Genetic recombination is important for generating diversity and to ensure faithful segregation of chromosomes atmeiosis. However, few crossovers (COs) are formed per meiosis despite an excess of DNA double-strand break precursors. This reflects the existence of active mechanisms that limitCOformation. We previously showed that AtFANCM is a meiotic anti-CO factor. The same genetic screen now identified AtMHF2 as another player of the same anti-CO pathway. FANCM and MHF2 are both Fanconi Anemia (FA) associated proteins, prompting us to test the other FA genes conserved in Arabidopsis for a role in CO control at meiosis. This revealed that among the FA proteins tested, only FANCM and its two DNA-binding co-factors MHF1 and MHF2 limit CO formation at meiosis. © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.
CITATION STYLE
Girard, C., Crismani, W., Froger, N., Mazel, J., Lemhemdi, A., Horlow, C., & Mercier, R. (2014). FANCM-associated proteins MHF1 and MHF2, but not the other Fanconi anemia factors, limit meiotic crossovers. Nucleic Acids Research, 42(14), 9087–9095. https://doi.org/10.1093/nar/gku614
Mendeley helps you to discover research relevant for your work.