| Literature DB >> 16973164 |
Michael Schlame1, Mindong Ren.
Abstract
Barth syndrome is an X-linked recessive disease caused by mutations in the tafazzin gene. Patients have reduced concentration and altered composition of cardiolipin, the specific mitochondrial phospholipid, and they have variable clinical findings, often including heart failure, myopathy, neutropenia, and growth retardation. This article provides an overview of the molecular basis of Barth syndrome. It is argued that tafazzin, a phospholipid acyltransferase, is involved in acyl-specific remodeling of cardiolipin, which promotes structural uniformity and molecular symmetry among the cardiolipin molecular species. Inhibition of this pathway leads to changes in mitochondrial architecture and function.Entities:
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Year: 2006 PMID: 16973164 DOI: 10.1016/j.febslet.2006.07.022
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124