期刊文献+

与小鼠小脑发育相关的一种长非编码RNA Gm2694的鉴定

Characterization of a novel lncRNA Gm2694 specifically expressed in mice cerebellum
下载PDF
导出
摘要 目的鉴定与小鼠小脑发育相关的长非编码RNA,并验证其各剪接变异体的存在。方法用芯片技术分析小鼠小脑发育不同阶段RNA的表达差异;用实时定量PCR技术对芯片结果加以验证;针对目的 RNA,验证其各剪接变异体的存在及在小鼠小脑中的表达量。结果 1)长非编码RNA Gm2694在小鼠小脑发育过程中呈动态变化趋势;2)其在小鼠小脑中特异性表达;3)在小鼠小脑中检测到Gm2694有8种表达水平各不相同的剪接变异体,其中除Ensembl数据库预测的7个之外,发现了1个新的表达于小脑的剪接变异体。结论 Gm2694是一种在小鼠小脑特异性表达的长非编码RNA,存在8种表达量各不相同的剪接变异体。 Objective To identify novel lncRNAs involved in cerebellar neurogenesis and validate the expression of related splice variants. Methods Microarray analysis of infant( P7) and adult( P28) mice cerebellar RNA was performed to discover novel lncRNAs involved in mice cerebellum neurogenesis. RT-q PCR was then performed to validate the expression of candidate lncRNAs and splice variants. Results A novel lncRNA,Gm2694,was found to be specifically expressed in mice cerebellum in a developmentally regulated manner. In total eight kinds of splice variants has been detected in cerebellum with various expression levels: besides 7 variants as predicted in the Ensembl databases,another novel variant was identified in mice cerebellum by RACE c DNA amplification. Conclusions Temporal spatial analysis reveals that Gm2694 is a novel lncRNA possibly involved in mice cerebellum neurogenesis.
出处 《基础医学与临床》 CSCD 2016年第4期492-497,共6页 Basic and Clinical Medicine
基金 国家自然科学基金(31471288)
关键词 长非编码RNA Gm2694 小鼠小脑发育 剪接变异体 long non-coding RNA Gm2694 mice cerebellar neurogenesis splice variant
  • 相关文献

参考文献12

  • 1Kapranov P, Cheng J, Dike S, et al. RNA maps reveal new RNA classes and a possible function for pervasive transcrip- tion [ J ]. Science, 2007, 316 : 1484-1488.
  • 2Huang Y, Liu N, Wang JP, et al. Regulatory long non- coding RNA and its functions [ J ]. J Physiol Biochem, 2012, 68:611-618.
  • 3Mortimer SA, Kidwell MA, Doudna JA. Insights into RNA structure and function from genome-wide studies [ J ]. Nat Rev Genet, 2014, 15:469-479.
  • 4Lin M, Pedrosa E, Shah A, et al. RNA-Seq of human neu- rons derived from iPS cells reveals candidate long non-cod- ing RNAs involved in neurogenesis and neuropsychiatric disorders[J]. PLoS One, 2011,6:e23356. doi: 10. 1371/ journal, pone. 0023356.
  • 5Qureshi IA, Mehler MF. Non-coding RNA networks under- lying cognitive disorders across the lifespan[ J]. Trends Mo! Med, 2011, 17:337-346.
  • 6Ziats MN, Rennert OM. Aberrant expression of long non- coding RNAs in autistic brain[J]. J Mol Neurosci, 2013, 49:589-593.
  • 7岳永松,张伟龙,刘春英,牛亚梅,佟伟民.长链非编码RNA Gm15577参与小鼠小脑神经元增殖与分化[J].中华病理学杂志,2015,44(7):504-508. 被引量:2
  • 8Moran VA, Perera R J, Khalil AM, et al. Emerging func- tional and mechanistic paradigms of mammalian long non- coding RNAs [ J]. Nucleic Acids Res, 2012, 40: 6391-6400.
  • 9Ng SY, Lin L, Soh BS, et al. Long noncoding RNAs in de- velopment and disease of the central nervous system [ J]. Trends Genet, 2013, 29:461-468.
  • 10Wang VY, Zoghbi HY. Genetic regulation of cerebellar development [ J ]. Nat Rev Neurosci, 2001, 2:484-491.

二级参考文献12

  • 1Varon R, Vissinga C, Platzer M, et al. Nibr/n, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome[ J]. Cell, 1998,93 (3) :467-476.
  • 2Frappart PO, Tong WM, Demuth I, et al. An essential function for NBS1 in the prevention of ataxia and cerebellar defects [ J ]. Nat Med, 2005,11 (5) :538-544.
  • 3Jones-Villeneuve EM, McBurney MW, Rogers KA, et al. Retinoic acid induces embryonal carcinoma cells to differentiate into neurons and glial cells [ J]. J Cell Biol, 1982, 94 (2) :253- 262.
  • 4Saeed AI, Bhagabati NK, Braisted JC, et al. TM4 microarray software suite [ J]. Methods Enzymol, 2006,411 : 134-193.
  • 5Wu C, Orozco C, Boyer J, et al. BioGPS : an extensible and customizable portal for querying and organizing gene annotation resources[ J]. Genome Biol, 2009,10 ( 11 ) : R130.
  • 6Kong L, Zhang Y, Ye ZQ, et al. CPC: assess the protein-coding potential of transcripts using sequence features and support vector machine[ J]. Nucleic Acids Res, 2007, 35 (Web Server issue) : W345-W349.
  • 7Wang L, Park HJ, Dasari S, et al. CPAT: Coding-Potential Assessment Tool using an alignment-free logistic regression model [J]. Nucleic Acids Res, 2013,41(6) : e74.
  • 8Pauli A, Rinn JL, Schier AF. Non-coding RNAs as regulators of embryogeuesis[J]. Nat Rev Genet, 2011,12(2) : 136-149.
  • 9Kanr P, Karolina DS, Sepramaniam S, et al. Expression profiling of RNA transcripts during neuronal maturation and ischemic injury [J]. PLoS One, 2014,9(7) : e103525.
  • 10Roussel MF, Hatten ME. Cerebellum development and medulloblastoma[ J]. Curt Top Dev Biol, 2011,94:235-282.

共引文献1

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