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We generated a mutant of the red fluorescent protein
drFP583. The mutant (E5) changes its fluorescence from green to red
overtime. The rate of color conversion is independent of protein
concentrationand therefore can be used to trace time-dependent
expression.We used in vivo labeling with E5 to measure expression from
theheat shock-dependent promoter in Caenorhabditis elegans
and fromthe Otx-2 promoter in developing Xenopus
embryos. Thus, E5 isa "fluorescent timer" that can be used to
monitor both activationand down-regulation of target promoters on the
whole-organismscale.
1 School of Medicine, Stanford University,
Stanford, CA 94305, USA.
2 Institute of Bioorganic
Chemistry, Russian Academy of Science, 117871 Moscow, Russia.
3 Center for Molecular Modeling, Center for
Information Technology, NIH, Building 12A, Bethesda, MD 20892, USA.
4 Clontech Laboratories, 1020 East Meadow Circle,
Palo Alto, CA 94303, USA.
*
To whom correspondence should be addressed. E-mail:
Alexey.Terskikh{at}Stanford.edu
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