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Evolution of human, chicken, alligator, frog, and zebrafish mineralocorticoid receptors: Allosteric influence on steroid specificity
Science Signaling ( IF 6.7 ) Pub Date : 2018-07-03 , DOI: 10.1126/scisignal.aao1520
Yoshinao Katsu 1, 2 , Kaori Oka 1 , Michael E. Baker 3
Affiliation  

Although multiple steroid ligands of the glucocorticoid, mineralocorticoid, and progestin families bind to and regulate the activity of mineralocorticoid receptors (MRs), the responses to these ligands differ across species. To understand how the different domains of MRs contribute to the ligand-induced activation or inhibition of MR activity, we studied the response to eight steroids (aldosterone, 11-deoxycorticosterone, 11-deoxycortisol, cortisol, corticosterone, progesterone, 19-norprogesterone, and spironolactone) of human, chicken, alligator, frog, and zebrafish full-length MRs and truncated MRs, which lacked the N-terminal domain (NTD) and DNA binding domain (DBD). Compared to full-length MRs, some truncated MRs were not activated by the steroids, and others required higher steroid concentrations for activation. Progesterone, 19-norprogesterone, and spironolactone did not activate full-length or truncated human, alligator, or frog MRs. However, at 10 nM, these steroids activated full-length chicken and zebrafish MRs, whereas at 100 nM, these steroids had little activity for truncated chicken MRs, but they retained activity for truncated zebrafish MRs. This suggests that regulation of the activation of the chicken MR by progestin resides in the NTD-DBD and that of the zebrafish MR resides in the hinge-LBD. Zebrafish and chicken MRs contain a serine corresponding to Ser810 in human MR, which is required for the antagonist activity of progesterone for human MR, suggesting a previously uncharacterized mechanism of regulation of progestin activation of chicken and zebrafish MRs. These findings suggest that progesterone may be a physiological activator of chicken and zebrafish MRs.



中文翻译:

人,鸡,扬子鳄,青蛙和斑马鱼盐皮质激素受体的进化:变构作用对类固醇特异性的影响

尽管糖皮质激素,盐皮质激素和孕激素家族的多个类固醇配体结合并调节盐皮质激素受体(MRs)的活性,但对这些配体的反应因物种而异。为了了解MR的不同域如何促进配体诱导的MR激活或抑制,我们研究了对八种类固醇的反应(醛固酮,11-脱氧皮质酮,11-脱氧皮质醇,皮质醇,皮质酮,孕酮,19-去甲孕酮和人,鸡,扬子鳄,青蛙和斑马鱼的MR(螺内酯)全长MR和截短MR,它们缺少N末端结构域(NTD)和DNA结合结构域(DBD)。与全长MR相比,某些截短的MR没有被类固醇激活,而另一些则需要更高的类固醇浓度才能激活。孕酮 19-去黄体酮和螺内酯不能激活全长或截短的人类,鳄鱼或蛙类MR。但是,在10 nM时,这些类固醇激活全长的鸡和斑马鱼MR,而在100 nM时,这些类固醇对截短的鸡MR几乎没有活性,但它们保留了对截短的斑马鱼MR的活性。这表明孕激素对鸡MR激活的调节存在于NTD-DBD中,而斑马鱼MR的调节存在于铰链LBD中。斑马鱼和鸡肉MR含有对应于Ser的丝氨酸 但它们保留了截短的斑马鱼MR的活性。这表明孕激素对鸡MR激活的调节存在于NTD-DBD中,而斑马鱼MR的调节存在于铰链LBD中。斑马鱼和鸡肉MR含有对应于Ser的丝氨酸 但它们保留了截短的斑马鱼MR的活性。这表明孕激素对鸡MR激活的调节存在于NTD-DBD中,而斑马鱼MR的调节存在于铰链LBD中。斑马鱼和鸡肉MR含有对应于Ser的丝氨酸孕激素对人MR的拮抗作用所必需的人类MR中的810提示了鸡和斑马鱼MR的孕激素活化调节的以前未知的机制。这些发现表明,孕酮可能是鸡和斑马鱼MR的一种生理激活剂。

更新日期:2018-07-04
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