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Function and regulation of the divisome for mitochondrial fission

Author

Listed:
  • Felix Kraus

    (Monash University
    Harvard Medical School)

  • Krishnendu Roy

    (Indian Institute of Science Education and Research)

  • Thomas J. Pucadyil

    (Indian Institute of Science Education and Research)

  • Michael T. Ryan

    (Monash University)

Abstract

Mitochondria form dynamic networks in the cell that are balanced by the flux of iterative fusion and fission events of the organelles. It is now appreciated that mitochondrial fission also represents an end-point event in a signalling axis that allows cells to sense and respond to external cues. The fission process is orchestrated by membrane-associated adaptors, influenced by organellar and cytoskeletal interactions and ultimately executed by the dynamin-like GTPase DRP1. Here we invoke the framework of the ‘mitochondrial divisome’, which is conceptually and operationally similar to the bacterial cell-division machinery. We review the functional and regulatory aspects of the mitochondrial divisome and, within this framework, parse the core from the accessory machinery. In so doing, we transition from a phenomenological to a mechanistic understanding of the fission process.

Suggested Citation

  • Felix Kraus & Krishnendu Roy & Thomas J. Pucadyil & Michael T. Ryan, 2021. "Function and regulation of the divisome for mitochondrial fission," Nature, Nature, vol. 590(7844), pages 57-66, February.
  • Handle: RePEc:nat:nature:v:590:y:2021:i:7844:d:10.1038_s41586-021-03214-x
    DOI: 10.1038/s41586-021-03214-x
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    Cited by:

    1. Chih-Wei Chen & Chi Su & Chang-Yu Huang & Xuan-Rong Huang & Xiaojing Cuili & Tung Chao & Chun-Hsiang Fan & Cheng-Wei Ting & Yi-Wei Tsai & Kai-Chien Yang & Ti-Yen Yeh & Sung-Tsang Hsieh & Yi-Ju Chen & , 2024. "NME3 is a gatekeeper for DRP1-dependent mitophagy in hypoxia," Nature Communications, Nature, vol. 15(1), pages 1-20, December.

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