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First published online 31 October 2007
doi: 10.1242/dev.010934
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1 Department of Molecular Biology, University of Copenhagen, Ole Maaløes
Vej 5, DK-2200 Copenhagen N, Denmark.
2 Department of Molecular Biology and Biochemistry, Rutgers University, Waksman
Institute, 190 Frelinghuysen Rd, Piscataway, NJ 08854-8020, USA.
3 Cell Biology and Metabolism Branch, NICHD, NIH, Bldg. 1, 8T, 18 Library Drive,
Bethesda, MD 20892, USA.
* Author for correspondence (e-mail: rdelotto{at}my.molbio.ku.dk)
Accepted 5 September 2007
In Drosophila, the NF-
B/REL family transcription factor,
Dorsal, redistributes from the cytoplasm to nuclei, forming a concentration
gradient across the dorsoventral axis of the embryo. Using live imaging
techniques in conjunction with embryos expressing a chimeric Dorsal-GFP, we
demonstrate that the redistribution of Dorsal from cytoplasm to nucleus is an
extremely dynamic process. Nuclear Dorsal concentration changes continuously
over time in all nuclei during interphase. While Dorsal appears to be
nuclearly localized primarily in ventral nuclei, it is actively shuttling into
and out of all nuclei, including nuclei on the dorsal side. Nuclear export is
blocked by leptomycin B, a potent inhibitor of Exportin 1 (CRM1)-mediated
nuclear export. We have developed a novel in vivo assay revealing the presence
of a functional leucine-rich nuclear export signal within the carboxyterminal
44 amino acids of Dorsal. We also find that diffusion of Dorsal is partially
constrained to cytoplasmic islands surrounding individual syncitial nuclei. A
model is proposed in which the generation and maintenance of the Dorsal
gradient is a consequence of an active process involving both restricted
long-range diffusion and the balancing of nuclear import with nuclear
export.
Key words: NF-
B, Gradient formation, Transcription factor dynamics, Drosophila
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