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

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-t...

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Autores principales: Hu, Jingsheng, Tian, Jianghai, Li, Fanchi, Xue, Bin, Hu, Jiahuan, Cheng, Xiaoyu, Li, Jinxin, Shen, Weide, Li, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278501/
https://www.ncbi.nlm.nih.gov/pubmed/28134300
http://dx.doi.org/10.1038/srep41563
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author Hu, Jingsheng
Tian, Jianghai
Li, Fanchi
Xue, Bin
Hu, Jiahuan
Cheng, Xiaoyu
Li, Jinxin
Shen, Weide
Li, Bing
author_facet Hu, Jingsheng
Tian, Jianghai
Li, Fanchi
Xue, Bin
Hu, Jiahuan
Cheng, Xiaoyu
Li, Jinxin
Shen, Weide
Li, Bing
author_sort Hu, Jingsheng
collection PubMed
description 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(2) 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(2) NPs showed no effect on the transcription of aaRS and content of free amino acids, suggesting that TiO(2) NPs promotes silk protein synthesis possibly by increasing the activity of fibroin synthase in silkworm.
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spelling pubmed-52785012017-02-03 Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori Hu, Jingsheng Tian, Jianghai Li, Fanchi Xue, Bin Hu, Jiahuan Cheng, Xiaoyu Li, Jinxin Shen, Weide Li, Bing Sci Rep Article 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(2) 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(2) NPs showed no effect on the transcription of aaRS and content of free amino acids, suggesting that TiO(2) NPs promotes silk protein synthesis possibly by increasing the activity of fibroin synthase in silkworm. Nature Publishing Group 2017-01-30 /pmc/articles/PMC5278501/ /pubmed/28134300 http://dx.doi.org/10.1038/srep41563 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hu, Jingsheng
Tian, Jianghai
Li, Fanchi
Xue, Bin
Hu, Jiahuan
Cheng, Xiaoyu
Li, Jinxin
Shen, Weide
Li, Bing
Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title_full Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title_fullStr Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title_full_unstemmed Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title_short Clone and functional analysis of Seryl-tRNA synthetase and Tyrosyl-tRNA synthetase from silkworm, Bombyx mori
title_sort clone and functional analysis of seryl-trna synthetase and tyrosyl-trna synthetase from silkworm, bombyx mori
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278501/
https://www.ncbi.nlm.nih.gov/pubmed/28134300
http://dx.doi.org/10.1038/srep41563
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