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Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes
The biology of sperm, its capability of fertilizing an egg and its role in sex ratio are the major biological questions in reproductive biology. To answer these question we integrated X and Y chromosome transcriptome across different species: Bos taurus and Sus scrofa and identified reproductive dri...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589591/ https://www.ncbi.nlm.nih.gov/pubmed/28903352 http://dx.doi.org/10.18632/oncotarget.17081 |
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author | Khan, Faheem Ahmed Liu, Hui Zhou, Hao Wang, Kai Qamar, Muhammad Tahir Ul Pandupuspitasari, Nuruliarizki Shinta Shujun, Zhang |
author_facet | Khan, Faheem Ahmed Liu, Hui Zhou, Hao Wang, Kai Qamar, Muhammad Tahir Ul Pandupuspitasari, Nuruliarizki Shinta Shujun, Zhang |
author_sort | Khan, Faheem Ahmed |
collection | PubMed |
description | The biology of sperm, its capability of fertilizing an egg and its role in sex ratio are the major biological questions in reproductive biology. To answer these question we integrated X and Y chromosome transcriptome across different species: Bos taurus and Sus scrofa and identified reproductive driver genes based on Weighted Gene Co-Expression Network Analysis (WGCNA) algorithm. Our strategy resulted in 11007 and 10445 unique genes consisting of 9 and 11 reproductive modules in Bos taurus and Sus scrofa, respectively. The consensus module calculation yields an overall 167 overlapped genes which were mapped to 846 DEGs in Bos taurus to finally get a list of 67 dual feature genes. We develop gene co-expression network of selected 67 genes that consists of 58 nodes (27 down-regulated and 31 up-regulated genes) enriched to 66 GO biological process (BP) including 6 GO annotations related to reproduction and two KEGG pathways. Moreover, we searched significantly related TF (ISRE, AP1FJ, RP58, CREL) and miRNAs (bta-miR-181a, bta-miR-17-5p, bta-miR-146b, bta-miR-146a) which targeted the genes in co-expression network. In addition we performed genetic analysis including phylogenetic, functional domain identification, epigenetic modifications, mutation analysis of the most important reproductive driver genes PRM1, PPP2R2B and PAFAH1B1 and finally performed a protein docking analysis to visualize their therapeutic and gene expression regulation ability. |
format | Online Article Text |
id | pubmed-5589591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55895912017-09-12 Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes Khan, Faheem Ahmed Liu, Hui Zhou, Hao Wang, Kai Qamar, Muhammad Tahir Ul Pandupuspitasari, Nuruliarizki Shinta Shujun, Zhang Oncotarget Research Paper The biology of sperm, its capability of fertilizing an egg and its role in sex ratio are the major biological questions in reproductive biology. To answer these question we integrated X and Y chromosome transcriptome across different species: Bos taurus and Sus scrofa and identified reproductive driver genes based on Weighted Gene Co-Expression Network Analysis (WGCNA) algorithm. Our strategy resulted in 11007 and 10445 unique genes consisting of 9 and 11 reproductive modules in Bos taurus and Sus scrofa, respectively. The consensus module calculation yields an overall 167 overlapped genes which were mapped to 846 DEGs in Bos taurus to finally get a list of 67 dual feature genes. We develop gene co-expression network of selected 67 genes that consists of 58 nodes (27 down-regulated and 31 up-regulated genes) enriched to 66 GO biological process (BP) including 6 GO annotations related to reproduction and two KEGG pathways. Moreover, we searched significantly related TF (ISRE, AP1FJ, RP58, CREL) and miRNAs (bta-miR-181a, bta-miR-17-5p, bta-miR-146b, bta-miR-146a) which targeted the genes in co-expression network. In addition we performed genetic analysis including phylogenetic, functional domain identification, epigenetic modifications, mutation analysis of the most important reproductive driver genes PRM1, PPP2R2B and PAFAH1B1 and finally performed a protein docking analysis to visualize their therapeutic and gene expression regulation ability. Impact Journals LLC 2017-04-13 /pmc/articles/PMC5589591/ /pubmed/28903352 http://dx.doi.org/10.18632/oncotarget.17081 Text en Copyright: © 2017 Khan et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Khan, Faheem Ahmed Liu, Hui Zhou, Hao Wang, Kai Qamar, Muhammad Tahir Ul Pandupuspitasari, Nuruliarizki Shinta Shujun, Zhang Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title | Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title_full | Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title_fullStr | Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title_full_unstemmed | Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title_short | Analysis of Bos taurus and Sus scrofa X and Y chromosome transcriptome highlights reproductive driver genes |
title_sort | analysis of bos taurus and sus scrofa x and y chromosome transcriptome highlights reproductive driver genes |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589591/ https://www.ncbi.nlm.nih.gov/pubmed/28903352 http://dx.doi.org/10.18632/oncotarget.17081 |
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