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Published on: January 26, 2018
The Lysine Methylase SMYD3 Modulates Mesendodermal Commitment during Development
Raffaella Fittipaldi1, Pamela Floris1, Valentina Proserpio1,2
1Department of Biosciences, University of Milan, Via Celoria 26, 20133 Milan, Italy.
Abstract:
SMYD3 (SET and MYND domain containing protein 3) is a methylase over-expressed in cancer cells and involved in oncogenesis. While several studies uncovered key functions for SMYD3 in cancer models, the SMYD3 role in physiological conditions has not been fully elucidated yet. Here, we dissect the role of SMYD3 at early stages of development, employing mouse embryonic stem cells (ESCs) and zebrafish as model systems. We report that SMYD3 depletion promotes the induction of the mesodermal pattern during in vitro differentiation of ESCs and is linked to an upregulation of cardiovascular lineage markers at later stages. In vivo, smyd3 knockdown in zebrafish favors the upregulation of mesendodermal markers during zebrafish gastrulation. Overall, our study reveals that SMYD3 modulates levels of mesendodermal markers, both in development and in embryonic stem cell differentiation.
Insights
SET and MYND domain containing protein 3 (SMYD3) regulates mesendodermal markers during early development. This study reveals SMYD3
Area of Science:
- Developmental Biology
- Epigenetics
- Cancer Biology
Background:
- SET and MYND domain containing protein 3 (SMYD3) is a methylase implicated in oncogenesis and overexpressed in cancer.
- Its role in normal physiological development remains largely uncharacterized.
Purpose of the Study:
- To investigate the function of SMYD3 during early embryonic development.
- To elucidate the role of SMYD3 in embryonic stem cell differentiation and zebrafish development.
Main Methods:
- Utilized mouse embryonic stem cells (ESCs) for in vitro differentiation studies.
- Employed zebrafish as an in vivo model system for genetic knockdown experiments.
Main Results:
- SMYD3 depletion in ESCs promoted mesodermal pattern induction and upregulated cardiovascular lineage markers.
- Knockdown of SMYD3 in zebrafish led to increased mesendodermal marker expression during gastrulation.
Conclusions:
- SMYD3 plays a crucial role in modulating mesendodermal marker levels during early development.
- These findings highlight a novel function for SMYD3 in developmental processes beyond its known oncogenic roles.
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