bims-cytox1 Biomed News
on Cytochrome oxidase subunit 1
Issue of 2023–04–09
two papers selected by
Gavin McStay, Liverpool John Moores University
  1. Protein translocation in mitochondria: Sorting out the Toms, Tims, Pams, Sams and Mia.
  2. CLPP inhibition triggers apoptosis in human ovarian granulosa cells via COX5A abnormality-Mediated mitochondrial dysfunction.
  1. FEBS Lett. 2023 Apr 05.
    Protein translocation in mitochondria: Sorting out the Toms, Tims, Pams, Sams and Mia.
    Johannes M Herrmann, Yury Bykov.
      Mitochondria contain 902 (yeast) to 1.136 (mouse, humans) verified proteins. Except for a very small number of mitochondrially encoded core components of the respiratory chain, mitochondrial proteins are encoded by nuclear genes and synthesized in the cytosol. Different import pathways direct proteins to their respective mitochondrial subcompartment (outer membrane, intermembrane space (IMS), inner membrane and matrix). Specific targeting signals in their sequence direct proteins to their target destination and allow the proteins to embark on their respective import pathway. The main import pathways are shown here on the poster and are introduced in the following, using the mitochondrial import system of the baker's yeast Saccharomyces cerevisiae as example. However, the mitochondrial import system of mammalian cells is highly similar and deviates only in minor aspects. Even the mitochondrial import machineries of less closely related eukaryotes, such as plants and trypanosomes, are very similar and adhere to the same general principles.
    Keywords:  Mitochondria; Protein Import; Protein translocation; Translocase of the inner membrane; Translocase of the outer membrane
    DOI:  https://doi.org/10.1002/1873-3468.14614
  2. Front Genet. 2023 ;14 1141167
    CLPP inhibition triggers apoptosis in human ovarian granulosa cells via COX5A abnormality-Mediated mitochondrial dysfunction.
    Xiong Yuan, Wenjie Ma, Shuping Chen, Huiyuan Wang, Chenyi Zhong, Li Gao, Yugui Cui, Danhua Pu, Rongrong Tan, Jie Wu.
      Premature ovarian insufficiency (POI) is characterized by early loss of ovarian function before the age of 40 years. It is confirmed to have a strong and indispensable genetic component. Caseinolytic mitochondrial matrix peptidase proteolytic subunit (CLPP) is a key inducer of mitochondrial protein quality control for the clearance of misfolded or damaged proteins, which is necessary to maintain mitochondrial function. Previous findings have shown that the variation in CLPP is closely related to the occurrence of POI, which is consistent with our findings. This study identified a novel CLPP missense variant (c.628G > A) in a woman with POI who presented with secondary amenorrhea, ovarian dysfunction, and primary infertility. The variant was located in exon 5 and resulted in a change from alanine to threonine (p.Ala210Thr). Importantly, Clpp was mainly localized in the cytoplasm of mouse ovarian granulosa cells and oocytes, and was relatively highly expressed in granulosa cells. Moreover, the overexpression of c.628G > A variant in human ovarian granulosa cells decreased the proliferative capacity. Functional experiments revealed that the inhibition of CLPP decreased the content and activity of oxidative respiratory chain complex IV by affecting the degradation of aggregated or misfolded COX5A, leading to the accumulation of reactive oxygen species and reduction of mitochondrial membrane potential, ultimately activating the intrinsic apoptotic pathways. The present study demonstrated that CLPP affected the apoptosis of granulosa cells, which might be one of the mechanisms by which CLPP aberrations led to the development of POI.
    Keywords:  CLPP; COX5A; POI; apoptosis; granulosa cell (GC)
    DOI:  https://doi.org/10.3389/fgene.2023.1141167
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