Literature DB >> 25129257

A novel frameshift mutation in BLM gene associated with high sister chromatid exchanges (SCE) in heterozygous family members.

Ghada Ben Salah1, Ikhlas Hadj Salem, Abderrahmen Masmoudi, Fakhri Kallabi, Hamida Turki, Faiza Fakhfakh, Hamadi Ayadi, Hassen Kamoun.   

Abstract

The Bloom syndrome (BS) is an autosomic recessive disorder comprising a wide range of abnormalities, including stunted growth, immunodeficiency, sun sensitivity and increased frequency of various types of cancer. Bloom syndrome cells display a high level of genetic instability, including a 10-fold increase in the sister chromatid exchanges (SCE) level. Bloom syndrome arises through mutations in both alleles of the BLM gene, which was identified as a member of the RecQ helicase family. In this study, we screened a Tunisian family with three BS patients. Cytogenetic analysis showed several chromosomal aberrations, and an approximately 14-fold elevated SCE frequency in BS cells. A significant increase in SCE frequency was observed in some family members but not reaching the BS patients values, leading to suggest that this could be due to the heterozygous profile. Microsatellite genotyping using four fluorescent dye-labeled microsatellite markers revealed evidence of linkage to BLM locus and the healthy members, sharing higher SCE frequency, showed heterozygous haplotypes as expected. Additionally, the direct BLM gene sequencing identified a novel homozygous frameshift mutation c.3617-3619delAA (p.K1207fsX9) in BS patients and a heterozygous BLM mutation in the family members with higher SCE frequency. Our findings suggest that this latter mutation likely leads to a reduced BLM activity explaining the homologous recombination repair defect and, therefore, the increase in SCE. Based on the present data, the screening of this mutation could contribute to the rapid diagnosis of BS. The genetic confirmation of the mutation in BLM gene provides crucial information for genetic counseling and prenatal diagnosis.

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Year:  2014        PMID: 25129257     DOI: 10.1007/s11033-014-3624-5

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  37 in total

1.  Binding and melting of D-loops by the Bloom syndrome helicase.

Authors:  A J van Brabant; T Ye; M Sanz; J L German III; N A Ellis; W K Holloman
Journal:  Biochemistry       Date:  2000-11-28       Impact factor: 3.162

2.  A simple method for DNA extraction from leukocytes for use in PCR.

Authors:  H A Lewin; J A Stewart-Haynes
Journal:  Biotechniques       Date:  1992-10       Impact factor: 1.993

3.  Sister chromatid exchange (SCE) and high-frequency cells (HFC) in peripheral blood lymphocytes of healthy Tunisian smokers.

Authors:  Ghada Ben Salah; Hassen Kamoun; Ahmed Rebai; Achraf Ben Youssef; Hajer Ayadi; Neila Belghith-Mahfoudh; Amine Fourati; Hamadi Ayadi; Faiza Fakhfakh
Journal:  Mutat Res       Date:  2010-09-29       Impact factor: 2.433

Review 4.  RecQ helicases: guardian angels of the DNA replication fork.

Authors:  Csanád Z Bachrati; Ian D Hickson
Journal:  Chromosoma       Date:  2008-01-11       Impact factor: 4.316

5.  The Bloom's syndrome helicase unwinds G4 DNA.

Authors:  H Sun; J K Karow; I D Hickson; N Maizels
Journal:  J Biol Chem       Date:  1998-10-16       Impact factor: 5.157

Review 6.  A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases.

Authors:  V Morozov; A R Mushegian; E V Koonin; P Bork
Journal:  Trends Biochem Sci       Date:  1997-11       Impact factor: 13.807

7.  The Werner and Bloom syndrome proteins help resolve replication blockage by converting (regressed) holliday junctions to functional replication forks.

Authors:  Amrita Machwe; Rajashree Karale; Xioahua Xu; Yilun Liu; David K Orren
Journal:  Biochemistry       Date:  2011-07-21       Impact factor: 3.162

8.  A conditional mouse model for measuring the frequency of homologous recombination events in vivo in the absence of essential genes.

Authors:  Adam D Brown; Alison B Claybon; Alexander J R Bishop
Journal:  Mol Cell Biol       Date:  2011-06-27       Impact factor: 4.272

9.  BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal.

Authors:  H Kaneko; K O Orii; E Matsui; N Shimozawa; T Fukao; T Matsumoto; A Shimamoto; Y Furuichi; S Hayakawa; K Kasahara; N Kondo
Journal:  Biochem Biophys Res Commun       Date:  1997-11-17       Impact factor: 3.575

Review 10.  RecQ helicases: caretakers of the genome.

Authors:  Ian D Hickson
Journal:  Nat Rev Cancer       Date:  2003-03       Impact factor: 60.716

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  5 in total

1.  A helical bundle in the N-terminal domain of the BLM helicase mediates dimer and potentially hexamer formation.

Authors:  Jing Shi; Wei-Fei Chen; Bo Zhang; San-Hong Fan; Xia Ai; Na-Nv Liu; Stephane Rety; Xu-Guang Xi
Journal:  J Biol Chem       Date:  2017-02-22       Impact factor: 5.157

2.  Genetics and genomic medicine in Tunisia.

Authors:  Houda Elloumi-Zghal; Habiba Chaabouni Bouhamed
Journal:  Mol Genet Genomic Med       Date:  2018-03       Impact factor: 2.183

Review 3.  Bloom syndrome: research and data priorities for the development of precision medicine as identified by some affected families.

Authors:  Mary Beth Campbell; Wesley C Campbell; James Rogers; Natalie Rogers; Zachary Rogers; Anne Marie van den Hurk; Annie Webb; Talon Webb; Paul Zaslaw
Journal:  Cold Spring Harb Mol Case Stud       Date:  2018-04-02

Review 4.  Rare Genetic Diseases with Defects in DNA Repair: Opportunities and Challenges in Orphan Drug Development for Targeted Cancer Therapy.

Authors:  Sonali Bhattacharjee; Saikat Nandi
Journal:  Cancers (Basel)       Date:  2018-09-01       Impact factor: 6.639

5.  Mechanism of Bloom syndrome complex assembly required for double Holliday junction dissolution and genome stability.

Authors:  Charlotte Hodson; Jason K K Low; Sylvie van Twest; Samuel E Jones; Paolo Swuec; Vincent Murphy; Kaima Tsukada; Matthew Fawkes; Rohan Bythell-Douglas; Adelina Davies; Jessica K Holien; Julienne J O'Rourke; Benjamin L Parker; Astrid Glaser; Michael W Parker; Joel P Mackay; Andrew N Blackford; Alessandro Costa; Andrew J Deans
Journal:  Proc Natl Acad Sci U S A       Date:  2022-02-08       Impact factor: 12.779

  5 in total

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