An ATM-like gene was identified in the genome of Caenorhabditis elegans. Th
e putative product of the gene, termed Ce-atl-1 (C. elegans ATM-like 1) con
sists of 2514 amino acid residues. The C-terminal sequence, which contains
a PI-3 kinase-like domain, showed good homology with the products of the ge
ne MEC1/ESR1 from budding yeast, the rad3(+) gene of fission yeast and mamm
alian A TR (ataxia-telangiectasia and rad3(+) related) genes. The results o
f RNA-mediated interference indicated that the major phenotype associated w
ith repression of Ce-atl-1 was lethality (approximately 50-80%) during earl
y embryogenesis. Among the surviving progeny, males (XO animals) arose at a
high frequency (2-30%). In addition, 5% of oocyte chromosomes demonstrated
aneuploidy due to a defect in pre-meiotic chromosomal segregation. Gene ex
pression analyses indicated that Ce-atl-1 mRNA was expressed in all larval
stages and that its level increased about fivefold in the adult stage. The
adult expression level was de creased in the glp-4 mutant, which is defecti
ve in germ line proliferation. Ce-atl-1 was strongly expressed in both the
mitotic and meiotic cells of adult gonads. In summary, Ce-atl-1 appears to
be important for early embryogenesis, and loss of its function results in a
defect in chromosome segregation, similar to what has been observed for AT
-related proteins.