Literature DB >> 8875256

Recombination and nondisjunction in humans and flies.

K E Koehler1, R S Hawley, S Sherman, T Hassold.   

Abstract

Recent studies of Drosophila and humans indicate that aberrant genetic recombination is an important component of nondisjunction in both species. In both, a proportion of nondisjunction is associated with failure to pair and/or recombine and in both, exchanges which are either too distal or too proximal increase the likelihood of malsegregation. In this review we provide two perspectives on these observations: first, a review of exchange and chromosome segregation in model organisms, focusing on Drosophila, and secondly an overview of nondisjunction in humans. This format allows us to describe the paradigms developed from studies of model organisms and to ask whether these paradigms apply to the human situation.

Entities:  

Mesh:

Year:  1996        PMID: 8875256     DOI: 10.1093/hmg/5.supplement_1.1495

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  62 in total

1.  Trisomic pregnancy and earlier age at menopause.

Authors:  J Kline; A Kinney; B Levin; D Warburton
Journal:  Am J Hum Genet       Date:  2000-06-28       Impact factor: 11.025

2.  The evolution of recombination in a heterogeneous environment.

Authors:  T Lenormand; S P Otto
Journal:  Genetics       Date:  2000-09       Impact factor: 4.562

3.  Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Authors:  Tiffany Renee Oliver; Stuart W Tinker; Emily Graves Allen; Natasha Hollis; Adam E Locke; Lora J H Bean; Reshmi Chowdhury; Ferdouse Begum; Mary Marazita; Vivian Cheung; Eleanor Feingold; Stephanie L Sherman
Journal:  Hum Genet       Date:  2011-12-09       Impact factor: 4.132

4.  Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction.

Authors:  Sue Ann Berend; Scott L Page; William Atkinson; Christopher McCaskill; Neil E Lamb; Stephanie L Sherman; Lisa G Shaffer
Journal:  Am J Hum Genet       Date:  2002-12-23       Impact factor: 11.025

5.  Pairing, connecting, exchanging, pausing and pulling chromosomes.

Authors:  Alex McDougall; David J Elliott; Neil Hunter
Journal:  EMBO Rep       Date:  2005-02       Impact factor: 8.807

Review 6.  Changing partners: moving from non-homologous to homologous centromere pairing in meiosis.

Authors:  Mara N Stewart; Dean S Dawson
Journal:  Trends Genet       Date:  2008-09-18       Impact factor: 11.639

7.  Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology?

Authors:  M V Zaragoza; E Millie; R W Redline; T J Hassold
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

Review 8.  New Solutions to Old Problems: Molecular Mechanisms of Meiotic Crossover Control.

Authors:  Gerald R Smith; Mridula Nambiar
Journal:  Trends Genet       Date:  2020-03-21       Impact factor: 11.639

9.  Pericentromere-Specific Cohesin Complex Prevents Meiotic Pericentric DNA Double-Strand Breaks and Lethal Crossovers.

Authors:  Mridula Nambiar; Gerald R Smith
Journal:  Mol Cell       Date:  2018-08-02       Impact factor: 17.970

Review 10.  Emerging roles for centromeres in meiosis I chromosome segregation.

Authors:  Gloria A Brar; Angelika Amon
Journal:  Nat Rev Genet       Date:  2008-12       Impact factor: 53.242

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.