Proteomics

Dataset Information

0

Acetylation of p73 in 293T cell


ABSTRACT: 293T cells ectopically expressing FLAG-tagged p73 were treated with AGK2 and p73 was immunoprecipitated. The precipitants were resuspended in deacetylation buffer (50 mM Tris-HCl pH 8.0, 140 mM NaCl, 2 mM MgCl 2 ) and incubated with recombinant SIRT2 protein (10 U). The reaction was terminated by boiling with SDS sample buffer and acetylation levels were determined by immunoblotting.

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: Tetsu Akiyama 

PROVIDER: PXD010411 | JPOST Repository | Mon Sep 10 00:00:00 BST 2018

REPOSITORIES: jPOST

Dataset's files

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Action DRS
140306iwa_Hayashi1_65min_TOP20_4ul.msf Msf
140306iwa_Hayashi1_65min_TOP20_4ul.raw Raw
140306iwa_Hayashi1_65min_TOP20_4ul.xlsx Xlsx
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Publications


Glioblastoma is one of the most aggressive forms of cancers and has a poor prognosis. Genomewide analyses have revealed that a set of core signaling pathways, the p53, RB, and RTK pathways, are commonly deregulated in glioblastomas. However, the molecular mechanisms underlying the tumorigenicity of glioblastoma are not fully understood. Here, we show that the lysine deacetylase SIRT2 is required for the proliferation and tumorigenicity of glioblastoma cells, including glioblastoma stem cells. Fu  ...[more]

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