Pvt1-encoded microRNAs in oncogenesis

被引:96
作者
Beck-Engeser, Gabriele B. [1 ]
Lum, Amy M. [2 ]
Huppi, Konrad [3 ]
Caplen, Natasha J. [3 ]
Wang, Bruce B. [2 ]
Wabl, Matthias [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Picobella LLC, Burlingame, CA 94010 USA
[3] NCI, Gene Silencing Sect, Genet Branch, Ctr Canc Res, Bethesda, MD 20892 USA
关键词
D O I
10.1186/1742-4690-5-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: The functional significance of the Pvt1 locus in the oncogenesis of Burkitt's lymphoma and plasmacytomas has remained a puzzle. In these tumors, Pvt1 is the site of reciprocal translocations to immunoglobulin loci. Although the locus encodes a number of alternative transcripts, no protein or regulatory RNA products were found. The recent identification of noncoding microRNAs encoded within the PVT1 region has suggested a regulatory role for this locus. Results: The mouse Pvt1 locus encodes several microRNAs. In mouse T cell lymphomas induced by retroviral insertions into the locus, the Pvt1 transcripts, and at least one of their microRNA products, mmu-miR-1204 are overexpressed. Whereas up to seven co-mutations can be found in a single tumor, in over 2,000 tumors none had insertions into both the Myc and Pvt1 loci. Conclusion: Judging from the large number of integrations into the Pvt1 locus-more than in the nearby Myc locus-Pvt1 and the microRNAs encoded by it are as important as Myc in T lymphomagenesis, and, presumably, in T cell activation. An analysis of the co-mutations in the lymphomas likely place Pvt1 and Myc into the same pathway.
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