Affiliation:
1. Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803
Abstract
ABSTRACT
Chromosomal sites of RNA polymerase III (Pol III) transcription have been demonstrated to have “extratranscriptional” functions, as the assembled Pol III complex can act as chromatin boundaries or pause sites for replication forks, can alter nucleosome positioning or affect transcription of neighboring genes, and can play a role in sister chromatid cohesion. Several studies have demonstrated that assembled Pol III complexes block the propagation of heterochromatin-mediated gene repression. Here we show that in
Saccharomyces cerevisiae
tRNA genes (tDNAs) and even partially assembled Pol III complexes containing only the transcription factor TFIIIC can exhibit chromatin boundary functions both as heterochromatin barriers and as insulators to gene activation. Both the
TRT2
tDNA and the
ETC4
site which binds only the TFIIIC complex prevented an upstream activation sequence from activating the
GAL
promoters in our assay system, effectively acting as chromatin insulators. Additionally, when placed downstream from the heterochromatic
HMR
locus,
ETC4
blocked the ectopic spread of Sir protein-mediated silencing, thus functioning as a barrier to repression. Finally, we show that
TRT2
and the
ETC6
site upstream of
TFC6
in their natural contexts display potential insulator-like functions, and
ETC6
may represent a novel case of a Pol III factor directly regulating a Pol II promoter. The results are discussed in the context of how the TFIIIC transcription factor complex may function to demarcate chromosomal domains in yeast and possibly in other eukaryotes.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology