Protein arginine methyltransferase Prmt5-Mep50 methylates histones H2A and H4 and the histone chaperone nucleoplasmin in Xenopus laevis eggs

Carola Wilczek, Raghu Chitta, Eileen Woo, Jeffrey Shabanowitz, Brian T. Chait, Donald F. Hunt, David Shechter

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Histone proteins carry information contained in post-translational modifications. Eukaryotic cells utilize this histone code to regulate the usage of the underlying DNA. In the maturing oocytes and eggs of the frog Xenopus laevis, histones are synthesized in bulk in preparation for deposition during the rapid early developmental cell cycles. During this key developmental time frame, embryonic pluripotent chromatin is established. In the egg, non-chromatin-bound histones are complexed with storage chaperone proteins, including nucleoplasmin. Here we describe the identification and characterization of a complex of the protein arginine methyltransferase 5 (Prmt5) and the methylosome protein 50 (Mep50) isolated from Xenopus eggs that specifically methylates predeposition histones H2A/H2A.X-F and H4 and the histone chaperone nucleoplasmin on a conserved motif (GRGXK). We demonstrate that nucleoplasmin (Npm), an exceedingly abundant maternally deposited protein, is a potent substrate for Prmt5-Mep50 and is monomethylated and symmetrically dimethylated at Arg-187. Furthermore, Npm modulates Prmt5-Mep50 activity directed toward histones, consistent with a regulatory role for Npm in vivo. We show that H2A and nucleoplasmin methylation appears late in oogenesis and is most abundant in the laid egg. We hypothesize that these very abundant arginine methylations are constrained to premid blastula transition events in the embryo and therefore may be involved in the global transcriptional repression found in this developmental time frame.

Original languageEnglish (US)
Pages (from-to)42221-42231
Number of pages11
JournalJournal of Biological Chemistry
Volume286
Issue number49
DOIs
StatePublished - Dec 9 2011

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Nucleoplasmins
Histone Chaperones
Protein-Arginine N-Methyltransferases
Xenopus laevis
Histones
Eggs
Proteins
Methylation
Ovum
Histone Code
Blastula
Oogenesis
Eukaryotic Cells
Post Translational Protein Processing
Anura
Chromatin
Oocytes
Arginine
Cell Cycle
Embryonic Structures

ASJC Scopus subject areas

  • Biochemistry
  • Cell Biology
  • Molecular Biology

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Protein arginine methyltransferase Prmt5-Mep50 methylates histones H2A and H4 and the histone chaperone nucleoplasmin in Xenopus laevis eggs. / Wilczek, Carola; Chitta, Raghu; Woo, Eileen; Shabanowitz, Jeffrey; Chait, Brian T.; Hunt, Donald F.; Shechter, David.

In: Journal of Biological Chemistry, Vol. 286, No. 49, 09.12.2011, p. 42221-42231.

Research output: Contribution to journalArticle

Wilczek, Carola ; Chitta, Raghu ; Woo, Eileen ; Shabanowitz, Jeffrey ; Chait, Brian T. ; Hunt, Donald F. ; Shechter, David. / Protein arginine methyltransferase Prmt5-Mep50 methylates histones H2A and H4 and the histone chaperone nucleoplasmin in Xenopus laevis eggs. In: Journal of Biological Chemistry. 2011 ; Vol. 286, No. 49. pp. 42221-42231.
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