Arginine methylation catalyzed by PRMT1 is required for B cell activation and differentiation
Publication Year 2017-10-12, Volume 8, Issue #1, Page 891
Journal Title
Naure Communications
Publication Type
Journal Article
Arginine methylation catalyzed by protein arginine methyltransferases (PRMT) is a common post-translational modification in mammalian cells, regulating many important functions including cell signalling, proliferation and differentiation. Here we show the role of PRMT1 in B-cell activation and differentiation. PRMT1 expression and activity in human and mouse peripheral B cells increases in response to in vitro or in vivo activation. Deletion of the Prmt1 gene in mature B cells establishes that although the frequency and phenotype of peripheral B cell subsets seem unaffected, immune responses to T-cell-dependent and -independent antigens are substantially reduced. In vitro activation of Prmt1-deficient B cells with a variety of mitogens results in diminished proliferation, differentiation and survival, effects that are correlated with altered signal transduction from the B cell receptor. Thus PRMT1 activity in B cells is required for correct execution of multiple processes that in turn are necessary for humoral immunity.PRMT1 is an arginine methyltransferase involved in a variety of cell functions. Here the authors delete PRMT1 specifically in mature B cells to show the importance of arginine methylation for B cell proliferation, differentiation and survival, and thereby for humoral immunity.
Springer Nature
WEHI Research Division(s)
Immunology; Molecular Immunology
PubMed ID
NHMRC Grants
Rights Notice
Refer to copyright notice on published article.

Creation Date: 2017-10-16 01:59:58
Last Modified: 2017-10-16 02:58:46
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