Tanguay R L, Gallie D R
Department of Biochemistry, University of California, Riverside 92521-0129, USA.
Mol Cell Biol. 1996 Jan;16(1):146-56. doi: 10.1128/MCB.16.1.146.
All polyadenylated mRNAs contain sequence of variable length between the coding region and the poly(A) tail. Little has been done to establish what role the length of the 3' untranslated region (3'UTR) plays in posttranscriptional regulation. Using firefly luciferase (luc) reporter mRNA in transiently transfected Chinese hamster ovary (CHO) cells, we observed that the addition of a poly(A) tail increased expression 97-fold when the length of the 3'UTR was 19 bases but that its stimulatory effect was only 2.3-fold when the length of the 3'UTR was increased to 156 bases. The effect of the luc 3'UTR on poly(A) tail function was orientation independent, suggesting that its length and not its primary sequence was the important factor. Increasing the length of the 3'UTR increased expression from poly(A)- mRNA but had little effect on poly(A)+ mRNA. To examine the effect of length on translational efficiency and mRNA stability, a 20-base sequence was introduced and reiterated downstream of the luc stop codon to generate a nested set of constructs in which the length of the 3'UTR increased from 4 to 104 bases. For poly(A)- reporter mRNA, translational efficiency in CHO cells increased 38-fold as the length of the 3'UTR increased from 4 to 104 bases. Increasing the length of the 3'UTR beyond 104 bases increased expression even further. Increasing the length of the 3'UTR also resulted in a 2.5-fold stabilization of the reporter mRNA. For poly(A)+ mRNA, the translational efficiency and mRNA half-life increased only marginally as the length of the 3'UTR increased from 27 to 161 bases. However, positioning the poly(A) tail only 7 bases downstream of the stop codon resulted in a 39-fold reduction in the rate of translation relative to a construct with a 27-base 3'UTR, which may be a consequence of the poly(A) tail-poly(A)-binding protein complex functioning as a steric block to translocating ribosomes as they approached the termination codon. The optimal length of the 3' noncoding region for maximal poly(A) tail-mediated stimulation of translation is approximately 27 bases. These data suggest that the length of the 3'UTR plays an important role in determining both the translational efficiency and the stability of an mRNA.
所有多聚腺苷酸化的mRNA在编码区和多聚(A)尾之间都含有长度可变的序列。关于3'非翻译区(3'UTR)的长度在转录后调控中起什么作用,目前所做的研究很少。在瞬时转染的中国仓鼠卵巢(CHO)细胞中使用萤火虫荧光素酶(luc)报告mRNA,我们观察到当3'UTR的长度为19个碱基时,添加多聚(A)尾使表达增加了97倍,但当3'UTR的长度增加到156个碱基时,其刺激作用仅为2.3倍。luc 3'UTR对多聚(A)尾功能的影响与方向无关,这表明其长度而非一级序列是重要因素。增加3'UTR的长度会增加来自多聚(A)- mRNA的表达,但对多聚(A)+ mRNA影响不大。为了研究长度对翻译效率和mRNA稳定性的影响,在luc终止密码子下游引入并重复一个20个碱基的序列,以生成一组嵌套构建体,其中3'UTR的长度从4个碱基增加到104个碱基。对于多聚(A)-报告mRNA,随着3'UTR的长度从4个碱基增加到104个碱基,CHO细胞中的翻译效率提高了38倍。将3'UTR的长度增加到104个碱基以上会进一步增加表达。增加3'UTR的长度还导致报告mRNA稳定了2.5倍。对于多聚(A)+ mRNA,随着3'UTR的长度从27个碱基增加到161个碱基,翻译效率和mRNA半衰期仅略有增加。然而,将多聚(A)尾定位在终止密码子下游仅7个碱基处,相对于具有27个碱基3'UTR的构建体,翻译速率降低了39倍,这可能是多聚(A)尾 - 多聚(A)结合蛋白复合物在核糖体接近终止密码子时作为空间障碍发挥作用的结果。3'非编码区实现多聚(A)尾介导的最大翻译刺激的最佳长度约为27个碱基。这些数据表明,3'UTR的长度在决定mRNA的翻译效率和稳定性方面都起着重要作用。