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Translation defects

Jonathan B Weitzman

Genome Biology 2001, 2:spotlight-20011114-01  doi:10.1186/gb-spotlight-20011114-01

The electronic version of this article is the complete one and can be found online at:

Published:14 November 2001

© 2001 BioMed Central Ltd

Research news

Analysis of patients with an inherited brain disease has provided the first link between translation initiation factors and human disease. Leukoencephalopathy with vanishing white matter (VWM) occurs during childhood and is a chronic-progressive disorder (involving rapid additional deterioration following febrile infection or minor head trauma). In the Advanced Online Publication of Nature Genetics, Leegwater et al. report mutations in VWM patients within two subunits of the eIF2B translation initiation factor (DOI: 10.1038/ng764). They identified a pedigree of nine families with a common haplotype (EN) to narrow down the hunt to a region of chromosome 3q27 containing around 25 genes. Genomic sequence analysis identified mutations in EIF2B5, encoding the ε subunit of eIF2B, a eukaryotic translation initiation factor. Analysis of genomic loci encoding other eIF2B subunits led the researchers to discover additional mutations in VWM families without linkage to chromosome 3q27, and these were due to mutations in the EIF2B2 gene on chromosome 14q24, encoding the eIF2B β-subunit. The activity of eIF2B is regulated by stress, and the authors suggest that the function of eIF2B in the heat-shock response might account for the neurological deterioration of VWM patients following fever conditions.


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    Leukoencephalopathy with vanishing white matter

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    Nature Genetics

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    Eukaryotic translation initiation factor 2B945

  4. Regulation of translation initiation factors by signal transduction.

    PubMed Abstract | Publisher Full Text OpenURL