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本文引用的文献

1
Engineering RNA-binding proteins for biology.工程 RNA 结合蛋白用于生物学。
FEBS J. 2013 Aug;280(16):3734-54. doi: 10.1111/febs.12375. Epub 2013 Jul 5.
2
A complex network of factors with overlapping affinities represses splicing through intronic elements.一个具有重叠亲和性的复杂因子网络通过内含子元件抑制剪接。
Nat Struct Mol Biol. 2013 Jan;20(1):36-45. doi: 10.1038/nsmb.2459. Epub 2012 Dec 16.
3
Engineering RNA endonucleases with customized sequence specificities.用定制的序列特异性工程 RNA 内切酶。
Nat Commun. 2012;3:1147. doi: 10.1038/ncomms2154.
4
Cyclin-dependent kinase control of the initiation-to-elongation switch of RNA polymerase II.细胞周期蛋白依赖性激酶对 RNA 聚合酶 II 起始延伸转换的调控。
Nat Struct Mol Biol. 2012 Nov;19(11):1108-15. doi: 10.1038/nsmb.2399. Epub 2012 Oct 14.
5
Triplet repeats in transcripts: structural insights into RNA toxicity.转录本中的三核苷酸重复:对 RNA 毒性的结构见解。
Biol Chem. 2012 Nov;393(11):1299-315. doi: 10.1515/hsz-2012-0218.
6
Promoter-proximal pausing of RNA polymerase II: emerging roles in metazoans.RNA 聚合酶 II 的启动子近端暂停:后生动物中的新兴作用。
Nat Rev Genet. 2012 Oct;13(10):720-31. doi: 10.1038/nrg3293.
7
Intronic splicing enhancers, cognate splicing factors and context-dependent regulation rules.内含子剪接增强子、同源剪接因子和依赖上下文的调控规则。
Nat Struct Mol Biol. 2012 Oct;19(10):1044-52. doi: 10.1038/nsmb.2377. Epub 2012 Sep 16.
8
Human Pumilio proteins recruit multiple deadenylases to efficiently repress messenger RNAs.人 Pumilio 蛋白招募多种脱腺苷酸化酶以有效抑制信使 RNA。
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9
A combinatorial amino acid code for RNA recognition by pentatricopeptide repeat proteins.五肽重复蛋白识别 RNA 的组合氨基酸密码。
PLoS Genet. 2012;8(8):e1002910. doi: 10.1371/journal.pgen.1002910. Epub 2012 Aug 16.
10
A eukaryotic translation initiation factor 4E-binding protein promotes mRNA decapping and is required for PUF repression.真核翻译起始因子 4E 结合蛋白促进 mRNA 去帽化,并且是 PUF 抑制所必需的。
Mol Cell Biol. 2012 Oct;32(20):4181-94. doi: 10.1128/MCB.00483-12. Epub 2012 Aug 13.

利用 Pumilio/fem-3 mRNA 结合因子支架工程化蛋白质来操纵 RNA 代谢。

Engineered proteins with Pumilio/fem-3 mRNA binding factor scaffold to manipulate RNA metabolism.

机构信息

Department of Pharmacology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

FEBS J. 2013 Aug;280(16):3755-67. doi: 10.1111/febs.12367. Epub 2013 Jun 24.

DOI:10.1111/febs.12367
PMID:23731364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3768134/
Abstract

Pumilio/fem-3 mRNA binding factor proteins are characterized by a sequence-specific RNA-binding domain. This unique single-stranded RNA recognition module, whose sequence specificity can be reprogrammed, has been fused with functional modules to engineer protein factors with various functions. We summarize the advances made with respect to developing RNA regulatory tools, as well as opportunities for the future.

摘要

Pumilio/fem-3 mRNA 结合因子蛋白的特征是具有序列特异性的 RNA 结合结构域。这个独特的单链 RNA 识别模块的序列特异性可以被重新编程,已经与功能模块融合,用于设计具有各种功能的蛋白质因子。我们总结了在开发 RNA 调控工具方面取得的进展,以及未来的机会。