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跨越枯草芽孢杆菌染色体复制终点的DNA限制酶切图谱。

Restriction map of DNA spanning the replication terminus of the Bacillus subtilis chromosome.

作者信息

Weiss A S, Wake R G

出版信息

J Mol Biol. 1983 Dec 5;171(2):119-37. doi: 10.1016/s0022-2836(83)80349-0.

Abstract

The Bacillus subtilis 168 dna-1 chromosome was labelled during sporulation with [3H]thymine for five minutes immediately before termination of replication. The isolated radioactive DNA was cleaved with BamHI (or SalI) and the resulting restriction fragments separated by agarose gel electrophoresis. The individual fragments, fractionated into a series of slices cut from the gel, were then cleaved with SalI (or BamHI) and the double-digest fragments identified by electrophoresis and fluorography. All major fragments and most minor ones present in a whole double-digest were assigned to BamHI and SalI parents. Such information enabled the construction of an unambiguous restriction map of 150 X 10(3) bases of the approximately 250 X 10(3) bases of DNA labelled in the five minutes. In conjunction with published data on the order of replication of restriction fragments as termination is approached, it was clear that most (105 X 10(3) bases) of the mapped DNA was replicated by a major fork moving in one direction towards a BamHI 24.8 X 10(3) base fragment. The 45 X 10(3) bases extending to the other side of this region were labelled only slightly, and presumably was replicated by a fork that approached the other in an opposite direction until its progress was blocked or severely impeded within this region at a site, referred to as terC, sometime (less than 5 min) earlier. The regions of the map replicated in the final 2.5 and 1.0 minute by the major fork were also identified.

摘要

在芽孢形成过程中,紧接复制终止前五分钟,用[³H]胸腺嘧啶标记枯草芽孢杆菌168 dna - 1染色体。分离出的放射性DNA用BamHI(或SalI)切割,所得的限制性片段通过琼脂糖凝胶电泳分离。将各个片段分成从凝胶上切下的一系列条带,然后用SalI(或BamHI)切割,通过电泳和荧光自显影鉴定双酶切片段。在整个双酶切中出现的所有主要片段和大多数次要片段都被归为BamHI和SalI亲本片段。这些信息使得能够构建出在这五分钟内标记的约250×10³个碱基中150×10³个碱基的明确限制性图谱。结合已发表的关于接近终止时限制性片段复制顺序的数据,很明显,所绘制图谱中的大部分DNA(105×10³个碱基)是由一个主要复制叉沿一个方向朝着一个24.8×10³碱基的BamHI片段复制的。延伸到该区域另一侧的45×10³个碱基仅被轻微标记,推测是由一个从相反方向接近另一个复制叉的复制叉复制的,直到其进程在该区域内的一个位点(称为terC)在某个时间(不到5分钟)之前被阻断或严重阻碍。还鉴定了主要复制叉在最后2.5分钟和1.0分钟复制的图谱区域。

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