BA (University of Cambridge, 1989), PhD (MRC Laboratory of Molecular Biology, Cambridge, 1994)
Personal Chair
- About
-
- Email Address
- a.d.donaldson@abdn.ac.uk
- Telephone Number
- +44 (0)1224 437316
- Office Address
Room 2:17 Institute of Medical Sciences Foresterhill University of Aberdeen Aberdeen AB25 2ZD Lab phone +44 (0)1224 437312
- School/Department
- School of Medicine, Medical Sciences and Nutrition
Biography
Anne Donaldson investigates how cells replicate their DNA—a process central to all life, since a complete copy of the genome must be passed to each daughter cell on every cell division. Anne’s research is funded by major grants from Cancer Research UK and the Wellcome Trust. Within the Institute of Medical Sciences Anne leads the 'Chromosome & Cellular Dynamics' Section, consisting of six research groups sharing interests in chromosome dynamics.
After her Bachelors degree in Natural Sciences at the University of Cambridge, Anne 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 where she began to study DNA replication. Anne established her lab as a Royal Society University Research Fellow at the University of Dundee, moving in 2003 to the University of Aberdeen Institute of Medical Sciences.
Anne served as Organizer of the Cold Spring Harbor Eukaryotic DNA Replication & Genome Maintenance meeting from 2014-2019, and on the Organizing Committee for the 2022 UK DNA Replication meeting.
Anne is a member of the Wellcome Trust Discovery Award Interview Committee.
Latest Publications
Dysregulated Alternative Splicing in Breast Cancer Subtypes of RIF1 and Other Transcripts
International Journal of Molecular Sciences, vol. 26, no. 15, 7308Contributions to Journals: ArticlesThe human RIF1-Long isoform interacts with BRCA1 to promote recombinational fork repair under DNA replication stress
Nature Communications, vol. 16, 5820Contributions to Journals: ArticlesCheckpoint phosphorylation sites on budding yeast Rif1 protect nascent DNA from degradation by Sgs1-Dna2
PLoS Genetics, vol. 19, no. 11, e1011044Contributions to Journals: ArticlesProtection of nascent DNA at stalled replication forks is mediated by phosphorylation of RIF1 intrinsically disordered region
eLife, vol. 11, e75047Contributions to Journals: ArticlesSAF-A promotes origin licensing and replication fork progression to ensure robust DNA replication
Journal of Cell Science, vol. 135, no. 2, jcs.258991Contributions to Journals: Articles
- Research
-
Research Overview
!!We have Postdoc and PhD positions available in the lab, funded by the Wellcome Trust and 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 molecular 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, biochemical, genomic and microscopy methods to investigate the cellular components that regulate these DNA replication and repair processes.
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
Wellcome Trust Discovery Award (£2,475,614) ‘Control of DNA Replication by Protein Dephosphorylation: the Role of Protein Phosphatase 1 and its Regulatory Interactors’
- Publications
-
Page 4 of 5 Results 31 to 40 of 42
Detection of replication origins using comparative genomics and recombinational ARS assay
DNA Replication: Methods and Protocols. Vengrova, S., Dalgaard, J. Z. (eds.). Humana Press, pp. 295-313, 19 pagesChapters in Books, Reports and Conference Proceedings: Chapters- [ONLINE] DOI: https://doi.org/10.1007/978-1-60327-815-7_16
- [ONLINE] View publication in Scopus
Release of yeast telomeres from the nuclear periphery is triggered by replication and maintained by suppression of Ku-mediated anchoring
Genes & Development, vol. 22, no. 23, pp. 3363-3374Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1101/gad.486208
Histone H3 lysine 56 acetylation by Rtt109 is crucial for chromosome positioning
Journal of Cell Biology, vol. 183, no. 4, pp. 641-651Contributions to Journals: ArticlesOriDB: a DNA replication origin database
Nucleic Acids Research, vol. 35, no. Database Issue, pp. D40-D46Contributions to Journals: ArticlesGenome-wide identification of replication origins in yeast by comparative genomics
Genes & Development, vol. 20, no. 14, pp. 1874-1879Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1101/gad.385306
The Ctf18 RFC-like complex positions yeast telomeres but does not specify their replication time
EMBO Journal, vol. 25, no. 7, pp. 1505-1514Contributions to Journals: ArticlesThe requirement of yeast replication origins for pre-replication complex proteins is modulated by transcription
Nucleic Acids Research, vol. 33, no. 8, pp. 2410-2420Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1093/nar/gki539
Shaping time: chromatin structure and the DNA replication programme
Trends in Genetics, vol. 21, pp. 444-449Contributions to Journals: Literature Reviews- [ONLINE] DOI: https://doi.org/10.1016/j.tig.2005.05.012
DNA replication: telling time with microarrays
Genome Biology, vol. 4, no. 2Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1186/gb-2003-4-2-204
Ku complex controls the replication time of DNA in telomere regions
Genes & Development, vol. 16, no. 19, pp. 2485-2490Contributions to Journals: Articles- [ONLINE] DOI: https://doi.org/10.1101/gad.231602