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使用联合酶消化/电喷雾电离质谱分析法研究TATA结合蛋白对TATA框中光产物形成的影响。

Use of a combined enzymatic digestion/ESI mass spectrometry assay to study the effect of TATA-binding protein on photoproduct formation in a TATA box.

作者信息

Wang Y, Gross M L, Taylor J S

机构信息

Department of Chemistry, Washington University, One Brookings Drive, St. Louis, Missouri 63130,USA.

出版信息

Biochemistry. 2001 Oct 2;40(39):11785-93. doi: 10.1021/bi0111552.

Abstract

Recently, it was reported that TATA-binding protein (TBP) enhances (6-4) photoproduct formation in a TATA box under UVC irradiation [Aboussekhra and Thoma (1999) EMBO J. 18, 433-443]. The conclusions of that study were based on an indirect enzymatic assay that was not specific for (6-4) photoproducts. Herein we report the use of a recently developed coupled enzymatic digestion/mass spectrometry assay [Wang et al. (1999) Chem. Res. Toxicol. 12, 1077-1082] to identify unambiguously and quantify the photoproducts formed in a TATA box-containing dodecamer duplex sequence in the presence or absence of TBP binding. Exposure of the adenovirus major late promoter TATA box to a high dose of UVC irradiation in the absence of the C-terminal domain of yeast TBP leads to predominant formation of the cis-syn dimer within the T(4) tract, whereas exposure in the presence of TBP leads to almost exclusive formation of the (6-4) photoproduct. In contrast, the (6-4) product is not detected at high doses of UVB irradiation in the absence of TBP but is detected in the presence of TBP, although the cis-syn product predominates. When the products of UVB irradiation were subsequently exposed to a high dose of UVC irradiation in the presence of TBP, the (6-4) photoproduct again becomes nearly the exclusive photoproduct, indicating that the cis-syn dimer is being reversed to TT by UVC light. Both cis-syn and (6-4) photoproducts are formed in approximately equal amounts upon irradiation with small doses of UVC in the presence of TBP, but the fraction of (6-4) photoproduct increases with dose. Through the use of a TATA box containing a site-specifically deuterated thymine, it was found that (6-4) photoproducts formed most selectively at the second and third positions of the T(4) tract upon either UVB or UVC irradiation in the presence of TBP. By using the same substrate, it was found that UVC-induced TA formation was inhibited by TBP binding and that TA formation was greatest at the 5' end of the TATA sequence.

摘要

最近,有报道称TATA结合蛋白(TBP)在紫外线C(UVC)照射下可增强TATA框中(6-4)光产物的形成[阿卜杜勒塞赫拉和托马(1999年),《欧洲分子生物学组织杂志》18卷,433 - 443页]。该研究的结论基于一种间接酶促测定法,该方法对(6-4)光产物不具有特异性。在此,我们报告使用一种最近开发的偶联酶消化/质谱分析法[王等人(1999年),《化学研究毒理学》12卷,1077 - 1082页],以明确鉴定和定量在存在或不存在TBP结合的情况下,在含TATA框的十二聚体双链序列中形成的光产物。在不存在酵母TBP的C末端结构域的情况下,将腺病毒主要晚期启动子TATA框暴露于高剂量的UVC照射下,会导致T(4)序列内顺式-顺式二聚体的主要形成,而在存在TBP的情况下暴露则会导致几乎 exclusively形成(6-4)光产物。相比之下,在不存在TBP的情况下,高剂量的紫外线B(UVB)照射未检测到(6-4)产物,但在存在TBP的情况下检测到了,尽管顺式-顺式产物占主导。当UVB照射的产物随后在存在TBP的情况下暴露于高剂量的UVC照射时,(6-4)光产物再次几乎成为唯一的光产物,这表明顺式-顺式二聚体被UVC光逆转为TT。在存在TBP的情况下,用小剂量的UVC照射时,顺式-顺式和(6-4)光产物的形成量大致相等,但(6-4)光产物的比例随剂量增加。通过使用含有位点特异性氘代胸腺嘧啶的TATA框,发现(6-4)光产物在存在TBP的情况下,在UVB或UVC照射时,最选择性地在T(4)序列的第二个和第三个位置形成。通过使用相同的底物,发现TBP结合抑制了UVC诱导的TA形成,并且TA形成在TATA序列的5'端最大。

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