1. Academic Validation
  2. Identification and characterization of the human mus81-eme1 endonuclease

Identification and characterization of the human mus81-eme1 endonuclease

  • J Biol Chem. 2003 Jul 4;278(27):25172-8. doi: 10.1074/jbc.M302882200.
Alberto Ciccia 1 Angelos Constantinou Stephen C West
Affiliations

Affiliation

  • 1 Cancer Research UK, London Research Institute, Clare Hall Laboratories, South Mimms, Hertfordshire EN6 3LD, United Kingdom.
Abstract

The faithful and complete replication of DNA is necessary for the maintenance of genome stability. It is known, however, that replication forks stall at lesions in the DNA template and need to be processed so that replication restart can occur. In fission yeast, the Mus81-Eme1 Endonuclease complex (Mus81-Mms4 in Saccharomyces cerevisiae) has been implicated in the processing of aberrant replication intermediates. In this report, we identify the human homolog of the Schizosaccharomyces pombe EME1 gene and have purified the human Mus81-Eme1 heterodimer. We show that Mus81-Eme1 is an Endonuclease that exhibits a high specificity for synthetic replication fork structures and 3'-flaps in vitro. The Nuclease cleaves Holliday junctions inefficiently ( approximately 75-fold less than FLAP or fork structures), although cleavage can be increased 6-fold by the presence of homologous sequences previously shown to permit base pair "breathing." We conclude that human Mus81-Eme1 is a FLAP/fork Endonuclease that is likely to play a role in the processing of stalled replication fork intermediates.

Figures