Email updates

Keep up to date with the latest news and content from BMC Plant Biology and BioMed Central.

Open Access Research article

Identification of functional cis-regulatory elements by sequential enrichment from a randomized synthetic DNA library

Mario Roccaro1*, Nahal Ahmadinejad13, Thomas Colby2 and Imre E Somssich1*

Author Affiliations

1 Department of Plant Microbe Interaction, Max Planck Institute for Plant Breeding Research, Carl-von-Linne-Weg 10, Cologne 50829, Germany

2 Mass Spectrometry Group, Max Planck Institute for Plant Breeding Research, Carl-von-Linne-Weg 10, Cologne 50829, Germany

3 Current address: INRES - Crop Bioinformatics, Universit├Ąt Bonn, Katzenburgweg 2, Bonn 53115, Germany

For all author emails, please log on.

BMC Plant Biology 2013, 13:164  doi:10.1186/1471-2229-13-164

Published: 18 October 2013

Abstract

Background

The identification of endogenous cis-regulatory DNA elements (CREs) responsive to endogenous and environmental cues is important for studying gene regulation and for biotechnological applications but is labor and time intensive. Alternatively, by taking a synthetic biology approach small specific DNA binding sites tailored to the needs of the scientist can be generated and rapidly identified.

Results

Here we report a novel approach to identify stimulus-responsive synthetic CREs (SynCREs) from an unbiased random synthetic element (SynE) library. Functional SynCREs were isolated by screening the SynE libray for elements mediating transcriptional activity in plant protoplasts. Responsive elements were chromatin immunoprecipitated by targeting the active Ser-5 phosphorylated RNA polymerase II CTD (Pol II ChIP). Using sequential enrichment, deep sequencing and a bioinformatics pipeline, candidate responsive SynCREs were identified within a pool of constitutively active DNA elements and further validated. These included bonafide biotic/abiotic stress-responsive motifs along with novel SynCREs. We tested several SynCREs in Arabidopsis and confirmed their response to biotic stimuli.

Conclusions

Successful isolation of synthetic stress-responsive elements from our screen illustrates the power of the described methodology. This approach can be applied to any transfectable eukaryotic system since it exploits a universal feature of the eukaryotic Pol II.

Keywords:
Chromatin immunoprecipitation (ChIP); Motif discovery; Plant protoplasts; Pol II CTD phosphorylation; Synthetic DNA elements