Literature DB >> 1765385

Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatch.

I Dianzani1, C Camaschella, G Saglio, S M Forrest, S Ramus, R G Cotton.   

Abstract

We used the chemical cleavage of mismatch (CCM) method to screen the beta-globin gene simultaneously for Mediterranean beta-thalassemia mutations. The beta-globin gene was amplified in two segments encompassing the whole gene and hybridized to a corresponding labeled PCR product from a normal subject. All the known mutations tested were identified and discriminated. Three beta-thalassemic subjects with previously undiagnosed mutations were identified as carriers of two rare DNA changes. The inheritance of the mutations could be traced in family studies, showing the reliability of the method even for prenatal diagnosis. The beta-globin gene polymorphisms were also detected and the framework was determined for most alleles. Our results suggest further applicability of the CCM method as a means to screen a gene simultaneously for multiple mutations.

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Year:  1991        PMID: 1765385     DOI: 10.1016/0888-7543(91)90100-s

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

Authors:  R Youil; B W Kemper; R G Cotton
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-03       Impact factor: 11.205

2.  Rapid detection of hemoglobin variants by mutagenically separated polymerase chain reaction (MS-PCR).

Authors:  J G Chang; C P Chang; C M Lu; J M Huang; J T Chen; H J Liu
Journal:  Ann Hematol       Date:  1995-08       Impact factor: 3.673

3.  Two new mutations in the dihydropteridine reductase gene in patients with tetrahydrobiopterin deficiency.

Authors:  I Dianzani; D W Howells; A Ponzone; J A Saleeba; P M Smooker; R G Cotton
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

4.  Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutation.

Authors:  I Dianzani; C Camaschella; G Saglio; G B Ferrero; S Ramus; A Ponzone; R G Cotton
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

5.  Efficient detection of Mediterranean β-thalassemia mutations by multiplex single-nucleotide primer extension.

Authors:  Biljana Atanasovska; Georgi Bozhinovski; Dijana Plaseska-Karanfilska; Lyubomira Chakalova
Journal:  PLoS One       Date:  2012-10-26       Impact factor: 3.240

6.  Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations.

Authors:  Chia-Cheng Hung; Yi-Ning Su; Chia-Yun Lin; Yin-Fei Chang; Chien-Hui Chang; Wen-Fang Cheng; Chi-An Chen; Chien-Nan Lee; Win-Li Lin
Journal:  BMC Biotechnol       Date:  2008-08-12       Impact factor: 2.563

  6 in total

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