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组蛋白修饰在神经系统疾病中的研究进展 被引量:1

Progress of Histone Modification in Nervous System Disease
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摘要 基因表达是一个受多因素调控的复杂过程。组蛋白是染色体的基本结构——核小体中的一个重要组成部分,其在N末端氨基酸残基上发生的乙酰化、甲基化、磷酸化、泛素化、多聚ADP糖基化等多种共价修饰作用。其改变染色质状态,使转录因子与组蛋白或DNA相互作用发生变化,从而发挥基因调控作用。神经系统中特异性的组蛋白修饰已经在多种神经系统疾病发病机制的解释及新型治疗方案的研究中得到应用。 Gene expression is a kind of complex process regulated by multiple factors. Histone is the important ingredient of nucleosome which is the basic unit of chromatin. Histone modifications are a number of covalent modifications including acetylation, methylation, phosphorylation, ubiquitination and poly-ADP glycosylation in its N-terminal amino acid residue including. These modifications influence chromatin condition and change the interaction between transcription factor and histone or transcription factor and DNA, thereby regulate gene expression. In the recent few years, neurologic researchers have paid more attention to specific histone modification in nervous system. Some kinds of mechanism of modifications have been used to explain the pathogenesis of multiple nervous system diseases and to study neotype treatment prescription.
作者 杨方 黄远桂
出处 《中国临床神经科学》 2006年第3期308-313,共6页 Chinese Journal of Clinical Neurosciences
关键词 组蛋白 共价修饰 特异性组蛋白修饰 神经系统疾病 histone covalent modification specific histone modification nervous system disease
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  • 1Allfrey VG, Faulkner R, Mirsky AE. Acetylation and methylation of histones and their possible role in the regulation of RNA synthesis[J].Proc Natl Acad Sci USA, 1964, 51:786-794
  • 2Sun ZW, Allis CD. Ubiquitination of histone H2B regulates, H3 methylation and gene silencing in yeast[J]. Nature, 2002, 418, 104-108
  • 3Felsenfeld G, Groudine M. Controlling the double helix[J]. Nature,2003, 421:448-453
  • 4Cheung P, Allis CD, Sassone-Corsi P. Signaling to chromatin through histone modifications[J]. Cell, 2000, 103, 263-271
  • 5Roth SY, Denu JM, Allis CD. Histone acetyltransferases[J]. Annu Rev Biochem, 2001, 70:81-120
  • 6Eberharter A, Becker PB. Histone acetylation: a switch between repressive and permissive chromatin[J]. EMBO Rep, 2002, 3:224-229
  • 7Vaziri H, Dessain SK, Ng Eaton E, et al. hSIR2(SIRT1) functions as an NAD-dependent p53 deacetylase[J]. Cell, 2001, 107:149-159
  • 8Legube G, Trouche D. Regulating histone acetyhransferases and deacetylases[J]. EMBO Rep, 2003, 4:944-947
  • 9Detich N, Bovenzi V, Szyf M. Valproate induces replication-independent active DNA demethylation[J]. J Biol Chem, 2003, 278:27586-27592
  • 10Eyal S, Yagen B, Sobo E, et al. The activity of antiepileptic drugs as histone deacetylase inhibitors[J]. Epilepsia, 2004, 45:737-744

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  • 1Vanderah TW. Pathophysiology of pain[J]. Med Clin North Am,2007,91:1 - 12.
  • 2Dworkin RH. An overview of neuropathic pain: syndromes, symptoms, signs, and several mechanisms[J]. Clin J Pain,2002,18:343- 349.
  • 3Denk F, MeMahon S B. Chronic pain: emerging evidence for the involvement of epigenetics[J]. Neuron,2012,73:435-444.
  • 4Borders AS, de Almeida L, Van Eldik L J, et al. The p38alpha mitogen- activated protein kinase as a central nervous system drug discovery target[J]. BMC Neurosci,2008,9:S 12.
  • 5Kondo T, Sakurai J, Miwa H, et al. Activation of p38 MAPK through trasient receptor potential A1 in a rat model of gastric distension- induced visceral pain[J]. Neuroreport,2013,24:68-72.
  • 6Piao Z G, Cho I H, Park C K, et al. Activation of glia and microglial p38 MAPK in medullary dorsal horn contributes to tactile hypersensitivity following trigeminal sensory nerve injury[J]. Pain,2006,12:219-231.
  • 7Vierck C J, Wong F, King CD, et al. Characteristics of sensitization associated with chronic pain conditions[J]. Clin J Pain,2014,30:119- 128.
  • 8Coronado RA, Simon CB, Valencia C, et al. Experimental pain responses support peripheral and central sensitization in patients with unilateral shoulder pain[J]. Clin J Pain,2014,30:143-151.
  • 9Ji RR, Suter MR. p38 MAPK, microglial signaling, and neuropathic pain[J]. Mol Pain,2007,3:33-42.
  • 10Cargnello M, Roux PP. Activation and function of the MAPKs and their substrates, the MAPK-activated protein kinases[J]. Microbiol Mol Biol Rev,2011,75:50-83.

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