Home LiteratureArticle Details
PMID: 15655350 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

How the cell deals with DNA nicks.

Cell cycle (Georgetown, Tex.) ·Vol. 4 ·No. 2 ·2005-02-00 ·Pages 221-4

Garg P, Burgers PM

Abstract

During lagging strand DNA replication, the Okazaki fragment maturation machinery is required to degrade the initiator RNA with high speed and efficiency, and to generate with great accuracy a proper DNA nick for closure by DNA ligase. Several operational parameters are important in generating and maintaining a ligatable nick. These are the strand opening capacity of the lagging strand DNA polymerase delta (Pol delta ), and its ability to limit strand opening to that of a few nucleotides. In the presence of the flap endonuclease FEN1, Pol delta rapidly hands off the strand-opened product for cutting by FEN1, while in its absence, the ability of DNA polymerase delta to switch to its 3'-->5'-exonuclease domain in order to degrade back to the nick position is important in maintaining a ligatable nick. This regulatory system has a built-in redundancy so that dysfunction of one of these activities can be tolerated in the cell. However, further dysfunction leads to uncontrolled strand displacement synthesis with deleterious consequences, as is revealed by genetic studies of exonuclease-defective mutants of S. cerevisiae Pol delta. These same parameters are also important for other DNA metabolic processes, such as base excision repair, that depend on Pol delta for synthesis.

MeSH Terms
Acetyltransferases DNA/physiology DNA Ligases/physiology DNA Polymerase III/genetics,physiology DNA Replication DNA Topoisomerases, Type I/physiology DNA, Fungal/genetics,metabolism Exodeoxyribonucleases/physiology Membrane Proteins/physiology Mutation Proliferating Cell Nuclear Antigen/physiology Protein Biosynthesis Saccharomyces cerevisiae/genetics,metabolism Saccharomyces cerevisiae Proteins/physiology
Chemicals
DNA, Fungal Membrane Proteins Okazaki fragments Proliferating Cell Nuclear Antigen Saccharomyces cerevisiae Proteins DNA Acetyltransferases ELO2 protein, S cerevisiae DNA Polymerase III Exodeoxyribonucleases DNA Topoisomerases, Type I DNA Ligases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Garg Parie
Department of Biochemistry and Molecular Physics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Burgers Peter M J
Article Info
Journal
Cell cycle (Georgetown, Tex.)
Abbr.
Cell Cycle
ISSN
1551-4005
Published
2005-02-00
Epub
2005-00-03
Pages
221-4
Language
English
Region
United States
NLM ID
101137841
Subset
IM
Grants
NIGMS NIH HHS · R01 GM032431 · United States
NIGMS NIH HHS · GM32431 · United States
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: [email protected]