| Literature DB >> 27012206 |
Claudia Solari1, Camila Vázquez Echegaray2, Carlos Luzzani3, María Soledad Cosentino4, Ariel Waisman5, María Victoria Petrone6, Marcos Francia7, Alina Sassone8, Jésica Canizo9, Gustavo Sevlever10, Lino Barañao11, Santiago Miriuka12, Alejandra Guberman13.
Abstract
Addition of methyl groups to arginine residues is catalyzed by a group of enzymes called Protein Arginine Methyltransferases (Prmt). Although Prmt1 is essential in development, its paralogue Prmt8 has been poorly studied. This gene was reported to be expressed in nervous system and involved in neurogenesis. In this work, we found that Prmt8 is expressed in mouse embryonic stem cells (ESC) and in induced pluripotent stem cells, and modulated along differentiation to neural precursor cells. We found that Prmt8 promoter activity is induced by the pluripotency transcription factors Oct4, Sox2 and Nanog. Moreover, endogenous Prmt8 mRNA levels were reduced in ESC transfected with Sox2 shRNA vector. As a whole, our results indicate that Prmt8 is expressed in pluripotent stem cells and its transcription is modulated by pluripotency transcription factors. These findings suggest that besides its known function in nervous system, Prmt8 could play a role in pluripotent stem cells.Entities:
Keywords: Embryonic stem cells; Induced pluripotent stem cells; Nanog; Oct4; Prmt8; Sox2
Mesh:
Substances:
Year: 2016 PMID: 27012206 DOI: 10.1016/j.bbrc.2016.03.077
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575