Literature DB >> 15279804

The role of the DNA double-strand break response network in meiosis.

Christine Richardson1, Nobuo Horikoshi, Tej K Pandita.   

Abstract

Organisms with sexual reproduction have two homologous copies of each chromosome. Meiosis is characterized by two successive cell divisions that result in four haploid sperms or eggs, each carrying a single copy of homologous chromosome. This process requires a coordinated reorganization of chromatin and a complex network of meiotic-specific signaling cascades. At the beginning of meiosis, each chromosome must recognize its homolog, then the two become intimately aligned along their entire lengths which allows the exchange of DNA strands between homologous sequences to generate genetic diversity. DNA double-strand breaks (DSBs) initiate meiotic recombination in a variety of organisms. Numerous studies have identified both the genomic loci of the initiating DSBs and the proteins involved in their formation. This review will summarize the activation and signaling networks required for the DSB response in meiosis.

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Year:  2004        PMID: 15279804     DOI: 10.1016/j.dnarep.2004.05.007

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  30 in total

1.  The role of MOF in the ionizing radiation response is conserved in Drosophila melanogaster.

Authors:  Manika P Bhadra; Nobuo Horikoshi; Sreerangam N C V L Pushpavallipvalli; Arpita Sarkar; Indira Bag; Anita Krishnan; John C Lucchesi; Rakesh Kumar; Qin Yang; Raj K Pandita; Mayank Singh; Utpal Bhadra; Joel C Eissenberg; Tej K Pandita
Journal:  Chromosoma       Date:  2011-11-10       Impact factor: 4.316

Review 2.  Double-strand breaks and the concept of short- and long-term epigenetic memory.

Authors:  Christian Orlowski; Li-Jeen Mah; Raja S Vasireddy; Assam El-Osta; Tom C Karagiannis
Journal:  Chromosoma       Date:  2010-12-21       Impact factor: 4.316

Review 3.  The cellular control of DNA double-strand breaks.

Authors:  Shaun P Scott; Tej K Pandita
Journal:  J Cell Biochem       Date:  2006-12-15       Impact factor: 4.429

4.  Tetrahymena meiotic nuclear reorganization is induced by a checkpoint kinase-dependent response to DNA damage.

Authors:  Josef Loidl; Kazufumi Mochizuki
Journal:  Mol Biol Cell       Date:  2009-03-18       Impact factor: 4.138

5.  MOF and histone H4 acetylation at lysine 16 are critical for DNA damage response and double-strand break repair.

Authors:  Girdhar G Sharma; Sairei So; Arun Gupta; Rakesh Kumar; Christelle Cayrou; Nikita Avvakumov; Utpal Bhadra; Raj K Pandita; Matthew H Porteus; David J Chen; Jacques Cote; Tej K Pandita
Journal:  Mol Cell Biol       Date:  2010-05-17       Impact factor: 4.272

6.  Ahp2 (Hop2) function in Arabidopsis thaliana (Ler) is required for stabilization of close alignment and synaptonemal complex formation except for the two short arms that contain nucleolus organizer regions.

Authors:  P Stronghill; N Pathan; H Ha; E Supijono; C Hasenkampf
Journal:  Chromosoma       Date:  2010-04-01       Impact factor: 4.316

7.  The DNA damage response induces IFN.

Authors:  Sabrina Brzostek-Racine; Chris Gordon; Sarah Van Scoy; Nancy C Reich
Journal:  J Immunol       Date:  2011-10-17       Impact factor: 5.422

Review 8.  The DNA-damage response in human biology and disease.

Authors:  Stephen P Jackson; Jiri Bartek
Journal:  Nature       Date:  2009-10-22       Impact factor: 49.962

Review 9.  Chromatin remodeling finds its place in the DNA double-strand break response.

Authors:  Tej K Pandita; Christine Richardson
Journal:  Nucleic Acids Res       Date:  2009-01-12       Impact factor: 16.971

10.  BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice.

Authors:  Yulong Liang; Hong Gao; Shiaw-Yih Lin; Guang Peng; Xingxu Huang; Pumin Zhang; John A Goss; Francis C Brunicardi; Asha S Multani; Sandy Chang; Kaiyi Li
Journal:  PLoS Genet       Date:  2010-01-22       Impact factor: 5.917

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