Stalled replication forks: Making ends meet for recognition and stabilization

Bioessays 32 (8):687-697 (2010)
  Copy   BIBTEX

Abstract

In bacteria, PriA protein, a conserved DEXH‐type DNA helicase, plays a central role in replication restart at stalled replication forks. Its unique DNA‐binding property allows it to recognize and stabilize stalled forks and the structures derived from them. Cells must cope with fork stalls caused by various replication stresses to complete replication of the entire genome. Failure of the stalled fork stabilization process and eventual restart could lead to various forms of genomic instability. The low viability of priA null cells indicates a frequent occurrence of fork stall during normal growth that needs to be properly processed. PriA specifically recognizes the 3′‐terminus of the nascent leading strand or the invading strand in a displacement (D)‐loop by the three‐prime terminus binding pocket (TT‐pocket) present in its unique DNA binding domain. Elucidation of the structural basis for recognition of arrested forks by PriA should provide useful insight into how stalled forks are recognized in eukaryotes.

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 91,853

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

Similar books and articles

Replication without replicators.Bence Nanay - 2011 - Synthese 179 (3):455-477.
Replication and mere replication.Michael Mulkay & G. Nigel Gilbert - 1986 - Philosophy of the Social Sciences 16 (1):21-37.

Analytics

Added to PP
2013-11-23

Downloads
22 (#708,419)

6 months
9 (#307,343)

Historical graph of downloads
How can I increase my downloads?

Citations of this work

No citations found.

Add more citations

References found in this work

Add more references