Author
Listed:
- Andrew S. Moore
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine
Howard Hughes Medical Institute, Janelia Research Campus)
- Stephen M. Coscia
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Cory L. Simpson
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Fabian E. Ortega
(Stanford University)
- Eric C. Wait
(Howard Hughes Medical Institute, Janelia Research Campus)
- John M. Heddleston
(Howard Hughes Medical Institute, Janelia Research Campus)
- Jeffrey J. Nirschl
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
- Christopher J. Obara
(Howard Hughes Medical Institute, Janelia Research Campus)
- Pedro Guedes-Dias
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine
Technische Universität München)
- C. Alexander Boecker
(University of Pennsylvania Perelman School of Medicine)
- Teng-Leong Chew
(Howard Hughes Medical Institute, Janelia Research Campus)
- Julie A. Theriot
(University of Washington
University of Washington)
- Jennifer Lippincott-Schwartz
(Howard Hughes Medical Institute, Janelia Research Campus)
- Erika L. F. Holzbaur
(University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine
University of Pennsylvania Perelman School of Medicine)
Abstract
Symmetric cell division requires the even partitioning of genetic information and cytoplasmic contents between daughter cells. Whereas the mechanisms coordinating the segregation of the genome are well known, the processes that ensure organelle segregation between daughter cells remain less well understood1. Here we identify multiple actin assemblies with distinct but complementary roles in mitochondrial organization and inheritance in mitosis. First, we find a dense meshwork of subcortical actin cables assembled throughout the mitotic cytoplasm. This network scaffolds the endoplasmic reticulum and organizes three-dimensional mitochondrial positioning to ensure the equal segregation of mitochondrial mass at cytokinesis. Second, we identify a dynamic wave of actin filaments reversibly assembling on the surface of mitochondria during mitosis. Mitochondria sampled by this wave are enveloped within actin clouds that can spontaneously break symmetry to form elongated comet tails. Mitochondrial comet tails promote randomly directed bursts of movement that shuffle mitochondrial position within the mother cell to randomize inheritance of healthy and damaged mitochondria between daughter cells. Thus, parallel mechanisms mediated by the actin cytoskeleton ensure both equal and random inheritance of mitochondria in symmetrically dividing cells.
Suggested Citation
Andrew S. Moore & Stephen M. Coscia & Cory L. Simpson & Fabian E. Ortega & Eric C. Wait & John M. Heddleston & Jeffrey J. Nirschl & Christopher J. Obara & Pedro Guedes-Dias & C. Alexander Boecker & Te, 2021.
"Actin cables and comet tails organize mitochondrial networks in mitosis,"
Nature, Nature, vol. 591(7851), pages 659-664, March.
Handle:
RePEc:nat:nature:v:591:y:2021:i:7851:d:10.1038_s41586-021-03309-5
DOI: 10.1038/s41586-021-03309-5
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Citations
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Cited by:
- Chang Qiao & Yunmin Zeng & Quan Meng & Xingye Chen & Haoyu Chen & Tao Jiang & Rongfei Wei & Jiabao Guo & Wenfeng Fu & Huaide Lu & Di Li & Yuwang Wang & Hui Qiao & Jiamin Wu & Dong Li & Qionghai Dai, 2024.
"Zero-shot learning enables instant denoising and super-resolution in optical fluorescence microscopy,"
Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Stephen M. Coscia & Andrew S. Moore & Cameron P. Thompson & Christian F. Tirrito & E. Michael Ostap & Erika L. F. Holzbaur, 2024.
"An interphase actin wave promotes mitochondrial content mixing and organelle homeostasis,"
Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Jingjing Zhao & Xiaojun Han, 2024.
"Investigation of artificial cells containing the Par system for bacterial plasmid segregation and inheritance mimicry,"
Nature Communications, Nature, vol. 15(1), pages 1-11, December.
- Ana Teresa López-Jiménez & Serge Mostowy, 2021.
"Emerging technologies and infection models in cellular microbiology,"
Nature Communications, Nature, vol. 12(1), pages 1-13, December.
- Peng Shi & Xiaoyu Ren & Jie Meng & Chenlu Kang & Yihe Wu & Yingxue Rong & Shujuan Zhao & Zhaodi Jiang & Ling Liang & Wanzhong He & Yuxin Yin & Xiangdong Li & Yong Liu & Xiaoshuai Huang & Yujie Sun & B, 2022.
"Mechanical instability generated by Myosin 19 contributes to mitochondria cristae architecture and OXPHOS,"
Nature Communications, Nature, vol. 13(1), pages 1-14, December.
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