The twist gene is a common target of retroviral integration and transcriptional deregulation in experimental nephroblastoma
Language English Country England, Great Britain Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
12569359
DOI
10.1038/sj.onc.1206105
PII: 1206105
Knihovny.cz E-resources
- MeSH
- 5' Untranslated Regions MeSH
- Transcription, Genetic physiology MeSH
- Virus Integration genetics MeSH
- Nuclear Proteins genetics MeSH
- Cloning, Molecular MeSH
- Chickens genetics MeSH
- Chick Embryo MeSH
- Polymerase Chain Reaction MeSH
- Promoter Regions, Genetic MeSH
- Gene Expression Regulation, Viral physiology MeSH
- Gene Expression Regulation, Neoplastic physiology MeSH
- Retroviridae genetics MeSH
- Twist-Related Protein 1 MeSH
- Transcription Factors * MeSH
- Up-Regulation MeSH
- Wilms Tumor genetics MeSH
- Animals MeSH
- Check Tag
- Chick Embryo MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 5' Untranslated Regions MeSH
- Nuclear Proteins MeSH
- Twist-Related Protein 1 MeSH
- Transcription Factors * MeSH
The genes involved in the transformation of kidney blastema cells were searched for in avian nephroblastomas induced by the MAV2 retrovirus. The twist gene was identified as a common site of provirus integration in tumor cells. Twist was rearranged by the MAV2 provirus in three out of 76 independent nephroblastoma samples. The MAV2 integration sites were localized within 40 nucleotides of the twist 5'UTR region, right upstream from the ATG initiation codon. The integrated proviruses were deleted at their 5'ends. As a consequence, twist transcription became controlled by the retroviral 3'LTR promoter and was strongly upregulated, more than 200 times. In addition, 2-100 times elevated twist transcription was also detected in the majority of other nephroblastoma samples not containing MAV2 in the twist locus. We propose that chicken nephroblastoma originates from a single blastemic cell in which the MAV retrovirus, through its integration, has deregulated specific combinations of genes controlling proliferation and differentiation. The activation of the twist gene expression appears to contribute to tumorigenesis, as there is an in vivo positive selection of tumor cell clones containing the twist gene hyperactivated by MAV2 sequences inserted within the twist promoter.
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