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Identification of a novel homozygous mutation (S144I) in a Malay patient with maple syrup urine disease

  • Ernie Zuraida Ali EMAIL logo , Zabedah Md Yunus , Norsiah Md Desa and Ngu Lock Hock
Published/Copyright: May 17, 2013

Abstract

Maple syrup urine disease (MSUD) is a rare autosomal recessive metabolic disorder of branched-chain amino acid metabolism caused by the defective function of branched-chain α-ketoacid dehydrogenase complex (BCKDH). It is characterised by increased plasma leucine, isoleucine, and valine levels, and mutations can be detected in any one of the BCKDHA, BCKDHB, and DBT genes. In this study, we describe the molecular basis of a novel mutation found in one MSUD Malay patient from consanguineous parents. A homozygous mutation has been detected in this patient whose both parents carried a heterozygous mutation at DNA coding region c.431G>T in exon 4, which resulted in a substitution of serine to isoleucine at codon 144 (p.S144I). In silico analysis predicted S144I to be potentially damaging. The mutation was located on the alpha helical region of the BCKDHA protein, and it is predicted to affect the stability of protein due to the loss of various polar interactions between local secondary structures. Homology analysis revealed that this mutation occurred in a highly conserved region (100%). This result indicates that S144I mutation is likely pathogenic and may contribute to the classic form of MSUD in this patient.


Corresponding author: Ernie Zuraida Ali, MSc, Molecular Diagnostics and Protein Unit, Specialised Diagnostics Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia, Phone: +603 26162568, Fax: +603 26162533, E-mail: ;

We thank the Director General of Health Malaysia for permission to publish this paper. Our special thanks to Dr. Shahnaz Murad (Director of IMR) and Dr. Rohani Md Yasin (Centre Head, SDC) for critical reading of the manuscripts and valuable comments. We would like to extend our gratitude to Mohd Heikkal Ismail and Nurul Farahana Rosli for their excellent technical assistance and Mohd Khairul Nizam for his support in the protein structural analysis. We are also grateful to all clinicians for their contributions in this study. This study was funded by Diagnostics Services, Institute for Medical Research, Ministry of Health.

Conflict of interest statement

Competing interests: The authors declare that they have no competing interests.

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Received: 2012-12-29
Accepted: 2013-4-4
Published Online: 2013-05-17
Published in Print: 2013-10-01

©2013 by Walter de Gruyter Berlin Boston

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