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Cloning and expression analysis of GATA1 gene in Carassius auratus red var
BACKGROUND: GATA1 is a key transcription factor in the GATA family, and promotes the differentiation and maturation of red blood cell, which is essential for normal hematopoiesis. RESULTS: Our results showed that the cDNA sequence of GATA1 was 2730 bp long encoding 443 amino acids. qRT-PCR analysis...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977614/ https://www.ncbi.nlm.nih.gov/pubmed/33736593 http://dx.doi.org/10.1186/s12863-021-00966-3 |
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author | Tian, Yusu Sun, Yuandong Ou, Mi Cui, Xiaojuan Zhou, Dinggang Che, Wen’an |
author_facet | Tian, Yusu Sun, Yuandong Ou, Mi Cui, Xiaojuan Zhou, Dinggang Che, Wen’an |
author_sort | Tian, Yusu |
collection | PubMed |
description | BACKGROUND: GATA1 is a key transcription factor in the GATA family, and promotes the differentiation and maturation of red blood cell, which is essential for normal hematopoiesis. RESULTS: Our results showed that the cDNA sequence of GATA1 was 2730 bp long encoding 443 amino acids. qRT-PCR analysis demonstrated that GATA1 had the highest expression in testis (T), followed by pituitary (P) and spleen (S). GATA1 gene expression in C. auratus red var. embryo from the neuroblast stage (N) to the embryo hatching (H) changes continuously; and the gene expression levels of nonylphenol (NP)-treated and those of control embryos were significantly different. Moreover, Methylation levels of GATA1 gene in NP-treated embryos were higher than those in control embryos, indicating that NP affected GATA1 methylation. CONCLUSIONS: Our study provides cues for further studying the roles of GATA1 gene in fish development, and suggested a potential molecular mechanism by which NP leads to abnormal development of fish embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-021-00966-3. |
format | Online Article Text |
id | pubmed-7977614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79776142021-03-22 Cloning and expression analysis of GATA1 gene in Carassius auratus red var Tian, Yusu Sun, Yuandong Ou, Mi Cui, Xiaojuan Zhou, Dinggang Che, Wen’an BMC Genom Data Research Article BACKGROUND: GATA1 is a key transcription factor in the GATA family, and promotes the differentiation and maturation of red blood cell, which is essential for normal hematopoiesis. RESULTS: Our results showed that the cDNA sequence of GATA1 was 2730 bp long encoding 443 amino acids. qRT-PCR analysis demonstrated that GATA1 had the highest expression in testis (T), followed by pituitary (P) and spleen (S). GATA1 gene expression in C. auratus red var. embryo from the neuroblast stage (N) to the embryo hatching (H) changes continuously; and the gene expression levels of nonylphenol (NP)-treated and those of control embryos were significantly different. Moreover, Methylation levels of GATA1 gene in NP-treated embryos were higher than those in control embryos, indicating that NP affected GATA1 methylation. CONCLUSIONS: Our study provides cues for further studying the roles of GATA1 gene in fish development, and suggested a potential molecular mechanism by which NP leads to abnormal development of fish embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12863-021-00966-3. BioMed Central 2021-03-18 /pmc/articles/PMC7977614/ /pubmed/33736593 http://dx.doi.org/10.1186/s12863-021-00966-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Tian, Yusu Sun, Yuandong Ou, Mi Cui, Xiaojuan Zhou, Dinggang Che, Wen’an Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title | Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title_full | Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title_fullStr | Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title_full_unstemmed | Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title_short | Cloning and expression analysis of GATA1 gene in Carassius auratus red var |
title_sort | cloning and expression analysis of gata1 gene in carassius auratus red var |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7977614/ https://www.ncbi.nlm.nih.gov/pubmed/33736593 http://dx.doi.org/10.1186/s12863-021-00966-3 |
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