A role for organ level dynamics in morphogenesis of the <i>C. elegans</i> hermaphrodite distal tip cell

The morphology of cells in vivo can arise from a variety of mechanisms. In the Caenorhabditis elegans hermaphrodite gonad, the distal tip cell (DTC) elaborates into a complex plexus over a relatively short developmental time period, but the mechanisms underlying this change in cell morphology are not well defined. We correlated the time of DTC elaboration with the L4-to-adult molt, but ruled out a relevant heterochronic pathway as a cue for DTC elaboration. Instead, we found that the timing of gonad elongation and aspects of underlying germline flux influence DTC elaboration. We propose a 'hitch and tow' aspect of organ-level dynamics that contributes to cellular morphogenesis, whereby germline flux drags the flexible DTC cell cortex away from its stationary cell body. More broadly, we speculate that this mechanism may contribute to cell shape changes in other contexts with implications for development and disease.

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Publication Details

Journal
Development
Published
2024-10-01
DOI
https://doi.org/10.1242/dev.203019
Citations
7
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
1.59

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article

A role for organ level dynamics in morphogenesis of the C. elegans hermaphrodite distal tip cell

E. Jane Albert Hubbard, Julia Burnett, Theadora Tolkin
7 citations
Development
Genetics, Aging, and Longevity in Model Organisms
1.59
article

A role for organ level dynamics in morphogenesis of the C. elegans hermaphrodite distal tip cell

E. Jane Albert Hubbard, Julia Burnett, Theadora Tolkin
article en
7 citations

Abstract

The morphology of cells in vivo can arise from a variety of mechanisms. In the Caenorhabditis elegans hermaphrodite gonad, the distal tip cell (DTC) elaborates into a complex plexus over a relatively short developmental time period, but the mechanisms underlying this change in cell morphology are not well defined. We correlated the time of DTC elaboration with the L4-to-adult molt, but ruled out a relevant heterochronic pathway as a cue for DTC elaboration. Instead, we found that the timing of gonad elongation and aspects of underlying germline flux influence DTC elaboration. We propose a 'hitch and tow' aspect of organ-level dynamics that contributes to cellular morphogenesis, whereby germline flux drags the flexible DTC cell cortex away from its stationary cell body. More broadly, we speculate that this mechanism may contribute to cell shape changes in other contexts with implications for development and disease.

DevelopmentVol. 151(19)
New York University (US)
American Cancer Society, National Institute on Aging, National Institute of General Medical Sciences
Openalex Percentile: Top 17%
Genetics, Aging, and Longevity in Model Organisms
1.59
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