Literature DB >> 2567277

The factor IX BamHI polymorphism: T-to-G transversion at the nucleotide sequence -561. The BamHI/MSPI haplotypes in blacks and Caucasians.

M Zhang1, S H Chen, C R Scott, A R Thompson.   

Abstract

The polymerase chain reaction (PCR) method was used to amplify a 356-bp DNA segment containing the suspected BamHI polymorphic site of the factor IX gene. Following the enzyme digestions and gel electrophoresis, polymorphic genotypes (-,+ and +/- types) were observed. The gene frequencies for the rare (+) allele are about 36% in blacks and 2% in Caucasians. The 356-bp DNA was further purified and sequenced. The sequencing gels revealed a single nucleotide substitution (T to G) at position -561 of the gene in blacks and Caucasians. The T-to-G transversion generated a new BamHI site (GGATCC,+type) from a nonenzymatic site, (TGATCC,-type).

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Year:  1989        PMID: 2567277     DOI: 10.1007/BF00291171

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


  6 in total

1.  MspI polymorphic site within the factor IX gene. Localization of the site and an improved method for detection.

Authors:  D L Freedenberg; S H Chen; K Kurachi; C R Scott
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

2.  Nucleotide sequence of the gene for human factor IX (antihemophilic factor B).

Authors:  S Yoshitake; B G Schach; D C Foster; E W Davie; K Kurachi
Journal:  Biochemistry       Date:  1985-07-02       Impact factor: 3.162

3.  Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier status.

Authors:  C W Hay; K A Robertson; S L Yong; A R Thompson; G H Growe; R T MacGillivray
Journal:  Blood       Date:  1986-05       Impact factor: 22.113

4.  An intragenic deletion of the factor IX gene in a family with hemophilia B.

Authors:  S H Chen; S Yoshitake; P F Chance; G L Bray; A R Thompson; C R Scott; K Kurachi
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

5.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

6.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

  6 in total
  12 in total

1.  Haemophilia B: database of point mutations and short additions and deletions.

Authors:  F Giannelli; P M Green; K A High; J N Lozier; D P Lillicrap; M Ludwig; K Olek; P H Reitsma; M Goossens; A Yoshioka
Journal:  Nucleic Acids Res       Date:  1990-07-25       Impact factor: 16.971

2.  An HhaI polymorphism is present in factor IX genes of Asian subjects.

Authors:  A P Reiner; A R Thompson
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

3.  A 50 bp polymorphic insertion in the factor IX gene is readily detected by amplification and is in equilibrium with other polymorphic sites.

Authors:  D P Bouvier; S H Chen; A R Thompson
Journal:  Nucleic Acids Res       Date:  1990-09-11       Impact factor: 16.971

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.  The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene.

Authors:  C D Bottema; R P Ketterling; E Vielhaber; H S Yoon; B Gostout; D P Jacobson; A Shapiro; S S Sommer
Journal:  Hum Genet       Date:  1993-06       Impact factor: 4.132

6.  CG dinucleotide transitions in the factor IX gene account for about half of the point mutations in hemophilia B patients: a Seattle series.

Authors:  S H Chen; M Zhang; E W Lovrien; C R Scott; A R Thompson
Journal:  Hum Genet       Date:  1991-06       Impact factor: 4.132

7.  The rates and patterns of deletions in the human factor IX gene.

Authors:  R P Ketterling; E L Vielhaber; T J Lind; E C Thorland; S S Sommer
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

Review 8.  Haemophilia: strategies for carrier detection and prenatal diagnosis.

Authors:  I R Peake; D P Lillicrap; V Boulyjenkov; E Briet; V Chan; E K Ginter; E M Kraus; R Ljung; P M Mannucci; K Nicolaides
Journal:  Bull World Health Organ       Date:  1993       Impact factor: 9.408

9.  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

10.  T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection.

Authors:  R P Ketterling; C D Bottema; D D Koeberl; S Ii; S S Sommer
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

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