Suyama Y
Department of Biology, University of Pennsylvania, Philadelphia 19104.
Curr Genet. 1986;10(5):411-20. doi: 10.1007/BF00418415.
Two dimensional (2D) urea-polyacrylamide gel electrophoresis of tRNA isolated from Tetrahymena mitochondria separated at least 36 spots, while more than 45 major and minor spots were resolved with cytosolic tRNA. Co-electrophoresis of mitochondrial and cytosolic tRNAs revealed that many spots co-migrate. When radioactive mitochondrial tRNA was hybridized to mtDNA under various conditions and tRNA melted from the hybrid was analyzed by 2D gel electrophoresis, only 10 tRNA spots were found. Identified as mtDNA-encoded were 2 spots for tRNA(leu), 2 for tRNA(met), and 1 each for tRNA(phe), tRNA(trp) and tRNA(tyr). The remaining three were unidentified. Mitochondrial tRNA spots that correspond to the tRNAs for arg, gly, ile, lys, ser, and val do not hybridize with mtDNA, and in gel positions they correspond to the cytoplasmic tRNA spots for the same respective amino acids. These mitochondrial tRNAs isolated from the gel can be acylated either by the mitochondrial or cytosolic enzymes. Mitochondrial tRNA isolated from a Tetrahymena cell homogenate which was pretreated with RNase A and Micrococcus nuclease exhibited the same 2D gel pattern as a non-treated control. Mitochondrial tRNAs from old and young cells showed generally similar tRNA spots in 2D gels, though more variable spots were seen with old cells. 3H-labeled whole-cell tRNA added to the cell homogenate prior to the mitochondrial isolation procedure did not remain associated with the final mitochondrial tRNA preparation. The present studies also showed mitochondrial tRNAs bound to the mitochondrial 80S monosome and polysome fractions. Radioactive tRNA added to the mitochondrial lysate does not adhere to the ribosomes, suggesting that the ribosome-bound tRNAs are not contaminating cytoplasmic tRNAs. These results are generally in good agreement with our previous data showing that only a small number of tRNAs are coded for by the mitochondrial DNA, while the others are a selected set of imported cytoplasmic tRNAs.
从嗜热四膜虫线粒体中分离得到的tRNA进行二维(2D)尿素-聚丙烯酰胺凝胶电泳,可分辨出至少36个斑点,而胞质tRNA则可分辨出45个以上的主要和次要斑点。线粒体和胞质tRNA的共电泳显示许多斑点迁移位置相同。当放射性线粒体tRNA在各种条件下与线粒体DNA杂交,并通过二维凝胶电泳分析从杂交体中解链的tRNA时,仅发现10个tRNA斑点。已确定为线粒体DNA编码的有2个tRNA(leu)斑点、2个tRNA(met)斑点,以及各1个tRNA(phe)、tRNA(trp)和tRNA(tyr)斑点。其余3个未鉴定。与精氨酸、甘氨酸、异亮氨酸、赖氨酸、丝氨酸和缬氨酸对应的线粒体tRNA斑点不与线粒体DNA杂交,在凝胶中的位置与相同氨基酸的胞质tRNA斑点相对应。从凝胶中分离得到的这些线粒体tRNA可用线粒体或胞质酶进行酰化。用核糖核酸酶A和微球菌核酸酶预处理的嗜热四膜虫细胞匀浆中分离得到的线粒体tRNA,其二维凝胶图谱与未处理的对照相同。老龄和幼龄细胞的线粒体tRNA在二维凝胶中通常显示出相似的tRNA斑点,不过老龄细胞中可见更多可变斑点。在进行线粒体分离之前,向细胞匀浆中添加的3H标记全细胞tRNA并未与最终的线粒体tRNA制剂结合。本研究还表明线粒体tRNA与线粒体80S单体和多聚体部分结合。添加到线粒体裂解物中的放射性tRNA不与核糖体结合,这表明与核糖体结合的tRNA不是污染的胞质tRNA。这些结果与我们之前的数据总体上非常一致,即线粒体DNA仅编码少数tRNA,而其他tRNA是一组经过挑选的导入胞质tRNA。