Literature DB >> 7635485

Two novel missense mutations in the cystathionine beta-synthase gene in homocystinuric patients.

L A Kluijtmans1, H J Blom, G H Boers, B A van Oost, F J Trijbels, L P van den Heuvel.   

Abstract

Direct sequencing of the coding region of the cystathionine beta-synthase (CBS) gene in two homocystinuric patients revealed the presence of two novel missense mutations. The first mutation, a 1111G-->A transition, resulted in the substitution of the evolutionary conserved valine-371 by a methionine residue (V371M) and created a new NlaIII restriction site. The second mutation, a G-->A transition at base-pair 494, resulted in an amino acid change from cysteine to tyrosine (C165Y) and abolished a BsoFI restriction site. Both mutations were found in a compound heterozygous state with the previously described 833T-->C transition.

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Year:  1995        PMID: 7635485     DOI: 10.1007/bf00207394

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  6 in total

1.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.

Authors:  P Chomczynski; N Sacchi
Journal:  Anal Biochem       Date:  1987-04       Impact factor: 3.365

2.  Methionine metabolism in mammals. Distribution of homocysteine between competing pathways.

Authors:  J D Finkelstein; J J Martin
Journal:  J Biol Chem       Date:  1984-08-10       Impact factor: 5.157

Review 3.  Komrower Lecture. Molecular basis of phenotype expression in homocystinuria.

Authors:  J P Kraus
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

4.  Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria.

Authors:  F L Hu; Z Gu; V Kozich; J P Kraus; V Ramesh; V E Shih
Journal:  Hum Mol Genet       Date:  1993-11       Impact factor: 6.150

5.  The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

Authors:  M Münke; J P Kraus; T Ohura; U Francke
Journal:  Am J Hum Genet       Date:  1988-04       Impact factor: 11.025

6.  Human cystathionine beta-synthase cDNA: sequence, alternative splicing and expression in cultured cells.

Authors:  J P Kraus; K Le; M Swaroop; T Ohura; T Tahara; L E Rosenberg; M D Roper; V Kozich
Journal:  Hum Mol Genet       Date:  1993-10       Impact factor: 6.150

  6 in total
  7 in total

Review 1.  Hyperhomocysteinaemia and associated disease.

Authors:  R C Bakker; D P Brandjes
Journal:  Pharm World Sci       Date:  1997-06

2.  Four novel mutations at the cystathionine beta-synthase locus causing homocystinuria.

Authors:  M Coudé; J Aupetit; M T Zabot; P Kamoun; B Chadefaux-Vekemans
Journal:  J Inherit Metab Dis       Date:  1998-12       Impact factor: 4.982

3.  Surrogate genetics and metabolic profiling for characterization of human disease alleles.

Authors:  Jacob A Mayfield; Meara W Davies; Dago Dimster-Denk; Nick Pleskac; Sean McCarthy; Elizabeth A Boydston; Logan Fink; Xin Xin Lin; Ankur S Narain; Michael Meighan; Jasper Rine
Journal:  Genetics       Date:  2012-01-20       Impact factor: 4.562

Review 4.  Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.

Authors:  A G Motulsky
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

5.  Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.

Authors:  L A Kluijtmans; G H Boers; E M Stevens; W O Renier; J P Kraus; F J Trijbels; L P van den Heuvel; H J Blom
Journal:  J Clin Invest       Date:  1996-07-15       Impact factor: 14.808

6.  High prevalence of a mutation in the cystathionine beta-synthase gene.

Authors:  M Y Tsai; M Bignell; K Schwichtenberg; N Q Hanson
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

7.  Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Authors:  L A Kluijtmans; L P van den Heuvel; G H Boers; P Frosst; E M Stevens; B A van Oost; M den Heijer; F J Trijbels; R Rozen; H J Blom
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

  7 in total

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