DNA damage signalling recruits RREB-1 to the p53 tumour suppressor promoter

2009 ◽  
Vol 422 (3) ◽  
pp. 543-551 ◽  
Author(s):  
Hanshao Liu ◽  
Hoi Chin Hew ◽  
Zheng-Guang Lu ◽  
Tomoko Yamaguchi ◽  
Yoshio Miki ◽  
...  

Transcriptional regulation of the p53 tumour suppressor gene plays an important role in the control of the expression of various target genes involved in the DNA damage response. However, the molecular basis of this regulation remains obscure. In the present study we demonstrate that RREB-1 (Ras-responsive-element-binding protein-1) efficiently binds to the p53 promoter via the p53 core promoter element and transactivates p53 expression. Silencing of RREB-1 significantly reduces p53 expression at both the mRNA and the protein levels. Notably, disruption of RREB-1-mediated p53 transcription suppresses the expression of the p53 target genes. We also show that, upon exposure to genotoxic stress, RREB-1 controls apoptosis in a p53-dependent manner. These findings provide evidence that RREB-1 participates in modulating p53 transcription in response to DNA damage.

2016 ◽  
Vol 9 (2) ◽  
pp. 181-197 ◽  
Author(s):  
Kevin B Myant ◽  
Patrizia Cammareri ◽  
Michael C Hodder ◽  
Jimi Wills ◽  
Alex Von Kriegsheim ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-16
Author(s):  
Xianmei Meng ◽  
Na Liu ◽  
Yanbin Jia ◽  
Kerui Gong ◽  
Jingjie Zhang ◽  
...  

Background. It is pretty well known that DNA methyltransferases (DNMTs) are actively involved in abnormal cell growth. The goal of the current study is to explore the correlation between DNMT expression and colorectal adenomatous polyps (CAPs). Method. Twenty pairs of CAP samples with a diameter≥10 mm and corresponding normal colorectal mucosa (NCM) tissues from patients were used in the present study. The expression levels and activity of DNA methyltransferases (DNMTs) were measured in the CAP tissues. The global methylation and the promoter methylation level of 3 kinds of tumour suppressor gene were detected. Results. mRNA and protein levels of DNMT3B were found to be elevated in the CAP tissues compared with the control tissue. Additionally, the methylation of long interspersed nuclear elements-1 (LINE-1/L1) was decreased in the CAP tissue. Furthermore, methylation of the promoter of a tumour suppressor gene Ras association domain family 1A (RASSF1A) was increased in the CAP tissues, while the mRNA levels of RASSF1A were decreased. Conclusions. These results suggest that the overexpression of DNMT3B may contribute to a role in the genesis of CAPs through the hypomethylation of chromosomes in the whole cell and promoter hypermethylation of RASSF1A.


2008 ◽  
Vol 36 (3) ◽  
pp. 472-478 ◽  
Author(s):  
Michelle J. Nyhan ◽  
Gerald C. O'Sullivan ◽  
Sharon L. McKenna

The VHL (von Hippel–Lindau) tumour-suppressor gene is inactivated in VHL disease and in sporadic cases of CCRCC [clear-cell RCC (renal cell carcinoma)]. pVHL (VHL protein) functions as part of an E3 ubiquitin ligase complex that targets proteins for proteasomal degradation. The best-characterized substrate is HIF-α (hypoxia-inducible factor-α). Loss of pVHL and subsequent up-regulation of HIF target genes has been attributed to the highly vascular nature of these neoplasms. However, pVHL does not just function as the executioner of HIF-α. Additional functions of pVHL that may be important in preventing CCRCC tumorigenesis have been identified, including primary cilium maintenance, assembly of the extracellular matrix and roles in the stabilization of p53 and Jade-1 (gene for apoptosis and differentiation in epithelia). Current evidence indicates that pVHL probably requires additional co-operating signalling pathways for CCRCC initiation and tumorigenesis.


Nephrology ◽  
2002 ◽  
Vol 7 (1) ◽  
pp. A5-A5
Author(s):  
Little M.H ◽  
Forrest A ◽  
Grimmond S ◽  
Lindsay M ◽  
Martinez G ◽  
...  

The Lancet ◽  
2005 ◽  
Vol 365 (9464) ◽  
pp. 1026-1027
Author(s):  
A BITTON ◽  
M NEUMAN ◽  
J BARNOYA ◽  
S GLANTZ

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