4.2 Article

Mitochondrial nucleoids from the yeast Candida parapsilosis: expansion of the repertoire of proteins associated with mitochondrial DNA

期刊

MICROBIOLOGY-SGM
卷 155, 期 -, 页码 1558-1568

出版社

SOC GENERAL MICROBIOLOGY
DOI: 10.1099/mic.0.027474-0

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资金

  1. Japan Society for the promotion of Science [16570055]
  2. Howard Hughes Medical Institute [55005622]
  3. Fogarty International Research Collaboration Award [2-R03-TW005654-04Al]
  4. Slovak research grant agencies [APVV 20-0016-04, VEGA 1/0132/09, APVV 0024-07, LPP-0164-06, VEGA 1/0219/08 (J.N.)]
  5. Grants-in-Aid for Scientific Research [16570055] Funding Source: KAKEN

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Molecules of mitochondrial DNA (mtDNA) are packed into nucleic acid-protein complexes termed mitochondrial nucleoids (mt-nucleoids). In this study, we analysed mt-nucleoids of the yeast Candida parapsilosis, which harbours a linear form of the mitochondrial genome. To identify conserved as well as specific features of mt-nucleoids in this species, we employed two strategies for analysis of their components. First, we investigated the protein composition of mt-nucleoids isolated from C. parapsilosis mitochondria, determined N-terminal amino acid sequences of 14 proteins associated with the mt-nucleoids and identified corresponding genes. Next, we complemented the list of mt-nucleoid components with additional candidates identified in the complete genome sequence of C. parapsilosis as homologues of Saccharomyces cerevisiae mt-nucleoid proteins. Our approach revealed several known mt-nucleoid proteins as well as additional components that expand the repertoire of proteins associated with these cytological structures. In particular, we identified and purified the protein Gcf1, which is abundant in the mt-nucleoids and exhibits structural features in common with the mtDNA packaging protein Abf2 from S. cerevisiae. We demonstrate that Gcf1 p co-localizes with mtDNA, has DNA-binding activity in vitro, and is able to stabilize mtDNA in the S. cerevisiae Delta abf2 mutant, all of which points to a role in the maintenance of the C. parapsilosis mitochondrial genome. Importantly, in contrast to Delta bf2p, in silico analysis of Gcf1 p predicted the presence of a coiled-coil domain and a single high-mobility group (HMG) box, suggesting that it represents a novel type of mitochondrial HMG protein.

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