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Identification and characterization of new molecular partners for the protein arginine methyltransferase 6 (PRMT6)

LO SARDO, ALESSANDRA
•
ALTAMURA, SANDRO
•
PEGORARO, SILVIA
altro
MANFIOLETTI, GUIDALBERTO
2013
  • journal article

Periodico
PLOS ONE
Abstract
To identify in an unbiased manner substrates and potential regulators of PRMT6 we have used a yeast two-hybrid approach. We identified 36 new putative partners for PRMT6 and we validated the interaction in vivo for 7 of them. In addition, using invitro methylation assay we identified 4 new substrates for PRMT6, extending the involvement of this enzyme to other cellular processes beyond its well-established role in gene expression regulation. Holistic approaches create molecular connections that allow to test functional hypotheses. The assembly of PRMT6 protein network allowed us to formulate functional hypotheses which led to the discovery of new molecular partners for the architectural transcription factor HMGA1a, a known substrate for PRMT6, and to provide evidences for a modulatory role of HMGA1a on the methyltransferase activity of PRMT6.
DOI
10.1371/journal.pone.0053750
WOS
WOS:000313552400040
Archivio
http://hdl.handle.net/11368/2759160
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84872250137
Diritti
metadata only access
Soggetti
  • Protein arginine meth...

  • HMGA

  • yeast two-hybrid

Web of Science© citazioni
10
Data di acquisizione
Mar 17, 2024
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