Cargando…
Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken
BACKGROUND: Henny feathering in chickens is determined by a dominant mutation that transforms male-specific plumage to female-like plumage. Previous studies indicated that this phenotype is caused by ectopic expression in skin of CYP19A1 encoding aromatase that converts androgens to estrogen and the...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712707/ https://www.ncbi.nlm.nih.gov/pubmed/31467598 http://dx.doi.org/10.1186/s13100-019-0181-4 |
_version_ | 1783446732614402048 |
---|---|
author | Li, Jingyi Davis, Brian W. Jern, Patric Dorshorst, Ben. J. Siegel, Paul B. Andersson, Leif |
author_facet | Li, Jingyi Davis, Brian W. Jern, Patric Dorshorst, Ben. J. Siegel, Paul B. Andersson, Leif |
author_sort | Li, Jingyi |
collection | PubMed |
description | BACKGROUND: Henny feathering in chickens is determined by a dominant mutation that transforms male-specific plumage to female-like plumage. Previous studies indicated that this phenotype is caused by ectopic expression in skin of CYP19A1 encoding aromatase that converts androgens to estrogen and thereby inhibits the development of male-specific plumage. A long terminal repeat (LTR) from an uncharacterized endogenous retrovirus (ERV) insertion was found in an isoform of the CYP19A1 transcript from henny feathering chicken. However, the complete sequence and the genomic position of the insertion were not determined. RESULTS: We used publicly available whole genome sequence data to determine the flanking sequences of the ERV, and then PCR amplified the entire insertion and sequenced it using Nanopore long reads and Sanger sequencing. The 7524 bp insertion contains an intact endogenous retrovirus that was not found in chickens representing 31 different breeds not showing henny feathering or in samples of the ancestral red junglefowl. The sequence shows over 99% sequence identity to the avian leukosis virus ev-1 and ev-21 strains, suggesting a recent integration. The ERV 3’LTR, containing a powerful transcriptional enhancer and core promoter with TATA box together with binding sites for EFIII and Ig/EBP inside the CYP19A1 5′ untranslated region, was detected partially in an aromatase transcript, which present a plausible explanation for ectopic expression of aromatase in non-ovarian tissues underlying the henny feathering phenotype. CONCLUSIONS: We demonstrate that the henny feathering allele harbors an insertion of an intact avian leukosis virus at the 5’end of CYP19A1. The presence of this ERV showed complete concordance with the henny feathering phenotype both within a pedigree segregating for this phenotype and across breeds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0181-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6712707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67127072019-08-29 Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken Li, Jingyi Davis, Brian W. Jern, Patric Dorshorst, Ben. J. Siegel, Paul B. Andersson, Leif Mob DNA Research BACKGROUND: Henny feathering in chickens is determined by a dominant mutation that transforms male-specific plumage to female-like plumage. Previous studies indicated that this phenotype is caused by ectopic expression in skin of CYP19A1 encoding aromatase that converts androgens to estrogen and thereby inhibits the development of male-specific plumage. A long terminal repeat (LTR) from an uncharacterized endogenous retrovirus (ERV) insertion was found in an isoform of the CYP19A1 transcript from henny feathering chicken. However, the complete sequence and the genomic position of the insertion were not determined. RESULTS: We used publicly available whole genome sequence data to determine the flanking sequences of the ERV, and then PCR amplified the entire insertion and sequenced it using Nanopore long reads and Sanger sequencing. The 7524 bp insertion contains an intact endogenous retrovirus that was not found in chickens representing 31 different breeds not showing henny feathering or in samples of the ancestral red junglefowl. The sequence shows over 99% sequence identity to the avian leukosis virus ev-1 and ev-21 strains, suggesting a recent integration. The ERV 3’LTR, containing a powerful transcriptional enhancer and core promoter with TATA box together with binding sites for EFIII and Ig/EBP inside the CYP19A1 5′ untranslated region, was detected partially in an aromatase transcript, which present a plausible explanation for ectopic expression of aromatase in non-ovarian tissues underlying the henny feathering phenotype. CONCLUSIONS: We demonstrate that the henny feathering allele harbors an insertion of an intact avian leukosis virus at the 5’end of CYP19A1. The presence of this ERV showed complete concordance with the henny feathering phenotype both within a pedigree segregating for this phenotype and across breeds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0181-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-28 /pmc/articles/PMC6712707/ /pubmed/31467598 http://dx.doi.org/10.1186/s13100-019-0181-4 Text en © The Author(s). 2019 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 Li, Jingyi Davis, Brian W. Jern, Patric Dorshorst, Ben. J. Siegel, Paul B. Andersson, Leif Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title | Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title_full | Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title_fullStr | Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title_full_unstemmed | Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title_short | Characterization of the endogenous retrovirus insertion in CYP19A1 associated with henny feathering in chicken |
title_sort | characterization of the endogenous retrovirus insertion in cyp19a1 associated with henny feathering in chicken |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712707/ https://www.ncbi.nlm.nih.gov/pubmed/31467598 http://dx.doi.org/10.1186/s13100-019-0181-4 |
work_keys_str_mv | AT lijingyi characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken AT davisbrianw characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken AT jernpatric characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken AT dorshorstbenj characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken AT siegelpaulb characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken AT anderssonleif characterizationoftheendogenousretrovirusinsertionincyp19a1associatedwithhennyfeatheringinchicken |