Nutrient signaling integrates and coordinates gene expression, metabolism and growth. In multicellular organisms, growth factors and hormones are ineffective in growth promotion without the support of nutrient signaling networks. However, surprisingly little is known about the primary nutrient signaling mechanisms in plants and animals. Plants play a central role in bridging the conversion of inorganic nitrogen to organic nitrogen in the global nitrogen cycle by assimilating inorganic nitrate to generate amino acids, nucleic acids, and organic nitrogen-carbon molecules, which are essential to build and sustain lives from plants and humans. Despite the fundamental and multifaceted regulatory roles of nitrate in gene expression, metabolism, growth and development, the molecular and cellular mechanisms of nitrate signaling remain mostly elusive in multicellular plants. Hampered by gene redundancy and mutant lethality, classical genetic screens had limited success for identifying key nitrate signaling components in plants over the past two decades. By taking integrated molecular, cellular, biochemical, functional genomic, chemical genetic and systems analyses, we have discovered a surprising molecular link between specific Ca2+-sensor protein kinases (CPKs) and the NODULE INCEPTION-LIKE PROTEIN (NLP) transcription factors as the primary regulators of the nitrate-signaling network in plants. Our research has demonstrated the unique role of nitrate as a central signaling molecule in transcriptome reprograming and shoot- root coordination to shape organ biomass and architecture. We propose to build on our new findings and innovative experimental platforms to elucidate the molecular and cellular basis of the nutrient-growth network that orchestrates system-wide transcription and modulates plant developmental processes. We will implement complementary strategies and methodologies to advance our understanding of nutrient signaling mechanisms via elucidating the biological functions of Ca2+-CPK signaling in nutrient-coupled transcription responses essential to all life forms. We will analyze the nitrate sensing and signaling mechanism by transporters/sensors, and uncover the cellular and molecular mechanism of novel nitrate signaling components. The proposed research on unraveling the signaling mechanisms mediated by the nitrate-CPK-NLP relay, transporter/sensor, and novel nutrient regulators will establish new paradigms in nutrient-mediated transcriptional and developmental regulation with sustained scientific impact beyond plant biology.
Aim 1. Elucidate the nitrate-CPK-NLP signaling relay in plant nutrient-growth network Aim 2. Analyze nitrate nutrient sensing and signaling mechanisms Aim 3. Uncover the molecular and cellular action of novel nitrate signaling components

Public Health Relevance

Our discovery on the nitrate signaling network controlled by two groups of evolutionarily conserved master regulators, the Ca2+-sensor/transducer CPKs and the NLP transcription factors, will help uncover the poorly understood molecular links in nutrient regulation of transcription, metabolism and organ growth in plants, which are the core to agricultural and bioenergy productivity for sustaining human life and the ecosystems on the planet. The new concepts and mechanisms revealed from nutrient-coupled Ca2+ signaling represent a paradigm shift in current research on nutrient regulation in multicellular organisms from plants to humans, and may aid the elucidation of transcriptional networks coupling metabolic regulation and organ growth pivotal to the health, longevity and diseases of animals and humans. As plants play a central role in bridging the conversion of inorganic nitrogen to organic nitrogen in the global nitrogen cycle, the proposed studies will lead to fundamental knowledge with sustained impact on nutrient signaling central to plant biology, environmental protection and human nutrient and health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM129093-02
Application #
9735314
Study Section
Cellular Signaling and Regulatory Systems Study Section (CSRS)
Program Officer
Reddy, Michael K
Project Start
2018-07-01
Project End
2022-05-31
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
2
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02114