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哺乳动物真核起始因子 4B 对细胞存活和增殖的控制。

Control of cell survival and proliferation by mammalian eukaryotic initiation factor 4B.

机构信息

Department of Biochemistry and Goodman Cancer Centre, McGill University, The Cancer Research Building, 1160 Pine Avenue West, Room 615, Montreal, Quebec H3A 1A3, Canada.

出版信息

Mol Cell Biol. 2010 Mar;30(6):1478-85. doi: 10.1128/MCB.01218-09. Epub 2010 Jan 19.

Abstract

Translation initiation plays an important role in cell growth, proliferation, and survival. The translation initiation factor eIF4B (eukaryotic initiation factor 4B) stimulates the RNA helicase activity of eIF4A in unwinding secondary structures in the 5' untranslated region (5'UTR) of the mRNA in vitro. Here, we studied the effects of eIF4B depletion in cells using RNA interference (RNAi). In agreement with the role of eIF4B in translation initiation, its depletion resulted in inhibition of this step. Selective reduction of translation was observed for mRNAs harboring strong to moderate secondary structures in their 5'UTRs. These mRNAs encode proteins, which function in cell proliferation (Cdc25C, c-myc, and ODC [ornithine decarboxylase]) and survival (Bcl-2 and XIAP [X-linked inhibitor of apoptosis]). Furthermore, eIF4B silencing led to decreased proliferation rates, promoted caspase-dependent apoptosis, and further sensitized cells to camptothecin-induced cell death. These results demonstrate that eIF4B is required for cell proliferation and survival by regulating the translation of proliferative and prosurvival mRNAs.

摘要

翻译起始在细胞生长、增殖和存活中起着重要作用。翻译起始因子 eIF4B(真核起始因子 4B)在体外刺激 eIF4A 的 RNA 解旋酶活性,解开 mRNA 5'非翻译区(5'UTR)中的二级结构。在这里,我们使用 RNA 干扰(RNAi)研究了细胞中 eIF4B 耗竭的影响。与 eIF4B 在翻译起始中的作用一致,其耗竭导致该步骤受到抑制。对于在其 5'UTR 中具有强至中等二级结构的 mRNA,观察到选择性的翻译减少。这些 mRNA 编码在细胞增殖(Cdc25C、c-myc 和 ODC[鸟氨酸脱羧酶])和存活(Bcl-2 和 XIAP[凋亡抑制因子 X 连接体])中起作用的蛋白质。此外,eIF4B 沉默导致增殖率降低、促进 caspase 依赖性细胞凋亡,并进一步使细胞对喜树碱诱导的细胞死亡敏感。这些结果表明,eIF4B 通过调节增殖和存活 mRNA 的翻译,对细胞增殖和存活是必需的。

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本文引用的文献

1
The helicase protein DHX29 promotes translation initiation, cell proliferation, and tumorigenesis.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22217-22. doi: 10.1073/pnas.0909773106. Epub 2009 Dec 11.
2
Targeting PI3K signalling in cancer: opportunities, challenges and limitations.
Nat Rev Cancer. 2009 Aug;9(8):550-62. doi: 10.1038/nrc2664.
3
Topology and regulation of the human eIF4A/4G/4H helicase complex in translation initiation.
Cell. 2009 Feb 6;136(3):447-60. doi: 10.1016/j.cell.2009.01.014.
4
Translation initiation on mammalian mRNAs with structured 5'UTRs requires DExH-box protein DHX29.
Cell. 2008 Dec 26;135(7):1237-50. doi: 10.1016/j.cell.2008.10.037.
5
BCL-2 family antagonists for cancer therapy.
Nat Rev Drug Discov. 2008 Dec;7(12):989-1000. doi: 10.1038/nrd2658.
6
IAP-targeted therapies for cancer.
Oncogene. 2008 Oct 20;27(48):6252-75. doi: 10.1038/onc.2008.302.
7
AGC kinases regulate phosphorylation and activation of eukaryotic translation initiation factor 4B.
Oncogene. 2009 Jan 8;28(1):95-106. doi: 10.1038/onc.2008.367. Epub 2008 Oct 6.
8
Drug discovery approaches targeting the PI3K/Akt pathway in cancer.
Oncogene. 2008 Sep 18;27(41):5511-26. doi: 10.1038/onc.2008.246.
9
Interactions between eIF4AI and its accessory factors eIF4B and eIF4H.
RNA. 2008 Oct;14(10):2136-48. doi: 10.1261/rna.1049608. Epub 2008 Aug 21.
10
DAP5 promotes cap-independent translation of Bcl-2 and CDK1 to facilitate cell survival during mitosis.
Mol Cell. 2008 May 23;30(4):447-59. doi: 10.1016/j.molcel.2008.03.018. Epub 2008 May 1.

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