Enhanced microtubule-dependent trafficking and p53 nuclear accumulation by suppression of microtubule dynamics
Puma
DOI:
10.1073/pnas.132275599
Publication Date:
2002-09-30T16:42:53Z
AUTHORS (8)
ABSTRACT
The tumor suppressor protein p53 localizes to microtubules (MT) and, in response DNA damage, is transported the nucleus via MT minus-end-directed motor dynein. Dynein also responsible for MT-mediated nuclear targeting of adenovirus type 2 (Ad2). Here we show that treatment with low concentrations MT-targeting compounds (MTCs) do not disrupt network but are known suppress dynamics enhanced accumulation, and activation p53-downstream target genes. accumulation required binding MTCs MTs induction p53-up-regulated modulator apoptosis (PUMA) mRNA on challenging cells DNA-damaging drug adriamycin. Low rate movement fluorescent Ad2 increased efficiency Ad2. We propose suppression by enhances MT-dependent trafficking toward minus ends facilitates targeting.
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