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(BBSRC DTP) Kinesin light chains: why so many?


Project Description

Kinesin-1 is a microtubule motor that moves many cargoes within cells, and this transport is crucial for life and health. It is vital in neurons, which rely on kinesin-1 to carry cargo such as secretory vesicles, mitochondria, proteins and mRNAs from the nerve cell body to the axon tip, which may be more than 1 metre away. Kinesin-1 is a tetramer of two motor subunits (KHCs) and two identical light chain polypeptides (KLCs). There are four KLC genes in vertebrates, and two in the nematode worm, C. elegans, and the different KLC proteins are highly conserved except at their C-termini, which are also subject to further alternate splicing. KLC variety therefore provides a mechanism for directing the motor to its many different cargoes. It is not known how kinesin-1 tetramers containing a single KLC isoform are assembled, but one possibility is that the mRNAs for each KLC isoform are packaged into separate, distinct mRNA granules (mRNPs) that also contain KHC mRNAs.
This project will provide an in-depth analysis of kinesin-1 function and assembly, and the role of the many different KLCs. We will use cultured human cells (non-neuronal and the neuron-like SH-SY-5Y) and the genetically tractable model organism, C. elegans. A wide range of cell and molecular biological, biochemical and genetic techniques will be used, including CRISPR/Cas9. We will image dynamic events in living cells and worms using lattice lightsheet microscopy, an advanced imaging technique that is available in only 5 UK Institutions. We will:
1. Test if the localisation of KHC and KLC mRNAs plays a part in the synthesis of kinesin-1 itself, using single molecule FISH, and assessing mRNA dynamics in live cells.
2. Investigate the hypothesis that kinesin supports protein synthesis throughout the neuron by transporting the MARS complex (the aminoacyl-tRNA synthetase complex that catalyses the attachment of amino acids to their corresponding tRNAs) to ensure a supply of tRNA for protein synthesis.
3. Determine the role of kinesin in localising the essential for neuronal pathfinding molecule NAV1 (Unc-53 in C. elegans), a microtubule plus end binding protein.
4. Investigate the function of KLCs 1 and 2 in C. elegans: do they have distinct or shared roles? Existing KLC1 and KLC2 mutants will be used to investigate the motility of kinesin-1 cargoes in vivo. The expression profile and distribution of KLCs 1 and 2 will be assessed by tagging the endogenous protein using CRISPR/Cas9.

https://www.research.manchester.ac.uk/portal/viki.allan.html
https://www.research.manchester.ac.uk/portal/gino.poulin.html
https://www.research.manchester.ac.uk/portal/mark.p.ashe.html

Entry Requirements:
Applications are invited from UK/EU nationals only. Applicants must have obtained, or be about to obtain, at least an upper second class honours degree (or equivalent) in a relevant subject.

Funding Notes

This project is to be funded under the BBSRC Doctoral Training Partnership. If you are interested in this project, please make direct contact with the Principal Supervisor to arrange to discuss the project further as soon as possible. You MUST also submit an online application form - full details on how to apply can be found on the BBSRC DTP website View Website

As an equal opportunities institution we welcome applicants from all sections of the community regardless of gender, ethnicity, disability, sexual orientation and transgender status. All appointments are made on merit.

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