Literature DB >> 12376747

Comparative study on deletions of the dystrophin gene in three Asian populations.

Poh-San Lai1, Yasuhiro Takeshima, Kayo Adachi, Khanh Van Tran, Hoan Thi Nguyen, Poh-Sim Low, Masafumi Matsuo.   

Abstract

The frequency and distribution of deletions of 19 deletion-prone exons clustered in two hot spots in the proximal and central regions of the dystrophin gene were compared in three populations from Singaporean, Japan, and Vietnam. DNA samples obtained from 105 Singaporean, 86 Japanese, and 34 Vietnamese Duchenne muscular dystrophy patients were examined by polymerase chain reaction amplification. Deletions of the examined exons were found in 51.2% of Japanese patients but in 40.0% or less of the Singaporeans and Vietnamese. About two thirds of the deletions were localized in the central region and the remaining deletions were clustered at the proximal region. The most commonly deleted exons at the central deletion hot spot were exon 50 in the Singaporean, exons 49 and 50 in the Japanese, and exon 51 in the Vietnamese population. At the proximal deletion hot spot, the most commonly deleted exons were exons 6 and 8 in the Singaporeans, exons 12 and 17 in the Japanese, and exons 8 and 12 in the Vietnamese. Two cases each from Singapore and Japan had large-scale gross mutations spanning both deletion hot spots. Our results suggest that, although the presence and frequency of the two deletion hot spots may be similar in the three Asian populations analyzed, the distribution and frequency of deletions among the different exons can vary as a result of population-specific intronic sequences that predispose individuals to preferential deletion breakpoints.

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Year:  2002        PMID: 12376747     DOI: 10.1007/s100380200084

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  4 in total

1.  Distribution of dystrophin gene deletions in a Chinese population.

Authors:  Yuanyuan Li; Zhuo Liu; Shengrong OuYang; Yanli Zhu; Liwen Wang; Jianxin Wu
Journal:  J Int Med Res       Date:  2016-01-19       Impact factor: 1.671

2.  Screening of Duchenne muscular dystrophy (DMD) mutations and investigating its mutational mechanism in Chinese patients.

Authors:  Chen Chen; Hongwei Ma; Feng Zhang; Lu Chen; Xuesha Xing; Shusen Wang; Xue Zhang; Yang Luo
Journal:  PLoS One       Date:  2014-09-22       Impact factor: 3.240

3.  Comparison of mutation profiles in the Duchenne muscular dystrophy gene among populations: implications for potential molecular therapies.

Authors:  Luz Berenice López-Hernández; Benjamín Gómez-Díaz; Alexandra Berenice Luna-Angulo; Mónica Anaya-Segura; David John Bunyan; Carolina Zúñiga-Guzman; Rosa Elena Escobar-Cedillo; Bladimir Roque-Ramírez; Luis Angel Ruano-Calderón; Héctor Rangel-Villalobos; Julia Angélica López-Hernández; Francisco Javier Estrada-Mena; Silvia García; Ramón Mauricio Coral-Vázquez
Journal:  Int J Mol Sci       Date:  2015-03-09       Impact factor: 5.923

4.  The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine.

Authors:  Kristy Iskandar; Ery Kus Dwianingsih; Linda Pratiwi; Alvin Santoso Kalim; Hasna Mardhiah; Alifiani H Putranti; Dian K Nurputra; Agung Triono; Elisabeth S Herini; Rusdy G Malueka; Poh San Lai
Journal:  BMC Res Notes       Date:  2019-10-28
  4 in total

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