Literature DB >> 7943010

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

N Zhong1, X Liu, S Gou, G E Houck, S Li, C Dobkin, W T Brown.   

Abstract

The CGG repeat size distribution of the fragile X mental retardation gene (FMR-1) was studied in a population of normal Chinese X chromosomes along with that of two proximal microsatellite polymorphic markers: FRAXAC1 and DXS548. The most common CGG repeat allele was 29 (47.2%) with 30 being second most common (26%). This distribution was different from that seen in Caucasian controls, where the most common allele was 30 repeats. Other differences with Caucasian controls included a secondary modal peak at 36 repeats and the absence of peaks at 20 or 23 repeats. There were only two FRAXAC1 and five DXS548 alleles found in the Chinese sample. A striking linkage disequilibrium of FMR-1 alleles with FRAXAC1 alleles was observed, in that 90% of the 29 CGG repeat alleles but only 41% of the 30 CGG repeat alleles had the FRAXAC1 152 bp allele (18 AC repeats). This disequilibrium suggests that slippage between the closely spaced normal CGG repeat alleles, 29 and 30, and between 152 and 154 FRAXAC1 alleles is very rare. This study lays the groundwork for an understanding of founder chromosome effects in comparing Asian and Caucasian populations.

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Year:  1994        PMID: 7943010     DOI: 10.1002/ajmg.1320510423

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  10 in total

1.  Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Authors:  D C Crawford; C E Schwartz; K L Meadows; J L Newman; L F Taft; C Gunter; W T Brown; N J Carpenter; P N Howard-Peebles; K G Monaghan; S L Nolin; A L Reiss; G L Feldman; E M Rohlfs; S T Warren; S L Sherman
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

2.  Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening.

Authors:  Tri Indah Winarni; Agustini Utari; Farmaditya E P Mundhofir; Tzuhan Tong; Blythe Durbin-Johnson; Sultana M H Faradz; Flora Tassone
Journal:  Genet Test Mol Biomarkers       Date:  2011-10-11

3.  Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution.

Authors:  W T Brown; N Zhong; C Dobkin
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

Review 4.  Fragile X syndrome: the FMR1 CGG repeat distribution among world populations.

Authors:  Emmanuel Peprah
Journal:  Ann Hum Genet       Date:  2011-12-21       Impact factor: 1.670

Review 5.  FMR1 triplet arrays: paying the price for perfection.

Authors:  M C Hirst
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

6.  Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

Authors:  D Z Loesch; R Huggins; V Petrovic; H Slater
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

7.  Fragile X CGG repeat variation in Tamil Nadu, South India: a comparison of radioactive and methylation-specific polymerase chain reaction in CGG repeat sizing.

Authors:  Nagarathinam Indhumathi; Deepika Singh; Samuel S Chong; B K Thelma; Ramesh Arabandi; C R Srikumari Srisailpathy
Journal:  Genet Test Mol Biomarkers       Date:  2011-10-24

8.  Fragile X gene instability: anchoring AGGs and linked microsatellites.

Authors:  N Zhong; W Yang; C Dobkin; W T Brown
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

9.  Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.

Authors:  Xiaoli Chen; Jingmin Wang; Hua Xie; Wenjuan Zhou; Ye Wu; Jun Wang; Jian Qin; Jin Guo; Qiang Gu; Xiaozhen Zhang; Taoyun Ji; Yu Zhang; Zhiming Xiong; Liwen Wang; Xiru Wu; Gary J Latham; Yuwu Jiang
Journal:  BMC Pediatr       Date:  2015-07-15       Impact factor: 2.125

10.  Haplotype Analysis of DXS548 and FRAXAC1 Microsatellite Loci in Iranian Patients with Fragile X Syndrome.

Authors:  Seyed Ahmad Aleyasin; Fatemeh Salamat; Mojgan Mirakhori
Journal:  Iran J Child Neurol       Date:  2018
  10 in total

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