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Molecular cloning, expression, and functional features of IGF1 splice variants in sheep
Insulin-like growth factor 1 (IGF1), also known as somatomedin C, is essential for the regulation of animal growth and development. In many species, the IGF1 gene can be alternatively spliced into multiple transcripts, encoding different pre-pro-IGF1 proteins. However, the exact alternative splicing...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Bioscientifica Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428077/ https://www.ncbi.nlm.nih.gov/pubmed/34319906 http://dx.doi.org/10.1530/EC-21-0181 |
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author | Song, Xu-Ting Zhang, Jia-Nan Zhao, Duo-Wei Zhai, Yu-Fei Lu, Qi Qi, Mei-Yu Lu, Ming-Hai Deng, Shou-Long Han, Hong-Bing Yang, Xiu-Qin Yao, Yu-Chang |
author_facet | Song, Xu-Ting Zhang, Jia-Nan Zhao, Duo-Wei Zhai, Yu-Fei Lu, Qi Qi, Mei-Yu Lu, Ming-Hai Deng, Shou-Long Han, Hong-Bing Yang, Xiu-Qin Yao, Yu-Chang |
author_sort | Song, Xu-Ting |
collection | PubMed |
description | Insulin-like growth factor 1 (IGF1), also known as somatomedin C, is essential for the regulation of animal growth and development. In many species, the IGF1 gene can be alternatively spliced into multiple transcripts, encoding different pre-pro-IGF1 proteins. However, the exact alternative splicing patterns of IGF1 and the sequence information of different splice variants in sheep are still unclear. In this study, four splice variants (class 1-Ea, class 1-Eb, class 2-Ea, and class 2-Eb) were obtained, but no IGF1 Ec, similar to that found in other species, was discovered. Bioinformatics analysis showed that the four splice variants shared the same mature peptide (70 amino acids) and possessed distinct signal peptides and E peptides. Tissue expression analysis indicated that the four splice variants were broadly expressed in all tested tissues and were most abundantly expressed in the liver. In most tissues and stages, the expression of class 1-Ea was highest, and the expression of other splice variants was low. Overall, levels of the four IGF1 splice variants at the fetal and lamb stages were higher than those at the adult stage. Overexpression of the four splice variants significantly increased fibroblast proliferation and inhibited apoptosis (P < 0.05). In contrast, silencing IGF1 Ea or IGF1 Eb with siRNA significantly inhibited proliferation and promoted apoptosis (P < 0.05). Among the four splice variants, class 1-Ea had a more evident effect on cell proliferation and apoptosis. In summary, the four ovine IGF1 splice variants have different structures and expression patterns and might have different biological functions. |
format | Online Article Text |
id | pubmed-8428077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84280772021-09-13 Molecular cloning, expression, and functional features of IGF1 splice variants in sheep Song, Xu-Ting Zhang, Jia-Nan Zhao, Duo-Wei Zhai, Yu-Fei Lu, Qi Qi, Mei-Yu Lu, Ming-Hai Deng, Shou-Long Han, Hong-Bing Yang, Xiu-Qin Yao, Yu-Chang Endocr Connect Research Insulin-like growth factor 1 (IGF1), also known as somatomedin C, is essential for the regulation of animal growth and development. In many species, the IGF1 gene can be alternatively spliced into multiple transcripts, encoding different pre-pro-IGF1 proteins. However, the exact alternative splicing patterns of IGF1 and the sequence information of different splice variants in sheep are still unclear. In this study, four splice variants (class 1-Ea, class 1-Eb, class 2-Ea, and class 2-Eb) were obtained, but no IGF1 Ec, similar to that found in other species, was discovered. Bioinformatics analysis showed that the four splice variants shared the same mature peptide (70 amino acids) and possessed distinct signal peptides and E peptides. Tissue expression analysis indicated that the four splice variants were broadly expressed in all tested tissues and were most abundantly expressed in the liver. In most tissues and stages, the expression of class 1-Ea was highest, and the expression of other splice variants was low. Overall, levels of the four IGF1 splice variants at the fetal and lamb stages were higher than those at the adult stage. Overexpression of the four splice variants significantly increased fibroblast proliferation and inhibited apoptosis (P < 0.05). In contrast, silencing IGF1 Ea or IGF1 Eb with siRNA significantly inhibited proliferation and promoted apoptosis (P < 0.05). Among the four splice variants, class 1-Ea had a more evident effect on cell proliferation and apoptosis. In summary, the four ovine IGF1 splice variants have different structures and expression patterns and might have different biological functions. Bioscientifica Ltd 2021-07-28 /pmc/articles/PMC8428077/ /pubmed/34319906 http://dx.doi.org/10.1530/EC-21-0181 Text en © The authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Research Song, Xu-Ting Zhang, Jia-Nan Zhao, Duo-Wei Zhai, Yu-Fei Lu, Qi Qi, Mei-Yu Lu, Ming-Hai Deng, Shou-Long Han, Hong-Bing Yang, Xiu-Qin Yao, Yu-Chang Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title | Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title_full | Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title_fullStr | Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title_full_unstemmed | Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title_short | Molecular cloning, expression, and functional features of IGF1 splice variants in sheep |
title_sort | molecular cloning, expression, and functional features of igf1 splice variants in sheep |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428077/ https://www.ncbi.nlm.nih.gov/pubmed/34319906 http://dx.doi.org/10.1530/EC-21-0181 |
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