Increased spontaneous mitotic segregation in MMS-sensitive mutants of Saccharomyces cerevisiae

Genetics
|October 1, 1977
PubMed

Insights

Methyl methanesulfonate (MMS)-sensitive yeast mutants significantly elevate spontaneous mitotic segregation rates. These findings highlight MMS sensitivity as a key indicator of DNA repair defects impacting genetic stability.

Area of Science:

  • Molecular Biology
  • Genetics
  • Yeast Genetics

Background:

  • DNA repair mechanisms are crucial for maintaining genomic integrity.
  • Methyl methanesulfonate (MMS) is a chemical mutagen used to study DNA damage response pathways.
  • Spontaneous mitotic segregation is a measure of genetic instability in yeast.

Purpose of the Study:

  • To investigate the role of MMS sensitivity in spontaneous mitotic segregation.
  • To characterize novel MMS-sensitive mutants in Saccharomyces cerevisiae.
  • To quantify the impact of specific mutations on genetic instability.

Main Methods:

  • Utilized Saccharomyces cerevisiae as a model organism.
  • Generated and analyzed homozygous MMS-sensitive mutants.
  • Assessed spontaneous mitotic segregation rates to canavanine resistance in heterozygous diploids.
  • Determined sensitivity to MMS, X-rays, and UV radiation for characterized mutants.

Main Results:

  • Four complementation groups of MMS-sensitive mutants were identified.
  • Homozygous mutants exhibited a 13- to 170-fold increase in spontaneous mitotic segregation rates.
  • The mms8-1 mutant showed the highest increase (170-fold) and sensitivity to MMS and X-rays.
  • Other mutants (mms9-1, mms13-1, mms21-1) displayed varying sensitivities and segregation rates.

Conclusions:

  • MMS sensitivity in yeast is strongly correlated with increased rates of spontaneous mitotic segregation.
  • Specific MMS-sensitive mutations confer distinct sensitivities to different DNA damaging agents.
  • These mutants provide valuable tools for dissecting DNA repair pathways and understanding genetic instability.

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