A tumor suppressor Retinoblastoma1 is essential for embryonic development in the sea urchin

Research output: Contribution to journalArticle

Authors

External Institution(s)

  • Brown University

Details

Original languageEnglish (US)
Pages (from-to)1273-1285
Number of pages13
JournalDevelopmental Dynamics
Volume248
Issue number12
StatusPublished - Dec 1 2019
Peer-reviewedYes

Abstract

Background: Embryonic cells and cancer cells share various cellular characteristics important for their functions. It has been thus proposed that similar mechanisms of regulation may be present in these otherwise disparate cell types. Results: To explore how regulative embryonic cells are fundamentally different from cancerous cells, we report here that a fine balance of a tumor suppressor protein Retinoblastoma1 (Rb1) and a germline factor Vasa are important for proper cell proliferation and differentiation of the somatic cells during embryogenesis of the sea urchin. Rb1 knockdown blocked embryonic development and induced Vasa accumulation in the entire embryo, while its overexpression resulted in a smaller-sized embryo with differentiated body structures. These results suggest that a titrated level of Rb1 protein may be essential for a proper balance of cell proliferation and differentiation during development. Vasa knockdown or overexpression, on the other hand, reduced or increased Rb1 protein expression, respectively. Conclusions: Taken together, it appears that Vasa protein positively regulates Rb1 protein while Rb1 protein negatively regulates Vasa protein, balancing the act of these two antagonistic molecules in somatic cells. This mechanism may provide a fine control of cell proliferation and differentiation, which is essential for regulative embryonic development.

    Research areas

  • Retinoblastoma1, cell differentiation, embryonic development, sea urchin

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Fernandez-Nicolas, A, Xu, D & Yajima, M 2019, 'A tumor suppressor Retinoblastoma1 is essential for embryonic development in the sea urchin', Developmental Dynamics, vol. 248, no. 12, pp. 1273-1285. https://doi.org/10.1002/dvdy.113