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GIY-YIG核酸酶超家族的系统基因组分析。

Phylogenomic analysis of the GIY-YIG nuclease superfamily.

作者信息

Dunin-Horkawicz Stanislaw, Feder Marcin, Bujnicki Janusz M

机构信息

Laboratory of Bioinformatics and Protein Engineering, International Institute of Molecular and Cell Biology, Trojdena 4, 02-109 Warsaw, Poland.

出版信息

BMC Genomics. 2006 Apr 28;7:98. doi: 10.1186/1471-2164-7-98.

Abstract

BACKGROUND

The GIY-YIG domain was initially identified in homing endonucleases and later in other selfish mobile genetic elements (including restriction enzymes and non-LTR retrotransposons) and in enzymes involved in DNA repair and recombination. However, to date no systematic search for novel members of the GIY-YIG superfamily or comparative analysis of these enzymes has been reported.

RESULTS

We carried out database searches to identify all members of known GIY-YIG nuclease families. Multiple sequence alignments together with predicted secondary structures of identified families were represented as Hidden Markov Models (HMM) and compared by the HHsearch method to the uncharacterized protein families gathered in the COG, KOG, and PFAM databases. This analysis allowed for extending the GIY-YIG superfamily to include members of COG3680 and a number of proteins not classified in COGs and to predict that these proteins may function as nucleases, potentially involved in DNA recombination and/or repair. Finally, all old and new members of the GIY-YIG superfamily were compared and analyzed to infer the phylogenetic tree.

CONCLUSION

An evolutionary classification of the GIY-YIG superfamily is presented for the very first time, along with the structural annotation of all (sub)families. It provides a comprehensive picture of sequence-structure-function relationships in this superfamily of nucleases, which will help to design experiments to study the mechanism of action of known members (especially the uncharacterized ones) and will facilitate the prediction of function for the newly discovered ones.

摘要

背景

GIY-YIG结构域最初是在归巢内切核酸酶中被鉴定出来的,后来在其他自私的移动遗传元件(包括限制酶和非LTR反转录转座子)以及参与DNA修复和重组的酶中也被发现。然而,迄今为止,尚未有关于GIY-YIG超家族新成员的系统搜索或这些酶的比较分析的报道。

结果

我们进行了数据库搜索,以识别已知GIY-YIG核酸酶家族的所有成员。将多个序列比对以及已鉴定家族的预测二级结构表示为隐马尔可夫模型(HMM),并通过HHsearch方法与COG、KOG和PFAM数据库中收集的未表征蛋白质家族进行比较。该分析使得GIY-YIG超家族得以扩展,纳入了COG3680的成员以及一些未归类于COG的蛋白质,并预测这些蛋白质可能作为核酸酶发挥作用,潜在地参与DNA重组和/或修复。最后,对GIY-YIG超家族的所有新旧成员进行了比较和分析,以推断系统发育树。

结论

首次呈现了GIY-YIG超家族的进化分类以及所有(亚)家族的结构注释。它提供了这个核酸酶超家族中序列-结构-功能关系的全面图景,这将有助于设计实验来研究已知成员(特别是未表征的成员)的作用机制,并将促进对新发现成员功能的预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c52/1564403/cc19c4144b1a/1471-2164-7-98-1.jpg

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