期刊文献+

Rotor-Gene链融解曲线法甲基化标记筛选技术的建立 被引量:1

Methylation-specific melting curve analysis with Rotor-Gene
下载PDF
导出
摘要 目的:建立基于Rotor-Gene的链融解曲线法的甲基化标记筛选技术,分析各种影响因素,评估其实用性。方法:克隆Hela细胞雄激素受体基因外显子-1的Bisulfite-PCR产物,挑出经测序证实的可以代表不同甲基化程度的一组质粒,并以之为模板,在Rotor-Gene3000实时定量PCR仪进行扩增和链融解,分析融链温度、链融解曲线与甲基化程度、甲基化模式的相关性及各种影响因素。结果:基于Rotor-Gene的链融解曲线法,不仅可以区分甲基化与非甲基化,而且能够鉴别片段内细微的甲基化差异;主要的影响因素有升温幅度、缓冲液离子强度、产物浓度等。结论:基于Rotor-Gene的链融解曲线法,可以集扩增和链融解于一体,是一种经济简便的甲基化分析技术,可用于样品的甲基化筛选。 Aim : To develop a simple methylation scanning technique using methylation specific melting curve analysis (MS-MCA) with Rotor-Gene. Mothods,Plasmid clones containing androgen receptor(AR) exon-1 bisulfite fragment which represented different methylation patterns were prepared. Melting curve of the PCR products amplified from these plasmids was analyzed with a Rotor-Gene 3 000 real time thermal cycler. Results: PCR products representing different methylation patterns could be distinguished clearly. Main factors that affected the melting curves included salt concentration, products concentration and temperature changing speed. The relationship between melting temperature, melting curve and methylation degree, methylation pattern and the influencing factors were analyzed. Conclusion: The methylatlon-specific melting curve analysis with Rotor-Gene simplifies methylation scanning of genomic DNA.
出处 《郑州大学学报(医学版)》 CAS 北大核心 2008年第1期116-119,共4页 Journal of Zhengzhou University(Medical Sciences)
关键词 DNA甲基化 链融解曲线法 亚硫酸氢盐 雄激素受体 DNA methylation melting curve analysis bisulfite androgen receptor
  • 相关文献

参考文献17

二级参考文献31

  • 1舒青,张素珍,魏亚宁,马群风.雄激素受体基因甲基化与食管癌的分级[J].肿瘤防治研究,2004,31(11):688-690. 被引量:2
  • 2Herman JG, Graff JR, Myohanen S, et al. Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands [J]. Proc Natl Acad Sci, 1996,93(18):9821-9826. 被引量:1
  • 3Katzenellenbogen RA, Baylin SB, Herman JG. Hypermethylation of the DAP-kinase CpG island is a common alteration in Bcell malignancies [J]. Blood, 1999,93 (12): 4347 -4353. 被引量:1
  • 4Kudo S, Fukuda M. Tissue-specific transcriptional regulation of human leukosialin (CD43) gene is achieved by DNA methylation [J]. Biol Chem, 1995, 270:13298-13302. 被引量:1
  • 5Esteller M, Sanchez CM, Rosell R, et al. Detection of aberrant promoter hypermethylation of tumor suppressor genes in serum DNA from non-small cell lung cancer patients [J]. Cancer Res,1999, 59(1):67-70. 被引量:1
  • 6Jesper W, Per G. DNA methylation: an epigenetic pathway to cancer and a promising target for anticancer therapy [J]. J Oral Pathology & Medicine, 2002, 31(8) :443-446. 被引量:1
  • 7Marcella M, Marco G, Antonio G. Genetic and epigenetic alterations as hallmarks of the intricate road to cancer [J]. Oncogene, 2003, (22) :6472-6478. 被引量:1
  • 8Cohen O, Feinstein E, Kimchi A. DAP-kinase is a Ca^2+/calmodulin-dependent, cytoskeletal-associated protein kinase, with cell death-inducing functions that depend on its catalytic activity [J]. EMBO J, 1997,16(5):998-1008. 被引量:1
  • 9Fraga MF, Esteller M. DNA methylation: a profile of methods and applications [J]. Biotechniques, 2002,33 (3): 632 - 634,636-649. 被引量:1
  • 10Milutinovic S, Knox JD, Szyf M. DNA methyltransferase inhibition induces the transcription of the tumor suppressor p21WAF1/CIP1/sdil [J]. J Biol Chem, 2000, (9) ,275: 6353-6359. 被引量:1

共引文献17

同被引文献10

引证文献1

二级引证文献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