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QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing

Mechanisms that regulate silk protein synthesis provide the basis for silkworm variety breeding and silk gland bioreactor optimization. Here, using the pooling sequencing-based methodology, we deciphered the genetic basis for the varied silk production in different silkworm strains. We identified 8...

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Autores principales: Li, Chunlin, Tong, Xiaoling, Zuo, Weidong, Luan, Yue, Gao, Rui, Han, Minjin, Xiong, Gao, Gai, Tingting, Hu, Hai, Dai, Fangyin, Lu, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740181/
https://www.ncbi.nlm.nih.gov/pubmed/29269837
http://dx.doi.org/10.1038/s41598-017-18277-y
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author Li, Chunlin
Tong, Xiaoling
Zuo, Weidong
Luan, Yue
Gao, Rui
Han, Minjin
Xiong, Gao
Gai, Tingting
Hu, Hai
Dai, Fangyin
Lu, Cheng
author_facet Li, Chunlin
Tong, Xiaoling
Zuo, Weidong
Luan, Yue
Gao, Rui
Han, Minjin
Xiong, Gao
Gai, Tingting
Hu, Hai
Dai, Fangyin
Lu, Cheng
author_sort Li, Chunlin
collection PubMed
description Mechanisms that regulate silk protein synthesis provide the basis for silkworm variety breeding and silk gland bioreactor optimization. Here, using the pooling sequencing-based methodology, we deciphered the genetic basis for the varied silk production in different silkworm strains. We identified 8 SNPs, with 6 on chromosome 11 and 1 each on chromosomes 22 and 23, that were linked with silk production. After conducting an association analysis between gene expression pattern, silk gland development and cocoon shell weight (CSW), BMGN011620 was found to be regulating silk production. BMGN011620 encodes the 60S ribosomal protein, L18, which is an indispensable component of the 60S ribosomal subunit; therefore we named it BmRPL18. Moreover, the clustering of linked SNPs on chromosome 11 and the analysis of differentially expressed genes reported in previous Omics studies indicated that the genes regulating silk protein synthesis may exhibit a clustering distribution in the silkworm genome. These results collectively advance our understanding of the regulation of silk production, including the role of ribosomal proteins and the clustered distribution of genes involved in silk protein synthesis.
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spelling pubmed-57401812018-01-03 QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing Li, Chunlin Tong, Xiaoling Zuo, Weidong Luan, Yue Gao, Rui Han, Minjin Xiong, Gao Gai, Tingting Hu, Hai Dai, Fangyin Lu, Cheng Sci Rep Article Mechanisms that regulate silk protein synthesis provide the basis for silkworm variety breeding and silk gland bioreactor optimization. Here, using the pooling sequencing-based methodology, we deciphered the genetic basis for the varied silk production in different silkworm strains. We identified 8 SNPs, with 6 on chromosome 11 and 1 each on chromosomes 22 and 23, that were linked with silk production. After conducting an association analysis between gene expression pattern, silk gland development and cocoon shell weight (CSW), BMGN011620 was found to be regulating silk production. BMGN011620 encodes the 60S ribosomal protein, L18, which is an indispensable component of the 60S ribosomal subunit; therefore we named it BmRPL18. Moreover, the clustering of linked SNPs on chromosome 11 and the analysis of differentially expressed genes reported in previous Omics studies indicated that the genes regulating silk protein synthesis may exhibit a clustering distribution in the silkworm genome. These results collectively advance our understanding of the regulation of silk production, including the role of ribosomal proteins and the clustered distribution of genes involved in silk protein synthesis. Nature Publishing Group UK 2017-12-21 /pmc/articles/PMC5740181/ /pubmed/29269837 http://dx.doi.org/10.1038/s41598-017-18277-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Chunlin
Tong, Xiaoling
Zuo, Weidong
Luan, Yue
Gao, Rui
Han, Minjin
Xiong, Gao
Gai, Tingting
Hu, Hai
Dai, Fangyin
Lu, Cheng
QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title_full QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title_fullStr QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title_full_unstemmed QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title_short QTL analysis of cocoon shell weight identifies BmRPL18 associated with silk protein synthesis in silkworm by pooling sequencing
title_sort qtl analysis of cocoon shell weight identifies bmrpl18 associated with silk protein synthesis in silkworm by pooling sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740181/
https://www.ncbi.nlm.nih.gov/pubmed/29269837
http://dx.doi.org/10.1038/s41598-017-18277-y
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