Literature DB >> 10430587

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

M E Zwick1, D J Cutler, C H Langley.   

Abstract

A maximum-likelihood method for the estimation of tetrad frequencies from single-spore data is presented. The multilocus exchange with interference and viability (MEIV) model incorporates a clearly defined model of exchange, interference, and viability whose parameters define a multinomial distribution for single-spore data. Maximum-likelihood analysis of the MEIV model (MEIVLA) allows point estimation of tetrad frequencies and determination of confidence intervals. We employ MEIVLA to determine tetrad frequencies among 15 X chromosomes sampled at random from Drosophila melanogaster natural populations in Africa and North America. Significant variation in the frequency of nonexchange, or E(0) tetrads, is observed within both natural populations. Because most nondisjunction arises from E(0) tetrads, this observation is quite unexpected given both the prevalence and the deleterious consequences of nondisjunction in D. melanogaster. Use of MEIVLA is also demonstrated by reanalyzing a recently published human chromosome 21 dataset. Analysis of simulated datasets demonstrates that MEIVLA is superior to previous methods of tetrad frequency estimation and is particularly well suited to analyze samples where the E(0) tetrad frequency is low and sample sizes are small, conditions likely to be met in most samples from human populations. We discuss the implications of our analysis for determining whether an achiasmate system exists in humans to ensure the proper segregation of E(0) tetrads.

Entities:  

Mesh:

Year:  1999        PMID: 10430587      PMCID: PMC1460678     

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


  44 in total

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Authors:  A WEINSTEIN
Journal:  J Cell Physiol Suppl       Date:  1955-05

2.  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

Review 3.  Human aneuploidy: incidence, origin, and etiology.

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Journal:  Environ Mol Mutagen       Date:  1996       Impact factor: 3.216

4.  Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

Authors:  N E Lamb; E Feingold; A Savage; D Avramopoulos; S Freeman; Y Gu; A Hallberg; J Hersey; G Karadima; D Pettay; D Saker; J Shen; L Taft; M Mikkelsen; M B Petersen; T Hassold; S L Sherman
Journal:  Hum Mol Genet       Date:  1997-09       Impact factor: 6.150

5.  Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster.

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

6.  Distributive disjunction of authentic chromosomes in Saccharomyces cerevisiae.

Authors:  V Guacci; D B Kaback
Journal:  Genetics       Date:  1991-03       Impact factor: 4.562

7.  Incipient speciation by sexual isolation in Drosophila melanogaster: extensive genetic divergence without reinforcement.

Authors:  H Hollocher; C T Ting; M L Wu; C I Wu
Journal:  Genetics       Date:  1997-11       Impact factor: 4.562

8.  Spontaneous X chromosome MI and MII nondisjunction events in Drosophila melanogaster oocytes have different recombinational histories.

Authors:  K E Koehler; C L Boulton; H E Collins; R L French; K C Herman; S M Lacefield; L D Madden; C D Schuetz; R S Hawley
Journal:  Nat Genet       Date:  1996-12       Impact factor: 38.330

9.  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

10.  African and North American populations of Drosophila melanogaster are very different at the DNA level.

Authors:  D J Begun; C F Aquadro
Journal:  Nature       Date:  1993-10-07       Impact factor: 49.962

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  8 in total

1.  Mapping functions.

Authors:  Yuan-De Tan; Myriam Fornage
Journal:  Genetica       Date:  2007-10-14       Impact factor: 1.082

2.  Heterochromatin-mediated association of achiasmate homologs declines with age when cohesion is compromised.

Authors:  Vijayalakshmi V Subramanian; Sharon E Bickel
Journal:  Genetics       Date:  2009-02-09       Impact factor: 4.562

3.  A Fine-Scale Genetic Map for Vervet Monkeys.

Authors:  Susanne P Pfeifer
Journal:  Mol Biol Evol       Date:  2020-07-01       Impact factor: 16.240

4.  Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster.

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

5.  Variation in meiotic recombination frequencies among human males.

Authors:  Fei Sun; Kiril Trpkov; Alfred Rademaker; Evelyn Ko; Renée H Martin
Journal:  Hum Genet       Date:  2004-12-01       Impact factor: 4.132

6.  Genetic control of mammalian meiotic recombination. I. Variation in exchange frequencies among males from inbred mouse strains.

Authors:  Kara E Koehler; Jonathan P Cherry; Audrey Lynn; Patricia A Hunt; Terry J Hassold
Journal:  Genetics       Date:  2002-09       Impact factor: 4.562

7.  Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth.

Authors:  Sujoy Ghosh; Eleanor Feingold; Sumita Chakraborty; Subrata Kumar Dey
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

Review 8.  Female Meiosis: Synapsis, Recombination, and Segregation in Drosophila melanogaster.

Authors:  Stacie E Hughes; Danny E Miller; Angela L Miller; R Scott Hawley
Journal:  Genetics       Date:  2018-03       Impact factor: 4.562

  8 in total

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