Literature DB >> 8528212

Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions.

J A Naylor1, D Buck, P Green, H Williamson, D Bentley, F Giannelli.   

Abstract

A region of intron 22 of the factor VIII gene, which contains factor VIII-associated gene A (F8A), is repeated twice more nearer the Xq telomere. It has been proposed that intrachromosomal homologous recombination occurs between the intron 22 repeat and either of the two extragenic copies, resulting in the recurrent inversions that cause almost half of all cases of severe haemophilia A. We have precisely defined the repeated region as 9.5 kb of DNA which we have termed int22h (intron 22 homologous region). The junctions of the inversions examined were shown to represent precise exchanges between the int22h repeats, thus providing conclusive evidence for homologous recombination. The three copies of int22h were compared along 8 kb of their length, using chemical mismatch analysis, and found to be 99.9% similar. The presence of such long, almost identical inverted repeats near the Xq telomere could account for the high frequency at which the inversions occur.

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Year:  1995        PMID: 8528212     DOI: 10.1093/hmg/4.7.1217

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  24 in total

1.  Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers.

Authors:  Irena Hudecova; Peiyong Jiang; Joanna Davies; Y M Dennis Lo; Rezan A Kadir; Rossa W K Chiu
Journal:  Blood       Date:  2017-05-10       Impact factor: 22.113

2.  The Bleeding Assessment Tool and laboratory data in the characterisation of a female with inherited haemophilia A.

Authors:  Viviana Daidone; Eva Galletta; Antonella Bertomoro; Alessandra Casonato
Journal:  Blood Transfus       Date:  2016-11-15       Impact factor: 3.443

3.  Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardation.

Authors:  J J Cox; S T Holden; S Dee; J I Burbridge; F L Raymond
Journal:  J Med Genet       Date:  2003-03       Impact factor: 6.318

4.  Mutation rates in humans. II. Sporadic mutation-specific rates and rate of detrimental human mutations inferred from hemophilia B.

Authors:  F Giannelli; T Anagnostopoulos; P M Green
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

5.  Accurate, simple, and inexpensive assays to diagnose F8 gene inversion mutations in hemophilia A patients and carriers.

Authors:  Debargh Dutta; Devi Gunasekera; Margaret V Ragni; Kathleen P Pratt
Journal:  Blood Adv       Date:  2016-12-14

6.  Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A.

Authors:  Richard D Bagnall; Karen L Ayres; Peter M Green; Francesco Giannelli
Journal:  Genome Res       Date:  2005-02       Impact factor: 9.043

7.  The Chapel Hill hemophilia A dog colony exhibits a factor VIII gene inversion.

Authors:  Jay N Lozier; Amalia Dutra; Evgenia Pak; Nan Zhou; Zhili Zheng; Timothy C Nichols; Dwight A Bellinger; Marjorie Read; Richard A Morgan
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-19       Impact factor: 11.205

8.  Inverted low-copy repeats and genome instability--a genome-wide analysis.

Authors:  Piotr Dittwald; Tomasz Gambin; Claudia Gonzaga-Jauregui; Claudia M B Carvalho; James R Lupski; Paweł Stankiewicz; Anna Gambin
Journal:  Hum Mutat       Date:  2012-10-11       Impact factor: 4.878

9.  Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

Authors:  Ravikanth Metlapally; Michel Michaelides; Anuradha Bulusu; Yi-Ju Li; Marianne Schwartz; Thomas Rosenberg; David M Hunt; Anthony T Moore; Stephan Züchner; Catherine Bowes Rickman; Terri L Young
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-12-20       Impact factor: 4.799

Review 10.  New insight into the molecular basis of hemophilia A.

Authors:  Johannes Oldenburg; Osman El-Maarri
Journal:  Int J Hematol       Date:  2006-02       Impact factor: 2.490

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