Literature DB >> 10083731

Novel mutations, including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patients with Tay-Sachs disease.

A Tanaka1, M Fujimaru, K Choeh, G Isshiki.   

Abstract

Two novel mutations of the beta-hexosaminidase alpha subunit gene were identified in Japanese patients with the infantile form of Tay-Sachs disease. One mutation was a one-base deletion at nt613C, which generated a stop codon at two codons downstream, in three unrelated patients. The other mutation was a one-base substitution of G-to-A at IVS 5, +1, which caused a splicing abnormality, in one patient. A missense mutation of R170W, which has already been reported in other ethnic groups, was also newly identified in one patient. In 1993, the most common mutation (IVS 5, -1G-->T) in Japanese patients with Tay-Sachs disease was reported as the major mutation in Japan accounting for 80% of 56 mutant alleles from 28 unrelated patients. The deletion of nt613C was the second most common mutation, accounting for 5% of the mutant alleles. The previously reported mutation IVS 5, -1G-->T and the nt613C deletion found in this study together accounted for 85% of the mutations causing Tay-Sachs disease among Japanese. Since these two mutations were located in or close to exon 6 and since they abolish Fok I (IVS 5, -1G-->T) and Sfa NI (nt613C deletion) restriction sites, respectively, they were screened rapidly by single polymerase chain reaction followed by digestion with these enzymes.

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Year:  1999        PMID: 10083731     DOI: 10.1007/s100380050116

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


  6 in total

1.  Structural basis of the GM2 gangliosidosis B variant.

Authors:  Fumiko Matsuzawa; Sei-ichi Aikawa; Hitoshi Sakuraba; Hoang Thi Ngoc Lan; Akemi Tanaka; Kousaku Ohno; Yuko Sugimoto; Haruaki Ninomiya; Hirofumi Doi
Journal:  J Hum Genet       Date:  2003-10-24       Impact factor: 3.172

2.  Tay-Sachs Disease Presenting as Refractory Epilepsy with Autistic Regression Secondary to a Novel Mutation in HEXA Gene.

Authors:  Vykuntaraju K Gowda; Varunvenkat M Srinivasan; Maya Bhat; Asha Benakappa
Journal:  Indian J Pediatr       Date:  2018-07-14       Impact factor: 1.967

3.  Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form.

Authors:  Akemi Tanaka; Lan Thi Ngcok Hoang; Yasuaki Nishi; Satoshi Maniwa; Makio Oka; Tsunekazu Yamano
Journal:  J Hum Genet       Date:  2003-10-18       Impact factor: 3.172

4.  Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India.

Authors:  Mehul Mistri; Sanjeev Mehta; Dhaval Solanki; Mahesh Kamate; Neerja Gupta; Madhulika Kabra; Ratna Puri; Katta Girisha; Sankar Hariharan; Sheela Nampoothiri; Frenny Sheth; Jayesh Sheth
Journal:  J Hum Genet       Date:  2019-08-06       Impact factor: 3.172

5.  Identification of novel mutations in HEXA gene in children affected with Tay Sachs disease from India.

Authors:  Mehul Mistri; Parag M Tamhankar; Frenny Sheth; Daksha Sanghavi; Pratima Kondurkar; Swapnil Patil; Susan Idicula-Thomas; Sarita Gupta; Jayesh Sheth
Journal:  PLoS One       Date:  2012-06-18       Impact factor: 3.240

6.  Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.

Authors:  Jayesh Sheth; Mehul Mistri; Chaitanya Datar; Umesh Kalane; Shekhar Patil; Mahesh Kamate; Harshuti Shah; Sheela Nampoothiri; Sarita Gupta; Frenny Sheth
Journal:  Mol Genet Metab Rep       Date:  2014-09-29
  6 in total

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