Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.celrep.2021.109326
Title: A balance between antagonizing PAR proteins specifies the pattern of asymmetric and symmetric divisions in C. elegans embryogenesis
Authors: Lim, Yen Wei
Wen, Fu-Lai
Shankar, Prabhat
Shibata, Tatsuo
Motegi, Fumio 
Keywords: asymmetric cell division
C. elegans
cell polarity
embryo
PAR proteins
symmetric cell division
Issue Date: 1-Jul-2021
Publisher: Elsevier B.V.
Citation: Lim, Yen Wei, Wen, Fu-Lai, Shankar, Prabhat, Shibata, Tatsuo, Motegi, Fumio (2021-07-01). A balance between antagonizing PAR proteins specifies the pattern of asymmetric and symmetric divisions in C. elegans embryogenesis. Cell Reports 36 (1) : 109326. ScholarBank@NUS Repository. https://doi.org/10.1016/j.celrep.2021.109326
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Coordination between cell differentiation and proliferation during development requires the balance between asymmetric and symmetric modes of cell division. However, the cellular intrinsic cue underlying the choice between these two division modes remains elusive. Here, we show evidence in Caenorhabditis elegans that the invariable lineage of the division modes is specified by the balance between antagonizing complexes of partitioning-defective (PAR) proteins. By uncoupling unequal inheritance of PAR proteins from that of fate determinants during cell division, we demonstrate that changes in the balance between PAR-2 and PAR-6 can be sufficient to re-program the division modes from symmetric to asymmetric and vice versa in two daughter cells. The division mode adopted occurs independently of asymmetry in cytoplasmic fate determinants, cell-size asymmetry, and cell-cycle asynchrony between sister cells. We propose that the balance between PAR proteins represents an intrinsic self-organizing cue for the specification of the two division modes during development. © 2021 The Authors
Source Title: Cell Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/233682
ISSN: 2211-1247
DOI: 10.1016/j.celrep.2021.109326
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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