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BID as a double agent in cell life and death.BID作为细胞生死的双重作用因子。
Cell Cycle. 2006 Mar;5(6):582-4. doi: 10.4161/cc.5.6.2575. Epub 2006 Mar 15.
2
Proapoptotic BID is an ATM effector in the DNA-damage response.促凋亡蛋白BID是DNA损伤反应中的一种ATM效应蛋白。
Cell. 2005 Aug 26;122(4):593-603. doi: 10.1016/j.cell.2005.06.014.
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A role for proapoptotic BID in the DNA-damage response.促凋亡蛋白BID在DNA损伤反应中的作用。
Cell. 2005 Aug 26;122(4):579-91. doi: 10.1016/j.cell.2005.06.022.
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Cloning and characterization of mouse E2F8, a novel mammalian E2F family member capable of blocking cellular proliferation.小鼠E2F8的克隆与鉴定,E2F8是一种能够阻断细胞增殖的新型哺乳动物E2F家族成员。
J Biol Chem. 2005 May 6;280(18):18211-20. doi: 10.1074/jbc.M501410200. Epub 2005 Feb 18.
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E2F4 deficiency promotes drug-induced apoptosis.E2F4 缺乏促进药物诱导的细胞凋亡。
Cancer Biol Ther. 2004 Dec;3(12):1262-9. doi: 10.4161/cbt.3.12.1239. Epub 2004 Dec 14.
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Entrez Gene: gene-centered information at NCBI.Entrez基因:美国国立医学图书馆国家生物技术信息中心的基因中心信息。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D54-8. doi: 10.1093/nar/gki031.
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E1A activates transcription of p73 and Noxa to induce apoptosis.E1A激活p73和Noxa的转录以诱导细胞凋亡。
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Role of Mtd/Bok in normal and neoplastic B-cell development in the bursa of Fabricius.Mtd/Bok在法氏囊中正常和肿瘤性B细胞发育中的作用。
Dev Comp Immunol. 2004 May 17;28(6):619-34. doi: 10.1016/j.dci.2003.09.017.
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E2F-7: a distinctive E2F family member with an unusual organization of DNA-binding domains.E2F-7:一种独特的E2F家族成员,其DNA结合结构域的组织方式不同寻常。
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PRDI-BF1 recruits the histone H3 methyltransferase G9a in transcriptional silencing.PRDI-BF1在转录沉默过程中募集组蛋白H3甲基转移酶G9a。
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Bok,与Bcl-2相关的卵巢杀手,受细胞周期调控并对应激诱导的细胞凋亡敏感。

Bok, Bcl-2-related Ovarian Killer, Is Cell Cycle-regulated and Sensitizes to Stress-induced Apoptosis.

作者信息

Rodriguez Jose M, Glozak Michele A, Ma Yihong, Cress W Douglas

机构信息

Molecular Oncology Program, H. Lee Moffitt Cancer Center and Research Institute, Department of Interdisciplinary Oncology, Cancer Biology Ph.D. Program, University of South Florida, Tampa, Florida 33612.

出版信息

J Biol Chem. 2006 Aug 11;281(32):22729-35. doi: 10.1074/jbc.M604705200. Epub 2006 Jun 13.

DOI:10.1074/jbc.M604705200
PMID:16772296
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2134790/
Abstract

Bok/Mtd (Bcl-2-related ovarian killer/Matador) is considered a pro-apoptotic member of the Bcl-2 family. Although identified in 1997, little is known about its biological role. We have previously demonstrated that Bok mRNA is up-regulated following E2F1 overexpression. In the current work, we demonstrate that Bok RNA is low in quiescent cells and rises upon serum stimulation. To determine the mechanism underlying this regulation, we cloned and characterized the mouse Bok promoter. We find that the mouse promoter contains a conserved E2F binding site (-43 to -49) and that a Bok promoter-driven luciferase reporter is activated by serum stimulation dependent on this site. Chromatin immunoprecipitation assays demonstrate that endogenous E2F1 and E2F3 associate with the Bok promoter in vivo. Surprisingly, we find that H1299 cells can stably express high levels of exogenous Bok protein. However, these cells are highly sensitive to chemotherapeutic drug treatment. Taken together these results demonstrate that Bok represents a cell cycle-regulated pro-apoptotic member of the Bcl-2 family, which may predispose growing cells to chemotherapeutic treatment.

摘要

Bok/Mtd(Bcl-2相关卵巢杀手/杀手)被认为是Bcl-2家族的促凋亡成员。尽管它于1997年被发现,但其生物学作用却鲜为人知。我们之前已经证明,在E2F1过表达后Bok mRNA会上调。在当前的研究中,我们证明Bok RNA在静止细胞中含量较低,而在血清刺激后会升高。为了确定这种调控的潜在机制,我们克隆并鉴定了小鼠Bok启动子。我们发现小鼠启动子包含一个保守的E2F结合位点(-43至-49),并且一个由Bok启动子驱动的荧光素酶报告基因在血清刺激下会依赖于该位点被激活。染色质免疫沉淀分析表明内源性E2F1和E2F3在体内与Bok启动子相关联。令人惊讶的是,我们发现H1299细胞能够稳定表达高水平的外源性Bok蛋白。然而,这些细胞对化疗药物治疗高度敏感。综合这些结果表明,Bok代表了Bcl-2家族中一个受细胞周期调控的促凋亡成员,这可能使生长中的细胞更容易受到化疗治疗。