Spatiotemporal analysis identifies ABF2 and ABF3 as key hubs of endodermal response to nitrate.

Fondo de Desarrollo de Areas Prioritarias, Center for Genome Regulation, 8370415 Santiago, Chile. Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, 8331010 Santiago, Chile. Agencia Nacional de Investigación y Desarrollo-Millennium Science Initiative Program, Millennium Institute for Integrative Biology, 7500565 Santiago, Chile. Centro de Genómica y Bioinformática, Facultad de Ciencias, Universidad Mayor, 8580745 Santiago, Chile. Escuela de Biotecnología, Facultad de Ciencias, Universidad Mayor, 8580745 Santiago, Chile. Department of Plant and Soil Sciences, Delaware Biotechnology Institute, University of Delaware, Newark, DE 19713. Centro de Biotecnología y Genómica de Plantas, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Universidad Politécnica de Madrid, 28040 Madrid, Spain. Center for Genomics and Systems Biology, New York University, New York, NY 10003. Department of Biology, Duke University, Durham, NC 27708. HHMI, Duke University, Durham, NC 27708. Fondo de Desarrollo de Areas Prioritarias, Center for Genome Regulation, 8370415 Santiago, Chile; rgutierrez@bio.puc.cl.

Proceedings of the National Academy of Sciences of the United States of America. 2022;(4)

Abstract

Nitrate is a nutrient and a potent signal that impacts global gene expression in plants. However, the regulatory factors controlling temporal and cell type-specific nitrate responses remain largely unknown. We assayed nitrate-responsive transcriptome changes in five major root cell types of the Arabidopsis thaliana root as a function of time. We found that gene-expression response to nitrate is dynamic and highly localized and predicted cell type-specific transcription factor (TF)-target interactions. Among cell types, the endodermis stands out as having the largest and most connected nitrate-regulatory gene network. ABF2 and ABF3 are major hubs for transcriptional responses in the endodermis cell layer. We experimentally validated TF-target interactions for ABF2 and ABF3 by chromatin immunoprecipitation followed by sequencing and a cell-based system to detect TF regulation genome-wide. Validated targets of ABF2 and ABF3 account for more than 50% of the nitrate-responsive transcriptome in the endodermis. Moreover, ABF2 and ABF3 are involved in nitrate-induced lateral root growth. Our approach offers an unprecedented spatiotemporal resolution of the root response to nitrate and identifies important components of cell-specific gene regulatory networks.