Award details

The novel gene 'Histone Deacetylase Complex 1' enhances plant growth and abiotic stress tolerance; where, when and with whom?

Reference	BB/K008218/1
Principal Investigator / Supervisor	Professor Anna Amtmann
Co-Investigators / Co-Supervisors
Institution	University of Glasgow
Department	College of Medical, Veterinary, Life Sci
Funding type	Research
Value (£)	331,240
Status	Completed
Type	Research Grant
Start date	01/02/2013
End date	31/01/2016
Duration	36 months

Abstract

The proposed project is based on our recent discovery of 'Histone de-acetylation complex 1' (HDC1), a novel gene from Arabidopsis thaliana. We found that over-expression of HDC1 led to hyposensitivity of germinating seeds to the 'stress' hormone ABA and to enhanced growth of mature plants, while HDC1 knockout had the opposite effects. Ancestral precursors of HDC1 in yeast are members of multi-protein histone de-acetylation (HD) complexes. Our working hypothesis is that HDC1 'titrates' the stability of a HD complex thereby modifying accessibility of the DNA to ABA-dependent transcriptional regulators and hence ABA-sensitivity. This is an exciting concept because it means that through HDC1 one could gain control over a whole suite of stress responses while maintaining the integrity of the underlying complex signalling network. However, to exploit the opportunities presented by HDC1 as an adjustable 'hormostat' we need to understand the composition of HD complexes and individual protein functions therein, both of which are completely unknown in plants. The proposed work programme will answer three questions: Does HDC1 form a multi-protein HD complex and what are the partners? Is HDC1 regulated, and how? Does HDC1 regulate other genes, and which ones? In the first work package, using pull-downs, Y2H, BiFC and molecular genetics, we will identify proteins that interact with HDC1 and characterize their functional inter-dependence. In the second work package, employing Western blots and mutants that inhibit or promote specific post-translational modifications, we will explore HDC1-regulation and its role for cross-talk between different hormonal pathways. In the third work package we will identify HDC1 target genes through microarray analysis and ChIP-Sequencing. The outcomes from this project can be expected to cause a gearshift in the way we think about endogenous and biotechnological manipulation of hormone pathways.

Summary

Climate change and a growing world population are expected to lead to water scarcity and food shortage in the near future. There is an urgent need to increase yield, water usage efficiency and stress tolerance of food crops. We propose to achieve this through controlled manipulation of plant sensitivity to the 'stress' hormone abscisic acid (ABA). The project builds on our recent discovery of a novel gene from Arabidopsis thaliana, which we called 'Histone de-acetylation complex 1' (HDC1). We found that over-expression of HDC1 led to decreased ABA-sensitivity of germinating seeds and to enhanced growth of mature plants, while deletion of HDC1 had the opposite effects. Thus HDC1 can be used as an adjustable 'hormostat'. This property makes HDC1 an attractive target for crop improvement. For example, in a drought-prone rain-fed field increasing ABA-sensitivity will aid plant recovery after dehydration whereas in an irrigated field decreasing ABA-sensitivity could be a means to sustain biomass production with reduced water input. The question is then; how does HDC1 change ABA-sensitivity? Ancestral precursors of HDC1 in yeast are members of large multi-protein complexes that biochemically modify (de-acetylate) histone proteins that are associated with DNA (chromatin). Histone de-acetylation (HD) determines the overall structure of the DNA which in turn exerts a hyper-level of control over gene activity. Our current hypothesis is that HDC1 'titrates' the stability of a chromatin complex thereby modifying accessibility of the DNA to ABA-dependent regulators and hence ABA-sensitivity. This is an exciting concept because it means that via HDC1 one could gain control over a whole suite of stress responses without the need to tinker with the underlying complex signalling network. However, to exploit the opportunities presented by HDC1 for crop improvement we need to understand exactly how HDC1 operates at the molecular level. For example, the composition of HD complexes andthe precise functions of proteins therein are completely unknown in plants. The aim of this project is to investigate the molecular function of HDC1 in the model plant Arabidopsis. This research will run in parallel to a crop development programme carried out by the Industrial Partner. Reciprocal information flow between the two research programmes will ensure that fundamental discoveries made in the model species can immediately be translated into crop improvement. The work programme has three parts. In the first work package we will use an antibody against HDC1 to identify 'by association' other members of the HDC1-complex in plant protein extracts. We will obtain mutant lines for some of the identified associates and cross them with the HDC1mutant lines. This work will lead to a first understanding of HD complexes in plants, and to the identification of proteins that limit or enhance HDC1 function within the complex. The second work package addresses the question whether HDC1 itself is regulated and how. In particular, we will investigate whether HDC1 is a target for 'hijacking' of the ABA pathways by other hormones ('cross talk') or by pathogens. For this purpose we will measure HDC1 protein levels in plant extracts treated with hormones and pathogen elicitors. In the third work package we will investigate which genes cause the effects of HDC1 on seed germination and growth - the 'targets' of HDC1. In the first instance we will identify all genes that are differentially expressed in wildtype and HDC1 mutant plants using gene chips. To identify the DNA regions that are directly targeted by HDc1 we will pull-down HDC1-associated chromatin with the HDC1-antibody. Finally, we will measure acetylation levels of the chromatin with antibodies that recognize acetylated histone tails. The combined outcomes from this work will greatly enhance our understanding of gene regulation in plants and directly contribute to improving yield and water usage efficiency in crops.

