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AP-2与ETS结构域家族成员的结合与人生长激素/绒毛膜促生长催乳素基因座超敏位点III区域的增强子活性相关。

Binding of AP-2 and ETS-domain family members is associated with enhancer activity in the hypersensitive site III region of the human growth hormone/chorionic somatomammotropin locus.

作者信息

Jin Yan, Norquay Lisa D, Yang Xiaoyang, Gregoire Scott, Cattini Peter A

机构信息

Department of Physiology, University of Manitoba, 730 William Avenue, Winnipeg, Manitoba, Canada R3E 3J7.

出版信息

Mol Endocrinol. 2004 Mar;18(3):574-87. doi: 10.1210/me.2003-0405. Epub 2003 Dec 12.

Abstract

The human GH gene family is specifically expressed in somatotrophs of the anterior pituitary and placental syncytiotrophoblast. Two nuclease-hypersensitive sites, HS III and HS V, are associated with a region of chromatin located 28 and 30 kb upstream of the pituitary GH gene transcription initiation site (+1) in both pituitary and placenta nuclei. A role for this region in pituitary GH gene expression has been reported, but the potential relevance to placental gene expression has not been determined. Deletion analysis of a 5.2-kb region (nucleotides - 27,568/-32,746) containing HS III to V-related sequences localized significant enhancer activity to a 574-bp HS III fragment (nucleotides -27,676/-28,249) in multiple transfected cell lines. Four nuclease-protected regions [footprints (FP) 1-4] were identified in the 574-bp fragment. FP2 and FP3 were detected with placenta cell nuclear protein, whereas FP1 and FP4 were observed with placental and nonplacental cell nuclear extract. Disruption of FP1 had no effect on heterologous promoter activity in transfected pituitary and placental cells, whereas loss of FP2 and FP3 resulted in modest increases in placental cells, reflecting the presence of repressor activity associated with these regions in vitro. In contrast, disruption of the FP4 region by mutation or deletion significantly reduced enhancer activity. As a result, 30-fold enhancer activity was localized to a 41-bp region in transfected placental tumor cells. Binding of candidate proteins, activator protein (AP)-2 (FP3) and Elk-1 (FP4), was confirmed using competition assays with specific oligonucleotides and antibodies. Moreover, these factors were associated with the hyperacetylated HS III region in human pituitary [activator protein 2 (AP-2) and Elk-1] and term placenta (AP-2) chromatin. These data implicate AP-2 and ETS-domain family members in the regulation of the GH/CS locus and raise the possibility that different complexes form in the HS III region in placenta and pituitary cells.

摘要

人类生长激素(GH)基因家族特异性表达于垂体前叶的生长激素细胞和胎盘合体滋养层细胞。在垂体和胎盘细胞核中,两个核酸酶超敏位点HS III和HS V与位于垂体GH基因转录起始位点(+1)上游28 kb和30 kb的染色质区域相关。该区域在垂体GH基因表达中的作用已有报道,但与胎盘基因表达的潜在相关性尚未确定。对包含HS III至V相关序列的5.2 kb区域(核苷酸-27,568 / -32,746)进行缺失分析,在多个转染细胞系中,将显著的增强子活性定位于一个574 bp的HS III片段(核苷酸-27,676 / -28,249)。在574 bp片段中鉴定出四个核酸酶保护区域[足迹(FP)1 - 4]。用胎盘细胞核蛋白检测到FP2和FP3,而用胎盘和非胎盘细胞核提取物观察到FP1和FP4。破坏FP1对转染的垂体和胎盘细胞中的异源启动子活性没有影响,而FP2和FP3的缺失导致胎盘细胞中的活性适度增加,反映出体外这些区域存在抑制活性。相反,通过突变或缺失破坏FP4区域会显著降低增强子活性。结果,在转染的胎盘肿瘤细胞中,30倍的增强子活性定位于一个41 bp的区域。使用特异性寡核苷酸和抗体的竞争试验证实了候选蛋白激活蛋白(AP)-2(FP3)和Elk-1(FP4)的结合。此外,这些因子与人垂体[激活蛋白2(AP-2)和Elk-1]和足月胎盘(AP-2)染色质中高度乙酰化的HS III区域相关。这些数据表明AP-2和ETS结构域家族成员参与了GH/CS基因座的调控,并增加了在胎盘和垂体细胞的HS III区域形成不同复合物的可能性。

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