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Molecular cloning and characterization of the endothelin 3 gene in black bone sheep
BACKGROUND: Black bone sheep was first discovered in Yunnan province of China in 1970, with unique black pigmentation on the body and internal organs. Endothelin 3 (EDN3) has been known as a key gene causing hyperpigmentation in black bone chicken, the Silky fowl. METHODS: In this study, EDN3 was em...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022492/ https://www.ncbi.nlm.nih.gov/pubmed/29988351 http://dx.doi.org/10.1186/s40104-018-0272-y |
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author | Darwish, Hesham Y. A. Zhang, Yuanyuan Cui, Kai Yang, Zu Han, Deping Dong, Xianggui Mao, Huaming Deng, Weidong Deng, Xuemei |
author_facet | Darwish, Hesham Y. A. Zhang, Yuanyuan Cui, Kai Yang, Zu Han, Deping Dong, Xianggui Mao, Huaming Deng, Weidong Deng, Xuemei |
author_sort | Darwish, Hesham Y. A. |
collection | PubMed |
description | BACKGROUND: Black bone sheep was first discovered in Yunnan province of China in 1970, with unique black pigmentation on the body and internal organs. Endothelin 3 (EDN3) has been known as a key gene causing hyperpigmentation in black bone chicken, the Silky fowl. METHODS: In this study, EDN3 was employed as a candidate gene for regulating black color pigmentation. First, EDN3 was cloned from sheep to obtain the full-length cDNA by using the rapid amplification of cDNA ends (RACE). Genomic EDN3 was screened and a total of thirty predicted single nucleotide polymorphisms (SNPs) were genotyped for allele and genotype frequency analysis in a case-control study involving two black bone sheep populations. Genomic copy number analysis of EDN3 in sheep was conducted to measure the variation in copy number. EDN3 expression levels were observed among the groups in adult liver, lymph node, and kidney tissues, as well as embryo kidney samples. Also, among the tissues of black bone and non-black bone sheep. RESULTS: The size of the full-length cDNA was 1,578 bp, which included 426 bp of 5′-untranslated region (5′-UTR), an open reading frame (ORF) of 639 bp encoding a protein of 212 amino acids, and a 3′-UTR of 513 bp. Genotype and allele frequencies of all the discovered SNPs were found insignificantly different in black bone and non-black bone sheep (P > 0.05). Genomic copy number analysis of EDN3 in sheep revealed no significant difference between the two sheep groups. No significant variations were found in the adult liver and kidney embryo samples. However, the expression in lymph node and kidney tissue was significantly higher in black bone sheep than that in non-black bone sheep (P < 0.05). Significant variations in the EDN3 expression levels were observed among the tissues of non-black bone sheep. CONCLUSIONS: The findings of the present study indicate that unlike in Silky chickens, EDN3 is not responsible for hyperpigmentation but may play a key functional role in immune and excretory systems of black bone sheep. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-018-0272-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6022492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60224922018-07-09 Molecular cloning and characterization of the endothelin 3 gene in black bone sheep Darwish, Hesham Y. A. Zhang, Yuanyuan Cui, Kai Yang, Zu Han, Deping Dong, Xianggui Mao, Huaming Deng, Weidong Deng, Xuemei J Anim Sci Biotechnol Research BACKGROUND: Black bone sheep was first discovered in Yunnan province of China in 1970, with unique black pigmentation on the body and internal organs. Endothelin 3 (EDN3) has been known as a key gene causing hyperpigmentation in black bone chicken, the Silky fowl. METHODS: In this study, EDN3 was employed as a candidate gene for regulating black color pigmentation. First, EDN3 was cloned from sheep to obtain the full-length cDNA by using the rapid amplification of cDNA ends (RACE). Genomic EDN3 was screened and a total of thirty predicted single nucleotide polymorphisms (SNPs) were genotyped for allele and genotype frequency analysis in a case-control study involving two black bone sheep populations. Genomic copy number analysis of EDN3 in sheep was conducted to measure the variation in copy number. EDN3 expression levels were observed among the groups in adult liver, lymph node, and kidney tissues, as well as embryo kidney samples. Also, among the tissues of black bone and non-black bone sheep. RESULTS: The size of the full-length cDNA was 1,578 bp, which included 426 bp of 5′-untranslated region (5′-UTR), an open reading frame (ORF) of 639 bp encoding a protein of 212 amino acids, and a 3′-UTR of 513 bp. Genotype and allele frequencies of all the discovered SNPs were found insignificantly different in black bone and non-black bone sheep (P > 0.05). Genomic copy number analysis of EDN3 in sheep revealed no significant difference between the two sheep groups. No significant variations were found in the adult liver and kidney embryo samples. However, the expression in lymph node and kidney tissue was significantly higher in black bone sheep than that in non-black bone sheep (P < 0.05). Significant variations in the EDN3 expression levels were observed among the tissues of non-black bone sheep. CONCLUSIONS: The findings of the present study indicate that unlike in Silky chickens, EDN3 is not responsible for hyperpigmentation but may play a key functional role in immune and excretory systems of black bone sheep. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-018-0272-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-25 /pmc/articles/PMC6022492/ /pubmed/29988351 http://dx.doi.org/10.1186/s40104-018-0272-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Darwish, Hesham Y. A. Zhang, Yuanyuan Cui, Kai Yang, Zu Han, Deping Dong, Xianggui Mao, Huaming Deng, Weidong Deng, Xuemei Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title_full | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title_fullStr | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title_full_unstemmed | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title_short | Molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
title_sort | molecular cloning and characterization of the endothelin 3 gene in black bone sheep |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022492/ https://www.ncbi.nlm.nih.gov/pubmed/29988351 http://dx.doi.org/10.1186/s40104-018-0272-y |
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