Impact Summary

A growing world population combined with unstable climate puts an urgent demand on plant scientists to apply their expertise to avert a pending food crisis. This issue is compounded by the threat of worldwide freshwater scarcity. Many communities worldwide already suffer from inadequate water supply for consumption, hygiene and irrigation. Southern parts of England regularly experience water shortages. UK government and RCUK have recognized the urgency of these problems and have made food and water security priority areas for research. The proposed project directly supports food and water security. Agriculture accounts for 70 percent of all water withdrawn from "blue water" sources. Any achievements in increasing food production must therefore be measured by the amount of water needed ('crop per drop'). Crop improvement programmes are faced with the dilemma that drought tolerance in plants usually comes at the cost of reduced growth rates due to endogenous hormonal signals that tell the plant to shift from vegetative growth towards protective mechanisms which carry a growth penalty. Recent work in the PI's laboratory has shown that over-expression of a novel gene (HDC1) in the model plant A. thaliana decreases plant sensitivity to the 'stress' hormone ABA and enhances plant growth. These results are of great interest to farmers and agri-food companies as they may provide us with a handle to titrate ABA sensitivity (in the context of intrinsic yield increase or yield preservation) and thus to achieve better growth with less water. The potential of HDC1 for improving growth and water efficiency in crops has been recognized by Bayer CropScience and their substantial financial support for this grant is evidence of the high potential impact of the proposed project. The Bayer team has already carried out independent phenotypic tests with HDC1-lines from the PI's lab and a common patent application (led by University of Glasgow) is pending. Bayer will embark on a crop focussed research programme which will progress in parallel to the fundamental research programme proposed here. Maximal impact is therefore guaranteed since both research programmes will inform and add value to each other. For instance, the enhancement or inhibition of HDC1-activity by molecular HDC1-interactors, discovered in A. thaliana, can immediately be used to fine-tune the approaches taken in the crop lines generated by Bayer. In turn, new phenotypic or molecular data generated from the crop lines may provide novel information on fundamental mechanisms to be explored in A. thaliana. Considering both the long timelines 'from gene to product' and the difficulties to translate findings from model plants to crops, early engagement of fundamental research with commercial crop research programmes, as proposed here, is crucial if we want to maximize the probability of success and avert a pending food and water crisis. The proposed project provides ample opportunities for additional gene discovery, especially among newly identified HDC1 target genes, which may encode plant growth regulators and tolerance factors. The project therefore has a strong potential for additional commercialisation opportunities, which will be aided by close interaction with the industrial partner. In case, Bayer does not exercise its option for these opportunities (e.g. outside of its crop or trait focus) then the university will be able to explore these with other agri-food companies. Research into epigenetic regulation of gene expression has gained enormous momentum over the last decade due to its fundamental importance for understanding development and adaptation to the environment not just in plants but in all organisms. The proposed project will explore the molecular properties of multi-protein complexes involved in epigenetic regulation and the results are expected to make important contributions to academic advancement in the life sciences.

Committee	Research Committee B (Plants, microbes, food & sustainability)
Research Topics	Plant Science
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	Industrial Partnership Award (IPA)

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