RNA-dependent stabilization of SUV39H1 at constitutive heterochromatin.
Abstract
Heterochromatin formed by the SUV39 histone methyltransferases represses transcription
from repetitive DNA sequences and ensures genomic stability. How SUV39 enzymes localize
to their target genomic loci remains unclear. Here, we demonstrate that chromatin-associated
RNA contributes to the stable association of SUV39H1 with constitutive heterochromatin
in human cells. We find that RNA associated with mitotic chromosomes is concentrated
at pericentric heterochromatin, and is encoded, in part, by repetitive α-satellite
sequences, which are retained in cis at their transcription sites. Purified SUV39H1
directly binds nucleic acids through its chromodomain; and in cells, SUV39H1 associates
with α-satellite RNA transcripts. Furthermore, nucleic acid binding mutants destabilize
the association of SUV39H1 with chromatin in mitotic and interphase cells - effects
that can be recapitulated by RNase treatment or RNA polymerase inhibition - and cause
defects in heterochromatin function. Collectively, our findings uncover a previously
unrealized function for chromatin-associated RNA in regulating constitutive heterochromatin
in human cells.
Type
ConferenceSubject
SUV39H1cell biology
chromatin
chromosomes
genes
heterochromatin
histone methylation
human
noncoding RNA
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https://hdl.handle.net/10161/15324Published Version (Please cite this version)
10.7554/eLife.25299Collections
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Show full item recordScholars@Duke
Beth Ann Sullivan
Professor of Molecular Genetics and Microbiology
Research in the Sullivan Lab is focused on chromosome organization, with a specific
emphasis on the genomics and epigenetics of the chromosomal locus called the centromere
and the formation and fate of chromosome abnormalities that are associated with birth
defects, reproductive abnormalities, and cancer. The centromere is a specialized chromosomal
site involved in chromosome architecture and movement, kinetochore function, heterochromatin
assembly, and sister chromatid cohesion.Our

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