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Ann Neurol. 2004 Nov;56(5):734-8.

Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation.

Author information

1
Metabolic Disease Unit, Shaare-Zedek Medical Center, Jerusalem, Israel.

Abstract

The mitochondrial respiratory chain comprises 85 subunits, 13 of which are mitochondrial encoded. The synthesis of these 13 proteins requires many nuclear-encoded proteins that participate in mitochondrial DNA replication, transcript production, and a distinctive mitochondrial translation apparatus. We report a patient with agenesis of corpus callosum, dysmorphism, and fatal neonatal lactic acidosis with markedly decreased complex I and IV activity in muscle and liver and a generalized mitochondrial translation defect identified in pulse-label experiments. The defect was associated with marked reduction of the 12S rRNA transcript level likely attributed to a nonsense mutation in the MRPS16 gene. A new group of mitochondrial respiratory chain disorders is proposed, resulting from mutations in nuclear encoded components of the mitochondrial translation apparatus.

PMID:
15505824
DOI:
10.1002/ana.20282
[Indexed for MEDLINE]

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