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Identification of a nuclear localization signal, RRMKWKK, in the homeodomain transcription factor PDX-1
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作者:

Moede, T
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Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden

Leibiger, B
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Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden

Pour, HG
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Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden

Berggren, PO
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Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden

Leibiger, IB
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Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden
机构:
[1] Karolinska Inst, Rolf Luft Ctr Diabet Res L6B 01, Dept Mol Med, S-17176 Stockholm, Sweden
关键词:
PDX-1;
transcription factor;
gene expression regulation;
nuclear localization signal;
D O I:
10.1016/S0014-5793(99)01446-5
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Pancreatic duodenal homeobox-containing transcription factor 1 (PDX-1) plays a crucial role in pancreas development and beta-cell gene regulation. Absence of PDX-1 leads to pancreas agenesis and its malfunction causes MODY4 diabetes mellitus. PDX-1 has been suggested to be involved in the glucose-dependent regulation of insulin gene transcription. Whereas DNA-binding and transactivation domains of PDX-1 are in the process of being characterized, protein sequences responsible for its nuclear translocation remain unknown, By combining site-directed mutagenesis of putative phosphorylation sites and nuclear localization signal (NLS) motifs with on-line monitoring of GFP-tagged PDX-1 translocation, we demonstrate that the NLS motif RRMKWKK is necessary and in conjunction with the integrity of the 'helix 3' domain of the PDX-1 homeodomain is sufficient for the nuclear import of PDX-1, Furthermore, we show that there is no glucose-dependent cytoplasmic-nuclear cycling of PDX-1. (C) 1999 Federation of European Biochemical Societies.
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页码:229 / 234
页数:6
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