Affiliation:
1. Division of Science and Mathematics, University of Minnesota—Morris, Morris, Minnesota 56267
2. Genetics, Dartmouth Medical School, Hanover, New Hampshire 03755
3. Departments of Biochemistry
Abstract
ABSTRACT
We report the complete reconstruction of the firefly
luciferase
gene, fully codon optimized for expression in
Neurospora crassa
. This reporter enhances light output by approximately 4 log orders over that with previously available versions, now producing light that is visible to the naked eye and sufficient for monitoring the activities of many poorly expressed genes. Time lapse photography of strains growing in race tubes, in which the
frq
or
eas/ccg-2
promoter is used to drive
luciferase
, shows the highest levels of luciferase activity near the growth front and newly formed conidial bands. Further, we have established a sorbose medium colony assay that will facilitate luciferase-based screens. The signals from sorbose-grown colonies of strains in which the
frq
promoter drives
luciferase
exhibit the properties of circadian rhythms and can be tracked for many days to weeks. This reporter now makes it possible to follow the clock in real time, even in strains or under conditions in which the circadian rhythm in conidial banding is not expressed. This property has been used to discover short, ca. 15-h period rhythms at high temperatures, at which banding becomes difficult to observe in race tubes, and to generate a high-resolution temperature phase-response curve.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
124 articles.
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