Chang K C, Hansen E, Foroni L, Lida J, Goldspink G
Unit of Veterinary Molecular and Cellular Biology, Royal Veterinary College, University of London, U.K.
Arch Virol. 1991;117(1-2):1-15. doi: 10.1007/BF01310488.
The virus- and interferon-inducible human MxA (IFI-78k) gene is a homologue of the murine influenza resistance gene Mx1. Three overlapping human cosmid clones covering most of the gene including its promoter region were isolated. Sequencing the 5' MxA cDNA derived by RT-PCR (reverse transcriptase-polymerase chain reaction) confirmed the most 5' putative transcriptional start site. The MxA promoter does not contain a TATA or CCAAT box but has three Interferon Stimulated Response Element (ISRE) motifs. Strong induction with type I interferons was demonstrated with a fragment containing only two ISREs in human L132 cells. This induced expression was not adversely affected by 2-aminopurine. However, the promoter showed constitutive expression in transiently or stably transfected murine LM cells.
病毒和干扰素诱导的人Mx A(IFI-78k)基因是鼠流感抗性基因Mx1的同源物。分离出三个重叠的人黏粒克隆,它们覆盖了该基因的大部分区域,包括其启动子区域。对通过逆转录聚合酶链反应(RT-PCR)获得的5'Mx A cDNA进行测序,证实了最5'端推定的转录起始位点。Mx A启动子不含TATA盒或CCAAT盒,但有三个干扰素刺激反应元件(ISRE)基序。在人L132细胞中,仅含有两个ISRE的片段显示出对I型干扰素的强烈诱导作用。这种诱导表达不受2-氨基嘌呤的不利影响。然而,该启动子在瞬时或稳定转染的鼠LM细胞中表现出组成型表达。