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家蚕丝氨酸 tRNA 合成酶和酪氨酸 tRNA 合成酶的克隆与功能分析。

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

机构信息

School of Basic Medicine and Biological Sciences, Soochow University, Suzhou, Jiangsu 215123, P.R. China.

National Engineering Laboratory for Modern Silk, Soochow University, Suzhou, Jiangsu 215123, P.R. China.

出版信息

Sci Rep. 2017 Jan 30;7:41563. doi: 10.1038/srep41563.

Abstract

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 TiO 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 TiO NPs showed no effect on the transcription of aaRS and content of free amino acids, suggesting that TiO NPs promotes silk protein synthesis possibly by increasing the activity of fibroin synthase in silkworm.

摘要

氨酰-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家蚕丝素的主要氨基酸。其中,丙氨酰-tRNA 合成酶(AlaRS)和甘氨酰-tRNA 合成酶(GlyRS)的基因已被克隆。本研究从家蚕中克隆了丝氨酰-tRNA 合成酶(SerRS)和酪氨酰-tRNA 合成酶(TyrRS)基因。它们的全长分别为 1709bp 和 1868bp,包含 1485bp 和 1575bp 的开放阅读框(ORF)。RT-PCR 检测表明,SerRS、TyrRS、AlaRS 和 GlyRS 的转录水平在丝腺中明显高于其他组织。此外,它们在中后部丝腺中的转录水平远高于前部丝腺。此外,用毒死蜱(一种抑制丝蛋白合成的抑制剂)而不是 TiO NP(一种促进丝蛋白合成的增强剂)处理家蚕,显著降低了后部丝腺中 aaRS 的转录水平和游离氨基酸含量,从而影响丝蛋白合成,这可能是毒死蜱致蚕病的机制。此外,低浓度的 TiO NPs 对 aaRS 的转录和游离氨基酸含量没有影响,表明 TiO NPs 可能通过增加家蚕丝素合成酶的活性来促进丝蛋白合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80f0/5278501/c68ae2bb52db/srep41563-f1.jpg

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