Literature DB >> 2884869

Population genetics of coagulant factor IX: frequencies of two DNA polymorphisms in five ethnic groups.

D B Lubahn, S T Lord, J Bosco, J Kirshtein, O J Jeffries, N Parker, C Levtzow, L M Silverman, J B Graham.   

Abstract

Two frequently used restriction-enzyme polymorphisms (RFLPs) of coagulant F.IX, TaqI and XmnI, have been examined in five ethnic groups: white Americans, black Americans, East Indians, Chinese, and Malays. There is a distinct "cline" in the frequencies of both polymorphisms, from white Americans to Malays. The rarer type 2 alleles of both polymorphisms, in which middle recognition sites are present--and which in our sample reach their highest frequencies in white Americans--are marginally higher in four groups of Europeans previously reported by others. The frequencies of the rarer alleles are significantly higher in Europeans than in black Americans and East Indians, and these alleles are essentially absent in Chinese and Malays. The frequency of heterozygosity diminishes in the same order, being zero in Malays for both polymorphisms. The polymorphisms are in strong linkage disequilibrium, and in all groups the type 1 allele for TaqI is disproportionately accompanied by the type 1 allele for XmnI. The paucity of type 2 alleles and the low rate of heterozygosity in four non-European groups suggest that the polymorphisms will be of little diagnostic value south of Gibraltar and east of Suez. This prediction is confirmed by the observed haplotype frequencies in the black American and the Oriental groups.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2884869      PMCID: PMC1684156     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  20 in total

1.  Factor IXAlabama: a point mutation in a clotting protein results in hemophilia B.

Authors:  L M Davis; R A McGraw; J L Ware; H R Roberts; D W Stafford
Journal:  Blood       Date:  1987-01       Impact factor: 22.113

Review 2.  Caucasian genes in American Negroes.

Authors:  T E Reed
Journal:  Science       Date:  1969-08-22       Impact factor: 47.728

3.  Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).

Authors:  G Camerino; K H Grzeschik; M Jaye; H De La Salle; P Tolstoshev; J P Lecocq; R Heilig; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1984-01       Impact factor: 11.205

4.  Isolation of a human anti-haemophilic factor IX cDNA clone using a unique 52-base synthetic oligonucleotide probe deduced from the amino acid sequence of bovine factor IX.

Authors:  M Jaye; H de la Salle; F Schamber; A Balland; V Kohli; A Findeli; P Tolstoshev; J P Lecocq
Journal:  Nucleic Acids Res       Date:  1983-04-25       Impact factor: 16.971

5.  Isolation and characterization of a cDNA coding for human factor IX.

Authors:  K Kurachi; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  1982-11       Impact factor: 11.205

6.  Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene.

Authors:  L Grunebaum; J P Cazenave; G Camerino; C Kloepfer; J L Mandel; P Tolstoshev; M Jaye; H De la Salle; J P Lecocq
Journal:  J Clin Invest       Date:  1984-05       Impact factor: 14.808

7.  Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

Authors:  F Giannelli; D S Anson; K H Choo; D J Rees; P R Winship; N Ferrari; C R Rizza; G G Brownlee
Journal:  Lancet       Date:  1984-02-04       Impact factor: 79.321

8.  Molecular cloning of the gene for human anti-haemophilic factor IX.

Authors:  K H Choo; K G Gould; D J Rees; G G Brownlee
Journal:  Nature       Date:  1982-09-09       Impact factor: 49.962

9.  Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.

Authors:  G Camerino; M G Mattei; J F Mattei; M Jaye; J L Mandel
Journal:  Nature       Date:  1983 Dec 15-21       Impact factor: 49.962

10.  The gene structure of human anti-haemophilic factor IX.

Authors:  D S Anson; K H Choo; D J Rees; F Giannelli; K Gould; J A Huddleston; G G Brownlee
Journal:  EMBO J       Date:  1984-05       Impact factor: 11.598

View more
  7 in total

1.  Prenatal diagnosis of haemophilia B by the use of polymerase chain reaction and direct sequencing.

Authors:  M Ludwig; H H Brackmann; K Olek
Journal:  Klin Wochenschr       Date:  1991-03-18

2.  Functionally important regions of the factor IX gene have a low rate of polymorphism and a high rate of mutation in the dinucleotide CpG.

Authors:  D D Koeberl; C D Bottema; J M Buerstedde; S S Sommer
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

3.  The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians.

Authors:  C D Bottema; R P Ketterling; H S Yoon; S S Sommer
Journal:  Am J Hum Genet       Date:  1990-11       Impact factor: 11.025

4.  The varying frequencies of five DNA polymorphisms of X-linked coagulant factor IX in eight ethnic groups.

Authors:  J B Graham; G R Kunkel; N K Egilmez; A Wallmark; D M Fowlkes; S T Lord
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

5.  Segments containing alternating purine and pyrimidine dinucleotides: patterns of polymorphism in humans and prevalence throughout phylogeny.

Authors:  G Sarkar; C Paynton; S S Sommer
Journal:  Nucleic Acids Res       Date:  1991-02-11       Impact factor: 16.971

6.  Variations among Japanese of the factor IX gene (F9) detected by PCR-denaturing gradient gel electrophoresis.

Authors:  C Satoh; N Takahashi; J Asakawa; K Hiyama; M Kodaira
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

7.  The Malmö polymorphism of coagulation factor IX, an immunologic polymorphism due to dimorphism of residue 148 that is in linkage disequilibrium with two other F.IX polymorphisms.

Authors:  J B Graham; D B Lubahn; S T Lord; J Kirshtein; I M Nilsson; A Wallmark; R Ljung; L D Frazier; J L Ware; S W Lin
Journal:  Am J Hum Genet       Date:  1988-04       Impact factor: 11.025

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.