Fmp30, Mdm31和Mdm32在低磷脂酰乙醇胺条件下ups1独立心磷脂积累中的作用

Contact Pub Date : 2018-01-01 DOI:10.1177/2515256418764043
Non Miyata, O. Kuge
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引用次数: 0

摘要

心磷脂(CL)水平的维持主要依赖于Ups1-Mdm35复合物介导的线粒体内磷脂酸转移。此外,在酿酒酵母中也存在另一种CL积累途径。该途径不依赖于Ups1-Mdm35复合物,并受Ups2缺失的刺激,Ups2与Mdm35形成复合物,介导磷脂酰丝氨酸的线粒体内转移以合成磷脂酰乙醇胺。最近,我们发现替代CL积累途径通过降低磷脂酰乙醇胺水平而不是通过丢失Ups2本身来增强,并且依赖于三种线粒体内膜蛋白,Fmp30, Mdm31和Mdm32。
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Fmp30, Mdm31, and Mdm32 Function in Ups1-Independent Cardiolipin Accumulation Under Low Phosphatidylethanolamine Conditions
Maintenance of the cardiolipin (CL) level largely depends on Ups1-Mdm35 complex-mediated intramitochondrial phosphatidic acid transfer. In addition, the presence of an alternative CL accumulation pathway has been suggested in the yeast Saccharomyces cerevisiae. This pathway is independent of the Ups1-Mdm35 complex and stimulated by loss of Ups2, which forms a complex with Mdm35 and mediates intramitochondrial transfer of phosphatidylserine for phosphatidylethanolamine synthesis. Recently, we found that the alternative CL accumulation pathway is enhanced by a lowered phosphatidylethanolamine level, not by loss of Ups2 per se, and depends on three mitochondrial inner membrane proteins, Fmp30, Mdm31, and Mdm32.
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