Literature DB >> 21645633

Chromosomal instability at the 7q11.23 region impacts on DNA-damage response in lymphocytes from Williams-Beuren syndrome patients.

Natalya V Savina1, Marharyta P Smal, Tatyana D Kuzhir, Tatyana M Egorova, Olga M Khurs, Anna D Polityko, Roza I Goncharova.   

Abstract

Williams-Beuren syndrome (WBS) is the chromosomal disorder arising from a hemizygous microdeletion at 7q11.23. The present study was focused on a comparative investigation of genomic integrity in WBS patients by use of cytogenetic methods and the alkaline comet assay. Lymphocytes of whole peripheral blood were cultured and metaphases were examined for frequency and spectrum of chromosome aberrations. A WBS-related microdeletion was detected by means of the FISH (fluorescence in situ hybridization) technique. The blood samples from patients who were carriers of this microdeletion, were tested in the comet assay. For this purpose, freshly collected lymphocytes were exposed to hydrogen peroxide (100μM, 1min, 4°C). The frequencies of endogenous and exogenous DNA damage, and the kinetics and efficiency of DNA repair were measured during three subsequent hours of incubation. Comparison of the two data sets in this group of patients demonstrated a slightly elevated average frequency of chromosome aberrations, significantly increased levels of endogenous and H(2)O(2)-induced DNA damage, and somewhat impaired DNA repair. The relationship between an abnormal DNA-damage response and the 7q11.23 hemizygous microdeletion was confirmed experimentally when comparing the comet assay data in FISH-positive and FISH-negative lymphocytes from WBS-suspected patients. Briefly, our results indicate the impact of chromosomal instability within this region on susceptibility towards DNA damage, which may contribute to pathogenesis of this disease. It was shown also that the comet assay, as well as an experimental design proposed here, seem to be useful tools for estimating genome integrity in WBS patients.
Copyright © 2011 Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Year:  2011        PMID: 21645633     DOI: 10.1016/j.mrgentox.2011.05.009

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  5 in total

1.  Evolution of the Cdk-activator Speedy/RINGO in vertebrates.

Authors:  Sangeeta Chauhan; Xinde Zheng; Yue Ying Tan; Boon-Hui Tay; Shuhui Lim; Byrappa Venkatesh; Philipp Kaldis
Journal:  Cell Mol Life Sci       Date:  2012-07-05       Impact factor: 9.261

2.  Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in non-Hodgkin lymphoma.

Authors:  David Guenat; Samuel Quentin; Carmelo Rizzari; Catarina Lundin; Tiziana Coliva; Patrick Edery; Helen Fryssira; Laurent Bermont; Christophe Ferrand; Jean Soulier; Christophe Borg; Pierre-Simon Rohrlich
Journal:  J Hematol Oncol       Date:  2014-11-07       Impact factor: 17.388

3.  DNA damage response defect in Williams-Beuren syndrome.

Authors:  David Guenat; Giuseppe Merla; Eric Deconinck; Christophe Borg; Pierre-Simon Rohrlich
Journal:  Int J Mol Med       Date:  2017-01-17       Impact factor: 4.101

4.  Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.

Authors:  Yu Xia; Shufang Huang; Yueheng Wu; Yongchao Yang; Shaoxian Chen; Ping Li; Jian Zhuang
Journal:  Mol Genet Genomic Med       Date:  2018-12-18       Impact factor: 2.183

5.  The Cellular Response to Oxidatively Induced DNA Damage and Polymorphism of Some DNA Repair Genes Associated with Clinicopathological Features of Bladder Cancer.

Authors:  Nataliya V Savina; Nataliya V Nikitchenko; Tatyana D Kuzhir; Alexander I Rolevich; Sergei A Krasny; Roza I Goncharova
Journal:  Oxid Med Cell Longev       Date:  2015-11-16       Impact factor: 6.543

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.