Home LiteratureArticle Details
PMID: 25447518 Published · ppublish English

Molecular architecture of the HerA-NurA DNA double-strand break resection complex.

FEBS letters ·Vol. 588 ·No. 24 ·2015-02-17

Byrne Robert Thomas, Schuller Jan Michael, Unverdorben Pia, Förster Friedrich, Hopfner Karl-Peter

Abstract

DNA double-strand breaks can be repaired by homologous recombination, during which the DNA ends are long-range resected by helicase-nuclease systems to generate 3' single strand tails. In archaea, this requires the Mre11-Rad50 complex and the ATP-dependent helicase-nuclease complex HerA-NurA. We report the cryo-EM structure of Sulfolobus solfataricus HerA-NurA at 7.4Å resolution and present the pseudo-atomic model of the complex. HerA forms an ASCE hexamer that tightly interacts with a NurA dimer, with each NurA protomer binding three adjacent HerA HAS domains. Entry to NurA's nuclease active sites requires dsDNA to pass through a 23Å wide channel in the HerA hexamer. The structure suggests that HerA is a dsDNA translocase that feeds DNA into the NurA nuclease sites.

Keywords
Cryo-electron microscopy DNA double-strand break repair DNA resection FtsK/HerA ATPase Nuclease
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
Published
2015-02-17
Indexed
2014-12-16
Updated
2014-12-16
Language
English
Country/Region
England
NLM ID
0155157
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com