ArticleGenetics1992
Ty element-induced temperature-sensitive mutations of Saccharomyces cerevisiae.
Article in Genetics, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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Who cites it
16 citing papers in PubMed, 33 citations in OpenAlex.
- Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use.Nucleic acids research · 2016Review
- A novel zinc-finger HIT protein with an additional PAPA-1-like region from Suaeda liaotungensis K. enhanced transgenic Arabidopsis drought and salt stresses tolerance.Molecular biotechnology · 2014Article
- Protein Hit1, a novel box C/D snoRNP assembly factor, controls cellular concentration of the scaffolding protein Rsa1 by direct interaction.Nucleic acids research · 2014Article
- Genome remodeling.Nature biotechnology · 2011Article
- A comprehensive analysis of translational missense errors in the yeast Saccharomyces cerevisiae.RNA (New York, N.Y.) · 2010Article
- Nuclear receptor-coregulator interaction profiling identifies TRIP3 as a novel peroxisome proliferator-activated receptor gamma cofactor.Molecular & cellular proteomics : MCP · 2009Article
- Eukaryotic wobble uridine modifications promote a functionally redundant decoding system.Molecular and cellular biology · 2008Article
- Solution structure of the zinc finger HIT domain in protein FON.Protein science : a publication of the Protein Society · 2007Article
- Dissecting the pet18 mutation in Saccharomyces cerevisiae: HTL1 encodes a 7-kDa polypeptide that interacts with components of the RSC complex.Molecular genetics and genomics : MGG · 2003Article
- Effect of frameshift-inducing mutants of elongation factor 1alpha on programmed +1 frameshifting in yeast.RNA (New York, N.Y.) · 1998Article
- Article
- Ribosomal frameshifting in yeast viruses.Yeast (Chichester, England) · 1995Review
- Special peptidyl-tRNA molecules can promote translational frameshifting without slippage.Molecular and cellular biology · 1994Article
- A member of a novel family of yeast 'zn-finger' proteins mediates the transition from stationary phase to cell proliferation.The EMBO journal · 1994Article
- Spermidine deficiency increases +1 ribosomal frameshifting efficiency and inhibits Ty1 retrotransposition in Saccharomyces cerevisiae.Proceedings of the National Academy of Sciences of the United States of America · 1994Article
- MSI3, a multicopy suppressor of mutants hyperactivated in the RAS-cAMP pathway, encodes a novel HSP70 protein of Saccharomyces cerevisiae.Molecular & general genetics : MGG · 1993Article
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
Temperature-sensitive mutants of Saccharomyces cerevisiae were isolated by insertional mutagenesis using the HIS3 marked retrotransposon TyH3HIS3. In such mutants, the TyHIS3 insertions are expected to identify loci which encode genes essential for cell growth at high temperatures but dispensable at low temperatures. Five mutations were isolated and named hit for high temperature growth. The hit1-1 mutation was located on chromosome X and conferred the pet phenotype. Two hit2 mutations, hit2-1 and hit2-2, were located on chromosome III and caused the deletion of the PET18 locus which has been shown to encode a gene required for growth at high temperatures. The hit3-1 mutation was located on chromosome VI and affected the CDC26 gene. The hit4-1 mutation was located on chromosome XIII. These hit mutations were analyzed in an attempt to identify novel genes involved in the heat shock response. The hit1-1 mutation caused a defect in synthesis of a 74-kD heat shock protein. Western blot analysis revealed that the heat shock protein corresponded to the SSC1 protein, a member of the yeast hsp70 family. In the hit1-1 mutant, the TyHIS3 insertion caused a deletion of a 3-kb DNA segment between the delta 1 and delta 4 sequences near the SUP4 locus. The 1031-bp wild-type HIT1 DNA which contained an open reading frame encoding a protein of 164 amino acids and the AGG arginine tRNA gene complemented all hit1-1 mutant phenotypes, indicating that the mutant phenotypes were caused by the deletion of these genes. The pleiotropy of the HIT1 locus was analyzed by constructing a disruption mutation of each gene in vitro and transplacing it to the chromosome. This analysis revealed that the HIT1 gene essential for growth at high temperatures encodes the 164-amino acid protein. The arginine tRNA gene, named HSX1, is essential for growth on a nonfermentable carbon source at high temperatures and for synthesis of the SSC1 heat shock protein.
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