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Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation
A lack of the complete pig proteome has left a gap in our knowledge of the pig genome and has restricted the feasibility of using pigs as a biomedical model. In this study, we developed a tissue-based proteome map using 34 major normal pig tissues. A total of 5841 unknown protein isoforms were ident...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170766/ https://www.ncbi.nlm.nih.gov/pubmed/33631433 http://dx.doi.org/10.1016/j.gpb.2021.02.002 |
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author | Zhao, Pengju Zheng, Xianrui Yu, Ying Hou, Zhuocheng Diao, Chenguang Wang, Haifei Kang, Huimin Ning, Chao Li, Junhui Feng, Wen Wang, Wen Liu, George E. Li, Bugao Smith, Jacqueline Chamba, Yangzom Liu, Jian-Feng |
author_facet | Zhao, Pengju Zheng, Xianrui Yu, Ying Hou, Zhuocheng Diao, Chenguang Wang, Haifei Kang, Huimin Ning, Chao Li, Junhui Feng, Wen Wang, Wen Liu, George E. Li, Bugao Smith, Jacqueline Chamba, Yangzom Liu, Jian-Feng |
author_sort | Zhao, Pengju |
collection | PubMed |
description | A lack of the complete pig proteome has left a gap in our knowledge of the pig genome and has restricted the feasibility of using pigs as a biomedical model. In this study, we developed a tissue-based proteome map using 34 major normal pig tissues. A total of 5841 unknown protein isoforms were identified and systematically characterized, including 2225 novel protein isoforms, 669 protein isoforms from 460 genes symbolized beginning with LOC, and 2947 protein isoforms without clear NCBI annotation in the current pig reference genome. These newly identified protein isoforms were functionally annotated through profiling the pig transcriptome with high-throughput RNA sequencing of the same pig tissues, further improving the genome annotation of the corresponding protein-coding genes. Combining the well-annotated genes that have parallel expression pattern and subcellular witness, we predicted the tissue-related subcellularlocations and potential functions for these unknown proteins. Finally, we mined 3081 orthologous genes for 52.7% of unknown protein isoforms across multiple species, referring to 68 KEGG pathways as well as 23 disease signaling pathways. These findings provide valuable insights and a rich resource for enhancing studies of pig genomics and biology, as well as biomedical model application to human medicine. |
format | Online Article Text |
id | pubmed-9170766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91707662022-06-08 Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation Zhao, Pengju Zheng, Xianrui Yu, Ying Hou, Zhuocheng Diao, Chenguang Wang, Haifei Kang, Huimin Ning, Chao Li, Junhui Feng, Wen Wang, Wen Liu, George E. Li, Bugao Smith, Jacqueline Chamba, Yangzom Liu, Jian-Feng Genomics Proteomics Bioinformatics Original Research A lack of the complete pig proteome has left a gap in our knowledge of the pig genome and has restricted the feasibility of using pigs as a biomedical model. In this study, we developed a tissue-based proteome map using 34 major normal pig tissues. A total of 5841 unknown protein isoforms were identified and systematically characterized, including 2225 novel protein isoforms, 669 protein isoforms from 460 genes symbolized beginning with LOC, and 2947 protein isoforms without clear NCBI annotation in the current pig reference genome. These newly identified protein isoforms were functionally annotated through profiling the pig transcriptome with high-throughput RNA sequencing of the same pig tissues, further improving the genome annotation of the corresponding protein-coding genes. Combining the well-annotated genes that have parallel expression pattern and subcellular witness, we predicted the tissue-related subcellularlocations and potential functions for these unknown proteins. Finally, we mined 3081 orthologous genes for 52.7% of unknown protein isoforms across multiple species, referring to 68 KEGG pathways as well as 23 disease signaling pathways. These findings provide valuable insights and a rich resource for enhancing studies of pig genomics and biology, as well as biomedical model application to human medicine. Elsevier 2021-10 2021-02-23 /pmc/articles/PMC9170766/ /pubmed/33631433 http://dx.doi.org/10.1016/j.gpb.2021.02.002 Text en © 2021 The Authors. Published by Elsevier B.V. and Science Press on behalf of Beijing Institute of Genomics, Chinese Academy of Sciences / China National Center for Bioinformation and Genetics Society of China. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Zhao, Pengju Zheng, Xianrui Yu, Ying Hou, Zhuocheng Diao, Chenguang Wang, Haifei Kang, Huimin Ning, Chao Li, Junhui Feng, Wen Wang, Wen Liu, George E. Li, Bugao Smith, Jacqueline Chamba, Yangzom Liu, Jian-Feng Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title | Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title_full | Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title_fullStr | Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title_full_unstemmed | Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title_short | Mining Unknown Porcine Protein Isoforms by Tissue-based Map of Proteome Enhances Pig Genome Annotation |
title_sort | mining unknown porcine protein isoforms by tissue-based map of proteome enhances pig genome annotation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170766/ https://www.ncbi.nlm.nih.gov/pubmed/33631433 http://dx.doi.org/10.1016/j.gpb.2021.02.002 |
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