Pol II docking and pausing at growth and stress genes in C. elegans.
Abstract
Fluctuations in nutrient availability profoundly impact gene expression. Previous
work revealed postrecruitment regulation of RNA polymerase II (Pol II) during starvation
and recovery in Caenorhabditis elegans, suggesting that promoter-proximal pausing
promotes rapid response to feeding. To test this hypothesis, we measured Pol II elongation
genome wide by two complementary approaches and analyzed elongation in conjunction
with Pol II binding and expression. We confirmed bona fide pausing during starvation
and also discovered Pol II docking. Pausing occurs at active stress-response genes
that become downregulated in response to feeding. In contrast, "docked" Pol II accumulates
without initiating upstream of inactive growth genes that become rapidly upregulated
upon feeding. Beyond differences in function and expression, these two sets of genes
have different core promoter motifs, suggesting alternative transcriptional machinery.
Our work suggests that growth and stress genes are both regulated postrecruitment
during starvation but at initiation and elongation, respectively, coordinating gene
expression with nutrient availability.
Type
Journal articleSubject
AnimalsCaenorhabditis elegans
Chromatin Immunoprecipitation
Gene Expression Regulation, Developmental
Genes, Helminth
Mutation
Promoter Regions, Genetic
RNA Caps
RNA Polymerase II
RNA, Helminth
Sequence Analysis, RNA
Stress, Physiological
Transcription Initiation Site
Transcription, Genetic
Transcriptional Elongation Factors
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https://hdl.handle.net/10161/10399Published Version (Please cite this version)
10.1016/j.celrep.2014.01.008Publication Info
Maxwell, Colin S; Kruesi, William S; Core, Leighton J; Kurhanewicz, Nicole; Waters,
Colin T; Lewarch, Caitlin L; ... Baugh, L Ryan (2014). Pol II docking and pausing at growth and stress genes in C. elegans. Cell Rep, 6(3). pp. 455-466. 10.1016/j.celrep.2014.01.008. Retrieved from https://hdl.handle.net/10161/10399.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
L. Ryan Baugh
Associate Professor of Biology
The Baugh Lab is interested in phenotypic plasticity and physiological adaptation
to variable environmental conditions. We are using the roundworm C. elegans to understand
how animals adapt to starvation using primarily genetic and genomic approaches. We
are studying how development is governed by nutrient availability, how animals survive
starvation, and the long-term consequences of starvation including adult disease and
transgenerational epigenetic inheritance.

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