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PMID: 8349113 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The genetic analysis of achiasmate segregation in Drosophila melanogaster. III. The wild-type product of the Axs gene is required for the meiotic segregation of achiasmate homologs.

Genetics ·Vol. 134 ·No. 3 ·1993-07-00 ·Pages 825-35

Whyte WL, Irick H, Arbel T, Yasuda G, French RL, Falk DR, Hawley RS

Abstract

The regular segregation of achiasmate chromosomes in Drosophila melanogaster females is ensured by two distinct segregational systems. The segregation of achiasmate homologs is assured by the maintenance of heterochromatic pairing; while the segregation of heterologous chromosomes is ensured by a separate mechanism that may not require physical association. AxsD (Aberrant X segregation) is a dominant mutation that specifically impairs the segregation of achiasmate homologs; heterologous achiasmate segregations are not affected. As a result, achiasmate homologs frequently participate in heterologous segregations at meiosis I. We report the isolation of two intragenic revertants of the AxsD mutation (Axsr2 and Axsr3) that exhibit a recessive meiotic phenotype identical to that observed in AxsD/AxsD females. A third revertant (Axsr1) exhibits no meiotic phenotype as a homozygote, but a meiotic defect is observed in Axsr1/Axsr2 females. Therefore mutations at the AxsD locus define a gene necessary and specific for homologous achiasmate segregation during meiosis. We also characterize the interactions of mutations at the Axs locus with two other meiotic mutations (ald and ncd). Finally, we propose a model in which Axs+ is required for the normal separation of paired achiasmate homologs. In the absence of Axs+ function, the homologs are often unable to separate from each other and behave as a single segregational unit that is free to segregate from heterologous chromosomes.

Related Genes
MeSH Terms
Animals Chromosome Mapping Chromosomes/physiology Drosophila melanogaster/genetics Female Genes, Recessive Male Meiosis/genetics Multigene Family Mutation Nondisjunction, Genetic
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Whyte W L
Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, New York 10461.
Irick H
Arbel T
Yasuda G
French R L
Falk D R
Hawley R S
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Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1993-07-00
Pages
825-35
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1205519
Subset
IM
Grants
NIGMS NIH HHS · 5T32-GM07491 · United States
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