de la Casa-Esperon, EL-O, J. C.; de Villena, F. P. M.; Briscoe, T. L.; Malette, J. M.; Vaughan, J. E.; Morgan, K.; Sapienza, C.,
Genetics,
161:1651-1659.
2002.
We observed that maternal meiotic drive favoring the inheritance of DDK alleles at the Om locus on mouse chromosome 11 was correlated with the X chromosome inactivation phenotype of (C57BL/6Pgk1(a) X DDK)F-1 mothers. The basis for this unexpected observation appears to lie in the well-documented effect of recombination on meiotic drive that results from nonrandom segregation of chromosomes. Our analysis of genome-wide levels of meiotic recombination in females that vary in their X-inactivation phenotype indicates that an allelic difference at an X-linked locus is responsible for modulating levels of recombination in oocytes.
https://www.geneconvenevi.org/wp-content/uploads/2020/04/Genetics-30.png300300Academic Web Pageshttps://www.geneconvenevi.org/wp-content/uploads/2024/08/fnih-rm-mid.pngAcademic Web Pages2002-01-19 00:00:002024-09-12 08:46:07X chromosome effect on maternal recombination and meiotic drive in the mouse