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Mitochondrial ribosomal protein L41 mediates serum starvation-induced cell-cycle arrest through an increase of p21WAF1/CIP1
被引:38
作者:
Kim, MJ
Yoo, YA
Kim, HJ
Kang, S
Kim, YG
Kim, JS
Yoo, YD
[1
]
机构:
[1] Korea Univ, Coll Med, Grad Sch Med, Seoul 136705, South Korea
[2] Korea Univ, Sch Life Sci & Biotechnol, Seoul 136705, South Korea
[3] Yonsei Univ, Dept Internal Med, Coll Med, Seoul 135270, South Korea
[4] Korea Univ, Coll Med, Div Brain Korea 21 Program Biomed Sci, Seoul 136705, South Korea
[5] Korea Univ, Coll Med, Dept Internal Med, Seoul 136705, South Korea
关键词:
MRPL41;
p21(WAF1/CIP1);
serum starvation;
p53;
cell cycle;
p27 (Kip1);
D O I:
10.1016/j.bbrc.2005.10.064
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:
Ribosomal proteins not only act as components of the translation apparatus but also regulate cell proliferation and apoptosis. A previous study reported that MRPL41 plays an important role in p53-dependent apoptosis. It also showed that MRPL41 arrests the cell cycle by stabilizing p27(Kip1) in the absence of p53. This study found that MRPL41 mediates the p21(WAF1/CIP1)-mediated G1 arrest in response to serum starvation. The cells were released from serum starvation-induced G1 arrest via the siRNA-mediated blocking of MRPL41 expression. Overall, these results suggest that MRPL41 arrests the cell cycle by increasing the p21(WAF1/CIP1) and P27(Kip1) levels under the growth inhibitory conditions. (c) 2005 Elsevier Inc. All rights reserved.
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页码:1179 / 1184
页数:6
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