Previous studies of Saccharomyces cerevisiae have identified several m
eiosis-specific genes whose products are required for wild-type levels
of meiotic recombination and for normal synaptonemal complex (SC) for
mation. Several of these mutants were examined in a physical assay des
igned to detect heteroduplex DNA (hDNA) intermediates in meiotic recom
bination. hDNA was not detected in the rec102, mei4 and hop1 mutants;
it was observed at reduced levels in red1, mek1 and mer1 strains and a
t greater than the wild-type level in zip1. These results indicate tha
t the REC102, MEI4, HOP1, RED1, MEK1 and MER1 gene products act before
hDNA formation in the meiotic recombination pathway, whereas ZIP1 act
s later. The same mutants assayed for hDNA formation were monitored fo
r meiotic chromosome pairing by in situ hybridization of chromosome-sp
ecific DNA probes to spread meiotic nuclei. Homolog pairing occurs at
wild-type levels in the zip1 and mek1 mutants, but is substantially re
duced in mei4, rec102 hop1, red1 and merl strains. Even mutants that f
ail to recombine or to make any SC or SC precursors undergo a signific
ant amount of meiotic chromosome pairing. The in situ hybridization pr
ocedure revealed defects in meiotic chromatin condensation in mer1, re
d1 and hop1 strains.