Transcription factors KANADI 1, MYB DOMAIN PROTEIN 44, and PHYTOCHROME INTERACTING FACTOR 4 regulate long intergenic noncoding RNAs expressed in Arabidopsis roots

Author:

Liu Li12ORCID,Heidecker Michel34ORCID,Depuydt Thomas12ORCID,Manosalva Perez Nicolas12ORCID,Crespi Martin34,Blein Thomas34ORCID,Vandepoele Klaas125ORCID

Affiliation:

1. Department of Plant Biotechnology and Bioinformatics, Ghent University , Technologiepark 71, 9052 Ghent , Belgium

2. VIB Center for Plant Systems Biology , Technologiepark 71, 9052 Ghent , Belgium

3. CNRS, INRAE, Institute of Plant Sciences Paris-Saclay (IPS2), Université Evry, Université Paris-Saclay , 91190 Gif-sur-Yvette , France

4. CNRS, INRAE, Institute of Plant Sciences Paris-Saclay (IPS2), Université Paris Cité , 91190 Gif-sur-Yvette , France

5. Bioinformatics Institute Ghent, Ghent University , Technologiepark 71, 9052 Ghent , Belgium

Abstract

Abstract Thousands of long intergenic noncoding RNAs (lincRNAs) have been identified in plant genomes. While some lincRNAs have been characterized as important regulators in different biological processes, little is known about the transcriptional regulation for most plant lincRNAs. Through the integration of 8 annotation resources, we defined 6,599 high-confidence lincRNA loci in Arabidopsis (Arabidopsis thaliana). For lincRNAs belonging to different evolutionary age categories, we identified major differences in sequence and chromatin features, as well as in the level of conservation and purifying selection acting during evolution. Spatiotemporal gene expression profiles combined with transcription factor (TF) chromatin immunoprecipitation (ChIP) data were used to construct a TF-lincRNA regulatory network containing 2,659 lincRNAs and 15,686 interactions. We found that properties characterizing lincRNA expression, conservation, and regulation differ between plants and animals. Experimental validation confirmed the role of 3 TFs, KANADI 1, MYB DOMAIN PROTEIN 44, and PHYTOCHROME INTERACTING FACTOR 4, as key regulators controlling root-specific lincRNA expression, demonstrating the predictive power of our network. Furthermore, we identified 58 lincRNAs, regulated by these TFs, showing strong root cell type-specific expression or chromatin accessibility, which are linked with genome-wide association studies genetic associations related to root system development and growth. The multilevel genome-wide characterization covering chromatin state information, promoter conservation, and chromatin immunoprecipitation-based TF binding, for all detectable lincRNAs across 769 expression samples, permits rapidly defining the biological context and relevance of Arabidopsis lincRNAs through regulatory networks.

Funder

Saclay Plant Sciences-SPS

China Scholarship Council

Fondation pour la Recherche Médicale

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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