Lethal Phenotype-Based Database Screening Identifies Ceramide as a Negative Regulator of Primitive Streak Formation

Author:

Pu Jing1,Kofuji Satoshi1ORCID,Okamoto-Uchida Yoshimi1,Danzaki Keiko1,Yu Ruoxing1,Suzuki Akira2,Kitajima Satoshi3,Nishina Hiroshi1

Affiliation:

1. Department of Developmental and Regenerative Biology, Medical Research Institute, Tokyo Medical and Dental University , Tokyo , Japan

2. Division of Molecular and Cellular Biology, Kobe University Graduate School of Medicine , Kobe , Japan

3. Division of Cellular and Molecular Toxicology, Center for Biological Safety and Research, National Institute of Health Sciences , Kawasaki , Japan

Abstract

Abstract In early embryogenesis, the primitive streak (PrS) generates the mesendoderm and is essential for organogenesis. However, because the PrS is a minute and transient tissue, elucidating the mechanism of its formation has been challenging. We performed comprehensive screening of 2 knockout mouse databases based on the fact that failure of PrS formation is lethal. We identified 812 genes involved in various cellular functions and responses that might be linked to PrS formation, with the category of greatest abundance being “Metabolism.” In this study, we focused on genes of sphingolipid metabolism and investigated their roles in PrS formation using an in vitro mouse ES cell differentiation system. We show here that elevated intracellular ceramide negatively regulates gene expression essential for PrS formation and instead induces neurogenesis. In addition, sphingosine-1-phosphate (a ceramide derivative) positively regulates neural maturation. Our results indicate that ceramide regulates both PrS formation and the induction of neural differentiation.

Funder

JSPS

Ministry of Health, Labour and Welfare

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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