Literature DB >> 6751934

Two cell division cycle mutants of Saccharomyces cerevisiae are defective in transmission of mitochondria to zygotes.

S K Dutcher.   

Abstract

Mutations in CDC genes of S. cerevisiae disrupt the cell cycle at specific stages. The experiments reported here demonstrate that two CDC genes, CDC5 and CDC27, are necessary for mitochondrial segregation as well as for nuclear division. The defect in the transmission of mitochondria was revealed by the examination of uninucleate and binucleate progeny of transient heterokaryons generated by using the kar1-1 mutation that disrupts nuclear fusion. One of the parents lacked mitochondrial DNA (rho(0)) whereas the other parent had functional mitochondria (rho(+)). When the parents of the heterokaryon were both wild-type (CDC), nearly all progeny received mitochondria at 21 degrees and at 34 degrees . Thirty-four of the 36 cdc mutations tested had no defect in transmission of mitochondria to zygotic progeny in crosses in which one parent was a cdc mutant and the other parent was not (CDC). However, the cdc5 and cdc27 mutations prevented the transmission of mitochondria to cdc progeny at 34 degrees but not at 21 degrees ; CDC progeny received mitochondria at either temperature. This defect was observed in crosses of cdc5 or cdc27 by wild-type cells regardless of which parent donated mitochondria to the zygote. The defect in mitochondrial transmission cosegregated in meiotic tetrads with the defect in mitosis demonstrating that both are likely to be caused by the same temperature-sensitive mutation. These results indicate that the CDC5 and CDC27 gene products are essential in two motility-related processes: mitochondrial movement from the zygote to the progeny and in mitosis.-Furthermore, the results suggest that the function performed by the CDC5 and CDC27 gene products for mitochondrial transmission differ in some fundamental way from the function performed for mitosis. The function necessary for mitosis can be supplied to the cdc5 (or cdc27) nucleus by the CDC5 (or CDC27) nucleus in the same heterokaryon but the function necessary for mitochondrial transmission cannot. Perhaps the function needed for mitochondrial transmission must be performed in the cell cycle preceding the actual segregation of mitochondria whereas the function needed for nuclear segregation can be performed at the time that mitosis occurs.

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Year:  1982        PMID: 6751934      PMCID: PMC1201927     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  10 in total

1.  EXTRANUCLEAR TRANSMISSION IN YEAST HETEROKARYONS.

Authors:  R E Wright; J Lederberg
Journal:  Proc Natl Acad Sci U S A       Date:  1957-10-15       Impact factor: 11.205

2.  SUPPRESSIVENESS: A NEW FACTOR IN THE GENETIC DETERMINISM OF THE SYNTHESIS OF RESPIRATORY ENZYMES IN YEAST.

Authors:  B Ephrussi; H de Margerie-Hottinguer; H Roman
Journal:  Proc Natl Acad Sci U S A       Date:  1955-12-15       Impact factor: 11.205

3.  The effect of zygotic bud position on the transmission of mitochondrial genes in Saccharomyces cerevisiae.

Authors:  R L Strausberg; P S Perlman
Journal:  Mol Gen Genet       Date:  1978-07-11

4.  The effects of colcemid inhibition and reversal on the fine structure of the mitotic apparatus of Chinese hamster cells in vitro.

Authors:  B R Brinkley; E Stubblefield; T C Hsu
Journal:  J Ultrastruct Res       Date:  1967-07

5.  Diploid spore formation and other meiotic effects of two cell-division-cycle mutations of Saccharomyces cerevisiae.

Authors:  D Schild; B Byers
Journal:  Genetics       Date:  1980-12       Impact factor: 4.562

6.  The role of S. cerevisiae cell division cycle genes in nuclear fusion.

Authors:  S K Dutcher; L H Hartwell
Journal:  Genetics       Date:  1982-02       Impact factor: 4.562

7.  Zygote heterogeneity and uniparental inheritance of mitochondrial genes in yeast.

Authors:  C W Birky
Journal:  Mol Gen Genet       Date:  1975-11-03

8.  Macromolecule synthesis in temperature-sensitive mutants of yeast.

Authors:  L H Hartwell
Journal:  J Bacteriol       Date:  1967-05       Impact factor: 3.490

9.  THE MECHANISM OF COLCHICINE INHIBITION OF MITOSIS. I. KINETICS OF INHIBITION AND THE BINDING OF H3-COLCHICINE.

Authors:  E W TAYLOR
Journal:  J Cell Biol       Date:  1965-04       Impact factor: 10.539

10.  Functions of cytoplasmic fibers in intracellular movements in BHK-21 cells.

Authors:  E Wang; R D Goldman
Journal:  J Cell Biol       Date:  1978-12       Impact factor: 10.539

  10 in total
  3 in total

1.  Mitochondrial DNA loss by yeast reentry-mutant cells conditionally unable to proliferate from stationary phase.

Authors:  M Filipak; M A Drebot; L S Ireland; R A Singer; G C Johnston
Journal:  Curr Genet       Date:  1992-12       Impact factor: 3.886

2.  Test for temporal or spatial restrictions in gene product function during the cell division cycle.

Authors:  S K Dutcher; L H Hartwell
Journal:  Mol Cell Biol       Date:  1983-07       Impact factor: 4.272

3.  p53 regulates mtDNA copy number and mitocheckpoint pathway.

Authors:  Mariola Kulawiec; Vanniarajan Ayyasamy; Keshav K Singh
Journal:  J Carcinog       Date:  2009
  3 in total

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