Welcome to the web pages of Kirsten Skarstad’s group
DNA replication and chromosome dynamics
Cancer cells are characterized by loss of regulation, allowing them to go through the cell cycle in an uncontrolled fashion. We study regulation of the cell cycle, and are interested in how initiation of replication and segregation is controlled and coordinated with cell growth and cell division. We also study replication fork collapse and repair which are processes that contribute to genome instability and cancer cell development. Most of our projects are basic science projects and we use the simple model organisms Escherichia coli and Vibrio cholerae.
Current research involves:
- The mechanisms of replication fork collapse and repair
- The roles of the beta clamp and PCNA proteins in replication fork rescue
- The role of SeqA in daughter chromosome segregation
- How replication is tied to cell division?
- The role of DnaA initiator protein in control of replication frequency
K. Skarstad is professor II at the Institute of Pharmacy, University of Oslo, and is reponsible for the course FRM5810.
Department of Molecular Cell Biology, Institute for Cancer Research,
The Norwegian Radium Hospital, Oslo University Hospital, Montebello, N-0379 Oslo, Norway
Phone +47 22 78 19 82 (Kirsten Skarstad), +47 22 78 12 68 (Dept. secretary), Fax: +47 22 78 19 95
Dr. Bastian Fromm – Postdoc in Flatmark group
Sep 26, 2016
Histone marks regulate maternal-to-zygotic transition
Sep 15, 2016
Aug 29, 2016
The DnaA Protein Is Not the Limiting Factor for Initiation of Replication in Escherichia coli
PLoS Genet, 11 (6), e1005276
Dynamic Escherichia coli SeqA complexes organize the newly replicated DNA at a considerable distance from the replisome
Nucleic Acids Res, 43 (5), 2730-43