首页> 外文期刊>Nucleic Acids Research >Determination of the recognition sequence of Mycobacterium smegmatis topoisomerase I on mycobacterial genomic sequences.
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Determination of the recognition sequence of Mycobacterium smegmatis topoisomerase I on mycobacterial genomic sequences.

机译:确定耻垢分枝杆菌拓扑异构酶I在分枝杆菌基因组序列上的识别序列。

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摘要

Mycobacterium smegmatis topoisomerase I has several distinctive features. The absence of the zinc finger motif found in other prokaryotic type I topoisomerases and the ability of the enzyme to recognise single-stranded and duplex DNA are unique characteristics of the enzyme. We have mapped the strong topoisomerase sites of the enzyme on genomic DNA sequences from Mycobacterium tuberculosis and M.smegmatis. The enzyme does not nick DNA in random fashion and DNA cleavage occurred at a few specific sites. Mapping of these sites revealed conservation of a pentanucleotide motif CG/TCT/T at the cleavage site (/ represents the cleavage site). The enzyme binds and cleaves consensus oligo-nucleotides having this sequence motif. The protein exhibits a very high preference for C or a G residue at the +2 position with respect to the cleavage site. Based on earlier and the present studies we propose that the enzyme functions in vivo mainly at these specific sites to carry out topological reactions.
机译:耻垢分枝杆菌拓扑异构酶I具有几个独特的特征。其他原核I型拓扑异构酶中不存在锌指基序,以及该酶识别单链和双链DNA的能力是该酶的独特特征。我们已经从结核分枝杆菌和耻垢分枝杆菌的基因组DNA序列上绘制了该酶的强拓扑异构酶位点。该酶不会以随机方式刻痕DNA,并且在某些特定位点会发生DNA切割。这些位点的图谱揭示了在切割位点(/代表切割位点)的五核苷酸基序CG / TCT / T的保守性。该酶结合并切割具有该序列基序的共有寡核苷酸。相对于切割位点,该蛋白质在+2位上表现出非常高的C或G残基偏好性。基于较早的和当前的研究,我们提出酶在体内主要在这些特定位点起作用以进行拓扑反应。

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