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一种裂殖酵母的多组分蛋白质,可促进同源DNA形成连接分子。

A multicomponent protein of a fission yeast that promotes joint molecule formation from homologous DNAs.

作者信息

Arai N, Kawasaki K, Shibata T

机构信息

Laboratory of Microbiology, RIKEN, Institute of Physical and Chemical Research, Saitama, Japan.

出版信息

J Biol Chem. 1992 Feb 15;267(5):3514-22.

PMID:1737802
Abstract

We developed a quantitative assay ("homologous pairing gel assay") adequate for the purification of the activity promoting the formation of joint molecules, an intermediate of homologous recombination ("homologous pairing"). With this assay, one can measure the extent of homologous pairing between a single-stranded DNA and a strand of 3H-labeled double-stranded DNA by crude enzyme preparations. Since the total activity did not significantly change during the sporulation process, we tried to purify the activity from a whole cell extract of mitotic cells of a fission yeast, (Schizosaccharomyces pombe). Through quantitative assaying of a single fraction or of mixed fractions, we obtained three fractions, all of which were required for the maximum level of the ATP-independent homologous pairing: Fractions 65, 100, and 30. In Fractions 100 and 30, polypeptides of approximately 100 and approximately 30 kDa (the 100- and 30-kDa polypeptides), respectively, were the sole detectable components. Fraction 65 contained a polypeptide of approximately 65 kDa (the 65-kDa polypeptide) as the major component and also small amounts of the 30- and 100-kDa polypeptides. Fraction 65 by itself promoted homologous pairing, but the reaction was saturated at a level of approximately 20% of the maximum level achieved with the recA protein. Even when added in excess, Fraction 30 or 100 alone did not promote detectable homologous pairing. A mixture of Fractions 65 and 100 at a rather strict optimum ratio only promoted homologous pairing, the level being 50-70% that with the recA protein, suggesting a stoichiometric complex of these polypeptides as the active form. Fraction 30 alone did not enhance the reaction with Fraction 65, but stimulated homologous pairing promoted by the optimum mixture of Fractions 65 and 100 to the maximum level achieved with the recA protein. Therefore, the homologous pairing-promoting protein from the fission yeast is likely to be a multicomponent protein.

摘要

我们开发了一种定量检测方法(“同源配对凝胶检测法”),该方法适用于纯化促进连接分子形成的活性物质,连接分子是同源重组(“同源配对”)的中间体。通过这种检测方法,可以用粗酶制剂来测量单链DNA与一条3H标记的双链DNA链之间的同源配对程度。由于在孢子形成过程中总活性没有显著变化,我们尝试从裂殖酵母(粟酒裂殖酵母)有丝分裂细胞的全细胞提取物中纯化该活性物质。通过对单个组分或混合组分进行定量检测,我们获得了三个组分,所有这些组分都是实现最大水平的不依赖ATP的同源配对所必需的:组分65、100和30。在组分100和30中,分别约100 kDa和约30 kDa的多肽(100 kDa和30 kDa多肽)是唯一可检测到的成分。组分65含有约65 kDa的多肽(65 kDa多肽)作为主要成分,还含有少量的30 kDa和100 kDa多肽。组分65自身就能促进同源配对,但反应在达到recA蛋白所实现的最大水平的约20%时就饱和了。即使过量添加,单独的组分30或100也不会促进可检测到的同源配对。组分65和100以相当严格的最佳比例混合时才促进同源配对,其水平为recA蛋白的50 - 70%,这表明这些多肽的化学计量复合物是活性形式。单独的组分30不会增强与组分65的反应,但能将由组分65和100的最佳混合物促进的同源配对刺激到recA蛋白所实现的最大水平。因此,裂殖酵母中促进同源配对的蛋白可能是一种多组分蛋白。

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