Literature DB >> 9187675

The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians.

S H Chen1, J M Schoof, N E Buroker, C R Scott.   

Abstract

We have evaluated the structure of the CGG repeat within the FMR1 gene of an Asian population and found the most common size of the repeat to be 29 and 30 with a minor population of 36 repeats. We have isolated and sequenced DNA containing the 36 repeats and found the basis sequence to be (CGG)9AGG(CGG)9AGG-(CGG)6AGG(CGG)9; with a (CGG)6)AGG insertion, designated as 9A9A6A9. Of 144 Asian chromosomes, 11 (8%) had sequences with this insertion. Six different variations of the basic sequence were observed in the population: 9A9A6A2A9, 9A9A6A11, 9A9A16, 9A9A15, 8A9A6A6A9, and 11A6A6A9. All but one of the chromosomes with the insertion had the haplotype of DXS548/ FRAXAC1: 194/D suggesting that the sequences with the 6A insertion arose from a single ancestral allele. We have not observed the insertion in the FMR1 gene of Caucasians or Native Americans. The (CGG)6AGG insertion may be unique to Asians.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9187675     DOI: 10.1007/s004390050450

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


  4 in total

1.  The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population.

Authors:  Hua-Hsien Chiu; Yi-Ting Tseng; Hui-Pin Hsiao; Hui-Hua Hsiao
Journal:  J Genet       Date:  2008-12       Impact factor: 1.166

Review 2.  Current Understanding of the Etiology, Symptomatology, and Treatment Options in Premature Ovarian Insufficiency (POI).

Authors:  Bunpei Ishizuka
Journal:  Front Endocrinol (Lausanne)       Date:  2021-02-25       Impact factor: 5.555

3.  Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population.

Authors:  Wen Huang; Qiuping Xia; Shiyu Luo; Hua He; Ting Zhu; Qian Du; Ranhui Duan
Journal:  Mol Genet Genomic Med       Date:  2015-05       Impact factor: 2.183

4.  Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP Haplotype.

Authors:  Pornprot Limprasert; Janpen Thanakitgosate; Kanoot Jaruthamsophon; Thanya Sripo
Journal:  Genet Res Int       Date:  2016-03-02
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.