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Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase

OBJECTIVE: Intestinal alkaline sphingomyelinase (alk-SMase) generates ceramide and inactivates platelet-activating factor associated with digestion and inhibition of cancer. There is few study to analyze the correlated function and characterize the genes related to alk-SMase comprehensively. We char...

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Autores principales: Zhu, Jiang, Wang, Lingqi, Guo, Zhongwu, Zhang, Tao, Zhang, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644495/
https://www.ncbi.nlm.nih.gov/pubmed/36348490
http://dx.doi.org/10.1186/s12935-022-02764-y
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author Zhu, Jiang
Wang, Lingqi
Guo, Zhongwu
Zhang, Tao
Zhang, Ping
author_facet Zhu, Jiang
Wang, Lingqi
Guo, Zhongwu
Zhang, Tao
Zhang, Ping
author_sort Zhu, Jiang
collection PubMed
description OBJECTIVE: Intestinal alkaline sphingomyelinase (alk-SMase) generates ceramide and inactivates platelet-activating factor associated with digestion and inhibition of cancer. There is few study to analyze the correlated function and characterize the genes related to alk-SMase comprehensively. We characterised transcriptome landscapes of intestine tissues from alk-SMase knockout (KO) mice aiming to identify novel associated genes and research targets. METHODS: We performed the high-resolution RNA sequencing of alk-SMase KO mice and compared them to wild type (WT) mice. Differentially expressed genes (DEGs) for the training group were screened. Functional enrichment analysis of the DEGs between KO mice and WT mice was implemented using the Database for Annotation, Visualization and Integrated Discovery (DAVID). An integrated protein–protein interaction (PPI) and Kyoto Encyclopedia of Genes and Genomes (KEGG) network was chose to study the relationship of differentially expressed gene. Moreover, quantitative real-time polymerase chain reaction (qPCR) was further used to validate the accuracy of RNA-seq technology. RESULTS: Our RNA-seq data found 97 differentially expressed mRNAs between the WT mice and alk-SMase gene NPP7 KO mice, in which 32 were significantly up-regulated and 65 were down-regulated, including protein coding genes, non-coding RNAs. Notably, the results of gene ontology functional enrichment analysis indicated that DEGs were functionally associated with the immune response, regulation of cell proliferation and development related terms. Additionally, an integrated network analysis was shown that some modules was significantly related to alk-SMase and with accordance of previously results. We chose 6 of these genes randomly were validated the accuracy of RNA-seq technology using qPCR and 2 genes showed difference significantly (P < 0.05). CONCLUSIONS: We investigated the potential biological significant of alk-SMase with high resolution genome-wide transcriptome of alk-SMase knockout mice. The results revealed new insight into the functional modules related to alk-SMase was involved in the intestinal related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02764-y.
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spelling pubmed-96444952022-11-15 Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase Zhu, Jiang Wang, Lingqi Guo, Zhongwu Zhang, Tao Zhang, Ping Cancer Cell Int Research OBJECTIVE: Intestinal alkaline sphingomyelinase (alk-SMase) generates ceramide and inactivates platelet-activating factor associated with digestion and inhibition of cancer. There is few study to analyze the correlated function and characterize the genes related to alk-SMase comprehensively. We characterised transcriptome landscapes of intestine tissues from alk-SMase knockout (KO) mice aiming to identify novel associated genes and research targets. METHODS: We performed the high-resolution RNA sequencing of alk-SMase KO mice and compared them to wild type (WT) mice. Differentially expressed genes (DEGs) for the training group were screened. Functional enrichment analysis of the DEGs between KO mice and WT mice was implemented using the Database for Annotation, Visualization and Integrated Discovery (DAVID). An integrated protein–protein interaction (PPI) and Kyoto Encyclopedia of Genes and Genomes (KEGG) network was chose to study the relationship of differentially expressed gene. Moreover, quantitative real-time polymerase chain reaction (qPCR) was further used to validate the accuracy of RNA-seq technology. RESULTS: Our RNA-seq data found 97 differentially expressed mRNAs between the WT mice and alk-SMase gene NPP7 KO mice, in which 32 were significantly up-regulated and 65 were down-regulated, including protein coding genes, non-coding RNAs. Notably, the results of gene ontology functional enrichment analysis indicated that DEGs were functionally associated with the immune response, regulation of cell proliferation and development related terms. Additionally, an integrated network analysis was shown that some modules was significantly related to alk-SMase and with accordance of previously results. We chose 6 of these genes randomly were validated the accuracy of RNA-seq technology using qPCR and 2 genes showed difference significantly (P < 0.05). CONCLUSIONS: We investigated the potential biological significant of alk-SMase with high resolution genome-wide transcriptome of alk-SMase knockout mice. The results revealed new insight into the functional modules related to alk-SMase was involved in the intestinal related diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02764-y. BioMed Central 2022-11-09 /pmc/articles/PMC9644495/ /pubmed/36348490 http://dx.doi.org/10.1186/s12935-022-02764-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zhu, Jiang
Wang, Lingqi
Guo, Zhongwu
Zhang, Tao
Zhang, Ping
Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title_full Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title_fullStr Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title_full_unstemmed Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title_short Transcriptome analysis of intestine from alk-SMase knockout mice reveals the effect of alk-SMase
title_sort transcriptome analysis of intestine from alk-smase knockout mice reveals the effect of alk-smase
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644495/
https://www.ncbi.nlm.nih.gov/pubmed/36348490
http://dx.doi.org/10.1186/s12935-022-02764-y
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