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O亚型叉头框蛋白质翻译后修饰研究进展

Research progress of post-translational modification of the forkhead box subtype O proteins
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摘要 O亚型叉头框[forkhead box (FOX) subtype O,FOXO]蛋白质是FOX蛋白质转录因子家族的重要亚家族成员,在诱导细胞凋亡、DNA损伤修复、拮抗氧化应激、抑制细胞增殖、延长寿命和抑制肿瘤方面发挥重要作用。磷酸化、乙酰化、去乙酰化、泛素化和甲基化等翻译后修饰在其转录活性调控中发挥关键性作用。本文将主要就FOXO蛋白质亚家族成员的翻译后修饰和转录活性调节机制等方面的研究进展作一综述。 Forkhead box subtype O (FOXO) proteins, important subfamily members of the forkhead transcription factors, play critical roles in apoptosis induction, DNA injury repair, oxidative stress antagonism, proliferation inhibition, lifespan elongation and tumor suppression. The post-translational modifications, including phosphorylation, acetylation, deacetylation, ubiquitination and methylation play key roles in the regulation of their transcriptional activities. This review will mainly focus on the research progressions of post-translational modifications and the regulatory mechanisms of transcriptional activities of the FOXO subfamily members.
出处 《生命的化学》 CAS CSCD 北大核心 2009年第6期826-829,共4页 Chemistry of Life
关键词 O亚型叉头框(FOXO)蛋白质 磷酸化 乙酰化 泛素化 甲基化 forkhead box subtype O (FOXO) protein phosphorylation acetylation ubiquitination methylation
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参考文献19

  • 1Obsilova Vet al. 14-3-3 protein interacts with nuclear localization sequence of forkhead transcription factor FoxO4. Biochemistry, 2005, 44:11608-11617.
  • 2Tsai KL et al. Crystal structure of the human FOXO3a-DBD/ DNA complex suggests the effects of post-translational modification. Nucleic Acids Res, 2007, 35:6984-6994.
  • 3Boura E et al. Both the N-terminal loop and wing W2 of the forkhead domain of transcription factor Foxo4 are important for DNA binding. J Biol Chem, 2007, 282:8265-8275.
  • 4Arteaga MF et al. Multiple translational isoforms give functional specificity to serum- and glucocorticoid-induced kinase 1. Mol Biol Cell, 2007, 18:2072-2080.
  • 5Huang H et al. CDK2-dependent phosphorylation of FOXO1 as an apoptotic response to DNA damage. Science, 2006, 314: 294-297.
  • 6Liu P et al. CDK1 promotes cell proliferation and survival via phosphorylation and inhibition of FOXO1 transcription factor. Oncogene, 2008, 27:4733-4744.
  • 7Hu MC et al. IkappaB kinase promotes tumorigenesis through inhibition of forkhead FOXO3a. Cell, 2004, 117:225-237.
  • 8Brunet A et al. Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase. Science, 2004, 303: 2011- 2015.
  • 9Kitamura YI et al. FoxO1 protects against pancreatic beta cell failure through NeuroD and MafA induction. Cell Metab, 2005, 2:153-163.
  • 10Lehtinen MK et al.A conserved MST-FOXO signaling pathway mediates oxidative-stress responses and extends life span. Cell, 2006, 125:987-1001.

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