Wang S S, Hopper A K
Department of Biological Chemistry, Milton S. Hershey Medical Center, Pennsylvania State University 17033.
Mol Cell Biol. 1988 Dec;8(12):5140-9. doi: 10.1128/mcb.8.12.5140-5149.1988.
To identify genes involved in pre-tRNA processing, we searched for yeast DNA sequences that specifically enhanced the expression of the SUP4(G37) gene. The SUP4(G37) gene possesses a point mutation at position 37 of suppressor tRNA(Tyr). This lesion results in a reduced rate of pre-tRNA splicing and a decreased level of nonsense suppression. A SUP4(G37) strain was transformed with a yeast genomic library, and the transformants were screened for increased suppressor activity. One transformant contained a plasmid that encoded an unessential gene, STP1, that in multiple copies enhanced the suppression of SUP4(G37) and caused increased production of mature SUP4(G37) product. Disruption of the genomic copy of STP1 resulted in a reduced efficiency of SUP4-mediated suppression and the accumulation of pre-tRNAs. Not all intron-containing pre-tRNAs were affected by the stp1-disruption. At least five of the nine families of pre-tRNAs were affected. Two other species, pre-tRNA(Ile) and pre-tRNA(3Leu), were not. We propose that STP1 encodes a tRNA species-specific product that functions as a helper for pre-tRNA splicing. The STP1 product may interact with pre-tRNAs to generate a structure that is efficiently recognized by splicing machinery.
为了鉴定参与前体tRNA加工的基因,我们搜索了能特异性增强SUP4(G37)基因表达的酵母DNA序列。SUP4(G37)基因在抑制性tRNA(Tyr)的第37位存在一个点突变。该损伤导致前体tRNA剪接速率降低和无义抑制水平下降。用酵母基因组文库转化SUP4(G37)菌株,并筛选具有增强抑制活性的转化体。一个转化体含有一个编码非必需基因STP1的质粒,该基因的多个拷贝增强了对SUP4(G37)的抑制作用,并导致成熟SUP4(G37)产物产量增加。破坏STP1的基因组拷贝导致SUP4介导的抑制效率降低和前体tRNA的积累。并非所有含内含子的前体tRNA都受stp1破坏的影响。九个前体tRNA家族中至少有五个受到影响。另外两个种类,前体tRNA(Ile)和前体tRNA(3Leu)不受影响。我们提出STP1编码一种tRNA种类特异性产物,其作为前体tRNA剪接的辅助因子发挥作用。STP1产物可能与前体tRNA相互作用以产生一种能被剪接机制有效识别的结构。