Department of Chemistry, University of Texas San Antonio, San Antonio, TX 78249, USA.
Proteomics. 2010 Jan;10(2):203-11. doi: 10.1002/pmic.200800693.
Controversy remains about the identity of the transcription factor(s) (TFs), which bind to the two E-box elements (CACGTG, proximal and distal) of the human telomerase (hTERT) gene promoter, the essential elements in the regulation of telomerase. Here, systematic oligonucleotide trapping supplemented with 2-DE and proteomic methods was used to identify E-box binding TFs. Although insufficient purity was obtained from the proximal E-box element trapping, further fractionation provided by 2-DE and specific identification from Southwestern blotting analysis allow us to clearly identify an E-box binding TF. The protein spot was cut from 2-DE and in-gel digested with trypsin for LC-nanospray ESI-MS/MS analysis. This identified upstream stimulatory factor 2 (USF2). Western blotting analysis with specific antibodies clearly shows USF2 present in the purified fraction and USF2 antibody supershifts the specific DNA-binding complex on non-denaturing gels. Furthermore, a novel method was developed in which the specific DNA-TF complex was separated on a non-denaturing gel, the band was cut and applied to SDS-PAGE for a second dimension. Western blots of this second gel also confirmed the presence of USF2.
关于转录因子(TFs)的身份仍然存在争议,这些转录因子与人类端粒酶(hTERT)基因启动子的两个 E 盒元件(CACGTG,近端和远端)结合,这是调节端粒酶的基本元件。在这里,系统的寡核苷酸捕获辅以 2-DE 和蛋白质组学方法用于鉴定 E 盒结合 TF。尽管从近端 E 盒元件捕获中获得的纯度不足,但 2-DE 提供的进一步分级和来自 Southwestern 印迹分析的特异性鉴定允许我们清楚地鉴定出 E 盒结合 TF。从 2-DE 中切下蛋白斑点,并在胶内用胰蛋白酶消化进行 LC-纳米喷雾 ESI-MS/MS 分析。这鉴定出上游刺激因子 2(USF2)。用特异性抗体进行的 Western blot 分析清楚地表明 USF2 存在于纯化的级分中,并且 USF2 抗体超转移非变性凝胶上的特异性 DNA 结合复合物。此外,开发了一种新方法,其中将特异性 DNA-TF 复合物在非变性凝胶上分离,切下该条带并应用于 SDS-PAGE 进行第二维。该第二凝胶的 Western blot 也证实了 USF2 的存在。