Literature DB >> 17706468

ATM, the Mre11/Rad50/Nbs1 complex, and topoisomerase I are concentrated in the nucleus of Purkinje neurons in the juvenile human brain.

Elena Gorodetsky1, Sarah Calkins, Julia Ahn, P J Brooks.   

Abstract

The genetic disease ataxia telangiectasia (AT) results from mutations in the ataxia telangiectasia mutated (ATM) gene. AT patients develop a progressive degeneration of cerebellar Purkinje neurons. Surprisingly, while ATM plays a criticial role in the cellular reponse to DNA damage, previous studies have localized ATM to the cytoplasm of rodent and human Purkinje neurons. Here we show that ATM is primarily localized to the nucleus in cerebellar Purkinje neurons in postmortem human brain tissue samples, although some light cytoplasmic ATM staining was also observed. No ATM staining was observed in brain tissue samples from AT patients, verifying the specificity of the antibody. We also found that antibodies against components of the Mre11/Rad50/Nbs1 (MRN) complex showed strong staining in Purkinje cell nuclei. However, while ATM is present in both the nucleoplasm and nucleolus, MRN proteins are excluded from the nucleolus. We also observed very high levels of topoisomerase 1 (TOP1) in the nucleus, and specifically the nucleolus, of human Purkinje neurons. Our results have direct implications for understanding the mechanisms of neurodegeneration in AT and AT-like disorder.

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Year:  2007        PMID: 17706468      PMCID: PMC2797317          DOI: 10.1016/j.dnarep.2007.06.011

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


  38 in total

1.  Changes in mobility account for camptothecin-induced subnuclear relocation of topoisomerase I.

Authors:  Morten O Christensen; Hans U Barthelmes; Silke Feineis; Birgitta R Knudsen; Anni H Andersen; Fritz Boege; Christian Mielke
Journal:  J Biol Chem       Date:  2002-03-20       Impact factor: 5.157

Review 2.  Cellular roles of DNA topoisomerases: a molecular perspective.

Authors:  James C Wang
Journal:  Nat Rev Mol Cell Biol       Date:  2002-06       Impact factor: 94.444

Review 3.  The DNA double-strand break response in the nervous system.

Authors:  Clint W Abner; Peter J McKinnon
Journal:  DNA Repair (Amst)       Date:  2004 Aug-Sep

4.  Deficiency of the Mre11 DNA repair complex in Alzheimer's disease brains.

Authors:  Elizabeth Jacobsen; Thomas Beach; Yong Shen; Rena Li; Yung Chang
Journal:  Brain Res Mol Brain Res       Date:  2004-09-10

Review 5.  The Mre11 complex and ATM: a two-way functional interaction in recognising and signaling DNA double strand breaks.

Authors:  Martin F Lavin
Journal:  DNA Repair (Amst)       Date:  2004-11-02

6.  Differentiation of Purkinje cells and their relationship to other components of developing cerebellar cortex in man.

Authors:  N Zecevic; P Rakic
Journal:  J Comp Neurol       Date:  1976-05-01       Impact factor: 3.215

Review 7.  Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.

Authors:  A M R Taylor; A Groom; P J Byrd
Journal:  DNA Repair (Amst)       Date:  2004 Aug-Sep

8.  Distinct effects of topoisomerase I and RNA polymerase I inhibitors suggest a dual mechanism of nucleolar/nucleoplasmic partitioning of topoisomerase I.

Authors:  Morten O Christensen; René M Krokowski; Hans U Barthelmes; Robert Hock; Fritz Boege; Christian Mielke
Journal:  J Biol Chem       Date:  2004-03-09       Impact factor: 5.157

9.  Requirement of the MRN complex for ATM activation by DNA damage.

Authors:  Tamar Uziel; Yaniv Lerenthal; Lilach Moyal; Yair Andegeko; Leonid Mittelman; Yosef Shiloh
Journal:  EMBO J       Date:  2003-10-15       Impact factor: 11.598

10.  Eukaryotic type I topoisomerase is enriched in the nucleolus and catalytically active on ribosomal DNA.

Authors:  M T Muller; W P Pfund; V B Mehta; D K Trask
Journal:  EMBO J       Date:  1985-05       Impact factor: 11.598

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  15 in total

1.  Terminally differentiated astrocytes lack DNA damage response signaling and are radioresistant but retain DNA repair proficiency.

Authors:  L Schneider; M Fumagalli; F d'Adda di Fagagna
Journal:  Cell Death Differ       Date:  2011-10-07       Impact factor: 15.828

Review 2.  Radiological imaging in ataxia telangiectasia: a review.

Authors:  Ishani Sahama; Kate Sinclair; Kerstin Pannek; Martin Lavin; Stephen Rose
Journal:  Cerebellum       Date:  2014-08       Impact factor: 3.847

3.  In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.

Authors:  Amy J Hawkins; Mark A Subler; Konstantin Akopiants; Jenny L Wiley; Shirley M Taylor; Ann C Rice; Jolene J Windle; Kristoffer Valerie; Lawrence F Povirk
Journal:  DNA Repair (Amst)       Date:  2009-02-10

Review 4.  Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity.

Authors:  James E Cleaver; Ernest T Lam; Ingrid Revet
Journal:  Nat Rev Genet       Date:  2009-10-07       Impact factor: 53.242

Review 5.  ATM-dependent pathways of chromatin remodelling and oxidative DNA damage responses.

Authors:  N Daniel Berger; Fintan K T Stanley; Shaun Moore; Aaron A Goodarzi
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2017-10-05       Impact factor: 6.237

6.  Dysmyelination not demyelination causes neurological symptoms in preweaned mice in a murine model of Cockayne syndrome.

Authors:  Ingrid Revet; Luzviminda Feeney; Amy A Tang; Eric J Huang; James E Cleaver
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-05       Impact factor: 11.205

Review 7.  DNA repair deficiency in neurodegeneration.

Authors:  Dennis Kjølhede Jeppesen; Vilhelm A Bohr; Tinna Stevnsner
Journal:  Prog Neurobiol       Date:  2011-04-30       Impact factor: 11.685

8.  Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease.

Authors:  P J Brooks
Journal:  DNA Repair (Amst)       Date:  2013-05-16

Review 9.  Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?

Authors:  P J Brooks; Tsu-Fan Cheng; Lori Cooper
Journal:  DNA Repair (Amst)       Date:  2008-03-12

10.  Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks.

Authors:  Claudia Kerzendorfer; Annabel Whibley; Gillian Carpenter; Emily Outwin; Shih-Chieh Chiang; Gillian Turner; Charles Schwartz; Sherif El-Khamisy; F Lucy Raymond; Mark O'Driscoll
Journal:  Hum Mol Genet       Date:  2010-01-11       Impact factor: 6.150

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