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Directed control of secretory vesicle fusion

Reference	BB/K015893/1
Principal Investigator / Supervisor	Professor Michael Blatt
Co-Investigators / Co-Supervisors
Institution	University of Glasgow
Department	College of Medical, Veterinary, Life Sci
Funding type	Research
Value (£)	440,626
Status	Completed
Type	Research Grant
Start date	17/06/2013
End date	16/06/2016
Duration	36 months

Abstract

This proposal builds on our discovery of a novel set of protein-protein interactions between conserved subsets of vesicle trafficking and ion channel proteins. We have shown that the interaction is essential for channel activity, K+ uptake and growth in Arabidopsis; we have since uncovered a complementary role in facilitating secretion. Thus the activities of these proteins appear to be coordinately regulated through interaction. We have localised the binding sites on both sets of proteins, demonstrating binding in Arabidopsis and tobacco, and have confirmed that these sites are highly conserved among the orthologous proteins of land plants. For the channels - the inward-rectifying subfamily of Kv-like K+ channels of plants - the binding site localises to the voltage sensor domains (VSDs) that are known to move within the membrane in response to voltage. Coupling to membrane voltage is especially important, because the voltage both drives and reports back on the activity of all transporters at the membrane, hence governing solute accumulation and turgor. It is an obvious signal for tempering secretory traffic such as during cell expansion. We know that secretion is affected by mutant VSDs with altered voltage sensitivities. What we do not know is whether the effects on traffic depend on binding/debinding with voltage or whether, when bound, VSD conformation affects secretory activity through the partner trafficking (so-called SNARE) proteins. I am also intent on bridging the gap in knowledge between these molecular events and the effects on cell and tissue growth that we have demonstrated by uncoupling the coordination between ion transport and secretory traffic. Here I propose a combination of molecular, cell biological and physiological studies to address these issues. Regardless of the outcomes, it is clear that understanding the dynamics of these interactions will inform on the mechanisms underpinning cell turgor and volume control in plants.

Summary

Control of volume and osmolarity - and of turgor in plants and fungi - lies at the very core of cellular homeostasis in all eukaryotes. In plants and fungi, strongly electrogenic H+-ATPases, and the substantial membrane voltages they foster, drive solute accumulation to generate steep osmotic gradients and turgor pressure for cell growth. Vesicle traffic adds surface area for cell expansion and contributes to wall remodelling as the cell grows. The transport of solutes (especially of K+ ions) must be controlled in concert with secretion for survival and to determine organismal form. Despite their fundamental importance we know little of how cells coordinate the rates membrane traffic and solute transport. This proposal builds on the discovery of new subsets of secretory and transport proteins that occur in the genomes of all plants described to date and, in the few species examined, are known to interact with one another. In Arabidopsis these interactions contribute to transport regulation, osmotic solute uptake and affect growth; in tobacco uncoupling these processes leads to hypotrophic cell growth and uncontrolled tissue expansion similar to that of a number of plant diseases (e.g. clubroot in Brassicas, scab disease in potato). The findings point to a basal level of coordination between secretion and transport for co-regulation of the two processes. The findings also indicate a potential mechanism by which secretion may be controlled. The transporter binding partners - a subset of ion channels - include semi-autonomous voltage-sensor domains (VSDs) that move in response to voltage. This movement is known to activate/deactivate the channels, coordinating their activity with all other transporters in the membrane. Secretory protein binding occurs at a conserved site on the VSDs, suggesting that voltage may affect secretion directly. Coupling to membrane voltage is especially significant, because voltage reports on the activity of all solute transport across theplant plasma membrane while governing solute accumulation and, hence, cell turgor and expansion. I am very excited by these findings. They offer critical evidence of a molecular mechanism that clearly will help unravel the connection between ion transport and secretion in plant growth. Furthermore, they support an entirely new model for regulated secretory traffic that will rewrite the textbooks on membrane traffic in eukaryotic cells. Until recently VSDs were thought unique as components and modulators of a few, well-studied families of ion channels in prokaryotes and eukaryotes, and of a small group of voltage-sensitive and membrane-bound phosphatases in marine tunicates. In each of these instances, however, the VSDs are incorporated as an integral part of the native protein structure; no examples of voltage-related control through direct, VSD binding have surfaced until now. Our evidence to date suggests that voltage-driven movement of the VSDs have been 'hijacked' to function as voltage sensors for this subset of plant SNAREs. Thus my working hypothesis is that the VSDs, through their binding to the secretory protein partners, govern vesicle traffic much as they do the activity of the channels. I now propose to test key elements of this hypothesis. This project will fully characterize the voltage-dependence of VSD binding in order to assess its association with voltage-dependent channel activity and secretion. I also propose selective manipulation and analysis of the interactions between the proteins, modifying VSD movement and secretory protein binding to determine the effects on secretion. Not only will the the results further our understanding of the link between osmotic solute transport and control of cell turgor and growth in plants, but they will also yield crucial information about what is clearly an entirely new mechanism linking membrane traffic with other physiological and pathological processes in plants.

Impact Summary

This proposal is for fundamental research developing new concepts at the core of ideas emerging within the international plant and cell biology communities. The research will stimulate thinking about the interface between traffic and transport in cell growth, plant development and pathology, and it should facilitate a paradigm shift in approach. These studies will also extend recent developments by the MRB laboratory of novel assays and imaging tools for molecular interaction analyses. Thus, the research is expected to benefit fundamental researchers as well as industry through conceptual developments as well as the introduction of new technologies for the analysis of multicomponent systems. The research will feed into higher education training programmes through capacity building at the postgraduate and postdoctoral levels. Additional impact is proposed through public displays and the development of schools resources building on the background work for this proposal. Finally the research will help guide future efforts in applications to agricultural/industrial systems. MRB has established links with industrial/technology transfer partners (Agrisera, Dualsystems, Plant Bioscience) and research institutes (JHI and JIC) to take advantage of these developments. Further details of these, and additional impacts will be found in Part 1 of the Case for Support and in the attached Impact Pathways.

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	X – not Funded via a specific Funding Scheme

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