Pause A, Sonenberg N
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
EMBO J. 1992 Jul;11(7):2643-54. doi: 10.1002/j.1460-2075.1992.tb05330.x.
eIF-4A is a translation initiation factor that exhibits bidirectional RNA unwinding activity in vitro in the presence of another translation initiation factor, eIF-4B and ATP. This activity is thought to be responsible for the melting of secondary structure in the 5' untranslated region of eukaryotic mRNAs to facilitate ribosome binding. eIF-4A is a member of a fast growing family of proteins termed the DEAD family. These proteins are believed to be RNA helicases, based on the demonstrated in vitro RNA helicase activity of two members (eIF-4A and p68) and their homology in eight amino acid regions. Several related biochemical activities were attributed to eIF-4A: (i) ATP binding, (ii) RNA-dependent ATPase and (iii) RNA helicase. To determine the contribution of the highly conserved regions to these activities, we performed site-directed mutagenesis. First we show that recombinant eIF-4A, together with recombinant eIF-4B, exhibit RNA helicase activity in vitro. Mutations in the ATPase A motif (AXXXXGKT) affect ATP binding, whereas mutations in the predicted ATPase B motif (DEAD) affect ATP hydrolysis. We report here that the DEAD region couples the ATPase with the RNA helicase activity. Furthermore, two other regions, whose functions were unknown, have also been characterized. We report that the first residue in the HRIGRXXR region is involved in ATP hydrolysis and that the SAT region is essential for RNA unwinding. Our results suggest that the highly conserved regions in the DEAD box family are critical for RNA helicase activity.
真核起始因子4A(eIF-4A)是一种翻译起始因子,在另一种翻译起始因子eIF-4B和ATP存在的情况下,它在体外表现出双向RNA解旋活性。这种活性被认为负责解开真核mRNA 5'非翻译区的二级结构,以促进核糖体结合。eIF-4A是一个快速增长的蛋白质家族(称为DEAD家族)的成员。基于两个成员(eIF-4A和p68)已证实的体外RNA解旋酶活性及其在八个氨基酸区域的同源性,这些蛋白质被认为是RNA解旋酶。几种相关的生化活性归因于eIF-4A:(i)ATP结合,(ii)RNA依赖性ATP酶和(iii)RNA解旋酶。为了确定高度保守区域对这些活性的贡献,我们进行了定点诱变。首先,我们表明重组eIF-4A与重组eIF-4B一起在体外表现出RNA解旋酶活性。ATP酶A基序(AXXXXGKT)中的突变影响ATP结合,而预测的ATP酶B基序(DEAD)中的突变影响ATP水解。我们在此报告,DEAD区域将ATP酶与RNA解旋酶活性联系起来。此外,另外两个功能未知的区域也已得到表征。我们报告说,HRIGRXXR区域中的第一个残基参与ATP水解,而SAT区域对于RNA解旋至关重要。我们的结果表明,DEAD盒家族中的高度保守区域对于RNA解旋酶活性至关重要。