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http://hdl.handle.net/1993/2912
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| Title: | Effects of mitogen-activated protein kinases on nuclear protein import |
| Authors: | Faustino, RS Rousseau, DC Landry, MN Kostenuk, AL Pierce, GN |
| Keywords: | mitogen activated protein kinase nuclear protein import cell proliferation nucleus cell growth PORE COMPLEX MAP KINASE TRANSPORT PHOSPHORYLATION INHIBITION PATHWAY RANGAP1 RAN NUCLEOPORINS INVOLVEMENT |
| Issue Date: | 30-Apr-2006 |
| Citation: | 0008-4212; CAN J PHYSIOL PHARMACOL, MAR-APR 2006, vol. 84, no. 39145, p.469 to 475. |
| Abstract: | ERK-2 MAP kinase activation induces inhibitory effects on nuclear protein import in vascular smooth muscle cells. The mechanism and characteristics of this effect of ERK-2 were investigated. An Unusual dose-dependent effect of ERK-2 on nuclear protein import was identified. At higher concentrations (1 mu g/mL) of ERK-2, nuclear protein import was stimulated. whereas lower concentrations (0.04 mu g/mL) inhibited import. Intermediate concentrations exerted intermediate effects. The stimulatory and inhibitory, effects at the 2 different ERK-2 concentrations were observed in both conventional. permeabilized cell assays of nuclear protein import and With in situ microinjection of smooth muscle cells. The biphasic effects of ERK-2 oil import were also found for the other 2 members of the MAPK family. p38 and JNK. Ran-GAP was identified by structural analysis as a candidate target protein responsible for mediating the effects of ERK-2. After pretreatment with high concentrations of ERK-2. RanGAP activity was significantly increased by similar to 50%. In contrast. low concentrations of ERK-2 significantly attenuated RanGAP activity. These results demonstrate that all 3 members of the MAPK family can alter nuclear protein import in opposite directions depending upon the concentration of ERK-2 Used. RanGAP represents the MAP kinase target whereby nuclear transport can be stimulated or inhibited. |
| URI: | http://hdl.handle.net/1993/2912 |
| Appears in Collections: | Research Publications (citation and abstract only)
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