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本文引用的文献

1
Actin-binding protein ABP140 is a methyltransferase for 3-methylcytidine at position 32 of tRNAs in Saccharomyces cerevisiae.肌动蛋白结合蛋白 ABP140 是酿酒酵母 tRNA 第 32 位 3-甲基胞苷的甲基转移酶。
RNA. 2011 Jun;17(6):1111-9. doi: 10.1261/rna.2653411. Epub 2011 Apr 25.
2
A domain of the actin binding protein Abp140 is the yeast methyltransferase responsible for 3-methylcytidine modification in the tRNA anti-codon loop.肌动蛋白结合蛋白 Abp140 的一个结构域是酵母甲基转移酶,负责 tRNA 反密码环中 3-甲基胞嘧啶的修饰。
RNA. 2011 Jun;17(6):1100-10. doi: 10.1261/rna.2652611. Epub 2011 Apr 25.
3
Cortical actin dynamics driven by formins and myosin V.由formin 和肌球蛋白 V 驱动的皮层肌动蛋白动力学。
J Cell Sci. 2011 May 1;124(Pt 9):1533-41. doi: 10.1242/jcs.079038. Epub 2011 Apr 12.
4
An RNA-zipcode-independent mechanism that localizes Dia1 mRNA to the perinuclear ER through interactions between Dia1 nascent peptide and Rho-GTP.一种通过 Dia1 新生肽和 Rho-GTP 之间的相互作用将 Dia1 mRNA 定位到核周 ER 的 RNA-zipcode 非依赖性机制。
J Cell Sci. 2011 Feb 15;124(Pt 4):589-99. doi: 10.1242/jcs.072421. Epub 2011 Jan 25.
5
Translational pausing ensures membrane targeting and cytoplasmic splicing of XBP1u mRNA.翻译暂停确保了 XBP1u mRNA 的膜靶向和细胞质剪接。
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A novel mRNA affinity purification technique for the identification of interacting proteins and transcripts in ribonucleoprotein complexes.一种新的 mRNA 亲和纯化技术,用于鉴定核糖核蛋白复合物中的相互作用蛋白和转录本。
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Mol Biol Cell. 2010 Aug 1;21(15):2685-95. doi: 10.1091/mbc.e10-03-0197. Epub 2010 Jun 9.
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ABP140mRNA 共翻译转运至酿酒酵母远端极。

Cotranslational transport of ABP140 mRNA to the distal pole of S. cerevisiae.

机构信息

Biozentrum, Universität Basel, Switzerland.

出版信息

EMBO J. 2011 Jul 26;30(17):3567-80. doi: 10.1038/emboj.2011.247.

DOI:10.1038/emboj.2011.247
PMID:21792172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3181485/
Abstract

In budding yeast, several mRNAs are selectively transported into the daughter cell in an actin-dependent manner by a specialized myosin system, the SHE machinery. With ABP140 mRNA, we now describe the first mRNA that is transported in the opposite direction and localizes to the distal pole of the mother cell, independent of the SHE machinery. Distal pole localization is not observed in mutants devoid of actin cables and can be disrupted by latrunculin A. Furthermore, localization of ABP140 mRNA requires the N-terminal actin-binding domain of Abp140p to be expressed. By replacing the N-terminal localization motif, ABP140 mRNA can be retargeted to different subcellular structures. In addition, accumulation of the mRNA at the distal pole can be prevented by disruption of polysomes. Using the MS2 system, the mRNA was found to associate with actin cables and to follow actin cable dynamics. We therefore propose a model of translational coupling, in which ABP140 mRNA is tethered to actin cables via its nascent protein product and is transported to the distal pole by actin retrograde flow.

摘要

在芽殖酵母中,几种 mRNA 被一种特殊的肌球蛋白系统(SHE 机器)以依赖于肌动蛋白的方式有选择地运输到子细胞中。现在,我们用 ABP140 mRNA 描述了第一个以相反方向运输并定位于母细胞远端极的 mRNA,该过程独立于 SHE 机器。在缺乏肌动蛋白纤维的突变体中观察不到远端极定位,Latrunculin A 可以破坏这种定位。此外,ABP140 mRNA 的定位需要表达 Abp140p 的 N 端肌动蛋白结合结构域。通过替换 N 端定位基序,ABP140 mRNA 可以被重新靶向到不同的亚细胞结构。此外,通过破坏多核糖体,可以防止 mRNA 在远端极的积累。使用 MS2 系统,发现该 mRNA 与肌动蛋白纤维结合,并跟随肌动蛋白纤维的动力学。因此,我们提出了一个翻译偶联模型,其中 ABP140 mRNA 通过其新生蛋白质产物与肌动蛋白纤维相连,并通过肌动蛋白逆行流被运输到远端极。