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Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions

Open access
Wang, Jayson, Shiels, Carol, Sasieni, Peter, Wu, Pei Jun, Islam, Suhail A., Freemont, Paul S., Sheer, Denise·2004·The Journal of Cell Biology

Abstract

The promyelocytic leukemia (PML) protein is aggregated into nuclear bodies that are associated with diverse nuclear processes. Here, we report that the distance between a locus and its nearest PML body correlates with the transcriptional activity and gene density around the locus. Genes on the active X chromosome are more significantly associated with PML bodies than their silenced homologues on the inactive X chromosome. We also found that a histone-encoding gene cluster, which is transcribed only in S-phase, is more strongly associated with PML bodies in S-phase than in G0/G1 phase of the cell cycle. However, visualization of specific RNA transcripts for several genes showed that PML bodies were not themselves sites of transcription for these genes. Furthermore, knock-down of PML bodies by RNA interference did not preferentially change the expression of genes closely associated with PML bodies. We propose that PML bodies form in nuclear compartments of high transcriptional activity, but they do not directly regulate transcription of genes in these compartments.

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Metadata

Authors
Wang, J., Shiels, C., Sasieni, P., Wu, P. J., Islam, S. A., Freemont, P. S., & Sheer, D.
Venue
The Journal of Cell Biology
Published
2004-02-16
Volume
164
Issue
4
Pages
515-526
ISSN
  • 0021-9525 (ISSN-L)
  • 1540-8140
OpenAlex
W2101871282
Cited by
224
References
1
FWCI
7.65
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions. https://app.cochat.ai/papers/10.1083/jcb.200305142
The paper
Wang, J., Shiels, C., Sasieni, P., Wu, P. J., Islam, S. A., Freemont, P. S., & Sheer, D. (2004). Promyelocytic leukemia nuclear bodies associate with transcriptionally active genomic regions. The Journal of Cell Biology. https://doi.org/10.1083/jcb.200305142

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