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
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.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (39)
CITATIONS (175)