Shiba K, Motegi H, Yoshida M, Noda T
Department of Cell Biology, Cancer Institute, Japanese Foundation for Cancer Research, 1-37-1 Kami-Ikebukuro, Toshima, Tokyo 170-8455, Japan.
Nucleic Acids Res. 1998 Nov 15;26(22):5045-51. doi: 10.1093/nar/26.22.5045.
We have cloned and sequenced a cDNA encoding human cytoplasmic asparaginyl-tRNA synthetase (AsnRS). The N-terminal appended domain of 112 amino acid represents the signature sequence for the eukaryotic AsnRS and is absent from archaebacterial or eubacterial enzymes. The canonical ortholog for AsnRS is absent from most archaebacterial and some eubacterial genomes, indicating that in those organisms, formation of asparaginyl-tRNA is independent of the enzyme. The high degree of sequence conservation among asparaginyl- and aspartyl-tRNA synthetases (AsxRS) made it possible to infer the evolutionary paths of the two enzymes. The data show the neighbor relationship between AsnRS and eubacterial aspartyl-tRNA synthetase, and support the occurrence of AsnRS early in the course of evolution, which is in contrast to the proposed late occurrence of glutaminyl-tRNA synthetase.
我们已经克隆并测序了编码人细胞质天冬酰胺-tRNA合成酶(AsnRS)的cDNA。112个氨基酸的N端附加结构域代表真核生物AsnRS的特征序列,古细菌或真细菌酶中不存在该结构域。大多数古细菌和一些真细菌基因组中不存在AsnRS的典型直系同源物,这表明在这些生物体中,天冬酰胺-tRNA的形成不依赖于该酶。天冬酰胺和天冬氨酰-tRNA合成酶(AsxRS)之间高度的序列保守性使得推断这两种酶的进化路径成为可能。数据显示了AsnRS与真细菌天冬氨酰-tRNA合成酶之间的亲缘关系,并支持AsnRS在进化过程早期出现,这与所提出的谷氨酰胺-tRNA合成酶较晚出现形成对比。