Literature DB >> 8328460

Characterization of the patterns of polymorphism in a "cryptic repeat" reveals a novel type of hypervariable sequence.

D P Jacobson1, P Schmeling, S S Sommer.   

Abstract

Alternating purine and pyrimidine repeats (RY(i)) are an abundant source of polymorphism. The subset with long tandem repeats of GT or AC (GT(i)) have been studied extensively, but cryptic RY(i) (i.e., no single tandem repeat predominates) have received little attention. The factor IX gene has a polymorphic cryptic RY(i) of 142-216 bp. Previously, there were four known polymorphic alleles, of the form AB, A2B, A2B2, and A3B2, where A = (GT)(AC)3(AT)3(GT)(AT)4 and B = A with an additional 3' AT dinucleotide. To further characterize this locus, we examined more than 1,700 additional human chromosomes and determined the sequences of the homologous sites in orangutans and chimpanzees. The novel alleles found in humans expand the repertoire of A/B alleles to A0-4B1 and A1-3B2. The AnB2 series are abundant in Caucasians but are absent in blacks and Asians. Conversely, the A0B1 allele is common in blacks but is not found in more than 1,700 Caucasian chromosomes. The data are compatible with a model in which recombination is more frequent than polymerase slippage at this locus. In orangutans, the RY(i) is present, but the sequence is markedly different. An A/B-type of pattern was discerned in which B differs from A by an additional six (AT) dinucleotides at the 3' end. In chimpanzees, the size of the RY(i) locus was greatly expanded, and the sequence showed a novel pattern of hypervariability in which there are many tandem repeats of the form (GT)n(AC)o(AT)p(GT)q(AT)s, where n, o, p, q, and s are different integers. The sequences of the factor IX intron 1 cryptic RY(i) in three primates provide perspective on the range of possible patterns of polymorphism. Analysis of the patterns suggests how the RY(i) can be conserved during evolution, while the precise sequence varies.

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Year:  1993        PMID: 8328460      PMCID: PMC1682338     

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


  23 in total

1.  RNA bulges and the helical periodicity of double-stranded RNA.

Authors:  A Bhattacharyya; A I Murchie; D M Lilley
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2.  Recurrent nonsense mutations at arginine residues cause severe hemophilia B in unrelated hemophiliacs.

Authors:  D D Koeberl; C D Bottema; G Sarkar; R P Ketterling; S H Chen; S S Sommer
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3.  Five polymorphic microsatellite VNTRs on the human X chromosome.

Authors:  J A Luty; Z Guo; H F Willard; D H Ledbetter; S Ledbetter; M Litt
Journal:  Am J Hum Genet       Date:  1990-04       Impact factor: 11.025

Review 4.  Population-based distributions of haemostatic variables.

Authors:  T W Meade; W R North; R Chakrabarti; A P Haines; Y Stirling
Journal:  Br Med Bull       Date:  1977-09       Impact factor: 4.291

5.  Evaluation of APTT reagent sensitivity to factor IX and factor IX assay performance. Results from the College of American Pathologists Survey Program.

Authors:  J T Brandt; C F Arkin; E G Bovill; W A Rock; D A Triplett
Journal:  Arch Pathol Lab Med       Date:  1990-02       Impact factor: 5.534

6.  Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms.

Authors:  P R Winship; D S Anson; C R Rizza; G G Brownlee
Journal:  Nucleic Acids Res       Date:  1984-12-11       Impact factor: 16.971

Review 7.  The chemistry and biology of left-handed Z-DNA.

Authors:  A Rich; A Nordheim; A H Wang
Journal:  Annu Rev Biochem       Date:  1984       Impact factor: 23.643

8.  d(TG)n.d(CA)n sequences upstream of the rat prolactin gene form Z-DNA and inhibit gene transcription.

Authors:  L H Naylor; E M Clark
Journal:  Nucleic Acids Res       Date:  1990-03-25       Impact factor: 16.971

9.  Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms.

Authors:  J L Weber
Journal:  Genomics       Date:  1990-08       Impact factor: 5.736

10.  A past mutation at isoleucine 397 is now a common cause of moderate/mild haemophilia B.

Authors:  C D Bottema; D D Koeberl; R P Ketterling; E J Bowie; S A Taylor; D Lillicrap; A Shapiro; G Gilchrist; S S Sommer
Journal:  Br J Haematol       Date:  1990-06       Impact factor: 6.998

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  3 in total

1.  On the nomenclature and evolutionary persistence of dinucleotide repeats.

Authors:  F W Schwaiger; J T Epplen
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

2.  The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX gene.

Authors:  R P Ketterling; E Vielhaber; S S Sommer
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

3.  "Cryptic" dinucleotide polymorphism in the 3' region of the factor IX gene shows substantial variation among different populations.

Authors:  S S Sommer; V L Tillotson; E L Vielhaber; R P Ketterling; C M Dutton
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

  3 in total

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