Montagne J, Béraud C, Crenon I, Lombard-Platet G, Gazzolo L, Sergeant A, Jalinot P
UMR 49 CNRS-ENS, Ecole Normale Supérieure de Lyon, France.
EMBO J. 1990 Mar;9(3):957-64. doi: 10.1002/j.1460-2075.1990.tb08194.x.
Activation of the HTLV-I promoter by the viral Tax1 transactivator is mediated by a 21 bp sequence motif imperfectly repeated three times and composed of three exactly conserved domains (A, B and C from 5' to 3'). We show here that the Tax1 response requires the integrity of the B domain and of at least one of the flanking A or C domains. We have identified three cellular proteins which bind specifically to the 21 bp motif. One of these is the already well-characterized transcription factor ATF. The other two, namely HEB1 and HEB2, are specific for the 21 bp motif. HEB1 can bind to either domain A or C, but binding of ATF and HEB2 is determined by domain B. However, neither domain B alone, nor ATF/CREB binding sites respond significantly to Tax1. We therefore propose that Tax1 induction of the 21 bp enhancer element requires interaction with the two different cellular proteins identified in this study: HEB1 and HEB2, rather than binding of the ATF factor.
病毒Tax1反式激活因子对HTLV-I启动子的激活作用,是由一段21bp的序列基序介导的,该基序不完全重复三次,由三个完全保守的结构域(从5'到3'依次为A、B和C)组成。我们在此表明,Tax1应答需要B结构域以及侧翼A或C结构域中至少一个的完整性。我们鉴定出三种与21bp基序特异性结合的细胞蛋白。其中一种是已被充分表征的转录因子ATF。另外两种,即HEB1和HEB2,对21bp基序具有特异性。HEB1可以与结构域A或C结合,但ATF和HEB2的结合由结构域B决定。然而,单独的结构域B或ATF/CREB结合位点对Tax1均无明显应答。因此,我们提出Tax1对21bp增强子元件的诱导需要与本研究中鉴定出的两种不同细胞蛋白相互作用:HEB1和HEB2,而不是ATF因子的结合。