The spindle-assembly checkpoint ensures that, during mitosis and meiosis, c
hromosomes do not segregate until they are properly attached to the microtu
bules of the spindle. Here we show that mdf-l and mdf-2 are components of t
he spindle-assembly checkpoint in Caenorhabditis elegans, and are essential
for the long-term survival and fertility of this organism. Loss of functio
n of either of these genes leads to the accumulation of a variety of defect
s, including chromosome abnormalities, X-chromosome non-disjunction or loss
, problems in gonad development, and embryonic lethality. Antibodies that r
ecognize the MDF-2 protein localize to nuclei of the cleaving embryo in a c
ell-cycle-dependent manner. mdf-l, a gene encoding a product that interacts
with MDF-2, is required for cell-cycle arrest and proper chromosome segreg
ation in premeiotic germ cells treated with nocodoazole, a microtubule-depo
lymerizing agent. In the absence of mdf gene products, errors in chromosome
segregation arise and accumulate, ultimately leading to genetic lethality.