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在多种DNA结合蛋白中鉴定出的AT钩基序。

AT-hook motifs identified in a wide variety of DNA-binding proteins.

作者信息

Aravind L, Landsman D

机构信息

Computational Biology Branch, National Center for Biotechnology Information, National Library of Medicine, NIH, Building 38A, Room 8N807, 8600 Rockville Pike, Bethesda, MD 20894, USA.

出版信息

Nucleic Acids Res. 1998 Oct 1;26(19):4413-21. doi: 10.1093/nar/26.19.4413.

Abstract

The AT-hook is a small DNA-binding protein motif which was first described in the high mobility group non-histone chromosomal protein HMG-I(Y). Since its discovery, this motif has been observed in other DNA-binding proteins from a wide range of organisms. Using pattern searches and position-dependent matrices, we have extracted the AT-hook motifs present in a non-redundant protein sequence database. We have classified these motifs into three types according to their sequence similarity and have found that they are prevalent in many eukaryotic nuclear proteins in single or multiple copies. Furthermore, AT-hook motifs are frequently associated with known functional domains seen in chromatin proteins and in DNA-binding proteins (e.g. histone folds, homeodomains and zinc fingers). In general, it appears that the AT-hook motif is an auxiliary protein motif cooperating with other DNA-binding activities and facilitating changes in the structure of the DNA either as a polypeptide on its own [e.g. HMG-I(Y)] or as part of a multidomain protein [e.g. Swi2p in Saccharomyces cerevisiae or HRX (ALL-1) in Homo sapiens]. It is most interesting that this motif seems to be quite specific to known or predicted chromosomal/DNA-binding proteins, suggesting that it may act as a versatile minor groove tether.

摘要

AT钩是一种小的DNA结合蛋白基序,最初是在高迁移率族非组蛋白染色体蛋白HMG-I(Y)中发现的。自发现以来,在来自多种生物的其他DNA结合蛋白中也观察到了这种基序。通过模式搜索和位置依赖矩阵,我们从一个非冗余蛋白序列数据库中提取了存在的AT钩基序。我们根据它们的序列相似性将这些基序分为三种类型,并发现它们以单拷贝或多拷贝形式普遍存在于许多真核细胞核蛋白中。此外,AT钩基序经常与染色质蛋白和DNA结合蛋白中已知的功能结构域相关联(例如组蛋白折叠、同源结构域和锌指)。一般来说,AT钩基序似乎是一种辅助蛋白基序,它与其他DNA结合活性协同作用,并作为单独的多肽[例如HMG-I(Y)]或作为多结构域蛋白的一部分[例如酿酒酵母中的Swi2p或人类中的HRX(ALL-1)]促进DNA结构的变化。最有趣的是,这种基序似乎对已知或预测的染色体/DNA结合蛋白具有相当的特异性,这表明它可能作为一种通用的小沟系链发挥作用。

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