期刊文献+

肿瘤组织中转化/转录域相关蛋白TRRAP点突变检测方法

A simple detect method for a point mutation of transformation/transcription domain-associated protein
下载PDF
导出
摘要 转录因子TRRAP是维系生命体正常活动的重要蛋白,目前对其功能作用还知之甚少,相关研究方兴未艾.2011年发现TRRAP一个多发点突变与肿瘤相关,该突变亟须在人群样品中进行检测,以增加对该分子与肿瘤发生关系的了解.本文设计了一个通过PCR扩增,然后酶切的检测方法,有助于了解肿瘤的发生机理. Transformation/ Transcription Domain-associated Protein; TRRAP, an important transcription factor, was found in 1998 by McMahon, it is still not very clear about its function and its company proteins to date. 2011, Wei found a recurrent point mutation in conserved site of TRRAP by exome sequencing. Here was a detect method for this specific point mutation by PCR and nuclear restriction enzyme digest, through detecting the re- currence mutation situation on tumor patients samples, we will get more comprehensions for this important transcription factor.
出处 《南阳师范学院学报》 CAS 2012年第12期50-51,121,共3页 Journal of Nanyang Normal University
关键词 转化 转录域相关蛋白 TRRAP 点突变 transformation/transcription domain-assciated protein TRRAP point mutation
  • 相关文献

参考文献6

  • 1Doyon Y,Selleck W,Lane W S,Tan S Cote J. Structural and functional conservation of the NuA4 histone acetyl-transferase complex from yeast to humans[J].Molecular and Cellular Biology,2004.1884-1896.
  • 2Fazzio T G,Huff J T,Panning B. An RNAi screen of chromatin proteins identifies Tip60-p400 as a regulator of embryonic stem cell identity[J].Cell,2008.162-174.
  • 3Herceg Z,Hulla W,Gell D,Cuenin C Lleonart M Jack-son S Wang Z-Q. Disruption of Trrap causes early em-bryonic lethality and defects in cell cycle progression[J].Nature Genetics,2001.206-211.
  • 4McMahon S B,Van Buskirk H A,Dugan K A,Copeland T D Cole M D. The novel ATM-related protein TRRAP is an essential cofactor for the c-myc and E2F oncopro-teins[J].Cell,1998.363-374.
  • 5Vassilev A,Yamauchi J,Kotani T,Prives C Avantaggiati M L Qin J Nakatani Y. The 400 kDa subunit of the PCAF histone acetylase complex belongs to the ATM su-perfamily[J].Molec Ce11,1998.869-875.
  • 6Wei X,Walia V,Lin J C,Teer J K Prickett T D Gartner J Davis S NISC Comparative Sequencing Program Stemke-Hale K Davies M A Gershenwald J E Rob-inson W Robinson S Rosenberg S A Samuels Y. Ex-ome sequencing identifies GRIN2A as frequently muta-ted in melanoma[J].Nature Genetics,2011.442-446.

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