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E1A介导的腺病毒E4启动子激活可独立于细胞转录因子E4F而发生。

E1A-mediated activation of the adenovirus E4 promoter can occur independently of the cellular transcription factor E4F.

作者信息

Jones C, Lee K A

机构信息

Clare Hall Laboratories, Imperial Cancer Research Fund, South Mimms, Hertfordshire, England.

出版信息

Mol Cell Biol. 1991 Sep;11(9):4297-305. doi: 10.1128/mcb.11.9.4297-4305.1991.

Abstract

The cellular factors E4F and ATF-2 (a member of the activating transcription factor [ATF] family) bind to common sites in the adenovirus E4 promoter and have both been suggested to mediate transcriptional activation by the viral E1A protein. To assess the role of E4F, we have introduced mutations into the E4F/ATF binding sites of the E4 promoter and monitored promoter activity in HeLa cells. We find that the core motif (TGACG) of the E4F/ATF binding site is important for E4 promoter activity. However, a point mutation adjacent to the core motif that reduces E4F binding (but has no effect on ATF binding) has no effect on E4 promoter activity. Together with previous results, these findings indicate that there are at least two cellular factors (a member of the ATF family and E4F) that can function with E1A to induce transcription of the E4 promoter. We also find that certain mutations strongly reduce E4 transcription in vivo but have no effect on ATF-2 binding in vitro. These results are therefore incompatible with the possibility that (with respect to members of the ATF family) ATF-2 alone can function with E1A to transactivate the E4 promoter in HeLa cells.

摘要

细胞因子E4F和ATF-2(激活转录因子[ATF]家族的成员)结合腺病毒E4启动子中的共同位点,并且两者都被认为介导病毒E1A蛋白的转录激活。为了评估E4F的作用,我们在E4启动子的E4F/ATF结合位点引入了突变,并监测了HeLa细胞中的启动子活性。我们发现E4F/ATF结合位点的核心基序(TGACG)对E4启动子活性很重要。然而,与核心基序相邻的一个点突变降低了E4F结合(但对ATF结合没有影响),对E4启动子活性没有影响。与先前的结果一起,这些发现表明至少有两种细胞因子(ATF家族的一个成员和E4F)可以与E1A一起发挥作用以诱导E4启动子的转录。我们还发现某些突变在体内强烈降低E4转录,但在体外对ATF-2结合没有影响。因此,这些结果与(就ATF家族成员而言)单独的ATF-2可以与E1A一起在HeLa细胞中反式激活E4启动子的可能性不相符。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fce/361290/3ab74568bff7/molcellb00033-0024-a.jpg

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