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CpG突变热点中的序列特异性。

Sequence specificity in CpG mutation hotspots.

作者信息

Ollila J, Lappalainen I, Vihinen M

机构信息

Department of Biosciences, Division of Biochemistry, University of Helsinki, Finland.

出版信息

FEBS Lett. 1996 Nov 4;396(2-3):119-22. doi: 10.1016/0014-5793(96)01075-7.

Abstract

CpG dinucleotides are efficiently methylated in vertebrate genomes except in the CpG islands having a high C+G content. Methylated CpGs are the single most mutated dinucleotide. Sequences surrounding disease causing CpG mutation sites were analyzed from locus-specific mutation databases. Both tetra- and heptanucleotide analyses indicated clear overall sequence preference for having pyrimidines 5' and purines 3' to the mutated 5-methylcytosine. The most mutated tetranucleotides are TCGA and TCGG, the former being also a frequent restriction and modification site. The results will help in elucidating the still controversial mutation mechanism of CpG doublets.

摘要

除了具有高C+G含量的CpG岛外,脊椎动物基因组中的CpG二核苷酸会被高效甲基化。甲基化的CpG是最易发生突变的二核苷酸。从位点特异性突变数据库中分析了导致疾病的CpG突变位点周围的序列。四核苷酸和七核苷酸分析均表明,对于突变的5-甲基胞嘧啶,5'端为嘧啶、3'端为嘌呤的序列具有明显的整体偏好。最易突变的四核苷酸是TCGA和TCGG,前者也是常见的限制和修饰位点。这些结果将有助于阐明仍存在争议的CpG双联体突变机制。

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