期刊文献+

基于遗传片段分析系统的转录起始位点分析技术:从预测到结果评估 被引量:2

Transcriptional start site analysis based on genetic fragment analysis system:from prediction to data evaluation
原文传递
导出
摘要 【目的】以遗传片段分析仪内标法替代传统放射性标记引物延伸技术进行样本转录起始位点(TSS)分析,并弥补引物延伸技术应用于未知样本缺乏前期预测和后期评估环节,形成一套基于遗传片段分析仪内标法分析未知样品TSS的完整技术方案。【方法】以粘球菌Myxococcus DK1622来源的双拷贝Gro ELs基因为素材;首先从预测出发,利用数据库进行启动子和转录起始位点预测;其次,根据预测结果设计合成荧光标记引物进行靶标m RNA的反转录;再次,应用遗传片段分析技术内标法鉴定分析粘球菌来源的双拷贝Gro ELs基因转录起始位点(TSS)及其丰度;最后,应用正态分布理论进行鉴定结果评估。【结果】明确了转录起始位点的数量、转录丰度及最可能的TSS位点:粘球菌DK1622基因组中Gro EL1拷贝存在1个启动子,TSS位点为TSS_(286);Gro EL2拷贝存在2个启动子,TSS位点分别为TSS_(548)和TSS_(502),其中TSS_(548)转录丰度是TSS_(502)的13.8倍,Gro EL1的TSS_(286)丰度是gro EL2的TSS_(548)丰度的14.3倍。【结论】预测结果指明了实验设计的范围,遗传片段分析仪内标检测法替代传统放射性标记法使实验更加简便、安全、自动、准确,正态分布理论进一步评估了实验结果的可信度,三者接合形成了完善的转录起始位点鉴定技术方案。 [Objective] To establish a pipeline for unknown transcriptional start site (TSS) identification without radioactivity, we used genetic fragment analysis system and replenished two steps regarding prediction and evaluation. [Methods] We used unknown TSSs of GroEL genes from M. xanthus as a case. Firstly, we predicted the potential TSSs through bioinformatics databases. According to the prediction, we designed and synthesized fluorescence labeled primers to carry out the reverse transcription reactions. Further, we took advantage of the genetic fragment analysis system to identify TSSs with internal standards. Finally, we applied the normal distribution theory to evaluate the data. [Results] We determined the numbers, abundances and accurate sites of the TSSs: GroEL1 has one promoter and the site is TSS286, whereas GroEL2 has two promoters, and the sites are TSS548 and TSS502. TSS286 is 14.3 times more abundant than TSS548 and TSS548 is 13.8 times more than TSS502. [Conclusion] The bioinformatics analyzing indicates the range for the experimental design. TSS determination through genetic fragment analysis system is safer, more automatic and accurate. Normal distribution theory further refines the reliability of results. Combination of the three techniques establishes a more complete pipeline of primer extension for unknown TSS determination.
作者 黎志凤 张文燕 刘杨 曲绍峰 王岩 朱丽萍 李越中 Zhifeng L Wenyan Zhang Yang Liu Shaofeng Qu Yan Wang Liping Zhu Yuezhong Li(State Key Laboratory of Microbial Technology, College of Life Science, Shandong University, Jinan 250100, Shandong Province, China School of Mathematics, Shandong University, Jinan 250100, Shandong Province, China)
出处 《微生物学报》 CAS CSCD 北大核心 2017年第2期254-263,共10页 Acta Microbiologica Sinica
基金 国家自然科学基金(31370123 30900027) 高等学校博士学科点专项科研基金(200804221017) 山东大学实验室建设软件项目(sy2008023)~~
关键词 片段分析系统 转录起始位点(TSS) 转录丰度 荧光标记引物 引物延伸 粘球菌 GROEL genetic fragment analysis system, transcriptional start site (TSS), transcriptional abundances,fluorescently labeled primer, primer extension, Myxococcus, GroEL
  • 相关文献

参考文献6

二级参考文献101

  • 1Kewei Zhang,Jianmei Wang,Guodong Yang,Xingqi Guo,Fujiang Wen,Decai Cui,Chengchao Zheng.Isolation of a strong matrix attachment region (MAR) and identification of its function in vitro and in vivo[J].Chinese Science Bulletin,2002,47(23):1999-2005. 被引量:2
  • 2[1]Cohen P, Bouaboula M, Bellis M, et al. Monitoring cellular responses to Listeria monocytogenes with oligonucleotide arrays. J Biol Chem, 2000, 275:11181 - 11190.
  • 3[2]Ichikawa J K, Norris A, Bangera M G, et al. Interaction of Pseudomonas aeruginosa with epithelial cells: identification of differentially regulated genes by expression microarray analysis of human eDNAs.Proc Natl Acad Sci USA, 2000, 97: 9659 - 9664.
  • 4[3]Rosenberger C M, Scott M G, Gold M R, et al. Salmonella typhimurium infection and lipopolysaccharide stimulation induce similar changes in macrophage gene expression. J Immunol, 2000, 164,5894 - 5904.
  • 5[4]Way S S, Sallustio S, Magliozzo R S, et al. Impact of either elevated or decreased levels of cytochrome bd expression on Shigella flexneri virulence. J Bacteriol, 1999, 181:1229 - 1237.
  • 6[5]Runyen-Janecky L J, Payne S M. Identification of chromosomal Shigella flexneri genes induced by the eukaryotic intracellular environment. Infect Immun, 2002,70:4379 - 4388.
  • 7[6]Staudinger B J, Oberdoerster M A, Lewis P J, et al. mRNA expression profiles for Escherichia coli ingested by normal and phagocyte oxidase-deficient human neutrophils. J Clin Invest, 2002, 110(8): 1151 - 1163.
  • 8[7]Jin Q, Yuan Z H, Xu J G, et al. Genome sequence of Shigella flexneri 2a: Insight into pathogenicity through comparison with genomes of Escherichia coli K12 and O157. Nucl Acid Res, 2002, 30(20): 4432-4441.
  • 9[10]Jun Y, Emmanuelle E O, Stephens A, et al. Inactivation of DsbA alters the behaviour of Shigella flexneri towards murine and humanderived macrophage - like cells. FEMS Microbiology Letters, 2001,204:81 - 88.
  • 10[11]Hale T L, Formal S B. Protein synthesis in HeLa or Henle 407 cells infected with Shigella dysenteriae 1, Shigella flexneri 2a, or Salmonella typhimurium W118. Infect Immun, 1981,32: 137- 144.

共引文献19

同被引文献6

引证文献2

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