» Articles » PMID: 17248974

Cytogenetic Behavior of Spore Killer Genes in Neurospora

Overview
Journal Genetics
Specialty Genetics
Date 1979 Nov 1
PMID 17248974
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Crosses heterozygous and homozygous for Sk-1, Sk-2 and Sk-3 were examined by light microscopy. All three Spore killers behave similarly. In heterozygous killer x sensitive crosses, meiosis and ascospore development are normal until after the second postmeiotic mitosis when four of the eight ascospores in each ascus stop developing and degenerate. The four surviving ascospores carry the killer. Death of sensitives thus occurs only after killer and sensitive alleles, Sk(K) and Sk(S), have segregated into separate ascospores. Homozygous killer x killer crosses do not show such a pattern of degeneration. Either all ascospores are normal or, if some fail to mature, they do not resemble the degenerating sensitive ascospores in heterozygous asci.--With Sk-2, it was shown that Sk(S) nuclei do not abort when both Sk(K) and Sk(S) are present in the same ascospore. Mutants affecting ascus development were used to obtain large ascospores enclosing both Sk(K) and Sk(S) meiotic products in a common cytoplasm. Sk(S) nuclei do not then undergo the degeneration that would be seen if they were sequestered into separate ascospores, and viable Sk(S) progeny are recovered in undiminished numbers when the mixed multinucleate large ascospores are germinated. In a four-spored mutant, where each ascospore encloses a single nucleus following meiosis, degeneration of Sk(S) ascospores nevertheless occurs, even though the third nuclear division is omitted. Cycloheximide and temperature treatments do not affect the expression of Sk(K).

Citing Articles

Recurrent breakdown and rebalance of segregation distortion in the genomes: battle for the transmission advantage.

Xia F, Ouyang Y aBIOTECH. 2022; 1(4):246-254.

PMID: 36304131 PMC: 9590546. DOI: 10.1007/s42994-020-00023-0.


Identification of , a Meiotic Driver Undergoing RNA Editing in .

Rhoades N, Harvey A, Samarajeewa D, Svedberg J, Yusifov A, Abusharekh A Genetics. 2019; 212(1):93-110.

PMID: 30918007 PMC: 6499513. DOI: 10.1534/genetics.119.302122.


Regulated Forms of Cell Death in Fungi.

Goncalves A, Heller J, Daskalov A, Videira A, Glass N Front Microbiol. 2017; 8:1837.

PMID: 28983298 PMC: 5613156. DOI: 10.3389/fmicb.2017.01837.


Neurospora Heterokaryons with Complementary Duplications and Deficiencies in Their Constituent Nuclei Provide an Approach to Identify Nucleus-Limited Genes.

Giri D, Rekha S, Kasbekar D G3 (Bethesda). 2015; 5(6):1263-72.

PMID: 25897010 PMC: 4478554. DOI: 10.1534/g3.115.017616.


A critical component of meiotic drive in Neurospora is located near a chromosome rearrangement.

Harvey A, Rehard D, Groskreutz K, Kuntz D, Sharp K, Shiu P Genetics. 2014; 197(4):1165-74.

PMID: 24931406 PMC: 4125391. DOI: 10.1534/genetics.114.167007.


References
1.
CROUSE H . The Controlling Element in Sex Chromosome Behavior in Sciara. Genetics. 1960; 45(10):1429-43. PMC: 1210016. DOI: 10.1093/genetics/45.10.1429. View

2.
Mange E . Temperature sensitivity of segregation-distortion in Drosophila melanogaster. Genetics. 1968; 58(3):399-413. PMC: 1211871. DOI: 10.1093/genetics/58.3.399. View

3.
Koltin Y, Day P . Inheritance of killer phenotypes and double-stranded RNA in Ustilago maydis. Proc Natl Acad Sci U S A. 1976; 73(2):594-8. PMC: 335957. DOI: 10.1073/pnas.73.2.594. View

4.
Padieu E, Bernet J . [Mode of action of the genes responsible for abortion of certain products of meiosis in the Ascomycete, Podospora anserina]. C R Acad Hebd Seances Acad Sci D. 1967; 264(19):2300-3. View