BA (University of Cambridge, 1989), PhD (MRC Laboratory of Molecular Biology, Cambridge, 1994)
Room 2:17 Institute of Medical Sciences Foresterhill University of Aberdeen Aberdeen AB25 2ZD Lab phone +44 (0)1224 437312
Anne Donaldson studied Natural Sciences at the University of Cambridge, completed her PhD at the MRC Laboratory of Molecular Biology, then moved as a NATO/SERC postdoctoral fellow to the University of Washington in Seattle. Anne established her lab as a Royal Society University Research Fellow at the University of Dundee, and in 2001 Anne was chosen as an EMBO Young Investigator. The Donaldson laboratory has been at the University of Aberdeen Institute of Medical Sciences since 2003. The lab is funded by Cancer Research UK.
Anne leads the 'Chromosome & Cellular Dynamics' Section within the Institute of Medical Sciences. She teaches on topics related to chromosome maintenance on several undergraduate and graduate-level courses.
Anne served as Organizer of the Cold Spring Harbor Eukaryotic DNA Replication & Genome Maintenance meeting from 2014-2019.
!!We have Postdoc and PhD positions available in the lab, funded by Cancer Research UK!!
Interested applicants please send CV to Anne Donaldson with an explanation of your interest in our research area and your related lab experience.
Human cells contain 1.8 metres of DNA in a nucleus only about 6 microns in diameter. During chromosome replication this entire length of DNA must be duplicated exactly once with perfect accuracy, so that the strands can be disentangled and precisely segregated to the daughter cells. The DNA is extremely vulnerable to damage during this process, and cells must deal with thousands of potentially lethal DNA damage events every single day. Members of the Donaldson lab investigate the controls over DNA replication and damage repair. Understanding chromosome maintenance will suggest new therapeutic strategies in the fight against cancer, as well as illuminating the basic mechanisms at the heart of the cell division cycle.
The budding yeast S. cerevisiae provides an excellent model organism for studying the fundamentals of chromosome biology, because of the remarkable molecular genetics tools available for this system. DNA replication initiates at multiple sites on each chromosome called replication origins. We use molecular genetics to understand the processes of yeast DNA replication, which we then investigate in human cells. Using this approach we have discovered several molecular mechanisms of replication control that operate throughout eukaryotic cells.
Our focus of interest is understanding the molecular machinery controlling origin initiation, replication fork progression, and chromosome maintenance. We use a combination of advanced proteomic, genomic and microscopy methods to investigate the cellular components that regulate these DNA replication and repair processes.
- Molecular Biology
- Molecular Genetics
Our research specialisms are based on the Higher Education Classification of Subjects (HECoS) which is HESA open data, published under the Creative Commons Attribution 4.0 International licence.
Funding and Grants
Cancer Research UK Programme Award (£1,561,000) ‘How does Rif1 regulate DNA replication and cell recovery after chemotherapeutic replication inhibition?' Grant to Prof Anne Donaldson & Dr Shin-ichiro Hiraga
Page 1 of 4 Results 1 to 10 of 38
Protection of nascent DNA at stalled replication forks is mediated by phosphorylation of RIF1 intrinsically disordered regioneLife, vol. 11, e75047Contributions to Journals: Articles
SAF-A promotes origin licensing and replication fork progression to ensure robust DNA replicationJournal of Cell Science, vol. 135, no. 2, jcs.258991Contributions to Journals: Articles
Protein phosphatase 1 acts as a RIF1 effector to suppress DSB resection prior to Shieldin actionCell Reports, vol. 36, no. 2, 109383Contributions to Journals: Articles
Replication timing maintains the global epigenetic state in human cellsScience, vol. 372, no. 6540, pp. 371-378Contributions to Journals: Articles
The RIF1-Long splice variant promotes G1 phase 53BP1 nuclear bodies to protect against replication stresseLife, vol. 9, e58020Contributions to Journals: Articles
Genome-wide analysis of DNA replication timing in single cells: Yes! We're all individualsGenome Biology, vol. 20, 111Contributions to Journals: Articles
Human RIF1-Protein Phosphatase 1 Prevents Degradation and Breakage of Nascent DNA on Replication StallingCell Reports, vol. 27, no. 9, pp. 2558-2566.e4Contributions to Journals: Articles
Identification of Elg1 interaction partners and effects on post-replication chromatin re-formationPLoS Genetics, vol. 14, no. 11, e1007783Contributions to Journals: Articles
Budding yeast Rif1 binds to replication origins and protects DNA at blocked replication forksEMBO reports, vol. 19, no. 9, e46222Contributions to Journals: Articles
- [ONLINE] DOI: https://doi.org/10.15252/embr.201846222
- [OPEN ACCESS] http://aura.abdn.ac.uk/bitstream/2164/11048/1/embr.201846222.full.pdf
Rif1 acts through Protein Phosphatase 1 but independent of replication timing to suppress telomere extension in budding yeastNucleic Acids Research, vol. 46, no. 8, pp. 3993-4003Contributions to Journals: Articles