Literature DB >> 17033731

DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity.

Ching-Wan Lam1, Sui-Fan Tong2, Keong Wong3, Y F Luo3, Hoi-Yin Tang4, Shau-Yin Ha5, Michael Ho-Ming Chan2.   

Abstract

Malignant osteopetrosis, a severe disease causing early infantile death in humans, is caused by mutations in the TCIRG1, CLCN7, or OSTM1 genes. We have established the molecular basis of malignant osteopetrosis in a Chinese family by means of whole-genome scans based on high-density single-nucleotide polymorphism (SNP) microarrays. Because the parents were consanguineous, the disease-causing locus should be located in an autozygous chromosomal region. Mapping revealed that among the three possible causal loci, only the CLCN7 gene was located in an autozygous region. Mutational analysis of the CLCN7 gene showed that the proband was homozygous for a novel missense mutation, p.I261F. p.I261 is located in helix F of the chloride channel, near a critical site for gating of the channel. This mapping study prepares the ground for future mutation studies by decreasing the burden of completely sequencing all possible loci for this disease. This approach can be used to standardize molecular investigations of genetic diseases due to consanguinity to a whole-genome scan and subsequent sequencing of the mapped disease gene.

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Year:  2006        PMID: 17033731     DOI: 10.1007/s10038-006-0075-4

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  10 in total

1.  X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity.

Authors:  Raimund Dutzler; Ernest B Campbell; Martine Cadene; Brian T Chait; Roderick MacKinnon
Journal:  Nature       Date:  2002-01-17       Impact factor: 49.962

2.  Gating the selectivity filter in ClC chloride channels.

Authors:  Raimund Dutzler; Ernest B Campbell; Roderick MacKinnon
Journal:  Science       Date:  2003-03-20       Impact factor: 47.728

3.  Analysis of polymerase chain reaction products by denaturing high-performance liquid chromatography.

Authors:  Ching-Wan Lam
Journal:  Methods Mol Biol       Date:  2006

4.  Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.

Authors:  J B Fan; X Chen; M K Halushka; A Berno; X Huang; T Ryder; R J Lipshutz; D J Lockhart; A Chakravarti
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

5.  Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human.

Authors:  Nader Chalhoub; Nadia Benachenhou; Venkatesh Rajapurohitam; Monica Pata; Mathieu Ferron; Annalisa Frattini; Anna Villa; Jean Vacher
Journal:  Nat Med       Date:  2003-03-10       Impact factor: 53.440

6.  Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man.

Authors:  U Kornak; D Kasper; M R Bösl; E Kaiser; M Schweizer; A Schulz; W Friedrich; G Delling; T J Jentsch
Journal:  Cell       Date:  2001-01-26       Impact factor: 41.582

7.  DNA-based diagnosis of xeroderma pigmentosum group C by Whole-genome scan using single-nucleotide polymorphism microarray.

Authors:  Ching-Wan Lam; Kitty Kit-Ting Cheung; Nai-Ming Luk; Shirley Wen Chan; Kuen-Kong Lo; Sui-Fan Tong
Journal:  J Invest Dermatol       Date:  2005-01       Impact factor: 8.551

8.  Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Authors:  E Cleiren; O Bénichou; E Van Hul; J Gram; J Bollerslev; F R Singer; K Beaverson; A Aledo; M P Whyte; T Yoneyama; M C deVernejoul; W Van Hul
Journal:  Hum Mol Genet       Date:  2001-12-01       Impact factor: 6.150

9.  Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysis.

Authors:  H Shalev; A Mishori-Dery; J Kapelushnik; A Moser; V C Sheffield; A McClain; R Carmi
Journal:  Prenat Diagn       Date:  2001-03       Impact factor: 3.050

10.  Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis.

Authors:  A Frattini; P J Orchard; C Sobacchi; S Giliani; M Abinun; J P Mattsson; D J Keeling; A K Andersson; P Wallbrandt; L Zecca; L D Notarangelo; P Vezzoni; A Villa
Journal:  Nat Genet       Date:  2000-07       Impact factor: 38.330

  10 in total
  3 in total

1.  The virulence gene and clinical phenotypes of osteopetrosis in the Chinese population: six novel mutations of the CLCN7 gene in twelve osteopetrosis families.

Authors:  Chun Wang; Hao Zhang; Jin-Wei He; Jie-Mei Gu; Wei-Wei Hu; Yun-Qiu Hu; Miao Li; Yu-Juan Liu; Wen-Zhen Fu; Hua Yue; Yao-Hua Ke; Zhen-Lin Zhang
Journal:  J Bone Miner Metab       Date:  2011-09-28       Impact factor: 2.626

2.  A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis.

Authors:  Nesrin Besbas; Markus Draaken; Michael Ludwig; Ozgur Deren; Diclehan Orhan; Yelda Bilginer; Fatih Ozaltin
Journal:  Eur J Pediatr       Date:  2009-02-24       Impact factor: 3.183

Review 3.  The Role of the Lysosomal Cl-/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration.

Authors:  Giovanni Zifarelli
Journal:  Cells       Date:  2022-01-21       Impact factor: 6.600

  3 in total

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