Bharadwaj Manish S, Zhou Yu, Molina Anthony J, Criswell Tracy, Lu Baisong
Section on Gerontology and Geriatric Medicine, Wake Forest University Health Sciences, Department of Internal Medicine, Medical Center Boulevard, Winston-Salem, NC 27157, USA.
Wake Forest Institute for Regenerative Medicine, Wake Forest University Health Sciences, Medical Center Boulevard, Winston-Salem, NC 27157, USA.
Redox Biol. 2014;2:1008-15. doi: 10.1016/j.redox.2014.08.006. Epub 2014 Aug 28.
Inner mitochondrial membrane peptidase 2-like (IMMP2L) protein is a mitochondrial inner membrane peptidase that cleaves the signal peptide sequences of cytochrome c1 (CYC1) and mitochondrial glycerol phosphate dehydrogenase (GPD2). Immp2l mutant mice show infertility and early signs of aging. It is unclear whether mitochondrial respiratory deficiency underlies this phenotype. Here we show that the intermediate forms of GPD2 and CYC1 have normal expression levels and enzymatic function in Immp2l mutants. Mitochondrial respiration is not diminished in isolated mitochondria and cells from mutant mice. Our data suggest that respiratory deficiency is not the cause of the observed Immp2l mutant phenotypes.
线粒体内膜肽酶2样(IMMP2L)蛋白是一种线粒体内膜肽酶,可切割细胞色素c1(CYC1)和线粒体甘油磷酸脱氢酶(GPD2)的信号肽序列。Immp2l突变小鼠表现出不育和衰老的早期迹象。目前尚不清楚线粒体呼吸缺陷是否是这种表型的基础。在这里,我们表明GPD2和CYC1的中间形式在Immp2l突变体中具有正常的表达水平和酶功能。突变小鼠分离的线粒体和细胞中的线粒体呼吸没有减弱。我们的数据表明,呼吸缺陷不是观察到的Immp2l突变体表型的原因。