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Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts 02111
The recognition and alignment of homologous chromosomes early in meiosis is essential for their
subsequent segregation at anaphase I; however, the
mechanism by which this occurs is unknown. We demonstrate here that, in the absence of the molecular motor, Kar3p, meiotic cells are blocked with prophase
monopolar microtubule arrays and incomplete synaptonemal complex (SC) formation. kar3 mutants exhibit
very low levels of heteroallelic recombination. kar3
mutants do produce double-strand breaks that act as
initiation sites for meiotic recombination in yeast, but
at levels severalfold reduced from wild-type. These
data are consistent with a meiotic role for Kar3p in the
events that culminate in synapsis of homologues.
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