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CATGGCCATG的晶体结构及其对A序列弯曲模型的影响。

Crystal structure of CATGGCCATG and its implications for A-tract bending models.

作者信息

Goodsell D S, Kopka M L, Cascio D, Dickerson R E

机构信息

Molecular Biology Institute, University of California, Los Angeles 90024.

出版信息

Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2930-4. doi: 10.1073/pnas.90.7.2930.

Abstract

The single-crystal x-ray analysis of orthorhombic CATGGCCATG has revealed a previously unrecognized mode of intrinsic bending in DNA. The decamer shows a smooth bend of 23 degrees over the central four base pairs, caused by preferential stacking interactions at guanine bases. The bend is produced by a roll of base pairs along their long axes, in a direction that compresses the wide major groove of the double helix. This major-groove-compressing bend at GGC, plus the abundant crystallographic evidence that runs of successive adenine bases (A-tracts) are straight and unbent, requires rethinking of the models most commonly invoked to explain A-tract bending. A decade of excellent experimental work involving gel migration experiments, cyclization kinetics, and nucleosome phasing has clearly established that introduction of short A-tracts into a general DNA sequence in synchrony with the natural repeat of the helix leads to bending. But it does not logically and inevitably follow that the actual bending is to be found within these introduced A-tracts or even at junctions with general-sequence B-DNA.

摘要

正交晶系CATGGCCATG的单晶X射线分析揭示了DNA中一种以前未被认识的固有弯曲模式。该十聚体在中央四个碱基对上呈现出23度的平滑弯曲,这是由鸟嘌呤碱基处优先的堆积相互作用引起的。这种弯曲是由碱基对沿着其长轴的滚动产生的,滚动方向压缩了双螺旋的宽主沟。GGC处这种压缩主沟的弯曲,加上大量晶体学证据表明连续腺嘌呤碱基序列(A序列)是直的且不弯曲,这就需要重新思考最常被用来解释A序列弯曲的模型。十年来,涉及凝胶迁移实验、环化动力学和核小体相位分析的出色实验工作已经明确证实,与螺旋的自然重复同步将短A序列引入一般DNA序列会导致弯曲。但从逻辑上并不能必然得出实际弯曲发生在这些引入的A序列内,甚至是在与一般序列B-DNA的连接处。

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