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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.
Amato,
RNAi mediated acute depletion of retinoblastoma protein (pRb) promotes aneuploidy in human primary cells via micronuclei formation.
2009, Pubmed
Amato,
RNAi mediated acute depletion of retinoblastoma protein (pRb) promotes aneuploidy in human primary cells via micronuclei formation.
2009,
Pubmed Andrikou,
Myogenesis in the sea urchin embryo: the molecular fingerprint of the myoblast precursors.
2013,
Pubmed
,
Echinobase Calestani,
Isolation of pigment cell specific genes in the sea urchin embryo by differential macroarray screening.
2003,
Pubmed
,
Echinobase Chang,
FGF9/FGFR2 increase cell proliferation by activating ERK1/2, Rb/E2F1, and cell cycle pathways in mouse Leydig tumor cells.
2018,
Pubmed Dimaras,
Retinoblastoma, the visible CNS tumor: A review.
2019,
Pubmed Dominado,
Rbf Regulates Drosophila Spermatogenesis via Control of Somatic Stem and Progenitor Cell Fate in the Larval Testis.
2016,
Pubmed Ettensohn,
Alx1, a member of the Cart1/Alx3/Alx4 subfamily of Paired-class homeodomain proteins, is an essential component of the gene network controlling skeletogenic fate specification in the sea urchin embryo.
2003,
Pubmed
,
Echinobase Fresques,
The diversity of nanos expression in echinoderm embryos supports different mechanisms in germ cell specification.
2016,
Pubmed
,
Echinobase Gustafson,
Post-translational regulation by gustavus contributes to selective Vasa protein accumulation in multipotent cells during embryogenesis.
2011,
Pubmed
,
Echinobase Hassler,
Crystal structure of the retinoblastoma protein N domain provides insight into tumor suppression, ligand interaction, and holoprotein architecture.
2007,
Pubmed Indovina,
Emerging roles of RB family: new defense mechanisms against tumor progression.
2013,
Pubmed Iovino,
RB acute loss induces centrosome amplification and aneuploidy in murine primary fibroblasts.
2006,
Pubmed Janic,
Ectopic expression of germline genes drives malignant brain tumor growth in Drosophila.
2010,
Pubmed Julian,
Tissue-specific targeting of cell fate regulatory genes by E2f factors.
2016,
Pubmed Kohno,
Retinoblastoma tumor suppressor functions shared by stem cell and cancer cell strategies.
2016,
Pubmed Lamber,
Structural insights into the mechanism of phosphoregulation of the retinoblastoma protein.
2013,
Pubmed Lin,
Genome editing in sea urchin embryos by using a CRISPR/Cas9 system.
2016,
Pubmed
,
Echinobase Miles,
Post-transcriptional gene expression control by NANOS is up-regulated and functionally important in pRb-deficient cells.
2014,
Pubmed Morris,
Retinoblastoma protein partners.
2001,
Pubmed Moser,
Control of the Restriction Point by Rb and p21.
2018,
Pubmed Poon,
Evolutionary modification of AGS protein contributes to formation of micromeres in sea urchins.
2019,
Pubmed
,
Echinobase Sage,
The retinoblastoma tumor suppressor and stem cell biology.
2012,
Pubmed Saunders,
Sub-circuits of a gene regulatory network control a developmental epithelial-mesenchymal transition.
2014,
Pubmed
,
Echinobase Shevidi,
Single nucleotide editing without DNA cleavage using CRISPR/Cas9-deaminase in the sea urchin embryo.
2017,
Pubmed
,
Echinobase Tu,
Generation of human embryonic stem cell line with heterozygous RB1 deletion by CRIPSR/Cas9 nickase.
2018,
Pubmed Voronina,
Vasa protein expression is restricted to the small micromeres of the sea urchin, but is inducible in other lineages early in development.
2008,
Pubmed
,
Echinobase Wei,
A database of mRNA expression patterns for the sea urchin embryo.
2006,
Pubmed
,
Echinobase Wikramanayake,
Nuclear beta-catenin-dependent Wnt8 signaling in vegetal cells of the early sea urchin embryo regulates gastrulation and differentiation of endoderm and mesodermal cell lineages.
2004,
Pubmed
,
Echinobase Yajima,
The DEAD-box RNA helicase Vasa functions in embryonic mitotic progression in the sea urchin.
2011,
Pubmed
,
Echinobase Yajima,
Essential elements for translation: the germline factor Vasa functions broadly in somatic cells.
2015,
Pubmed
,
Echinobase Yajima,
Ars insulator protects transgenes from long-term silencing in sea urchin larva.
2007,
Pubmed
,
Echinobase Yajima,
Piwi regulates Vasa accumulation during embryogenesis in the sea urchin.
2014,
Pubmed
,
Echinobase Zhao,
RETINOBLASTOMA RELATED1 mediates germline entry in Arabidopsis.
2017,
Pubmed