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甲基化强烈增强大肠杆菌染色体复制起始区域的DNA弯曲。

Methylation strongly enhances DNA bending in the replication origin region of the Escherichia coli chromosome.

作者信息

Kimura T, Asai T, Imai M, Takanami M

机构信息

Institute for Chemical Research, Kyoto University, Japan.

出版信息

Mol Gen Genet. 1989 Oct;219(1-2):69-74. doi: 10.1007/BF00261159.

Abstract

Two-dimensional gel electrophoresis, at high and low temperatures, and gel mobilities of circularly permuted DNA segments showed a large bending locus about 50 bp downstream from the right border of the 245 bp oriC box, a minimal essential region of autonomous replication on the Escherichia coli chromosome. Bending was strongly enhanced by Dam methylation. In DNA from a Dam- strain, the mobility anomaly arising from altered conformation was much reduced, but was raised to the original level by methylation in vivo or in vitro. Enhancement of the mobility anomaly was also observed by hybrid formation of the Dam- strand with the Dam+ strand. Near the bending center, GATC, the target of Dam methylase, occurs seven times arranged essentially on the same face of the helix with 10.5 bp per turn. We concluded that small bends at each Dam site added up to the large bending detectable by gel electrophoresis.

摘要

二维凝胶电泳显示,在高温和低温下,环状排列的DNA片段的凝胶迁移率在大肠杆菌染色体上自主复制的最小必需区域——245 bp oriC框右边界下游约50 bp处出现一个大的弯曲位点。Dam甲基化强烈增强了弯曲。在来自Dam-菌株的DNA中,由构象改变引起的迁移率异常大大降低,但通过体内或体外甲基化可提高到原始水平。通过Dam-链与Dam+链的杂交形成也观察到迁移率异常的增强。在弯曲中心附近,Dam甲基化酶的靶标GATC出现7次,基本上排列在螺旋的同一面上,每圈10.5 bp。我们得出结论,每个Dam位点的小弯曲加起来形成了凝胶电泳可检测到的大弯曲。

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