We have identified MS12 as a gene of Saccharomyces cerevisiae which, w
hen on a multicopy vector, suppresses the heat shock sensitivity cause
d by the loss of the IRA1 product, a negative regulator of the RAS pro
tein. The multicopy MS12 also suppresses the heat shock sensitivity of
cells with the RAS2(vol19) mutation but not those with the bcyl mutat
ion, suggesting that the MS12 protein may interfere with the activity
of the RAS protein. The sequence analysis of MS12 reveals that it is i
dentical to LTE1 belonging to the CDC25 family: CDC25, SCD25 and BUDS,
each of which encodes a guanine nucleotide exchange factor for the ra
s superfamily gene products. Deletion of the entire MS12 coding region
reveals that MS12 is not essential but the disruptant shows a cold-se
nsitive phenotype. Under the non-permissive conditions, more than 70%
of the msi2 disruptants arrested at telophase as large budded cells wi
th two nuclei divided completely and elongated spindles, indicating th
at the msi2 deletion is a cell division cycle mutation. These results
suggest that MS12 is involved in the termination of M phase and that t
his process is regulated by a ras superfamily gene product.