Affiliation:
1. Institute of Molecular Biology, University of Oregon, Eugene, OR 97403
Abstract
Repression of facultative heterochromatin is essential for developmental processes in numerous organisms. Methylation of histone H3 lysine 27 (H3K27) by Polycomb repressive complex 2 is a prominent feature of facultative heterochromatin in both fungi and higher eukaryotes. Although this methylation is frequently associated with silencing, the detailed mechanism of repression remains incompletely understood. We utilized a forward genetics approach to identify genes required to maintain silencing at facultative heterochromatin genes in
Neurospora crassa
and identified three previously uncharacterized genes that are important for silencing:
sds3
(
NCU01599
),
rlp1
(
RPD3L protein 1
;
NCU09007
), and
rlp2
(
RPD3L protein 2
;
NCU02898
). We found that SDS3, RLP1, and RLP2 associate with
N. crassa
homologs of the
Saccharomyces cerevisiae
Rpd3L complex and are required for repression of a subset of H3K27-methylated genes. Deletion of these genes does not lead to loss of H3K27 methylation but increases acetylation of histone H3 lysine 14 at up-regulated genes, suggesting that RPD3L-driven deacetylation is a factor required for silencing of facultative heterochromatin in
N. crass
a, and perhaps in other organisms.
Funder
HHS | NIH | National Institute of General Medical Sciences
Publisher
Proceedings of the National Academy of Sciences