| Literature DB >> 25590558 |
Shunxin Wang1, Denise Zickler, Nancy Kleckner, Liangran Zhang.
Abstract
During meiosis, crossover recombination is tightly regulated. A spatial patterning phenomenon known as interference ensures that crossovers are well-spaced along the chromosomes. Additionally, every pair of homologs acquires at least one crossover. A third feature, crossover homeostasis, buffers the system such that the number of crossovers remains steady despite decreases or increases in the number of earlier recombinational interactions. Here we summarize recent work from our laboratory supporting the idea that all 3 of these aspects are intrinsic consequences of a single basic process and suggesting that the underlying logic of this process corresponds to that embodied in a particular (beam-film) model.Keywords: BF, beam-film; CO, crossover; DDF, designation driving force; DSBs, double-strand breaks; NCO, noncrossover; SC, synaptonemal complex; STUbL, SUMO-targeted ubiquitin ligase; beam-film model; crossover; crossover homeostasis; crossover interference; meiosis; obligatory crossover; recombination
Mesh:
Year: 2015 PMID: 25590558 PMCID: PMC4353236 DOI: 10.4161/15384101.2014.991185
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534