Cargando…

Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands

BACKGROUND: Using the piggyBac-mediated GAL4/UAS transgenic system established in the silkworm, Bombyx mori, we have previously reported that overexpression of the Ras1(CA) oncogene specifically in the posterior silk gland (PSG) improved cell growth, fibroin synthesis, and thus silk yield. However,...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Li, Ma, Qian, Li, Xuan, Cheng, Leilei, Li, Kai, Li, Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029079/
https://www.ncbi.nlm.nih.gov/pubmed/24606580
http://dx.doi.org/10.1186/1471-2164-15-182
_version_ 1782317156360257536
author Ma, Li
Ma, Qian
Li, Xuan
Cheng, Leilei
Li, Kai
Li, Sheng
author_facet Ma, Li
Ma, Qian
Li, Xuan
Cheng, Leilei
Li, Kai
Li, Sheng
author_sort Ma, Li
collection PubMed
description BACKGROUND: Using the piggyBac-mediated GAL4/UAS transgenic system established in the silkworm, Bombyx mori, we have previously reported that overexpression of the Ras1(CA) oncogene specifically in the posterior silk gland (PSG) improved cell growth, fibroin synthesis, and thus silk yield. However, the detailed molecular mechanism remains to be fully elucidated. To achieve this goal, Illumina sequencing was used in the present study to compare the transcriptomes of the Ras1(CA)-overexpressed and wildtype PSGs. RESULTS: The transcriptomic sequencing results in 56 million reads following filtering steps. Most of the reads (~70%) are successfully mapped to the Bombyx genome. The mapped reads are situated within at least 9,133 predicted genes, covering 62.46% genes of the Bombyx genome. GO annotation shows that 2512 of the 2,636 differentially expressed genes (DEGs) are mostly distributed in metabolic process, cell and cell part, and binding, and KEGG annotation shows that 1,941 DEGs are mapped into 277 pathways. Importantly, Ras1(CA) overexpression in the PSG upregulated many DEGs distributed in “pathways in cancer”, “insulin signaling pathway”, and “MAPK signaling pathway” as well as “purine metabolism” and “pyrimidine metabolism”. Transcriptional regulation of these DEGs was verified by quantitative real-time PCR. Moreover, injection of small-molecule chemical inhibitors of the Ras1 downstream effectors into the Ras1(CA)-overexpressed silkworms revealed that both Raf-MAPK and PI3K-TORC1 pathways are required for the Ras1-induced DEG expression. CONCLUSION: The transcriptomic analysis illustrates that, apart from phosphorylational regulation, Ras1 activates its downstream Raf-MAPK and PI3K-TORC1 pathways at the transcriptional level. Meanwhile, Ras1 increases DNA content and induces endoreplication, at least in part, by upregulating genes in “nucleotide metabolism” and “cell cycle”. This study provides further insights into the molecular mechanism of how Ras1(CA) overexpression in the PSG improves silk yield. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-182) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4029079
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-40290792014-05-22 Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands Ma, Li Ma, Qian Li, Xuan Cheng, Leilei Li, Kai Li, Sheng BMC Genomics Research Article BACKGROUND: Using the piggyBac-mediated GAL4/UAS transgenic system established in the silkworm, Bombyx mori, we have previously reported that overexpression of the Ras1(CA) oncogene specifically in the posterior silk gland (PSG) improved cell growth, fibroin synthesis, and thus silk yield. However, the detailed molecular mechanism remains to be fully elucidated. To achieve this goal, Illumina sequencing was used in the present study to compare the transcriptomes of the Ras1(CA)-overexpressed and wildtype PSGs. RESULTS: The transcriptomic sequencing results in 56 million reads following filtering steps. Most of the reads (~70%) are successfully mapped to the Bombyx genome. The mapped reads are situated within at least 9,133 predicted genes, covering 62.46% genes of the Bombyx genome. GO annotation shows that 2512 of the 2,636 differentially expressed genes (DEGs) are mostly distributed in metabolic process, cell and cell part, and binding, and KEGG annotation shows that 1,941 DEGs are mapped into 277 pathways. Importantly, Ras1(CA) overexpression in the PSG upregulated many DEGs distributed in “pathways in cancer”, “insulin signaling pathway”, and “MAPK signaling pathway” as well as “purine metabolism” and “pyrimidine metabolism”. Transcriptional regulation of these DEGs was verified by quantitative real-time PCR. Moreover, injection of small-molecule chemical inhibitors of the Ras1 downstream effectors into the Ras1(CA)-overexpressed silkworms revealed that both Raf-MAPK and PI3K-TORC1 pathways are required for the Ras1-induced DEG expression. CONCLUSION: The transcriptomic analysis illustrates that, apart from phosphorylational regulation, Ras1 activates its downstream Raf-MAPK and PI3K-TORC1 pathways at the transcriptional level. Meanwhile, Ras1 increases DNA content and induces endoreplication, at least in part, by upregulating genes in “nucleotide metabolism” and “cell cycle”. This study provides further insights into the molecular mechanism of how Ras1(CA) overexpression in the PSG improves silk yield. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-182) contains supplementary material, which is available to authorized users. BioMed Central 2014-03-09 /pmc/articles/PMC4029079/ /pubmed/24606580 http://dx.doi.org/10.1186/1471-2164-15-182 Text en © Ma et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Ma, Li
Ma, Qian
Li, Xuan
Cheng, Leilei
Li, Kai
Li, Sheng
Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title_full Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title_fullStr Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title_full_unstemmed Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title_short Transcriptomic analysis of differentially expressed genes in the Ras1(CA)-overexpressed and wildtype posterior silk glands
title_sort transcriptomic analysis of differentially expressed genes in the ras1(ca)-overexpressed and wildtype posterior silk glands
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029079/
https://www.ncbi.nlm.nih.gov/pubmed/24606580
http://dx.doi.org/10.1186/1471-2164-15-182
work_keys_str_mv AT mali transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands
AT maqian transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands
AT lixuan transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands
AT chengleilei transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands
AT likai transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands
AT lisheng transcriptomicanalysisofdifferentiallyexpressedgenesintheras1caoverexpressedandwildtypeposteriorsilkglands