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颌下腺核蛋白与肾素启动子DNA结合的物种差异。

Species differences in binding of submandibular nuclear proteins to renin promoter DNA.

作者信息

Loudon J A, Fukamizu A, Murakami K, Morris B J

机构信息

Department of Physiology, University of Sydney, New South Wales, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1993 May;20(5):283-8. doi: 10.1111/j.1440-1681.1993.tb01684.x.

Abstract
  1. Renin is highly expressed in submandibular gland (SMG) of mouse, which has two genes, Ren-1d and Ren-2d, but not at all in rat SMG. Differences in nuclear protein binding to renin promoter DNA were, therefore, explored. 2. Rat -169 to +23 renin DNA formed complexes with both mouse and rat extract, whereas a corresponding fragment of mouse Ren-1d DNA (-121 to +4) bound with rat extract, but much less so with mouse extract. Rat extract bound a -704 to -450 fragment of the Ren-1d promoter. For Ren-2d -578 to -383 and -786 to -718 DNA bound with mouse extract and -383 to +11 and -664 to -578 DNA bound with rat extract. 3. The results support a role for differences in presence or binding of species-specific trans-acting factors in the differential regulation of the renin gene in SMG of mouse and rat. Strong binding near the rat RNA polymerase II binding site could repress transcription in rat SMG, and binding peculiar to the Ren-2d B2 element might contribute to high expression in mouse SMG.
摘要
  1. 肾素在小鼠颌下腺(SMG)中高度表达,小鼠有两个肾素基因,即Ren-1d和Ren-2d,但在大鼠颌下腺中完全不表达。因此,研究了核蛋白与肾素启动子DNA结合的差异。2. 大鼠-169至+23的肾素DNA与小鼠和大鼠的提取物均形成复合物,而小鼠Ren-1d DNA的相应片段(-121至+4)与大鼠提取物结合,但与小鼠提取物的结合较少。大鼠提取物与Ren-1d启动子的-704至-450片段结合。对于Ren-2d,-578至-383和-786至-718的DNA与小鼠提取物结合,-383至+11和-664至-578的DNA与大鼠提取物结合。3. 结果支持物种特异性反式作用因子的存在或结合差异在小鼠和大鼠颌下腺肾素基因差异调节中起作用。大鼠RNA聚合酶II结合位点附近的强结合可能抑制大鼠颌下腺中的转录,而Ren-2d B2元件特有的结合可能有助于小鼠颌下腺中的高表达。

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