Cheng J, Belgrader P, Zhou X, Maquat L E
Department of Human Genetics, Roswell Park Cancer Institute, Buffalo, New York 14263.
Mol Cell Biol. 1994 Sep;14(9):6317-25. doi: 10.1128/mcb.14.9.6317-6325.1994.
The translation of human triosephosphate isomerase (TPI) mRNA normally terminates at codon 249 within exon 7, the final exon. Frameshift and nonsense mutations of the type that cause translation to terminate prematurely at or upstream of codon 189 within exon 6 reduce the level of nuclear TPI mRNA to 20 to 30% of normal by a mechanism that is not a function of the distance of the nonsense codon from either the translation initiation or termination codon. In contrast, frameshift and nonsense mutations of another type that cause translation to terminate prematurely at or downstream of codon 208, also within exon 6, have no effect on the level of nuclear TPI mRNA. In this work, quantitations of RNA that derived from TPI alleles in which nonsense codons had been generated between codons 189 and 208 revealed that the boundary between the two types of nonsense codons resides between codons 192 and 195. The analysis of TPI gene insertions and deletions indicated that the positional feature differentiating the two types of nonsense codons is the distance of the nonsense codon upstream of intron 6. For example, the movement of intron 6 to a position downstream of its normal location resulted in a concomitant downstream movement of the boundary between the two types of nonsense codons. The analysis of intron 6 mutations indicated that the intron 6 effect is stipulated by the 88 nucleotides residing between the 5' and 3' splice sites. Since the deletion of intron 6 resulted in only partial abrogation of the nonsense codon-mediated reduction in the level of TPI mRNA, other sequences within TPI pre-mRNA must function in the effect. One of these sequences may be intron 2, since the deletion of intron 2 also resulted in partial abrogation of the effect. In experiments that switched introns 2 and 6, the replacement of intron 6 with intron 2 was of no consequence to the effect of a nonsense codon within either exon 1 or exon 6. In contrast, the replacement of intron 2 with intron 6 was inconsequential to the effect of a nonsense codon in exon 6 but resulted in partial abrogation of a nonsense codon in exon 1.
人类磷酸丙糖异构酶(TPI)mRNA的翻译通常在最后一个外显子即外显子7内的密码子249处终止。导致翻译在位于外显子6内密码子189处或其上游提前终止的移码突变和无义突变,通过一种与无义密码子距翻译起始密码子或终止密码子的距离无关的机制,将细胞核TPI mRNA的水平降低至正常水平的20%至30%。相比之下,另一种导致翻译在同样位于外显子6内的密码子208处或其下游提前终止的移码突变和无义突变,对细胞核TPI mRNA的水平没有影响。在这项研究中,对来自TPI等位基因的RNA进行定量分析,这些等位基因在密码子189和208之间产生了无义密码子,结果显示这两种无义密码子之间的界限位于密码子192和195之间。对TPI基因插入和缺失的分析表明,区分这两种无义密码子的位置特征是无义密码子位于内含子6上游的距离。例如将内含子6移至其正常位置下游,会导致两种无义密码子之间的界限随之向下游移动。对内含子6突变的分析表明,内含子6的作用由位于5'和3'剪接位点之间的88个核苷酸决定。由于缺失内含子6仅部分消除了无义密码子介导的TPI mRNA水平降低,TPI前体mRNA中的其他序列必定也参与了这一作用。其中一个序列可能是内含子2,因为缺失内含子2也会部分消除这种作用。在交换内含子2和6的实验中,用内含子2替换内含子6对在外显子1或外显子6内的无义密码子的作用没有影响。相比之下,用内含子6替换内含子2对外显子6内无义密码子的作用没有影响,但会部分消除外显子1内无义密码子的作用。