DNA(cDNA)为探针,从小鼠129SvEv基因组文库中分离出编码NURR1的基因组DNA。NURR1基因约6.2千碱基对(kb)长,由7个外显子和6个内含子组成。对NURR1的结构分析表明,该基因与核受体NUR77/NGF1 - B具有相似的结构。与NUR77一样,NURR1的启动子区域缺乏可识别的TATA框,但富含GC。近端启动子区域还包含一个ATF/CREB共有结合位点,可能参与cAMP介导的对这种即刻早期基因产物的诱导。NURR1基因的分离和结构表征为该基因进一步的发育和转录调控研究提供了信息。

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