GEN1 from a Thermophilic Fungus Is Functionally Closely Similar to Non-Eukaryotic Junction-Resolving Enzymes

JOURNAL OF MOLECULAR BIOLOGY

卷:426

Article

Freeman, Alasdair D. J.¹  Liu, Yijin¹  Declais, Anne-Cecile¹  Gartner, Anton¹  Lilley, David M. J.¹ 

[1] Univ Dundee, Canc Res UK Nucle Acid Struct Res Grp, Dundee DD1 5EH, Scotland

关键词: DNA recombination and repair;    Holliday junction resolution;    Chaetomium thermophilum;    FEN1;    thermophilic proteins;   

DOI  :  10.1016/j.jmb.2014.10.008

来源: Elsevier

【 摘 要 】

Processing of Holliday junctions is essential in recombination. We have identified the gene for the junction-resolving enzyme GEN1 from the thermophilic fungus Chaetomium thermophilum and expressed the N-terminal 487-amino-acid section. The protein is a nuclease that is highly selective for four-way DNA junctions, cleaving 1 nt 3' to the point of strand exchange on two strands symmetrically disposed about a diagonal axis. CtGEN1 binds to DNA junctions as a discrete homodimer with nanomolar affinity. Analysis of the kinetics of cruciform cleavage shows that cleavage of the second strand occurs an order of magnitude faster than the first cleavage so as to generate a productive resolution event. All these properties are closely similar to those described for bacterial, phage and mitochondrial junction-resolving enzymes. CtGEN1 is also similar in properties to the human enzyme but lacks the problems with aggregation that currently prevent detailed analysis of the latter protein. CtGEN1 is thus an excellent enzyme with which to engage in biophysical and structural analysis of eukaryotic GEN1. (C) 2014 MRC Laboratory of Molecular Biology. Published by Elsevier Ltd.

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