Tolkunova E, Park H, Xia J, King M P, Davidson E
Department of Biochemistry and Molecular Pharmacology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
J Biol Chem. 2000 Nov 10;275(45):35063-9. doi: 10.1074/jbc.M006265200.
Two cDNAs encoding human lysyl-tRNA synthetase have been identified. One encodes the cytoplasmic form of the enzyme identified previously. The second cDNA contains the same sequence but with a 180-bp insertion at the 5'-end of the mRNA. This results in a predicted protein whose carboxyl 576 amino acids are identical to those of the cytoplasmic enzyme but with a different amino terminus of 49 amino acids that contains a putative mitochondrial targeting sequence. Expression of the two lysyl-tRNA synthetase-green fluorescent protein gene fusions in a human cell line confirmed that the cytoplasmic form was targeted to the cytoplasm and the mitochondrial form to mitochondria. The genomic lysyl-tRNA synthetase gene consisted of 15 exons. The two isoforms were created by alternative splicing of the first three exons of the gene. The cytoplasmic form was created by splicing exon 1 to exon 3. The inclusion of exon 2 between exons 1 and 3 produced an mRNA encoding the mitochondrial isoform with an additional upstream small open reading frame, consisting mainly of a portion of the 5' coding region of the cytoplasmic isoform. This is the first example of mitochondrial targeting sequence being encoded on the second exon of a gene. Ribonuclease protection analysis showed that the mRNA encoding the cytoplasmic isoform makes up approximately 70%, and the mitochondrial isoform approximately 30%, of the mature transcripts from the lysyl-tRNA synthetase gene. The mitochondrial form of the enzyme, purified after expression in Escherichia coli, aminoacylated in vitro transcripts corresponding to both the cytoplasmic and mitochondrial tRNA(Lys), despite the difference in the discriminator base sequence in the acceptor stems of these tRNAs.
已鉴定出两个编码人赖氨酰 - tRNA合成酶的cDNA。其中一个编码先前鉴定出的该酶的细胞质形式。第二个cDNA包含相同的序列,但在mRNA的5'端有一个180bp的插入片段。这导致预测的蛋白质,其羧基端的576个氨基酸与细胞质酶的相同,但有一个不同的49个氨基酸的氨基末端,其中包含一个假定的线粒体靶向序列。在人细胞系中两种赖氨酰 - tRNA合成酶 - 绿色荧光蛋白基因融合体的表达证实,细胞质形式定位于细胞质,而线粒体形式定位于线粒体。基因组赖氨酰 - tRNA合成酶基因由15个外显子组成。这两种同工型是由该基因的前三个外显子的可变剪接产生的。细胞质形式是通过将外显子1剪接到外显子3产生的。在外显子1和3之间包含外显子2产生了一种编码线粒体同工型的mRNA,其具有一个额外的上游小开放阅读框,主要由细胞质同工型的5'编码区的一部分组成。这是线粒体靶向序列在基因的第二个外显子上编码的第一个例子。核糖核酸酶保护分析表明,编码细胞质同工型的mRNA约占赖氨酰 - tRNA合成酶基因成熟转录本的70%,而线粒体同工型约占30%。在大肠杆菌中表达后纯化的该酶的线粒体形式,尽管这些tRNA的受体茎中鉴别碱基序列不同,但仍能使对应于细胞质和线粒体tRNA(Lys)的体外转录本氨基酰化。