Literature DB >> 8349113

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.

W L Whyte1, H Irick, T Arbel, G Yasuda, R L French, D R Falk, R S Hawley.   

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.

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Year:  1993        PMID: 8349113      PMCID: PMC1205519     

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


  18 in total

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Authors:  A T Carpenter
Journal:  Cell       Date:  1991-03-08       Impact factor: 41.582

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Authors:  H Wald
Journal:  Genetics       Date:  1936-05       Impact factor: 4.562

3.  The lethal(1)TW-6cs mutation of Drosophila melanogaster is a dominant antimorphic allele of nod and is associated with a single base change in the putative ATP-binding domain.

Authors:  R S Rasooly; C M New; P Zhang; R S Hawley; B S Baker
Journal:  Genetics       Date:  1991-10       Impact factor: 4.562

4.  A meiotic mutant defective in distributive disjunction in Drosophila melanogaster.

Authors:  A T Carpenter
Journal:  Genetics       Date:  1973-03       Impact factor: 4.562

5.  Nonexchange alignment: a meiotic process revealed by a synthetic meiotic mutant of Drosophila melanogaster.

Authors:  L G Robbins
Journal:  Mol Gen Genet       Date:  1971

6.  The characterization of chromosome breaks in Drosophila melanogaster. I. Mass isolation of deficiencies which have an end point in the 14A-15A region.

Authors:  D R Falk; L Roselli; S Curtiss; D Halladay; C Klufas
Journal:  Mutat Res       Date:  1984-03       Impact factor: 2.433

7.  A kinesin-like protein required for distributive chromosome segregation in Drosophila.

Authors:  P Zhang; B A Knowles; L S Goldstein; R S Hawley
Journal:  Cell       Date:  1990-09-21       Impact factor: 41.582

8.  Identification and characterization of a gene encoding a kinesin-like protein in Drosophila.

Authors:  H B McDonald; L S Goldstein
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

9.  Mutants of the microtubule motor protein, nonclaret disjunctional, affect spindle structure and chromosome movement in meiosis and mitosis.

Authors:  M Hatsumi; S A Endow
Journal:  J Cell Sci       Date:  1992-03       Impact factor: 5.285

10.  Separation of meiotic and mitotic effects of claret non-disjunctional on chromosome segregation in Drosophila.

Authors:  D J Komma; A S Horne; S A Endow
Journal:  EMBO J       Date:  1991-02       Impact factor: 11.598

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  10 in total

1.  The mechanism of secondary nondisjunction in Drosophila melanogaster females.

Authors:  Youbin Xiang; R Scott Hawley
Journal:  Genetics       Date:  2006-07-02       Impact factor: 4.562

2.  Genetic and molecular analysis of wings apart-like (wapl), a gene controlling heterochromatin organization in Drosophila melanogaster.

Authors:  F Vernì; R Gandhi; M L Goldberg; M Gatti
Journal:  Genetics       Date:  2000-04       Impact factor: 4.562

3.  Identification of novel Drosophila meiotic genes recovered in a P-element screen.

Authors:  J J Sekelsky; K S McKim; L Messina; R L French; W D Hurley; T Arbel; G M Chin; B Deneen; S J Force; K L Hari; J K Jang; A C Laurençon; L D Madden; H J Matthies; D B Milliken; S L Page; A D Ring; S M Wayson; C C Zimmerman; R S Hawley
Journal:  Genetics       Date:  1999-06       Impact factor: 4.562

4.  Double or nothing: a Drosophila mutation affecting meiotic chromosome segregation in both females and males.

Authors:  D P Moore; W Y Miyazaki; J E Tomkiel; T L Orr-Weaver
Journal:  Genetics       Date:  1994-03       Impact factor: 4.562

5.  Heterochromatin-Associated Proteins HP1a and Piwi Collaborate to Maintain the Association of Achiasmate Homologs in Drosophila Oocytes.

Authors:  Christopher C Giauque; Sharon E Bickel
Journal:  Genetics       Date:  2016-03-16       Impact factor: 4.562

6.  Dynein promotes achiasmate segregation in Schizosaccharomyces pombe.

Authors:  Luther Davis; Gerald R Smith
Journal:  Genetics       Date:  2005-03-31       Impact factor: 4.562

7.  Classic Weinstein: tetrad analysis, genetic variation and achiasmate segregation in Drosophila and humans.

Authors:  M E Zwick; D J Cutler; C H Langley
Journal:  Genetics       Date:  1999-08       Impact factor: 4.562

Review 8.  The Interchromosomal Effect: Different Meanings for Different Organisms.

Authors:  Danny E Miller
Journal:  Genetics       Date:  2020-11       Impact factor: 4.562

9.  mei-38 is required for chromosome segregation during meiosis in Drosophila females.

Authors:  Changjian Wu; Vinod Singaram; Kim S McKim
Journal:  Genetics       Date:  2008-08-30       Impact factor: 4.562

10.  Aging predisposes oocytes to meiotic nondisjunction when the cohesin subunit SMC1 is reduced.

Authors:  Vijayalakshmi V Subramanian; Sharon E Bickel
Journal:  PLoS Genet       Date:  2008-11-14       Impact factor: 5.917

  10 in total

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