Katoh I, Yoshinaka Y, Ikawa Y
Tsukuba Life Science Center, Institute of Chemical and Physical Research, Ibaraki, Japan.
EMBO J. 1989 Feb;8(2):497-503. doi: 10.1002/j.1460-2075.1989.tb03403.x.
The genome of bovine leukemia virus (BLV) encodes a transcriptional trans-activator p38tax (also referred to as pXBL-I) which amplifies the virus gene expression driven by its long terminal repeat (LTR). It was proposed that activation of cellular gene expression by p38tax might be involved in the mechanism of B-cell transformation caused in vivo by BLV infection. Here, we report that the U3 region of BLV LTR contains multiple regulatory elements responsive to p38tax. A core element composing the p38tax-inducible U3 structure is suggested to be a heptanucleotide motif of 5'TGACGTCA3', the consensus sequence proposed for a cAMP-responsive element (CRE) and for the binding sites of a cellular transcription factor (ATF). Adenovirus-5 E3 and E4, c-fos and somatostatin regulatory regions containing CRE/ATF-element exhibited responsiveness to p38tax in a chloramphenicol acetyltransferase transient expression assay. These suggest that in BLV-infected cells, cellular gene expression might be induced abnormally by the virus trans-activator through ATF or ATF-like factors.
牛白血病病毒(BLV)的基因组编码一种转录反式激活因子p38tax(也称为pXBL-I),它能增强由其长末端重复序列(LTR)驱动的病毒基因表达。有人提出,p38tax对细胞基因表达的激活可能参与了BLV感染在体内引起的B细胞转化机制。在此,我们报告BLV LTR的U3区域包含多个对p38tax有反应的调控元件。构成p38tax诱导型U3结构的核心元件被认为是一个5'TGACGTCA3'的七核苷酸基序,这是为cAMP反应元件(CRE)和细胞转录因子(ATF)的结合位点所提出的共有序列。在氯霉素乙酰转移酶瞬时表达试验中,含有CRE/ATF元件的腺病毒5型E3和E4、c-fos和生长抑素调控区域对p38tax有反应。这些表明,在BLV感染的细胞中,病毒反式激活因子可能通过ATF或类似ATF的因子异常诱导细胞基因表达。