4.6 Review

A 5′-upstream short open reading frame encoded peptide regulates angiotensin type 1a receptor production and signalling via the β-arrestin pathway

期刊

JOURNAL OF PHYSIOLOGY-LONDON
卷 594, 期 6, 页码 1601-1605

出版社

WILEY-BLACKWELL
DOI: 10.1113/JP270567

关键词

-

资金

  1. American Heart Association
  2. National Institutes of Health (NIH) [HL121456, AG/HL-19291, HL-066023]
  3. Nova Southeastern University, NIH [HL-113905]
  4. Pilot Award from Translational Technologies Component of the Georgetown/Howard Universities Center for Clinical and Translational Science [UL1TR000101]
  5. American Heart Association (Midwest Affiliate) [10GRNT4470043]

向作者/读者索取更多资源

AUG sequences and short open reading frames are commonly present in the 5-leader sequence of G protein-coupled receptor mRNAs. The presence of these upstream AUG sequences has been demonstrated to inhibit downstream receptor translation efficiency and, most recently, receptor signal transduction. A seven amino acid peptide encoded by a short open reading frame in exon 2 of the angiotensin type 1a receptor has been shown to inhibit non-G protein-coupled signalling of angiotensin II, without altering the classical G protein-coupled pathway activated by the ligand. This finding may lead to the development of a new class of angiotensin receptor antagonists with activities biased for one, but not all, of the signalling cascades activated by angiotensin II, which could have therapeutic implications for the myriad hormones and neurotransmitters that signal through G protein-coupled receptors.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据