RSS-Feed abonnieren
DOI: 10.1055/s-0038-1650589
Two New Frequent Dimorphisms in the Protein S (PROS1) Gene*
Publikationsverlauf
Received 28. Februar 1996
Accepted after resubmission 14. Mai 1996
Publikationsdatum:
10. Juli 2018 (online)
Summary
Two new polymorphisms were identified in the proteinS gene (PR0S1): an intronic T/A-dimorphism (PIPS1) in intron K, and an exonic C/A-dimorphism (PEPS2), located in the 3'untranslated trailer of exon 15. Allelic frequencies of 24% (PIPS 1-A) and 17% (PEPS2-A) respectively, were determined in the normal population. The identification of an intronic and an exonic PR0S1 dimorphism, in addition to the known BstXI dimorphism, enlarges the molecular tool box for gene analysis and transcript quantification in hereditary protein S deficiency. Haplotype analysis showed that variability of both new polymorphisms occurred almost exclusively in the A-allele of the known intragenic BstXI dimorphism. Therefore, PEPS2 and PIPS1 are especially valuable in individuals homozygous for the BstXI A-variant.
-
References
- 1 Pabinger I, Brücker S, Kyrle PA, Schneider B, Kominger HC, Niessner H, Lechner K. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening. Blood Coagul Fibrinol 1992; 3: 547-553
- 2 Ploos van Amstel JK, van der Zanden AL, Bakker E, Reitsma PH, Bertina RM. Two genes homologous with human protein S cDNA are located on chromosome 3. Thromb Haemost 1987; 58: 982-987
- 3 Ploos van Amstel HK, Reitsma PH, Bertina RM. The human protein S locus: Identification of the PS alpha gene as a site of liver protein S messenger RNA synthesis. Biochem Biophys Res Commun 1988; 157: 1033-1038
- 4 Schmidel DK, Tatro AV, Phelps LG, Tomczak JA, Long GL. Organization of the human protein S genes. Biochemistry 1990; 29: 7845-7852
- 5 Ploos van Amstel HK, Reitsma PH, van der Logt CP, Bertina RM. Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolution. Biochemistry 1990; 29: 7853-7861
- 6 Edenbrandt CM, Lundwall A, Wydro R, Stenflo J. Molecular analysis of the gene for vitamin K dependent protein S and its pseudogene. Cloning and partial gene organization. Biochemistry 1990; 29: 7861-7868
- 7 Hayashi T, Nishioka J, Shigekiyo T, Saito S, Suzuki K. ProteinS Tokushima: Abnormal molecule with substitution of glu for lys-155 in the second epidermal growth factor-like domain of protein S. Blood 1994; 83: 683-690
- 8 Reitsma PH, Ploos van Amstel HK, Bertina RM. Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I. J Clin Invest 1994; 93: 486-492
- 9 Gomez E, Ledford MR, Pegelow CH, Reitsma PH, Bertina RM. Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene. Thromb Haemost 1994; 71: 723-726
- 10 Gomez E, Poort SR, Bertina RM, Reitsma PH. Identification of eight point mutations in protein S deficiency type I- analysis of 15 pedigrees. Thromb Haemost 1995; 73: 750-755
- 11 Yamazaki T, Hamaguchi M, Katsumi A, Kagami K, Kojima T, Takamatsu J, Saito H. A quantitative protein S deficiency associated with a novel nonsense mutation and markedly reduced levels of RNA. Thromb Haemost 1995; 74: 590-595
- 12 Mustafa S, Pabinger I, Mannhalter C. Protein S deficiency type I: identification of point mutations in 9 of 10 families. Blood 1995; 86: 3444-3451
- 13 Borgel D, Gandrille S, Gouault-Heilmann M, Aiach M. First frame shift mutation in the active protein S gene associated with a quantitative hereditary deficiency. Blood Coagul Fibrinol 1994; 5: 593-600
- 14 Gandrille S, Borgel D, Eschwege-Gufflet V, Aillaud MF, Dreyfus M, Matheron C, Gaussem P, Abgrall JF, Jude B, Sié P, Toulon P, Aiach M. Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene. Blood 1995; 85: 130-138
- 15 Aiach M, Gandrille S, Emmerich J. A review of mutations causing deficiencies of antithrombin, protein C and protein S. Thromb Haemost 1995; 74: 81-89
- 16 Formstone CJ, Wacay AI, Berg L-P, Rahman S, Bevan D, Rowley M, Voke J, Bemardi F, Legnani C, Simioni P, Girolami A, Tuddenham EGD, Kakkar VV, Cooper DN. Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-poly-merase chain reaction as a mutation screening strategy. Blood 1995; 86: 2632-2641
- 17 Ploos van Amstel HK, Diepstraten CM, Reitsma PH, Bertina RM. Analysis of platelet protein S mRNA suggests silent alleles as frequent cause of hereditary protein S deficiency type I. Abstract in Thromb Haemost 1991; 65: 808
- 18 Sacchi E, Pinotti M, Marchetti G, Merati G, Tagliabue L, Mannucci PM, Bemardi F. Protein S mRNA in patients with protein S deficiency. Thromb Haemost 1995; 73: 746-749
- 19 Diepstraten CM, Ploos van Amstel HK, Reitsma PH, Bertina RM. A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PS-alpha (PROS 1). Nucleic Acids Res 1991; 19: 5091
- 20 Marchetti G, Legnani C, Patracchini P, Gemmati D, Ferrati M, Palareti G, Coccheri S, Bemardi F. Study of a protein S polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency. Brit J Haematol 1993; 85: 173-175
- 21 Svensson PJ, Dahlbäck B. Resistance to activated protein C is a basis for venous thrombosis. N Engl J Med 1994; 330: 517-521
- 22 Kunkel LM, Smith KD, Boyer SH, Borgaonkar DS, Wachtel SS, Miller OJ, Breg WR, Jones Jr HW, Rary JM. Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA 1977; 74: 1245-1249