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SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits
Retrotransposon is an important component of the mammalian genome. Previous studies have shown that the expression of protein-coding genes was affected by the insertion of retrotransposon into the proximal genes, and the phenotype variations would be related to the retrotransposon insertion polymorp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407865/ https://www.ncbi.nlm.nih.gov/pubmed/36011333 http://dx.doi.org/10.3390/genes13081422 |
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author | Wang, Xiaoyan Chi, Chengling He, Jia Du, Zhanyu Zheng, Yao D’Alessandro, Enrico Chen, Cai Moawad, Ali Shoaib Asare, Emmanuel Song, Chengyi |
author_facet | Wang, Xiaoyan Chi, Chengling He, Jia Du, Zhanyu Zheng, Yao D’Alessandro, Enrico Chen, Cai Moawad, Ali Shoaib Asare, Emmanuel Song, Chengyi |
author_sort | Wang, Xiaoyan |
collection | PubMed |
description | Retrotransposon is an important component of the mammalian genome. Previous studies have shown that the expression of protein-coding genes was affected by the insertion of retrotransposon into the proximal genes, and the phenotype variations would be related to the retrotransposon insertion polymorphisms (RIPs). In this study, leptin (LEP), leptin receptor (LEPR), and leptin receptor overlapping transcript (LEPROT), which play important roles in the regulation of fat synthesis and body weight, were screened to search for the RIPs and their effect on phenotype and gene expression, as well as to further study the function of the insertion. The results showed that three RIPs located in intron 1 of LEPROT and intron 2 and 21 of LEPR were identified, and they were all SINEA1, which was one type of retrotransposon. The SINE insertion at the LEPROT was the dominant allele in native pig breeds. The age of 100 kg body weight of SINE+/+ Large White individuals was significantly higher than those of SINE+/− and SINE−/− individuals (p < 0.05). The LEPROT gene expression in the liver and suet of 30-day-old SINE−/− Sujiang piglets were significantly higher than those of SINE+/+ and SINE+/− piglets (p < 0.01). The dual-luciferase reporter gene assay showed that SINE insertion in PK15 and 3T3-L1 cells significantly reduced the promoter activity of the LEPROT gene (p < 0.01). Therefore, SINE insertion can be a repressor to reduce the expression of LEPROT and could be a useful molecular marker for assisted selection of growth traits in pig breeding. |
format | Online Article Text |
id | pubmed-9407865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94078652022-08-26 SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits Wang, Xiaoyan Chi, Chengling He, Jia Du, Zhanyu Zheng, Yao D’Alessandro, Enrico Chen, Cai Moawad, Ali Shoaib Asare, Emmanuel Song, Chengyi Genes (Basel) Article Retrotransposon is an important component of the mammalian genome. Previous studies have shown that the expression of protein-coding genes was affected by the insertion of retrotransposon into the proximal genes, and the phenotype variations would be related to the retrotransposon insertion polymorphisms (RIPs). In this study, leptin (LEP), leptin receptor (LEPR), and leptin receptor overlapping transcript (LEPROT), which play important roles in the regulation of fat synthesis and body weight, were screened to search for the RIPs and their effect on phenotype and gene expression, as well as to further study the function of the insertion. The results showed that three RIPs located in intron 1 of LEPROT and intron 2 and 21 of LEPR were identified, and they were all SINEA1, which was one type of retrotransposon. The SINE insertion at the LEPROT was the dominant allele in native pig breeds. The age of 100 kg body weight of SINE+/+ Large White individuals was significantly higher than those of SINE+/− and SINE−/− individuals (p < 0.05). The LEPROT gene expression in the liver and suet of 30-day-old SINE−/− Sujiang piglets were significantly higher than those of SINE+/+ and SINE+/− piglets (p < 0.01). The dual-luciferase reporter gene assay showed that SINE insertion in PK15 and 3T3-L1 cells significantly reduced the promoter activity of the LEPROT gene (p < 0.01). Therefore, SINE insertion can be a repressor to reduce the expression of LEPROT and could be a useful molecular marker for assisted selection of growth traits in pig breeding. MDPI 2022-08-10 /pmc/articles/PMC9407865/ /pubmed/36011333 http://dx.doi.org/10.3390/genes13081422 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Xiaoyan Chi, Chengling He, Jia Du, Zhanyu Zheng, Yao D’Alessandro, Enrico Chen, Cai Moawad, Ali Shoaib Asare, Emmanuel Song, Chengyi SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title | SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title_full | SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title_fullStr | SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title_full_unstemmed | SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title_short | SINE Insertion May Act as a Repressor to Affect the Expression of Pig LEPROT and Growth Traits |
title_sort | sine insertion may act as a repressor to affect the expression of pig leprot and growth traits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407865/ https://www.ncbi.nlm.nih.gov/pubmed/36011333 http://dx.doi.org/10.3390/genes13081422 |
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