Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (5)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Smeds, J.
Right arrow Articles by Hemminki, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smeds, J.
Right arrow Articles by Hemminki, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Mutagenesis, Vol. 16, No. 6, 547-550, November 2001
© 2001 UK Environmental Mutagen Society/Oxford University Press

Polymorphic insertion of additional repeat within an area of direct 8 bp tandem repeats in the 5'-untranslated region of the p53R2 gene and cancer risk

Johanna Smeds,1, Rajiv Kumar and Kari Hemminki

Department of Biosciences, Karolinska Institute, Novum, 141 57 Huddinge, Sweden

p53R2 is a recently cloned gene that functions in p53-induced DNA repair. In the 5'-untranslated region of the p53R2 gene two direct tandem 8 bp repeats are located. Within the region of these 8 bp direct repeats we have detected the insertion of an additional repeat. In order to determine a possible association of this novel polymorphism with any cancer or population, we carried out genotyping of 843 European and Asian controls and patients with various cancer types. In addition, 26 cancer cell lines were included in the study. No significant difference in polymorphic frequency could be demonstrated for any of the cancer types, although the allelic frequency in melanoma patients was lower than in controls ({chi}2 = 3.28; P = 0.07; OR = 0.32; 95% CI 0.07–1.26). A significantly higher frequency of the polymorphism was detected in the compiled Caucasian individuals compared with Asians ({chi}2 = 9.19; P = 0.002; OR = 3.13; 95% CI 1.39–7.43). In one tumour cell line we observed two extra inserted copies of the 8 bp repeat. The functional effect of the insertion polymorphism on the p53R2 gene transcription remains to be determined.

1 To whom correspondence should be addressed. Email: johanna.smeds{at}cnt.ki.se


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
L. Chang, B. Zhou, S. Hu, R. Guo, X. Liu, S. N. Jones, and Y. Yen
ATM-mediated serine 72 phosphorylation stabilizes ribonucleotide reductase small subunit p53R2 protein against MDM2 to DNA damage
PNAS, November 25, 2008; 105(47): 18519 - 18524.
[Abstract] [Full Text] [PDF]


Home page
MutagenesisHome page
Z. Ye and J. M. Parry
The discovery and confirmation of single nucleotide polymorphisms in the human p53R2 gene by EST database analysis
Mutagenesis, September 1, 2002; 17(5): 361 - 364.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.