Published June 3, 2011 | Version v1
Journal article

The activation of p38 MAPK primarily contributes to UV-induced RhoB expression by recruiting the c-Jun and p300 to the distal CCAAT box of the RhoB promoter

  • 1. Department of Microbiology, Chungnam National University, Daejeon 305-764 (Korea, Republic of)
  • 2. Genome Research Center, KRIBB, Daejeon 305-806 (Korea, Republic of)
  • 3. Laboratory of Cytogenetics and Tissue Regeneration, KIRAMS, Seoul 139-706 (Korea, Republic of)
  • 4. Functional Genomics, Korea University of Science and Technology, Daejeon 305-350 (Korea, Republic of)

Description

Highlights: → Regulation of transcriptional activation of RhoB is still unclear. → We examine the effect of p38 MAPK inhibition, and c-Jun and RhoB depletion on UV-induced RhoB expression and apoptosis. → We identify the regions of RhoB promoter necessary to confer UV responsiveness using pRhoB-luciferase reporter assays. → c-Jun, ATF2 and p300 are dominantly associated with NF-Y on the distal CCAAT box. → The activation of p38 MAPK primarily contribute to UV-induced RhoB expression by recruiting the c-Jun and p300 proteins on distal CCAAT box of RhoB promoter. -- Abstract: The Ras-related small GTP-binding protein RhoB is rapidly induced in response to genotoxic stresses caused by ionizing radiation. It is known that UV-induced RhoB expression results from the binding of activating transcription factor 2 (ATF2) via NF-Y to the inverted CCAAT box (-23) of the RhoB promoter. Here, we show that the association of c-Jun with the distal CCAAT box (-72) is primarily involved in UV-induced RhoB expression and p38 MAPK regulated RhoB induction through the distal CCAAT box. UV-induced RhoB expression and apoptosis were markedly attenuated by pretreatment with the p38 MAPK inhibitor. siRNA knockdown of RhoB, ATF2 and c-Jun resulted in decreased RhoB expression and eventually restored the growth of UV-irradiated Jurkat cells. In the reporter assay using luciferase under the RhoB promoter, inhibition of RhoB promoter activity by the p38 inhibitor and knockdown of c-Jun using siRNA occurred through the distal CCAAT box. Immunoprecipitation and DNA affinity protein binding assays revealed the association of c-Jun and p300 via NF-YA and the dissociation of histone deacetylase 1 (HDAC1) via c-Jun recruitment to the CCAAT boxes of the RhoB promoter. These results suggest that the activation of p38 MAPK primarily contributes to UV-induced RhoB expression by recruiting the c-Jun and p300 proteins to the distal CCAAT box of the RhoB promoter in Jurkat cells.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2011.04.121

Additional details

Identifiers

DOI
10.1016/j.bbrc.2011.04.121;
PII
S0006-291X(11)00728-5;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
409
Journal Issue
2
Journal Page Range
p. 211-216
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45025852
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
APOPTOSIS; BIOLOGICAL STRESS; CELL PROLIFERATION; DISSOCIATION; DNA; GENE REGULATION; INHIBITION; IRRADIATION; LUCIFERASE; PROMOTERS; TRANSCRIPTION FACTORS; ULTRAVIOLET RADIATION
Descriptors DEC
ELECTROMAGNETIC RADIATION; ENZYMES; NUCLEIC ACIDS; ORGANIC COMPOUNDS; OXIDASES; OXIDOREDUCTASES; PROTEINS; RADIATIONS

Optional Information

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