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Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem?
BACKGROUND: Pigment regression is an intriguing phenomenon that can be caused by disorders in melanin metabolism or endocrine regulation, or by autoimmune disorders. Albino animals serve as excellent models for the study of the genetic determination of morphology, particularly the evolution of and m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742363/ https://www.ncbi.nlm.nih.gov/pubmed/36518250 http://dx.doi.org/10.3389/fendo.2022.1053732 |
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author | Chang, Liming Zhu, Wei Jiang, Jianping |
author_facet | Chang, Liming Zhu, Wei Jiang, Jianping |
author_sort | Chang, Liming |
collection | PubMed |
description | BACKGROUND: Pigment regression is an intriguing phenomenon that can be caused by disorders in melanin metabolism or endocrine regulation, or by autoimmune disorders. Albino animals serve as excellent models for the study of the genetic determination of morphology, particularly the evolution of and molecular mechanisms underlying chromatophore-related diseases in animals and humans. MATERIAL AND METHODS: The artificial culture of Andrias davidianus, the largest extant amphibian, is flourishing in China due to the great ecological and economic value of this animal. Approximately 0.1% of individuals express an albino phenotype accompanied by delayed somatic growth and mortality at early developmental stages. In this study, brain and skin transcriptomics were conducted to study the underlying molecular basis of the phenotype. RESULTS: The results indicated decreased transcription of genes of melanin synthesis. Interestingly, MHC I isotypes and immune-related pathways accounted for the primary transcriptional differences between groups, suggesting that the albino phenotype represents a systematic immune problem to a far greater extent than a pigmentation defect. Albino individuals exhibited shifted transcription of MHC I isotypes, and the albino-specific isotype was characterized by increased charges and decreased space in the antigen- binding pocket, implying a drastic change in antigen specificity and a potential risk of autoimmune disorders. CONCLUSION: These results suggest an association between the albino phenotype and MHC I variants in A. davidianus, which could serve as a convenient model for vitiligo or other autoimmune diseases. |
format | Online Article Text |
id | pubmed-9742363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97423632022-12-13 Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? Chang, Liming Zhu, Wei Jiang, Jianping Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Pigment regression is an intriguing phenomenon that can be caused by disorders in melanin metabolism or endocrine regulation, or by autoimmune disorders. Albino animals serve as excellent models for the study of the genetic determination of morphology, particularly the evolution of and molecular mechanisms underlying chromatophore-related diseases in animals and humans. MATERIAL AND METHODS: The artificial culture of Andrias davidianus, the largest extant amphibian, is flourishing in China due to the great ecological and economic value of this animal. Approximately 0.1% of individuals express an albino phenotype accompanied by delayed somatic growth and mortality at early developmental stages. In this study, brain and skin transcriptomics were conducted to study the underlying molecular basis of the phenotype. RESULTS: The results indicated decreased transcription of genes of melanin synthesis. Interestingly, MHC I isotypes and immune-related pathways accounted for the primary transcriptional differences between groups, suggesting that the albino phenotype represents a systematic immune problem to a far greater extent than a pigmentation defect. Albino individuals exhibited shifted transcription of MHC I isotypes, and the albino-specific isotype was characterized by increased charges and decreased space in the antigen- binding pocket, implying a drastic change in antigen specificity and a potential risk of autoimmune disorders. CONCLUSION: These results suggest an association between the albino phenotype and MHC I variants in A. davidianus, which could serve as a convenient model for vitiligo or other autoimmune diseases. Frontiers Media S.A. 2022-11-28 /pmc/articles/PMC9742363/ /pubmed/36518250 http://dx.doi.org/10.3389/fendo.2022.1053732 Text en Copyright © 2022 Chang, Zhu and Jiang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Chang, Liming Zhu, Wei Jiang, Jianping Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title | Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title_full | Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title_fullStr | Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title_full_unstemmed | Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title_short | Albinism in the largest extant amphibian: A metabolic, endocrine, or immune problem? |
title_sort | albinism in the largest extant amphibian: a metabolic, endocrine, or immune problem? |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742363/ https://www.ncbi.nlm.nih.gov/pubmed/36518250 http://dx.doi.org/10.3389/fendo.2022.1053732 |
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