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小鼠Ms6-hm高变微卫星形成一个发夹结构和两个异常的四重结构。

The mouse Ms6-hm hypervariable microsatellite forms a hairpin and two unusual tetraplexes.

作者信息

Weitzmann M N, Woodford K J, Usdin K

机构信息

Section on Genomic Structure and Function, Laboratory of Molecular and Cellular Biology, NIDDK, National Institutes of Health, Bethesda, Maryland 20892-0830, USA.

出版信息

J Biol Chem. 1998 Nov 13;273(46):30742-9. doi: 10.1074/jbc.273.46.30742.

Abstract

The mouse Ms6-hm microsatellite consists of a tandem array of the pentamer d(CAGGG)n. This microsatellite is extremely hypervariable, showing a germ line mutation rate of 2.5%/gamete. The mechanism responsible for this instability is not known. The ability to form intrastrand structures is a conserved feature of many hypervariable sequences, and it has been suggested that the formation of such structures might account for instability by affecting DNA replication, repair, or recombination. Here we show that this microsatellite is able to form intrastrand structures as well. Under physiological conditions, the Ms6-hm microsatellite forms a hairpin as well as two different unusual intrastrand tetraplexes. The hairpin forms in the absence of monovalent cation and contains G.A, G.C, and G.G base pairs in a 1:1:1 ratio. In the presence of K+, a tetraplex is formed in which the adenines are unpaired and extrahelical, and the cytosines are involved in C.C pairs. In Na+, a tetraplex forms that contains C.C+ pairs, with the adenines being intrahelical and hydrogen-bonded to guanines. Tetraplex formation in the presence of Na+ requires both cytosines and adenines and might reflect the altered internal dimensions of this tetraplex, perhaps resulting from the ability of the C.C+ pairs to become intercalated in this sequence context. Our demonstration of the stabilization of tetraplexes by hydrogen bonding between adenines and guanines expands the hydrogen-bonding possibilities for tetraplexes and suggests that the category of sequences with tetraplex-forming potential may be larger than previously appreciated.

摘要

小鼠Ms6-hm微卫星由五聚体d(CAGGG)n的串联阵列组成。该微卫星具有极高的变异性,其生殖系突变率为2.5%/配子。导致这种不稳定性的机制尚不清楚。形成链内结构的能力是许多高变序列的一个保守特征,有人提出,这种结构的形成可能通过影响DNA复制、修复或重组来解释不稳定性。在这里,我们表明这个微卫星也能够形成链内结构。在生理条件下,Ms6-hm微卫星形成一个发夹结构以及两种不同的异常链内四链体。发夹结构在没有单价阳离子的情况下形成,并且含有比例为1:1:1的G.A、G.C和G.G碱基对。在K+存在的情况下,形成一种四链体,其中腺嘌呤未配对且位于螺旋外,而胞嘧啶参与C.C配对。在Na+存在的情况下,形成一种含有C.C+配对的四链体,腺嘌呤位于螺旋内并与鸟嘌呤形成氢键。在Na+存在的情况下四链体的形成需要胞嘧啶和腺嘌呤两者,这可能反映了这种四链体内部尺寸的改变,可能是由于C.C+配对能够在这个序列环境中插入的能力。我们关于腺嘌呤和鸟嘌呤之间通过氢键稳定四链体的证明扩展了四链体的氢键可能性,并表明具有四链体形成潜力的序列类别可能比以前认识的更大。

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