Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression

Polycomb repressor complex 2 (PRC2) tri-methylates histone 3 at lysine 27 (H3K27me3), a post translational modification that induces heterochromatin formation and transcriptional repression. Survivin (also known as BIRC5) is a nucleocytoplasmic shuttling protein that is kept out of the nucleus in clement conditions, but that accumulates there in times of stress and in certain specialised cells. Although the cytoplasmic functions of survivin are well documented, there is comparatively less understanding of its roles within the nucleus. Here, we investigated whether nuclear survivin can affect transcriptional programming. Using interaction analyses and qPCR, we report that it binds to the enzymatic subunit of PRC2 (EZH2) and H3K27me3, and causes depression of its target genes in a variety of human cells.

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Publication Details

Journal
Journal of Cell Science
Published
2026-01-30
DOI
https://doi.org/10.1242/jcs.264572
Citations
1
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
22.24

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article

Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression

Sally P. Wheatley, Alexander J. Fezovich, Adesh D. Vaidya
1 citations
Journal of Cell Science
Genomics and Chromatin Dynamics
22.24
article

Interplay between nuclear survivin and the PRC2 complex and its impact on H3K27me3-directed transcriptional repression

Sally P. Wheatley, Alexander J. Fezovich, Adesh D. Vaidya
article en
1 citations

Abstract

Polycomb repressor complex 2 (PRC2) tri-methylates histone 3 at lysine 27 (H3K27me3), a post translational modification that induces heterochromatin formation and transcriptional repression. Survivin (also known as BIRC5) is a nucleocytoplasmic shuttling protein that is kept out of the nucleus in clement conditions, but that accumulates there in times of stress and in certain specialised cells. Although the cytoplasmic functions of survivin are well documented, there is comparatively less understanding of its roles within the nucleus. Here, we investigated whether nuclear survivin can affect transcriptional programming. Using interaction analyses and qPCR, we report that it binds to the enzymatic subunit of PRC2 (EZH2) and H3K27me3, and causes depression of its target genes in a variety of human cells.

Journal of Cell ScienceVol. 139(12)
University of Nottingham (GB)
Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 2%
Genomics and Chromatin Dynamics
22.24
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