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Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm Bombyx mori

机译:家蚕丝氨酰-tRNA合成酶和酪氨酰-tRNA合成酶的克隆及功能分析

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摘要

Aminoacyl-tRNA synthetases are the key enzymes for protein synthesis. Glycine, alanine, serine and tyrosine are the major amino acids composing fibroin of silkworm. Among them, the genes of alanyl-tRNA synthetase (AlaRS) and glycyl-tRNA synthetase (GlyRS) have been cloned. In this study, the seryl-tRNA synthetase (SerRS) and tyrosyl-tRNA synthetase (TyrRS) genes from silkworm were cloned. Their full length are 1709 bp and 1868 bp and contain open reading frame (ORF) of 1485 bp and 1575 bp, respectively. RT-PCR examination showed that the transcription levels of SerRS, TyrRS, AlaRS and GlyRS are significantly higher in silk gland than in other tissues. In addition, their transcription levels are much higher in middle and posterior silk gland than in anterior silk gland. Moreover, treatment of silkworms with phoxim, an inhibitor of silk protein synthesis, but not TiO2 NP, an enhancer of silk protein synthesis, significantly reduced the transcription levels of aaRS and content of free amino acids in posterior silk gland, therefore affecting silk protein synthesis, which may be the mechanism of phoxim-silking disorders. Furthermore, low concentration of TiO2 NPs showed no effect on the transcription of aaRS and content of free amino acids, suggesting that TiO2 NPs promotes silk protein synthesis possibly by increasing the activity of fibroin synthase in silkworm.
机译:氨酰基-tRNA合成酶是蛋白质合成的关键酶。甘氨酸,丙氨酸,丝氨酸和酪氨酸是构成蚕丝蛋白的主要氨基酸。其中,已经克隆了丙氨酰-tRNA合成酶(AlaRS)和甘氨酰-tRNA合成酶(GlyRS)的基因。在这项研究中,克隆了家蚕的丝氨酰tRNA合成酶(SerRS)和酪氨酰tRNA合成酶(TyrRS)基因。它们的全长分别为1709 bp和1868 bp,并分别包含1485 bp和1575 bp的开放阅读框(ORF)。 RT-PCR检查显示丝腺中SerRS,TyrRS,AlaRS和GlyRS的转录水平显着高于其他组织。另外,它们的转录水平在中部和后部丝腺中比在前部丝腺中高得多。此外,用辛硫磷(一种蚕丝蛋白合成抑制剂)而不是TiO2 NP(一种蚕丝蛋白合成增强剂)处理蚕,可显着降低后蚕丝腺中aaRS的转录水平和游离氨基酸含量,从而影响蚕丝蛋白合成,这可能是辛硫磷镇静障碍的机制。此外,低浓度的TiO2 NPs对aaRS的转录和游离氨基酸的含量没有影响,这表明TiO2 NPs可能通过增加蚕丝蛋白合成酶的活性来促进蚕丝蛋白的合成。

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