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HOXA10通过人子宫内膜基质细胞中三个连续的TTAT单元抑制p/CAF启动子活性。

HOXA10 suppresses p/CAF promoter activity via three consecutive TTAT units in human endometrial stromal cells.

作者信息

Sun Haixiang, Chen Linjun, Yan Guijun, Wang Ruina, Diao Zhenyu, Hu Yali, Li Chaojun

机构信息

College of Life Sciences, Nanjing Normal University, Nanjing, PR China.

出版信息

Biochem Biophys Res Commun. 2009 Jan 30;379(1):16-21. doi: 10.1016/j.bbrc.2008.11.144. Epub 2008 Dec 11.

Abstract

Implantation is the first maternal-embryo crosstalk that only occurs during a finite period called the 'implantation window'. HOXA10, a homeobox transcription factor, plays an important regulatory role during this period. However, the target genes of HOXA10 involved in implantation and decidualization have not been identified. Using a chromatin immunoprecipitation screen, we identified the p300/CBP-associated factor (p/CAF) as a direct HOXA10 target gene in vivo. Adenovirus-mediated overexpression and siRNA-specific knockdown of HOXA10 altered p/CAF promoter activity via interaction with the three consecutive TTAT element units in human endometrial cells. These results indicate that p/CAF is a novel HOXA10 target gene, and HOXA10 promotes human endometrial development, at least in part, through the regulation of p/CAF gene.

摘要

植入是母体与胚胎之间的首次相互作用,且仅在被称为“植入窗”的有限时期内发生。同源框转录因子HOXA10在此期间发挥重要的调节作用。然而,参与植入和蜕膜化过程的HOXA10靶基因尚未得到鉴定。通过染色质免疫沉淀筛选,我们在体内鉴定出p300/CBP相关因子(p/CAF)是HOXA10的直接靶基因。腺病毒介导的HOXA10过表达和siRNA特异性敲低通过与人子宫内膜细胞中三个连续的TTAT元件单元相互作用,改变了p/CAF启动子活性。这些结果表明,p/CAF是一个新的HOXA10靶基因,并且HOXA10至少部分地通过调节p/CAF基因来促进人子宫内膜的发育。

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