Jj. Mulero et al., PET112, A SACCHAROMYCES-CEREVISIAE NUCLEAR GENE REQUIRED TO MAINTAIN RHO(-DNA() MITOCHONDRIAL), Current genetics, 25(4), 1994, pp. 299-304
The nuclear gene PET112 was originally identified by a mutation (pet11
2-1) that specifically blocked accumulation of cytochrome c oxidase su
bunit II. The mutation causes a post-transcriptional defect since the
level of COX2 mRNA in the mutant is the same as in the wildtype. Howev
er, PET112 does not have a function similar to that of PET111, a COX2
mRNA-specific translational activator: while pet111 mutations are supp
ressed by chimeric COX2 mRNAs bearing 5'leaders of other mitochondrial
mRNAs, pet112-1 is not. The PET112 gene was isolated and shown to cod
e a protein of 541 residues (62 kDa) with no significant homology to k
nown amino-acid sequences. By hybridization to defined genomic clones
the gene was mapped to chromosome II between cdc25 and ilsl. Disruptio
n of the PET112 open reading frame destabilized the mitochondrial geno
me, causing cells to become rho(-). This finding suggests that PET112
has an important general function in mitochondrial gene expression, pr
obably in translation.