Cell type-specific regulation by different cytokinetic pathways in the early embryo

Cytokinesis, the physical division of one cell into two, is typically assumed to use the same molecular process across animal cells. However, regulation of cell division can vary significantly among different cell types, even within the same multicellular organism. Using six fast-acting temperature-sensitive (ts) cytokinesis-defective mutants, we found that each had unique cell type-specific profiles in the early 2-cell through 8-cell <i>C. elegans</i> embryo. Certain cell types were more sensitive than others to actomyosin and spindle signaling disruptions, disrupting two members of the same complex could result in different phenotypes, and protection against actomyosin inhibition did not always protect against spindle signaling inhibition.

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Journal
PubMed
Published
2024-08-08
DOI
https://doi.org/10.17912/micropub.biology.001316
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Cell type-specific regulation by different cytokinetic pathways in the early embryo

Julien Dumont, Caroline Q. Connors, Mimi Shirasu‐Hiza, Julie C. Canman et al.
1 links
PubMed
Pluripotent Stem Cells Research
article

Cell type-specific regulation by different cytokinetic pathways in the early embryo

Julien Dumont, Caroline Q. Connors, Mimi Shirasu‐Hiza, Julie C. Canman, Sophia L. Martin
article en

Abstract

Cytokinesis, the physical division of one cell into two, is typically assumed to use the same molecular process across animal cells. However, regulation of cell division can vary significantly among different cell types, even within the same multicellular organism. Using six fast-acting temperature-sensitive (ts) cytokinesis-defective mutants, we found that each had unique cell type-specific profiles in the early 2-cell through 8-cell <i>C. elegans</i> embryo. Certain cell types were more sensitive than others to actomyosin and spindle signaling disruptions, disrupting two members of the same complex could result in different phenotypes, and protection against actomyosin inhibition did not always protect against spindle signaling inhibition.

PubMedVol. 2024
Centre National de la Recherche Scientifique (FR), Université Paris Cité (FR), Columbia University Irving Medical Center (US), Institut Jacques Monod (FR)
National Institutes of Health, Office of Research Infrastructure Programs, National Institutes of Health
Openalex Percentile: Top 82%
Pluripotent Stem Cells Research
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