Rossini M
Virology. 1983 Nov;131(1):49-58. doi: 10.1016/0042-6822(83)90532-9.
The role of the adenovirus early region 1A (E1A) in the regulation of expression of early regions 2A (E2A) and 1B (E1B) has been investigated by microinjection of cloned segments of viral DNA into cultured cells. Plasmids carrying adenoviral sequences that code for the DNA binding protein (DBP) associated with either the early or the late E2A promoter (at map coordinates 75 and 72, respectively), or both promoters, were injected into cell nuclei in the presence or absence of a plasmid DNA containing early region 1A. The injected cells were scored for the expression of the DNA binding protein by indirect immunofluorescence using specific antisera. These studies suggest that the product(s) encoded by early region 1A differentially control the expression of the DNA binding protein. DBP produced from the early promoter is stimulated by addition of the E1A region. By contrast E1A gene product(s) inhibit the synthesis of the DBP species transcribed from the late promoter. It has been shown previously by a variety of studies that E1A regulates E1B expression. However, experiments in which E1B DNA was microinjected together with E1A and E2A suggest that the DNA binding protein may have a stimulatory effect on the synthesis of E1B products.
通过将病毒DNA的克隆片段显微注射到培养细胞中,研究了腺病毒早期区域1A(E1A)在调节早期区域2A(E2A)和1B(E1B)表达中的作用。携带编码与早期或晚期E2A启动子相关的DNA结合蛋白(DBP)(分别位于图谱坐标75和72处)或两个启动子的腺病毒序列的质粒,在存在或不存在含有早期区域1A的质粒DNA的情况下被注射到细胞核中。使用特异性抗血清通过间接免疫荧光对注射的细胞进行DNA结合蛋白表达评分。这些研究表明,早期区域1A编码的产物差异地控制DNA结合蛋白的表达。早期启动子产生的DBP通过添加E1A区域而受到刺激。相比之下,E1A基因产物抑制从晚期启动子转录的DBP种类的合成。先前通过各种研究表明E1A调节E1B表达。然而,将E1B DNA与E1A和E2A一起显微注射的实验表明,DNA结合蛋白可能对E1B产物的合成具有刺激作用。