Literature DB >> 23849264

Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy.

Yan-Yan Ma1, Tong-Fei Wu2, Yu-Peng Liu2, Qiao Wang2, Xi-Yuan Li2, Yuan Ding2, Jin-Qing Song2, Xiu-Yu Shi1, Wei-Na Zhang1, Meng Zhao1, Ling-Yan Hu1, Jun Ju1, Zhi-Long Wang3, Yan-Ling Yang4, Li-Ping Zou5.   

Abstract

OBJECTIVE: To investigate respiratory chain complex II deficiency resulted from mutation in succinate dehydrogenase gene (SDH) encoding complex II subunits in China.
METHODS: An 11-year-old boy was admitted to our hospital. He had a history of progressive psychomotor regression and weakness since the age of 4years. His cranial magnetic resonance imaging revealed focal, bilaterally symmetrical lesions in the basal ganglia and thalamus, indicating mitochondrial encephalopathy. The activities of mitochondrial respiratory chain enzymes I-V in peripheral leukocytes were determined via spectrophotometry. Mitochondrial DNA and the succinate dehydrogenase A (SDHA) gene were analyzed by direct sequencing.
RESULTS: Complex II activity in the leukocytes had decreased to 33.07nmol/min/mg mitochondrial protein (normal control 71.8±12.9); the activities of complexes I, III, IV and V were normal. The entire sequence of the mitochondrial DNA was normal. The SDHA gene showed two heterozygous frame-shift mutations: c.G117G/del in exon 2 and c.T220T/insT in exon 3, which resulted in stop codons at residues 56 and 81, respectively.
CONCLUSIONS: We have described the first Chinese case of mitochondrial respiratory chain complex II deficiency, which was diagnosed using enzyme assays and gene analysis. Two novel, compound, frame-shift mutations, c.G117G/del in exon 2 and c.T220T/insT in exon 3 of the SDHA gene, were found in our patient.
Copyright © 2013 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Frame-shift mutation; Respiratory chain complex II deficiency; SDHA gene

Mesh:

Substances:

Year:  2013        PMID: 23849264     DOI: 10.1016/j.braindev.2013.06.003

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  5 in total

1.  SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors.

Authors:  G Herma Renkema; Saskia B Wortmann; Roel J Smeets; Hanka Venselaar; Marion Antoine; Gepke Visser; Tawfeg Ben-Omran; Lambert P van den Heuvel; Henri J L M Timmers; Jan A Smeitink; Richard J T Rodenburg
Journal:  Eur J Hum Genet       Date:  2014-04-30       Impact factor: 4.246

2.  Progressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum.

Authors:  Beattie R H Sturrock; Ellen F Macnamara; Peter McGuire; Shannon Kruk; Ivan Yang; Jennifer Murphy; Cyndi J Tifft; Eliza Gordon-Lipkin
Journal:  Mol Genet Genomic Med       Date:  2021-05-07       Impact factor: 2.183

3.  A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency.

Authors:  Charlotte L Alston; Camilla Ceccatelli Berti; Emma L Blakely; Monika Oláhová; Langping He; Colin J McMahon; Simon E Olpin; Iain P Hargreaves; Cecilia Nolli; Robert McFarland; Paola Goffrini; Maureen J O'Sullivan; Robert W Taylor
Journal:  Hum Genet       Date:  2015-05-26       Impact factor: 4.132

4.  Clinical diagnosis and mutation analysis of four Chinese families with succinic semialdehyde dehydrogenase deficiency.

Authors:  Ping Wang; Fengying Cai; Lirong Cao; Yizheng Wang; Qianqian Zou; Peng Zhao; Chao Wang; Yuqin Zhang; Chunquan Cai; Jianbo Shu
Journal:  BMC Med Genet       Date:  2019-05-22       Impact factor: 2.103

Review 5.  The genetic basis of isolated mitochondrial complex II deficiency.

Authors:  Millie Fullerton; Robert McFarland; Robert W Taylor; Charlotte L Alston
Journal:  Mol Genet Metab       Date:  2020-10-03       Impact factor: 4.797

  5 in total

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