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 Cell Biology, Institute for Cancer Research,
The Norwegian Radium Hospital, Oslo University Hospital, Montebello, N-0310 Oslo, Norway
Phone +47 22 78 19 82 (Kirsten Skarstad), +47 22 78 12 68 (Dept. secretary), Fax: +47 22 78 19 95
“Linking genotype to phenotype in cancer: proteostasis and metabolic reprogramming"
Sep 12, 2014
The Escherichia coli datA site promotes proper regulation of cell division
Microbiology, 160 (Pt 4), 703-10
DNA compaction in the early part of the SOS response is dependent on RecN and RecA
Microbiology, 160 (Pt 5), 872-82
The Fis protein has a stimulating role in initiation of replication in Escherichia coli in vivo
PLoS One, 8 (12), e83562