4.6 Review

Branching out: meiotic recombination and its regulation

Journal

TRENDS IN CELL BIOLOGY
Volume 17, Issue 9, Pages 448-455

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tcb.2007.07.007

Keywords

-

Categories

Funding

  1. NIGMS NIH HHS [R01 GM032194, R01 GM031693] Funding Source: Medline
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM031693, R01GM032194] Funding Source: NIH RePORTER

Ask authors/readers for more resources

Homologous recombination is a dynamic process by which DNA sequences and strands are exchanged. In meiosis, the reciprocal DNA recombination events called crossovers are central to the generation of genetic diversity in gametes and are required for homolog segregation in most organisms. Recent studies have shed light on how meiotic crossovers and other recombination products form, how their position and number are regulated and how the DNA molecules undergoing recombination are chosen. These studies indicate that the long-dominant, unifying model of recombination proposed by Szostak et al applies, with modification, only to a subset of recombination events. Instead, crossover formation and its control involve multiple pathways, with considerable variation among model organisms. These observations force us to 'branch out' in our thinking about meiotic recombination.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available