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.2011.03.028Additional 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
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45025787
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CELL PROLIFERATION; FIBROBLASTS; HALF-LIFE; IN VIVO; INHIBITION; KNOCK-OUT REACTIONS; MESSENGER-RNA; MICE; NEOPLASMS; ONCOGENES; PHOSPHORYLATION; PROTEOLYSIS; RECEPTORS; SERINE; THREONINE
- Descriptors DEC
- AMINO ACIDS; ANIMAL CELLS; ANIMALS; CARBOXYLIC ACIDS; CHEMICAL REACTIONS; CONNECTIVE TISSUE CELLS; DECOMPOSITION; DIRECT REACTIONS; DISEASES; GENES; HYDROXY ACIDS; MAMMALS; MEMBRANE PROTEINS; NUCLEAR REACTIONS; NUCLEIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PROTEINS; RNA; RODENTS; SOMATIC CELLS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.