Literature DB >> 7001477

Preferential inclusion of extrachromosomal genetic elements in yeast meiotic spores.

B J Brewer, W L Fangman.   

Abstract

During meiosis and sporulation in the yeast Saccharomyces cerevisiae, extrachromosomal traits are efficiently transmitted to haploid spores. Although the pattern of inheritance of chromosomal traits reflects the mechanism of regular chromosomal segregation in meiosis, it is not known what processes are reflected by the efficient inheritance of extrachromosomal traits. Because extrachromosomal genetic elements in yeast are present in multiple copies, perpetuation of an extrachromosomal trait could occur by the passive envelopment of a subset of copies or by an active sequestering of all or a subset of copies within the four spores. We show that only subsets of the four extrachromosomal nucleic acids commonly found in yeast are transmitted through meiosis--55% of mitochondrial DNA copies, 82% of the 2-micron DNA plasmids, and about 70% of the L and M double-stranded RNAs. However, electron micrographs of serial sections through yeast asci indicate that the four spore enclose only 30% of the total ascus material. Thus these extrachromosomal elements are preferentially included within the spores, indicating that their inheritance is not a random process. Transmission of mitochondrial DNA can be accounted for by the observed enclosure of 52% of the mitochondrial volume within the spores. The high transmission frequencies of the double-stranded RNAs (which exist as virus-like particles in the cytoplasm) and 2-micron DNA must indicate that either these nucleic acids are actively recruited from the cytoplasm by some mechanism or they are associated in some way with the nucleus during meiosis.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 7001477      PMCID: PMC350062          DOI: 10.1073/pnas.77.9.5380

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  14 in total

1.  Behavior of spindles and spindle plaques in the cell cycle and conjugation of Saccharomyces cerevisiae.

Authors:  B Byers; L Goetsch
Journal:  J Bacteriol       Date:  1975-10       Impact factor: 3.490

2.  Naturally occurring cross-links in yeast chromosomal DNA.

Authors:  M A Forte; W L Fangman
Journal:  Cell       Date:  1976-07       Impact factor: 41.582

3.  Control of Saccharomyces cerevisiae 2microN DNA replication by cell division cycle genes that control nuclear DNA replication.

Authors:  D M Livingston; D M Kupfer
Journal:  J Mol Biol       Date:  1977-10-25       Impact factor: 5.469

4.  Inheritance of the 2 micrometer m DNA plasmid from Saccharomyces.

Authors:  D M Livingston
Journal:  Genetics       Date:  1977-05       Impact factor: 4.562

5.  Macromolecule synthesis and breakdown in relation to sporulation and meiosis in yeast.

Authors:  A K Hopper; P T Magee; S K Welch; M Friedman; B D Hall
Journal:  J Bacteriol       Date:  1974-08       Impact factor: 3.490

6.  Localization and quantification of circular DNA in yeast.

Authors:  G D Clark-Walker; G L Miklos
Journal:  Eur J Biochem       Date:  1974-01-16

7.  Sporulation of yeast harvested during logarithmic growth.

Authors:  R Roth; H O Halvorson
Journal:  J Bacteriol       Date:  1969-05       Impact factor: 3.490

8.  Biochemical and physiological studies of the yeast virus-like particle.

Authors:  S G Oliver; S J McCREADY; C Holm; P A Sutherland; C S McLaughlin; B S Cox
Journal:  J Bacteriol       Date:  1977-06       Impact factor: 3.490

9.  Fine structure of ascospore development in the yeast Saccharomyces cerevisiae.

Authors:  P B Moens
Journal:  Can J Microbiol       Date:  1971-04       Impact factor: 2.419

10.  Spindles, spindle plaques, and meiosis in the yeast Saccharomyces cerevisiae (Hansen).

Authors:  P B Moens; E Rapport
Journal:  J Cell Biol       Date:  1971-08       Impact factor: 10.539

View more
  28 in total

1.  Yeast L double-stranded ribonucleic acid is synthesized during the G1 phase but not the S phase of the cell cycle.

Authors:  V A Zakian; D W Wagner; W L Fangman
Journal:  Mol Cell Biol       Date:  1981-08       Impact factor: 4.272

2.  Interactions among prions and prion "strains" in yeast.

Authors:  Michael E Bradley; Herman K Edskes; Joo Y Hong; Reed B Wickner; Susan W Liebman
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-30       Impact factor: 11.205

3.  Defective Interference in the Killer System of Saccharomyces cerevisiae.

Authors:  S P Ridley; R B Wickner
Journal:  J Virol       Date:  1983-02       Impact factor: 5.103

4.  A nuclear mutation reversing a biased transmission of yeast mitochondrial DNA.

Authors:  S G Zweifel; W L Fangman
Journal:  Genetics       Date:  1991-06       Impact factor: 4.562

5.  Isolation and characterization of yeast mitochondrial mutants defective in spore germination.

Authors:  A Hartig; R Schroeder; E Mucke; M Breitenbach
Journal:  Curr Genet       Date:  1981-09       Impact factor: 3.886

6.  Mitochondrial circular RNAs are absent in sporulating cells of Saccharomyces cerevisiae.

Authors:  R Schroeder; M Breitenbach; R J Schweyen
Journal:  Nucleic Acids Res       Date:  1983-03-25       Impact factor: 16.971

Review 7.  Double-stranded ribonucleic acid killer systems in yeasts.

Authors:  D J Tipper; K A Bostian
Journal:  Microbiol Rev       Date:  1984-06

8.  Behaviour of nucleolus organizing regions (NORs) and nucleoli during mitotic and meiotic divisions in budding yeast.

Authors:  Jörg Fuchs; Josef Loidl
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

9.  Germination conditions that require mitochondrial function in Saccharomyces cerevisiae: utilization of acetate and galactose.

Authors:  C Donnini; N Artoni; N Marmiroli
Journal:  J Bacteriol       Date:  1986-12       Impact factor: 3.490

10.  Septin stability and recycling during dynamic structural transitions in cell division and development.

Authors:  Michael A McMurray; Jeremy Thorner
Journal:  Curr Biol       Date:  2008-08-14       Impact factor: 10.834

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.