@article {111866,
	title = {Mutations in Saccharomyces cerevisiae that block meiotic prophase chromosome metabolism and confer cell cycle arrest at pachytene identify two new meiosis-specific genes SAE1 and SAE3.},
	journal = {Genetics},
	volume = {146},
	number = {3},
	year = {1997},
	month = {1997 Jul},
	pages = {817-34},
	abstract = {Two new meiosis-specific genes, SAE1 and SAE3, have been identified in a screen for mutations that confer an intermediate block in meiotic prophase. Such mutations confer a block to spore formation that is circumvented by addition of a mutation that eliminates meiotic recombination initiation and other aspects of chromosome metabolism, i.e., spo11. We show that sae1-1 and sae3-1 mutations each confer a distinct defect in meiotic recombination. sae1-1 produces recombinants but very slowly and ultimately to less than half the wild-type level; sae3-1 makes persistent hyper-resected meiotic double-strand breaks and has a severe defect in formation of recombinants. Both mutants arrest at the pachytene stage of meiotic prophase, sae1-1 temporarily and sae3-1 permanently. The phenotypes conferred by sae3-1 are similar to those conferred by mutation of the yeast RecA homologue DMC1, suggesting that SAE3 and DMC1 act at the same step(s) of chromosome metabolism. These results provide further evidence that intermediate blocks to prophase chromosome metabolism cause cell-cycle arrest. SAE1 encodes a 208-residue protein homologous to vertebrate mRNA cap-binding protein 20. SAE3 corresponds to a meiosis-specific RNA encoding an unusually short open reading frame of 50 codons.},
	keywords = {Amino Acid Sequence, Animals, Base Sequence, Chromosomes, Fungal, Cloning, Molecular, DNA Primers, DNA, Fungal, Fungal Proteins, Genes, cdc, Humans, Meiosis, Molecular Sequence Data, Mutagenesis, Site-Directed, Nuclear Cap-Binding Protein Complex, Phenotype, Phosphoproteins, Prophase, Recombinases, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Sequence Homology, Amino Acid, Transcription, Genetic},
	issn = {0016-6731},
	author = {McKee, A H and Kleckner, N}
}
