Eleswarapu Satyanaryana, Gu Zhiliang, Jiang Honglin
Department of Animal and Poultry Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, USA.
Endocrinology. 2008 May;149(5):2230-40. doi: 10.1210/en.2007-1344. Epub 2008 Feb 14.
The transcription factor signal transducer and activator of transcription (STAT)-5 mediates GH stimulation of IGF-I gene expression in the liver. Previous studies suggested that STAT5 might exert this effect by binding to an IGF-I intron 2 region and a distal 5'-flanking region each containing two STAT5 binding sites. Here we report the identification of three additional chromosomal regions containing a total of five putative STAT5 binding sites that may mediate GH-induced STAT5 activation of IGF-I gene expression in the mouse liver. By comparing an 170-kb mouse genomic DNA containing the IGF-I gene with the corresponding human sequence, we identified 19 putative STAT5 binding sites that bear the consensus sequence of STAT5 binding site and are conserved across the two species. Chromatin immunoprecipitation assays indicated that five chromosomal regions containing a total of nine of the 19 putative STAT5 binding sites were bound by STAT5 in the mouse liver in response to GH administration and that these bindings preceded or coincided with GH-increased IGF-I gene transcription. Two of the five chromosomal regions correspond to those previously identified in other species, and the three new chromosomal regions that contain a total of five putative STAT5 binding sites are IGF-I intron 3 regions located at least 26 kb from the transcription start site. Gel-shift assays confirmed the binding of the five new putative STAT5 binding sites as well as three of the four previously identified STAT5 binding sites to GH-activated STAT5 from the mouse liver. Cotransfection analyses indicated that, although each of the five chromosomal regions was able to mediate STAT5 activation of reporter gene expression, together they mediated greater STAT5 activation of reporter gene expression in response to GH. Overall, these results suggest that GH-induced STAT5 activation of IGF-I gene expression in the mouse liver might be collectively mediated by at least eight STAT5 binding sites located in distal intronic and 5'-flanking regions of the IGF-I gene.
转录因子信号转导子与转录激活子(STAT)-5介导生长激素(GH)对肝脏中胰岛素样生长因子-I(IGF-I)基因表达的刺激作用。先前的研究表明,STAT5可能通过与IGF-I内含子2区域和一个远端5'侧翼区域结合来发挥这种作用,这两个区域各含有两个STAT5结合位点。在此,我们报告鉴定出另外三个染色体区域,总共含有五个假定的STAT5结合位点,它们可能介导GH诱导的小鼠肝脏中IGF-I基因表达的STAT5激活。通过将包含IGF-I基因的170 kb小鼠基因组DNA与相应的人类序列进行比较,我们鉴定出19个假定的STAT5结合位点,它们具有STAT5结合位点的共有序列,并且在这两个物种中保守。染色质免疫沉淀分析表明,在给予GH后小鼠肝脏中五个染色体区域(总共包含19个假定的STAT5结合位点中的九个)被STAT5结合,并且这些结合先于或与GH诱导的IGF-I基因转录同时发生。五个染色体区域中的两个与先前在其他物种中鉴定出的区域相对应,而总共含有五个假定的STAT5结合位点的三个新染色体区域是位于距转录起始位点至少26 kb的IGF-I内含子3区域。凝胶迁移分析证实了五个新的假定STAT5结合位点以及四个先前鉴定出的STAT5结合位点中的三个与来自小鼠肝脏的GH激活的STAT5结合。共转染分析表明,尽管五个染色体区域中的每一个都能够介导报告基因表达的STAT5激活,但它们共同介导对GH的反应中报告基因表达的更大STAT5激活。总体而言,这些结果表明,GH诱导的小鼠肝脏中IGF-I基因表达的STAT5激活可能由位于IGF-I基因远端内含子和5'侧翼区域的至少八个STAT5结合位点共同介导。