Published April 8, 2011 | Version v1
Journal article

STRAP regulates c-Jun ubiquitin-mediated proteolysis and cellular proliferation

  • 1. Department of Cancer Biology, Vanderbilt University, School of Medicine, Nashville, TN (United States)
  • 2. Department of Biostatistics, Vanderbilt University, School of Medicine, Nashville, TN (United States)
  • 3. Department of Surgery, Vanderbilt University, School of Medicine, Nashville, TN (United States)

Description

Highlights: → STRAP is specifically correlated with c-Jun expression and activation in fibroblasts. → STRAP inhibits c-Jun ubiquitylation in vivo and prolongs the half-life of c-Jun. → STRAP expression increases expression of the AP-1 target gene, cyclin D1, and promotes cell autonomous growth. -- Abstract: STRAP is a ubiquitous WD40 protein that has been implicated in tumorigenesis. Previous studies suggest that STRAP imparts oncogenic characteristics to cells by promoting ERK and pRb phosphorylation. While these findings suggest that STRAP can activate mitogenic signaling pathways, the effects of STRAP on other MAPK pathways have not been investigated. Herein, we report that STRAP regulates the expression of the c-Jun proto-oncogene in mouse embryonic fibroblasts. Loss of STRAP expression results in reduced phospho-c-Jun and total c-Jun but does not significantly reduce the level of two other early response genes, c-Myc and c-Fos. STRAP knockout also decreases expression of the AP-1 target gene, cyclin D1, which is accompanied by a reduction in cell growth. No significant differences in JNK activity or basal c-Jun mRNA levels were observed between wild type and STRAP null fibroblasts. However, proteasomal inhibition markedly increases c-Jun expression in STRAP knockout MEFs and STRAP over-expression decreases the ubiquitylation of c-Jun in 293T cells. Loss of STRAP accelerates c-Jun turnover in fibroblasts and ectopic over-expression of STRAP in STRAP null fibroblasts increases c-Jun expression. Collectively, our findings indicate that STRAP regulates c-Jun stability by decreasing the ubiquitylation and proteosomal degradation of c-Jun.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2011.03.028

Additional details

Identifiers

DOI
10.1016/j.bbrc.2011.03.028;
PII
S0006-291X(11)00401-3;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
407
Journal Issue
2
Journal Page Range
p. 372-377
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.