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可视化染色质重塑蛋白Rad54在单个DNA分子上的移位。

Visualization of Rad54, a chromatin remodeling protein, translocating on single DNA molecules.

作者信息

Amitani Ichiro, Baskin Ronald J, Kowalczykowski Stephen C

机构信息

Section of Microbiology, University of California, 95616, USA.

出版信息

Mol Cell. 2006 Jul 7;23(1):143-8. doi: 10.1016/j.molcel.2006.05.009.

Abstract

Rad54 protein plays an important role in the recombinational repair of double-strand DNA (dsDNA) breaks. It is a dsDNA-dependent ATPase that belongs to the Swi2/Snf2 family of chromatin-remodeling proteins. Rad54 remodels (1) DNA structure, (2) chromatin structure, and (3) Rad51-dsDNA complexes. These abilities imply that Rad54 moves along DNA. Here, we provide direct evidence of Rad54 translocation by visualizing its movement along single molecules of dsDNA. When compared to the remodeling processes, translocation is unexpectedly rapid, occurring at 301 +/- 22 bp/s at 25 degrees C. Rad54 binds randomly along the dsDNA and moves in either of the two possible directions with a velocity dependent on ATP concentration (K(m) = 97 +/- 28 microM). Movement is also surprisingly processive: the average distance traveled is approximately 11,500 bp, with molecules traversing up to 32,000 bp before stopping. The mechanistic implications of this vigorous Rad54 translocase activity in chromatin and protein-DNA complex remodeling are discussed.

摘要

Rad54蛋白在双链DNA(dsDNA)断裂的重组修复中起重要作用。它是一种依赖于dsDNA的ATP酶,属于染色质重塑蛋白的Swi2/Snf2家族。Rad54可重塑(1)DNA结构、(2)染色质结构以及(3)Rad51-dsDNA复合物。这些能力表明Rad54可沿DNA移动。在此,我们通过观察Rad54沿dsDNA单分子的移动,提供了其易位的直接证据。与重塑过程相比,易位速度出乎意料地快,在25℃时为301±22 bp/s。Rad54随机结合在dsDNA上,并以依赖于ATP浓度(K(m)=97±28 microM)的速度沿两个可能方向中的任意一个移动。移动也具有惊人的持续性:平均移动距离约为11,500 bp,分子在停止前可穿越多达32,000 bp。本文讨论了这种活跃的Rad54转位酶活性在染色质和蛋白质-DNA复合物重塑中的机制意义。

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