Journal
JOURNAL OF CELL BIOLOGY
Volume 194, Issue 5, Pages 721-735Publisher
ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201010118
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Funding
- Ministry of Health, Labor, and Welfare
- Japan Science and Technology Agency
- Naito Foundation
- Uehara Memorial Foundation
- Grants-in-Aid for Scientific Research [22590428] Funding Source: KAKEN
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Although pericentromeric heterochromatin is essential for chromosome segregation, its role in humans remains controversial. Dissecting the function of HIV-1-encoded Vpr, we unraveled important properties of heterochromatin during chromosome segregation. In Vpr-expressing cells, hRad21, hSgo1, and hMis12, which are crucial for proper chromosome segregation, were displaced from the centromeres of mitotic chromosomes, resulting in premature chromatid separation (PCS). Interestingly, Vpr displaced heterochromatin protein 1-alpha (HP1-alpha) and HP1-gamma from chromatin. RNA interference (RNAi) experiments revealed that down-regulation of HP1-alpha and/or HP1-gamma induced PCS, concomitant with the displacement of hRad21. Notably, Vpr stimulated the acetylation of histone H3, whereas p300 RNAi attenuated the Vpr-induced displacement of HP1-alpha and PCS. Furthermore, Vpr bound to p300 that was present in insoluble regions of the nucleus, suggesting that Vpr aberrantly recruits the histone acetyltransferase activity of p300 to chromatin, displaces HP1-alpha, and causes chromatid cohesion defects. Our study reveals for the first time centromere cohesion impairment resulting from epigenetic disruption of higher-order structures of heterochromatin by a viral pathogen.
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