Home LiteratureArticle Details
PMID: 320093 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The effect of ochre suppression on meiosis and ascospore formation in Saccharomyces.

Genetics ·Vol. 85 ·No. 1 ·1977-01-00 ·Pages 35-54

Rothstein RJ, Esposito RE, Esposito MS

Abstract

The effect of altered tyrosyl-tRNAs on the developmental process of sporulation was examined. Mutations in eight independent loci resulting in tyrosine-inserting nonsense suppressor were tested for their effects on sporulation. Different levels of inhibition were found ranging from SUP3-omicron, which caused the greatest reduction of sporulation (7-17% of wild type), to SUP11-omicron which caused no reduction in sporulation. Since the SUP3-omicron mutation exhibited the greatest effect, it was studied in detail. Although SUP3-omicron is a dominant nonsense suppressor, its effect on sporulation is recessive. Expression of the sporulation deficiency is dependent upon the stage of transfer from glucose growth medium (i.e., log, early stationary, etc.) to sporulation medium. SUP3-omicron/SUP3-omicron diploid cells transferred from log or early stationary phase are capable of sporulation, whereas cells transferred after early stationary phase (i.e., after adaptation to respiration) exhibit poor sporulative ability. Sporulation events were examined under restrictive conditions to observe those events completed by SUP3-omicron/SUP3-omicron diploids. The early events of sporulation occur in these cells. Later events are completed by progressively fewer cells. Premeiotic DNA synthesis occurred in approximately 40% of the cells, nuclear segregation occurred in 20%, and finally, only 2% formed asci. The fact that fewer late-sporulation events occur under restrictive conditions can be explained by increased efficiency of suppression.

MeSH Terms
Meiosis Mutation Peptide Chain Termination, Translational RNA, Transfer/metabolism Saccharomyces cerevisiae/physiology Spores, Fungal Suppression, Genetic Time Factors Tyrosine/metabolism
Chemicals
Tyrosine RNA, Transfer
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rothstein R J
Esposito R E
Esposito M S
References (10)
10 references, click to expand
  1. Transfer RNA and cell differentiation.
    Prog Nucleic Acid Res Mol Biol. 1970;10:23-55 PMID: 4986276
  2. Nuclear and mitochondrial DNA synthesis during yeast sporulation.
    Exp Cell Res. 1974 Feb;83(2):231-8 PMID: 4593582
  3. Protein synthesis in relation to sporulation and meiosis in yeast.
    J Bacteriol. 1974 Sep;119(3):952-60 PMID: 4604981
  4. Regulation of tRNA.
    Annu Rev Biochem. 1973;42:439-70 PMID: 4199854
  5. Biochemical changes in yeast during sporulation. I. Fate of nucleic acids and related compounds.
    Dev Growth Differ. 1971 Feb;12(4):273-83 PMID: 5554639
  6. Yeast super-suppressors are altered tRNAs capable of translating a nonsense codon in vitro.
    Cell. 1975 Nov;6(3):269-77 PMID: 802681
  7. Nonsense suppressors of Saccharomyces cerevisiae can be generated by mutation of the tyrosine tRNA anticodon.
    Nature. 1976 Aug 26;262(5571):757-61 PMID: 785283
  8. Yeast suppressors of UAA and UAG nonsense codons work efficiently in vitro via tRNA.
    Cell. 1976 Mar;7(3):381-90 PMID: 947546
  9. [Relationship between physiological state and ability to sporulate in yeasts].
    Z Allg Mikrobiol. 1971;11(8):671-8 PMID: 4947987
  10. Super-suppressors in Saccharomyces cerevisiae.
    Genetics. 1967 Aug;56(4):641-58 PMID: 6061656
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1977-01-00
Pages
35-54
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1213618
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com