Arrays for replication

DNA microarrays are normally used to detect variation in mRNA abundance. But in the August 15 Proceedings of the National Academy of Sciences Khodursky et al. use the arrays to track the progress of replication forks in Escherichia coli (Proc Natl Acad Sci USA 2000, 97:9419-9424). In a bacterial culture that is replicating synchronously, genomic DNA from replicated regions gives a stronger array signal than unreplicated DNA. Khodursky et al. use this signal variation to show that normal replicat

William Wells(wells@biotext.com)
Aug 20, 2000

DNA microarrays are normally used to detect variation in mRNA abundance. But in the August 15 Proceedings of the National Academy of Sciences Khodursky et al. use the arrays to track the progress of replication forks in Escherichia coli (Proc Natl Acad Sci USA 2000, 97:9419-9424). In a bacterial culture that is replicating synchronously, genomic DNA from replicated regions gives a stronger array signal than unreplicated DNA. Khodursky et al. use this signal variation to show that normal replication forks progress at 45 kb/min, whereas those in bacteria lacking functional gyrase slow to 14 kb/min, and eventually stop. The residual activity seems to be provided by topoisomerase IV (topo IV). When both gyrase and topo IV are inhibited, replication forks halt almost immediately. In the past, the importance of topo IV in replication has been masked by non-specific gyrase inhibitors. The speed of the halt in...

Interested in reading more?

Become a Member of

Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member?