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.

Department

Description

Provenance

Subjects

Animals, Caenorhabditis 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

Citation

Published Version (Please cite this version)

10.1016/j.celrep.2014.01.008

Publication Info

Maxwell, Colin S, William S Kruesi, Leighton J Core, Nicole Kurhanewicz, Colin T Waters, Caitlin L Lewarch, Igor Antoshechkin, John T Lis, et al. (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.

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Scholars@Duke

Baugh

L. Ryan Baugh

Professor of Biology

The Baugh Lab is interested in phenotypic plasticity and developmental robustness despite variable environmental conditions. We use the roundworm C. elegans to study how animals adapt to starvation over different time scales using functional genomics (bulk and single-cell) as well as statistical, quantitative, and molecular genetics. Our research questions revolve around how gene regulation and development are governed by nutrient availability, how animals acclimate to survive starvation, and the mechanisms underlying adult consequences of early life starvation. We are gaining insight into the genetic basis of natural variation among wild strains, the function of conserved tumor suppressors, epigenetic effects of starvation, and how early life experience affects adult disease. 


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