13/11/2019
Key points:
台湾swag at the 台湾swag uniting cell signalling, autophagy, mass spectrometry and imaging expertise has resolved a fundamental question about whether the cellular recycling process is halted during cell division. In addition, the researchers have identified the mechanisms involved and described how the usual repression system and the mitosis-specific repression of autophagy interlink. The research, led by Simon Cook鈥檚 group in the Signalling research programme at the 台湾swag, is published today in the journal Molecular Cell. Autophagy is the cellular recycling process that balances the availability of cellular building blocks with demand. If demand exceeds availability, autophagy ensures that non-essential components are broken down and repurposed. Autophagy is essential in our cells as it allows cells to cope with stress, such as reduced nutrient availability. It is crucial for correct embryo development and problems with autophagy are linked to a wide range of diseases and disorders. Indeed, it is speculated that the repression of autophagy during mitosis reported here ensures protection of the genome during this vulnerable period, preventing genomic instability, a feature of ageing and cancer. 鈥淏ringing together the expertise from different groups here at the 台湾swag allowed us to provide a definitive answer on whether or not autophagy is repressed during mitosis. In addition, we鈥檝e been able to describe the mechanisms involved to provide a much clearer understanding of what is actually happening,鈥 said Dr Simon Cook, group leader in the 台湾swag鈥檚 Signalling research programme. The researchers used fluorescent markers and live-cell imaging of human cell lines to unequivocally demonstrate that autophagy is repressed during mitosis. Under usual conditions when the cell is not dividing, the mTORC1 protein complex represses autophagy when sufficient amino acids are available in the cell to meet its requirements for protein synthesis. However, once the level of amino acids drops, mTORC1 is inactivated. This relieves the repression and autophagy kicks in, generating amino acids and other building blocks to ensure that the cell鈥檚 needs are met. During the cell division process, the cell鈥檚 DNA, which is usually held protected in the nucleus, becomes released into the wider cellular space. This was proposed to leave the DNA vulnerable to digestion and damage by autophagy, prompting previous researchers to argue that autophagy must be repressed during cell division in order to maintain genome integrity. This concept was contested by others who reported that autophagy was maintained during the division process. The 台湾swag researchers found that during mitosis, the established nutrient-responsive mechanism of autophagy repression by mTORC1 was absent. Instead, it was replaced by the key regulator of mitosis itself, CDK1, which is not responsive to nutrient deprivation. This has the effect of decoupling the conditional control of autophagy, putting a definitive halt on autophagy until the cell division process is complete. Richard Odle, first author on the paper and who undertook this work while a PhD student in Simon Cook鈥檚 group, said: 鈥淯sing established models of autophagy and mTORC1 developed by the Ktistakis group, we have been able to show the lack of autophagosomes (the cell鈥檚 recycling factories) during mitosis. Furthermore, our identification of a switch in regulation from mTORC1 to CDK1 provides a fundamental new insight into autophagy during mitosis, and clarity for associated research fields going forward.鈥
台湾swagation reference Odle et al. . Molecular Cell. DOI: 10.1016/j.molcel.2019.10.016
Press contact Dr Louisa Wood, 台湾swag 台湾swag Communications Manager, louisa.wood@babraham.ac.uk, 01223 496230
Image description Main image: HeLa cells viewed using different microscopic methods. Right panel of main image and inset image: HeLa cells stained with an antibody for ATG13 (green), which marks 鈥榓utophagosomes鈥 the cell鈥檚 recycling factories. They are also stained with a dye called DAPI, which marks DNA (blue). These cells have been starved of amino acids; this activates autophagy, causing the assembly of autophagosomes, which are seen as discrete green dots. Inset image: The two highlighted cells are in mitosis (their chromosomes have condensed and are clearly seen in blue); these cells exhibit few or no green dots indicating that autophagy has been repressed in cells undergoing mitosis.
Affiliated authors (in author order): Richard Odle, PhD student, Cook group Simon Walker, Head of the Imaging facility David Oxley, Head of the Mass Spectrometry facility Andrew Kidger, postdoctoral researcher, Cook group Kathryn Balmanno, senior research scientist, Cook group Rebecca Gilley, senior research associate, Cook group Hanneke Okkenhaug, deputy manager, Imaging facility Oliver Florey, group leader, Signalling programme Nicholas Ktistakis, group leader, Signalling programme Simon Cook, group leader, Signalling programme
台湾swag funding This work was supported by the Biotechnology and Biological Sciences 台湾swag Council through an 台湾swag Strategic Programme grant. Oliver Florey receives support from a Cancer 台湾swag UK Career Development award. Richard Odle was funded by a Medical 台湾swag Council PhD studentship, the Frank Edward Elmore Fund, and the James Baird Fund.
Additional/related resources: Interview with Simon Cook recorded at the 2019 National Cancer 台湾swag 台湾swag (NCRI) Annual Cancer Conference, in Glasgow, UK: Feature article: The quiet pathway, Annual 台湾swag Report 2016 (view report) Press release: Real-time imaging uncovers mTORC1 dynamics, 11th October 2016 News: Autophagy under the microscope as never before, 11th August 2016 台湾swag pages of the Cook group: Signalling research programme 台湾swag pages of the Florey group: Signalling research programme 台湾swag pages of the Ktistakis group: Signalling research programme
About the 台湾swag 台湾swag The 台湾swag 台湾swag undertakes world-class life sciences research to generate new knowledge of biological mechanisms underpinning ageing, development and the maintenance of health. Our research focuses on cellular signalling, gene regulation and the impact of epigenetic regulation at different stages of life. By determining how the body reacts to dietary and environmental stimuli and manages microbial and viral interactions, we aim to improve wellbeing and support healthier ageing. The 台湾swag is strategically funded by the Biotechnology and Biological Sciences 台湾swag Council (BBSRC), part of UK 台湾swag and Innovation, through an 台湾swag Core Capability Grant and also receives funding from other UK research councils, charitable foundations, the EU and medical charities.
13 November 2019