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分化特异性元件:一种顺式作用的发育开关,在激素诱导3T3-L1成纤维细胞向脂肪细胞分化过程中,对于血管紧张素原基因的持续转录表达是必需的。

Differentiation-specific element: a cis-acting developmental switch required for the sustained transcriptional expression of the angiotensinogen gene during hormonal-induced differentiation of 3T3-L1 fibroblasts to adipocytes.

作者信息

McGehee R E, Ron D, Brasier A R, Habener J F

机构信息

Laboratory of Molecular Endocrinology, Massachusetts General Hospital, Boston 02114.

出版信息

Mol Endocrinol. 1993 Apr;7(4):551-60. doi: 10.1210/mend.7.4.7684818.

DOI:10.1210/mend.7.4.7684818
PMID:7684818
Abstract

The gene encoding angiotensinogen, the glycoprotein precursor for the vasopressor angiotensin II, is under coordinate tissue-specific, developmental, and hormonal regulation. We show here that the irreversible, developmentally regulated increase in angiotensinogen gene expression during the hormonal (dexamethasone, insulin, and isobutylmethylxanthine) differentiation of fibroblast-like 3T3-L1 cells into adipocytes is mediated by a 14-base pair cis-acting element located at -1000 in the 5'-flanking region of the gene. The sequence of this differentiation-specific element (DSE) is similar to sites that bind the homeotic and pou class of transcription factors found in the promoters of other genes known to be regulated during differentiation. Furthermore, we show that there are several high affinity DSE-specific binding proteins present in preadipocyte nuclear extracts that are competed with known homeotic and pou transcription factor DNA binding sequences. Thus the DSE appears to serve as a developmental switch for the expression of the angiotensinogen gene during the differentiation of fibroblasts to adipocytes and may be a binding site for one or more of the pou-homeodomain class of transcription factors.

摘要

血管紧张素原是血管升压素血管紧张素II的糖蛋白前体,编码该蛋白的基因受到组织特异性、发育过程及激素的协同调控。我们在此表明,在成纤维细胞样3T3-L1细胞经激素(地塞米松、胰岛素和异丁基甲基黄嘌呤)诱导分化为脂肪细胞的过程中,血管紧张素原基因表达呈现出不可逆的、受发育调控的增加,这是由位于该基因5'侧翼区 -1000处的一个14碱基对的顺式作用元件介导的。这个分化特异性元件(DSE)的序列与在其他已知在分化过程中受调控的基因启动子中发现的、能结合同源异型和POU类转录因子的位点相似。此外,我们还表明,前脂肪细胞核提取物中存在几种高亲和力的DSE特异性结合蛋白,它们能与已知的同源异型和POU转录因子DNA结合序列相互竞争。因此,DSE似乎是成纤维细胞向脂肪细胞分化过程中血管紧张素原基因表达的一个发育开关,可能是POU-同源异型结构域类转录因子中一个或多个的结合位点。

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