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Updated: May 4, 2026

A Deep-sequencing-assisted, Spontaneous Suppressor Screen in the Fission Yeast Schizosaccharomyces pombe
Published on: March 7, 2019
Meiotic recombination-deficient mutants of Schizosaccharomyces pombe
1Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Abstract:
A mutant screen employing the ade6-M26 recombination hotspot was developed and used to isolate Schizosaccharomyces pombe mutants deficient in meiotic recombination. Nine rec mutations were recessive, defining six complementation groups, and reduced ade6 meiotic recombination 3-fold to greater than or equal to 300-fold when homozygous. Three recessive rec mutations analyzed further also reduced meiotic intragenic recombination at ura4 on chromosome III and intergenic recombination between pro2 and arg3 on chromosome I. The observed non-co-ordinate reductions of the recombinant frequencies in the three test intervals suggest a degree of locus (or intragenic vs. intergenic) specificity of the corresponding rec+ gene products. None of the mutations specifically inactivated the ade6-M26 hotspot. Additional rec genes may be identified with these methods.
Insights
Researchers identified new genes controlling meiotic recombination in Schizosaccharomyces pombe. These mutations significantly reduced genetic recombination, offering insights into the process and potential locus specificity.
Area of Science:
- Genetics
- Molecular Biology
- Cell Biology
Background:
- Meiotic recombination is crucial for genetic diversity and proper chromosome segregation.
- Understanding the genes involved in meiotic recombination is essential for comprehending genome stability and evolution.
Purpose of the Study:
- To identify and characterize genes essential for meiotic recombination in the fission yeast Schizosaccharomyces pombe.
- To investigate the specificity of gene products involved in regulating recombination frequencies.
Main Methods:
- A mutant screen utilizing the ade6-M26 recombination hotspot in Schizosaccharomyces pombe.
- Complementation analysis to group recessive mutations.
- Analysis of meiotic recombination frequencies at multiple genetic loci (ade6, ura4, pro2-arg3).
Main Results:
- Nine recessive mutations (rec) affecting meiotic recombination were isolated, defining six complementation groups.
- Homozygous rec mutations reduced ade6 meiotic recombination 3-fold to over 300-fold.
- Three analyzed mutations also reduced intragenic and intergenic recombination at other loci, suggesting locus specificity.
Conclusions:
- The study successfully identified novel genes involved in regulating meiotic recombination in S. pombe.
- The results indicate that some recombination gene products exhibit specificity for different genomic locations or types of recombination (intragenic vs. intergenic).
- The ade6-M26 hotspot was not specifically inactivated by any of the identified mutations.
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