期刊文献+

关注和跟踪表观遗传研究在眼科疾病诊治中的应用 被引量:4

Epigenetics,diseases and therapy in ophthalmology
下载PDF
导出
摘要 不涉及修改基因编码序列的、可遗传的基因表达变化称为表观遗传改变,眼科表观遗传学是当前生物医学研究的热点之一.表观遗传机制主要包括DNA甲基化、组蛋白修饰、染色质重排及非编码RNA.异常的DNA甲基化和组蛋白修饰与许多年龄相关性疾病密切关联,如癌症、自身免疫性疾病和其他疾病.近年来,表观遗传对眼科疾病发生和发展的调控机制及其在治疗中的作用日益引起研究者的关注,不仅加深了人们对相关眼病发病机制的理解,而且由于表观遗传性改变是可逆的,因此对与相关眼病有关的基因标志进行修饰也为这些疾病的预防、早期诊断和治疗提供了新的思路.我们讨论眼科表观遗传学的机制及表观遗传改变在眼病发生和发展过程中的作用,希望眼科研究人员重视基因表达改变与环境因素的相互作用及其对眼部发育和眼部疾病发病过程的影响,更重要的是应将这些研究成果更好地用于眼科疾病的预防和治疗. Heritable changes in gene expression are regarded as epigenetics,which do not involve coding sequence modifications.The study of ophthalmology epigenetics is a rapidly growing area in biomedical research.Epigenetic mechanisms principally include DNA methylation,histone modification,chromatin remodeling and noncoding RNA.Aberrant DNA methylation and histone modification are linked to a number of age-related disorders,such as cancer,autoimmune and others.In recent years,the modulations of epigenetic changes on the pathogenesis of eye disorders and their roles in therapeutic interventions are drawing more and more attention,and these studies deepen the understanding of relevant diseases.Since the epigenetic alterations are reversible,modifying epigenetic marks contributing to eye diseases provide a new approach to the development of disease prevention,diagnosis and therapies.Herein we discuss the roles of epigenetic changes in eye disease development,hoping that ophthalmologists and researchers pay attention to these researching cues in pathogenesis of eye disorders caused by genetic expression alterations in response to environmental changes,importantly,to the implication for relevant eye disease therapy and prevention.
出处 《中华实验眼科杂志》 CAS CSCD 北大核心 2015年第8期673-677,共5页 Chinese Journal Of Experimental Ophthalmology
关键词 表观遗传学 眼/遗传学 眼病/治疗 DNA甲基化 组蛋白 微小RNA Epigenesis, genetic Eye/genetlc Eye disorder/therapy DNA methylation Histones MicroRNA
  • 相关文献

参考文献25

  • 1Cvekl A, Ashery-Padan R. The cellular and molecular mechanisms of vertebrate lens development [ J ]. Development ,2014,141 ( 23 ) : 4432-4447. doi : 10. 1242/dev. 107953.
  • 2Jing Z, Gangalum RK, Mock DC, et al. A gene-speeific non-enhancer sequence is critical for expression from the promoter of the small heat shock protein gene alphaB-crystallin [ J/OL ]. Hum Genomics, 2014, 8 : 5 [ 2015-05-23 ]. http ://www. humgenomics, corncontent815. doi: 10.1186/1479-7364-8-5.
  • 3Nasonkin IO,Lazo K, Hambright D, et al. Distinct nuclear localization patterns of DNA methyltransferases in developing and mature mammalian retina[ Jl. J Comp Neuro1,2011,519 (10) : 1914-1930. doi: 10. 1002/ cne. 22613.
  • 4Tittle RK, Sze R, Ng A, et al. Uhrfl and Dnmtl are required for development and maintenance of the zebrafish lens[ J] Dev Biol,2011, 350 ( 1 ) : 50-63. doi : 10. 1016/j. ydbio. 2010.11. 009.
  • 5Ral K, Chidester S, Zavala CV, et al. Dnmt2 functions in the cytoplasm to promote liver,brain, and retina development in zebrafish [J]. Genes Dev,2007,21 ( 3 ) : 261-266. doi : 10.1101/gad. 1472907.
  • 6Seritrakul P,Gross JM. Expression of the de novo DNA methyltransferases (dnmt3-dnmt8) during zebrafish lens development [ J ]. Dev Dyn, 2014,243 ( 2 ) : 350-356. doi : 10. 1002/dvdy. 24077.
  • 7Zhou P, Luo Y, Liu X, et al. Down-regulation and CpG island hypermethylation of CRYAA in age-related nuclear cataract[ J]. FASEB J,2012,26(12) :4897-4902. doi:10. 1096/fj. 12-213702.
  • 8Zhou X, Ji F, An J, et al. Experimental routine myopia induces collagen type Ialphal (COL1AI) DNA methylation and altered COL1AI messenger RNA expression in sclera[ J]. Mol Vis ,2012,18:1312-1324.
  • 9Seddon JM, Reynolds R, Shah HR, et al. Smoking, dietary betaine, methionine, and vitamin D in monozygotic twins with discordant macular degeneration: epigenetic implications [ J ]. Ophthalmology, 2011, 118(7) :1386-1394. doi:10. 1016/j. ophtha. 2010.12.020.
  • 10Gardner JG, Escalante-Semerena JC. In Bacillus subtilis, the sirtuin protein deacetylase, encoded by the srtN gene ( formerly yhdZ), and functions encoded by the acuABC genes control the activity of acetyl coenzyrne A synthetase[ J]. J Bacteriol,2009,191 (6) : 1749- 1755. doi : 10.1128/JB. 01674-08.

同被引文献11

引证文献4

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部