Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate

The genome-wide recombination rate varies between individuals, but the mechanism controlling this variation in humans has remained elusive. A genome-wide search identified sequence variants in the 4p16.3 region correlated with recombination rate in both males and females. These variants are located...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2008-03, Vol.319 (5868), p.1398-1401
Hauptverfasser: Kong, Augustine, Thorleifsson, Gudmar, Stefansson, Hreinn, Masson, Gisli, Helgason, Agnar, Gudbjartsson, Daniel F., Jonsdottir, Gudrun M., Gudjonsson, Sigurjon A., Sverrisson, Sverrir, Thorlacius, Theodora, Jonasdottir, Aslaug, Hardarson, Gudmundur A., Palsson, Stefan T., Frigge, Michael L., Gulcher, Jeffrey R., Thorsteinsdottir, Unnur, Stefansson, Kari
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Sprache:eng
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Zusammenfassung:The genome-wide recombination rate varies between individuals, but the mechanism controlling this variation in humans has remained elusive. A genome-wide search identified sequence variants in the 4p16.3 region correlated with recombination rate in both males and females. These variants are located in the RNF212 gene, a putative ortholog of the ZHP-3 gene that is essential for recombinations and chiasma formation in Caenorhabditis elegans. It is noteworthy that the haplotype formed by two single-nucleotide polymorphisms (SNPs) associated with the highest recombination rate in males is associated with a low recombination rate in females. Consequently, if the frequency of the haplotype changes, the average recombination rate will increase for one sex and decrease for the other, but the sex-averaged recombination rate of the population can stay relatively constant.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.1152422