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The Arabidopsis Mediator complex subunits MED16, MED14 and MED2 regulate Mediator and RNA polymerase II recruitment to CBF-responsive cold-regulated genes.

Hemsley, P.A. and Hurst, C.H. and Kaliyadasa, E. and Lamb, R. and Knight, M.R. and De Cothi, E.A. and Steele, J.F. and Knight, H. (2014) 'The Arabidopsis Mediator complex subunits MED16, MED14 and MED2 regulate Mediator and RNA polymerase II recruitment to CBF-responsive cold-regulated genes.', Plant cell., 26 (1). pp. 465-484.

Abstract

The Mediator16 (MED16; formerly termed SENSITIVE TO FREEZING6 [SFR6]) subunit of the plant Mediator transcriptional coactivator complex regulates cold-responsive gene expression in Arabidopsis thaliana, acting downstream of the C-repeat binding factor (CBF) transcription factors to recruit the core Mediator complex to cold-regulated genes. Here, we use loss-of-function mutants to show that RNA polymerase II recruitment to CBF-responsive cold-regulated genes requires MED16, MED2, and MED14 subunits. Transcription of genes known to be regulated via CBFs binding to the C-repeat motif/drought-responsive element promoter motif requires all three Mediator subunits, as does cold acclimation–induced freezing tolerance. In addition, these three subunits are required for low temperature–induced expression of some other, but not all, cold-responsive genes, including genes that are not known targets of CBFs. Genes inducible by darkness also required MED16 but required a different combination of Mediator subunits for their expression than the genes induced by cold. Together, our data illustrate that plants control transcription of specific genes through the action of subsets of Mediator subunits; the specific combination defined by the nature of the stimulus but also by the identity of the gene induced.

Item Type:Article
Additional Information:Open access to the published version of this article and to supplemental data is available from the publisher's website: http://www.plantcell.org/content/early/2014/01/09/tpc.113.117796.short?rss=1
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Status:Peer-reviewed
Publisher Web site:http://dx.doi.org/10.1105/tpc.113.117796
Date accepted:17 December 2013
Date deposited:09 August 2016
Date of first online publication:10 January 2014
Date first made open access:09 August 2016

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