Some plant cytoplasms express novel mitochondrial genes that cause male sterility. Nuclear genes that disrupt the accumulation of the corresponding mitochondrial gene products can restore fertility to such plants. The Texas (T) cytoplasm mitochondrial genome of maize expresses a novel protein, URF13, which is necessary for T cytoplasm-induced male sterility. Working in concert, functional alleles of two nuclear genes, rf1 and rf2 , can restore fertility to T cytoplasm plants. Rf1 alleles, but not Rf2 alleles, reduce the accumulation of URF13. Hence, Rf2 differs from typical nuclear restorers in that it does not alter the accumulation of the mitochondrial protein necessary for T cytoplasm-induced male sterility. This study established that the rf2 gene encodes a soluble protein that accumulates in the mitochondrial matrix. Three independent lines of evidence establish that the RF2 protein is an aldehyde dehydrogenase (ALDH). The finding that T cytoplasm plants that are homozygous for the rf2-R213 allele are male sterile but accumulate normal amounts of RF2 protein that lacks normal mitochondrial (mt) ALDH activity provides strong evidence that rf2 -encoded mtALDH activity is required to restore male fertility to T cytoplasm maize. Detailed genetic analyses have established that the rf2 gene also is required for anther development in normal cytoplasm maize. Hence, it appears that the rf2 gene was recruited recently to function as a nuclear restorer. ALDHs typically have very broad substrate specificities. Indeed, the RF2 protein is capable of oxidizing at least three aldehydes. Hence, the specific metabolic pathway(s) within which the rf2 -encoded mtALDH acts remains to be discovered.
INTRODUCTIONMaternally inherited cytoplasmic male sterility (CMS) occurs in many plant species and is widely used to facilitate the production of hybrid seed because it eliminates the need for emasculation by hand. Mitochondrial defects account for all instances in which the nature of the lesion responsible for CMS has been identified (reviewed in Mackenzie et al., 1994;Schnable and Wise, 1998). In many species, the deleterious effects of these mitochondrial defects can be avoided or overcome by the action of nuclear genes, termed nuclear restorers. However, the specific mechanisms by which restoration can occur are only poorly understood.The male-sterile Texas (T) cytoplasm (cms-T) was used to produce ف 85% of U.S. hybrid maize seed until the 1970 epidemic of southern corn leaf blight (Ullstrup, 1972;Pring and Lonsdale, 1989). cms-T maize is highly sensitive to a hostselective toxin (T toxin) produced by race T of Cochliobolus heterostrophus , the causal organism of southern corn leaf blight (Hooker et al., 1970; Comstock and Scheffer, 1973; Yoder, 1973). The genomes of T cytoplasm mitochondria contain a unique mitochondrial gene, urf13 , which encodes the URF13 protein. URF13 accumulates in the inner membrane of the mitochondria (Forde and Leaver, 1980; Dewey et al., 1986;Wise et al., 1987a;Hack et al., 1991;Korth et al., 1991;...