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PMID: 2203538 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Meiotic gene conversion and crossing over: their relationship to each other and to chromosome synapsis and segregation.

Cell ·Vol. 62 ·No. 5 ·1990-09-07 ·Pages 927-37

Engebrecht J, Hirsch J, Roeder GS

Abstract

The yeast mer1 mutant produces inviable spores and is defective in both meiotic recombination and chromosome pairing. A gene called MER2 partially suppresses the mer1 phenotype when present in high copy number. Both gene conversion and chromosome pairing are completely restored in mer1 strains overexpressing MER2; however, reciprocal crossing over and spore viability are not restored. The data presented are consistent with a model in which chromosome pairing is a direct consequence of a homology search mediated through gene conversion. Analysis of random viable spores indicates that the crossovers that occur in mer1 strains overexpressing MER2 are more effective in ensuring meiosis I disjunction than those that occur in mer1 strains. One interpretation of this result is that only those crossovers that occur in the context of the synaptonemal complex lead to the establishment of functional chiasmata. The MER2 gene product is essential for meiosis.

MeSH Terms
Cell Nucleus/ultrastructure Chromosomes, Fungal Crossing Over, Genetic Gene Conversion Genes, Fungal Genotype Meiosis Mutation Plasmids Recombination, Genetic Saccharomyces cerevisiae/cytology,genetics,physiology Spores, Fungal/physiology Suppression, Genetic
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Engebrecht J
Department of Biology, Yale University, New Haven, Connecticut 06511-8112.
Hirsch J
Roeder G S
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1990-09-07
Pages
927-37
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NIGMS NIH HHS · GM28904 · United States
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