| Literature DB >> 34626131 |
Jiajia Ji1, Miriam L Greenberg1.
Abstract
Cardiolipin (CL) is the signature phospholipid (PL) of mitochondria and plays a pivotal role in mitochondrial and cellular function. Disruption of the CL remodeling gene tafazzin (TAZ) causes the severe genetic disorder Barth syndrome (BTHS). Our current understanding of the function of CL and the mechanism underlying the disease has greatly benefited from studies utilizing the powerful yeast model Saccharomyces cerevisiae. In this review, we discuss important findings on the function of CL and its remodeling from yeast studies and the implications of these findings for BTHS, highlighting the potential physiological modifiers that may contribute to the disparities in clinical presentation among BTHS patients.Entities:
Keywords: Barth syndrome; cardiolipin; mitochondrial disease; tafazzin; yeast
Mesh:
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Year: 2021 PMID: 34626131 PMCID: PMC8755574 DOI: 10.1002/jimd.12447
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982