Literature DB >> 20456353

Purification of FANCD2 sub-complexes.

Gang Zhi1, Xiaoyong Chen, William Newcomb, Jay Brown, Oliver J Semmes, Gary M Kupfer.   

Abstract

Fanconi anaemia (FA) is a recessive genetic disorder characterized by bone marrow failure, birth defects and cancer. Cells from FA patients are particularly defective in removing DNA interstrand crosslinks. We have developed a working chromatography purification scheme for FANCD2, a pivotal player in the FA DNA repair pathway, to facilitate identification of FANCD2 interacting partners. In doing so, at least three distinct FANCD2 subcomplexes were found to be present, designated as large, middle, and small complexes. The small complex is composed of tetramer of FANCD2 polypeptides, which may be the building block for other FANCD2 subcomplexes.

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Year:  2010        PMID: 20456353      PMCID: PMC5912677          DOI: 10.1111/j.1365-2141.2010.08217.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  16 in total

1.  The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway.

Authors:  Sebastian M B Nijman; Tony T Huang; Annette M G Dirac; Thijn R Brummelkamp; Ron M Kerkhoven; Alan D D'Andrea; René Bernards
Journal:  Mol Cell       Date:  2005-02-04       Impact factor: 17.970

Review 2.  Homologous recombination in DNA repair and DNA damage tolerance.

Authors:  Xuan Li; Wolf-Dietrich Heyer
Journal:  Cell Res       Date:  2008-01       Impact factor: 25.617

3.  Genetic subtyping of Fanconi anemia by comprehensive mutation screening.

Authors:  Najim Ameziane; Abdellatif Errami; France Léveillé; Chantal Fontaine; Yne de Vries; Rosalina M L van Spaendonk; Johan P de Winter; Gerard Pals; Hans Joenje
Journal:  Hum Mutat       Date:  2008-01       Impact factor: 4.878

4.  A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network.

Authors:  José Antonio Casado; Elsa Callén; Ariana Jacome; Paula Río; Maria Castella; Stephan Lobitz; Teresa Ferro; Arturo Muñoz; Julián Sevilla; Angeles Cantalejo; Elena Cela; José Cervera; Jesús Sánchez-Calero; Isabel Badell; Jesús Estella; Angeles Dasí; Teresa Olivé; Juan José Ortega; Antonia Rodriguez-Villa; María Tapia; Antonio Molinés; Luis Madero; José C Segovia; Kornelia Neveling; Reinhard Kalb; Detlev Schindler; Helmut Hanenberg; Jordi Surrallés; Juan A Bueren
Journal:  J Med Genet       Date:  2006-11-14       Impact factor: 6.318

5.  Fanconi anemia proteins stabilize replication forks.

Authors:  Lily Chien Wang; Stacie Stone; Maureen Elizabeth Hoatlin; Jean Gautier
Journal:  DNA Repair (Amst)       Date:  2008-09-25

Review 6.  Fanconi anemia: causes and consequences of genetic instability.

Authors:  R Kalb; K Neveling; I Nanda; D Schindler; H Hoehn
Journal:  Genome Dyn       Date:  2006

7.  Measurement of globular protein molecules by electron microscopy.

Authors:  C E HALL
Journal:  J Biophys Biochem Cytol       Date:  1960-07

8.  Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.

Authors:  Agata Smogorzewska; Shuhei Matsuoka; Patrizia Vinciguerra; E Robert McDonald; Kristen E Hurov; Ji Luo; Bryan A Ballif; Steven P Gygi; Kay Hofmann; Alan D D'Andrea; Stephen J Elledge
Journal:  Cell       Date:  2007-04-05       Impact factor: 41.582

9.  HTLV-1 Tax oncoprotein subverts the cellular DNA damage response via binding to DNA-dependent protein kinase.

Authors:  Sarah S Durkin; Xin Guo; Kimberly A Fryrear; Valia T Mihaylova; Saurabh K Gupta; S Mehdi Belgnaoui; Abdelali Haoudi; Gary M Kupfer; O John Semmes
Journal:  J Biol Chem       Date:  2008-10-27       Impact factor: 5.157

Review 10.  The Fanconi anemia pathway and ubiquitin.

Authors:  Céline Jacquemont; Toshiyasu Taniguchi
Journal:  BMC Biochem       Date:  2007-11-22       Impact factor: 4.059

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  5 in total

1.  Ubiquitin-like protein UBL5 promotes the functional integrity of the Fanconi anemia pathway.

Authors:  Yasuyoshi Oka; Simon Bekker-Jensen; Niels Mailand
Journal:  EMBO J       Date:  2015-04-09       Impact factor: 11.598

2.  Functional and physical interaction between the mismatch repair and FA-BRCA pathways.

Authors:  Stacy A Williams; James B Wilson; Allison P Clark; Alyssa Mitson-Salazar; Andrei Tomashevski; Sahana Ananth; Peter M Glazer; O John Semmes; Allen E Bale; Nigel J Jones; Gary M Kupfer
Journal:  Hum Mol Genet       Date:  2011-08-24       Impact factor: 6.150

3.  Functional cross talk between the Fanconi anemia and ATRX/DAXX histone chaperone pathways promotes replication fork recovery.

Authors:  Maya Raghunandan; Jung Eun Yeo; Ryan Walter; Kai Saito; Adam J Harvey; Stacie Ittershagen; Eun-A Lee; Jihyeon Yang; Maureen E Hoatlin; Anja K Bielinsky; Eric A Hendrickson; Orlando Schärer; Alexandra Sobeck
Journal:  Hum Mol Genet       Date:  2020-05-08       Impact factor: 6.150

4.  Coordinate nuclear targeting of the FANCD2 and FANCI proteins via a FANCD2 nuclear localization signal.

Authors:  Rebecca A Boisvert; Meghan A Rego; Paul A Azzinaro; Maurizio Mauro; Niall G Howlett
Journal:  PLoS One       Date:  2013-11-21       Impact factor: 3.240

5.  FANCD2-FANCI is a clamp stabilized on DNA by monoubiquitination of FANCD2 during DNA repair.

Authors:  Pablo Alcón; Shabih Shakeel; Zhuo A Chen; Juri Rappsilber; Ketan J Patel; Lori A Passmore
Journal:  Nat Struct Mol Biol       Date:  2020-02-17       Impact factor: 15.369

  5 in total

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