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Functional microRNA targeting without seed pairing

delete2025-10-28
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PRE
AI
H
Hall, Matthew H.
P
Peter Y. Wang
T
Thy Pham
D
David P. Bartel *
DOI:10.1093/nar/gkaf1018delete
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摘要

摘要

En 中文
微小RNA (miRNAs) 与Argonaute (AGO) 蛋白结合,充当引导分子,指导其与信使RNA (mRNA) 中部分互补位点结合,最终导致转录后抑制。与miRNA种子区(miRNA第2-7个核苷酸)的互补性通常是抑制所必需且充分的。在此,我们研究了与miRNA 3'区域(第9个核苷酸及以后)具有广泛互补性但与种子区无互补性的非同寻常位点。这些仅3'位点的顶级实例结合能力与顶级规范位点相当,并能产生相似的抑制效果,这种效果可由多达2-3对额外的种子区配对进一步增强。尽管存在这些相似性,但仅3'位点的结合和解离速率比种子匹配位点更慢。它们还会赋予结合的AGO-miRNA复合物不同的构象,而种子匹配位点则不会。此外,不同miRNA在与其各自的仅3'位点结合方面的能力存在显著差异。因此,种子配对并非总是绑定和抑制所必需的,或对于靶标获得引导分子3'区域的访问权限而言也非必需。对于识别仅3'位点的miRNA而言,这些位点据估计仅占内源性靶位点的<1%,这一比例与3'-补偿位点等其他罕见但功能性位点的比例相似。
Keyword:
MAMMALIAN MICRORNAS
STRUCTURAL BASIS
RNA RECOGNITION
ARGONAUTE
GUIDE
REVEALS
DETERMINANTS
SPECIFICITY
COMPLEX

期刊

Nucleic Acids Research 封面图
Nucleic Acids Research
IF:
13.1
论文数:
3.6W
被引数:
29.0W

机构

H
Howard Hughes Medical Institute
学者数:
1.2W
论文数: 7.8K
被引数: 6.0W
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