High fidelity of RecA-catalyzed recombination: a watchdog of genetic diversity

Details High fidelity of RecA-catalyzed recombination: a watchdog of genetic diversity High fidelity of RecA-catalyzed recombination: a watchdog of genetic diversity

2010-08-03

arxiv.org/abs/1008.0523v1

Nucleic Acids Research, 2006, Vol. 34, No. 18 5021-5031

Biology

Quantitative Biology

Biomolecules

http://www.weizmann.ac.il/complex/tlusty/papers/NuclAcidRes2006.pdf http://nar.oxfordjournals.org/cgi/content/short/34/18/5021

Scientific paper

10.1093/nar/gkl586

Homologous recombination plays a key role in generating genetic diversity, while maintaining protein functionality. The mechanisms by which RecA enables a single-stranded segment of DNA to recognize a homologous tract within a whole genome are poorly understood. The scale by which homology recognition takes place is of a few tens of base pairs, after which the quest for homology is over. To study the mechanism of homology recognition, RecA-promoted homologous recombination between short DNA oligomers with different degrees of heterology was studied in vitro, using fluorescence resonant energy transfer. RecA can detect single mismatches at the initial stages of recombination, and the efficiency of recombination is strongly dependent on the location and distribution of mismatches. Mismatches near the 5' end of the incoming strand have a minute effect, whereas mismatches near the 3' end hinder strand exchange dramatically. There is a characteristic DNA length above which the sensitivity to heterology decreases sharply. Experiments with competitor sequences with varying degrees of homology yield information about the process of homology search and synapse lifetime. The exquisite sensitivity to mismatches and the directionality in the exchange process support a mechanism for homology recognition that can be modeled as a kinetic proofreading cascade.

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