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Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens

BACKGROUND: miRNAs regulate circadian patterns by modulating the biological clocks of animals. In our previous study, we found that the clock gene exhibited a cosine expression pattern in the fallopian tube of chicken uterus. Clock-controlled miRNAs are present in mammals and Drosophila; however, wh...

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Autores principales: Cui, Zhifu, Zhang, Zhichao, Amevor, Felix Kwame, Du, Xiaxia, Li, Liang, Tian, Yaofu, Kang, Xincheng, Shu, Gang, Zhu, Qing, Wang, Yan, Li, Diyan, Zhang, Yao, Zhao, Xiaoling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547053/
https://www.ncbi.nlm.nih.gov/pubmed/34702171
http://dx.doi.org/10.1186/s12864-021-08074-3
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author Cui, Zhifu
Zhang, Zhichao
Amevor, Felix Kwame
Du, Xiaxia
Li, Liang
Tian, Yaofu
Kang, Xincheng
Shu, Gang
Zhu, Qing
Wang, Yan
Li, Diyan
Zhang, Yao
Zhao, Xiaoling
author_facet Cui, Zhifu
Zhang, Zhichao
Amevor, Felix Kwame
Du, Xiaxia
Li, Liang
Tian, Yaofu
Kang, Xincheng
Shu, Gang
Zhu, Qing
Wang, Yan
Li, Diyan
Zhang, Yao
Zhao, Xiaoling
author_sort Cui, Zhifu
collection PubMed
description BACKGROUND: miRNAs regulate circadian patterns by modulating the biological clocks of animals. In our previous study, we found that the clock gene exhibited a cosine expression pattern in the fallopian tube of chicken uterus. Clock-controlled miRNAs are present in mammals and Drosophila; however, whether there are clock-controlled miRNAs in the chicken uterus and, if so, how they regulate egg-laying rhythms is unclear. In this study, we selected 18 layer hens with similar ovipositional rhythmicity (each of three birds were sacrificed for study per 4 h throughout 24 h); their transcriptomes were scanned to identify the circadian miRNAs and to explore regulatory mechanisms within the uterus of chickens. RESULTS: We identified six circadian miRNAs that are mainly associated with several biological processes including ion trans-membrane transportation, response to calcium ion, and enrichment of calcium signaling pathways. Verification of the experimental results revealed that miR-449c-5p exhibited a cosine expression pattern in the chicken uterus. Ca(2+)-transporting ATPase 4 (ATP2B4) in the plasma membrane is the predicted target gene of circadian miR-449c-5p and is highly enriched in the calcium signaling pathway. We speculated that clock-controlled miR-449c-5p regulated Ca(2+) transportation during eggshell calcification in the chicken uterus by targeting ATP2B4. ATP2B4 mRNA and protein were rhythmically expressed in the chicken uterus, and dual-luciferase reporter gene assays confirmed that ATP2B4 was directly targeted by miR-449c-5p. The expression of miR-449c-5p showed an opposite trend to that of ATP2B4 within a 24 h cycle in the chicken uterus; it inhibited mRNA and protein expression of ATP2B4 in the uterine tubular gland cells. In addition, overexpression of ATP2B4 significantly decreased intracellular Ca(2+) concentration (P < 0.05), while knockdown of ATP2B4 accelerated intracellular Ca(2+) concentrations. We found similar results after ATP2B4 knockdown by miR-449c-5p. Taken together, these results indicate that ATP2B4 promotes uterine Ca(2+) trans-epithelial transport. CONCLUSIONS: Clock-controlled miR-449c-5p regulates Ca(2+) transport in the chicken uterus by targeting ATP2B4 during eggshell calcification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08074-3.
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spelling pubmed-85470532021-10-26 Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens Cui, Zhifu Zhang, Zhichao Amevor, Felix Kwame Du, Xiaxia Li, Liang Tian, Yaofu Kang, Xincheng Shu, Gang Zhu, Qing Wang, Yan Li, Diyan Zhang, Yao Zhao, Xiaoling BMC Genomics Research BACKGROUND: miRNAs regulate circadian patterns by modulating the biological clocks of animals. In our previous study, we found that the clock gene exhibited a cosine expression pattern in the fallopian tube of chicken uterus. Clock-controlled miRNAs are present in mammals and Drosophila; however, whether there are clock-controlled miRNAs in the chicken uterus and, if so, how they regulate egg-laying rhythms is unclear. In this study, we selected 18 layer hens with similar ovipositional rhythmicity (each of three birds were sacrificed for study per 4 h throughout 24 h); their transcriptomes were scanned to identify the circadian miRNAs and to explore regulatory mechanisms within the uterus of chickens. RESULTS: We identified six circadian miRNAs that are mainly associated with several biological processes including ion trans-membrane transportation, response to calcium ion, and enrichment of calcium signaling pathways. Verification of the experimental results revealed that miR-449c-5p exhibited a cosine expression pattern in the chicken uterus. Ca(2+)-transporting ATPase 4 (ATP2B4) in the plasma membrane is the predicted target gene of circadian miR-449c-5p and is highly enriched in the calcium signaling pathway. We speculated that clock-controlled miR-449c-5p regulated Ca(2+) transportation during eggshell calcification in the chicken uterus by targeting ATP2B4. ATP2B4 mRNA and protein were rhythmically expressed in the chicken uterus, and dual-luciferase reporter gene assays confirmed that ATP2B4 was directly targeted by miR-449c-5p. The expression of miR-449c-5p showed an opposite trend to that of ATP2B4 within a 24 h cycle in the chicken uterus; it inhibited mRNA and protein expression of ATP2B4 in the uterine tubular gland cells. In addition, overexpression of ATP2B4 significantly decreased intracellular Ca(2+) concentration (P < 0.05), while knockdown of ATP2B4 accelerated intracellular Ca(2+) concentrations. We found similar results after ATP2B4 knockdown by miR-449c-5p. Taken together, these results indicate that ATP2B4 promotes uterine Ca(2+) trans-epithelial transport. CONCLUSIONS: Clock-controlled miR-449c-5p regulates Ca(2+) transport in the chicken uterus by targeting ATP2B4 during eggshell calcification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-08074-3. BioMed Central 2021-10-26 /pmc/articles/PMC8547053/ /pubmed/34702171 http://dx.doi.org/10.1186/s12864-021-08074-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Cui, Zhifu
Zhang, Zhichao
Amevor, Felix Kwame
Du, Xiaxia
Li, Liang
Tian, Yaofu
Kang, Xincheng
Shu, Gang
Zhu, Qing
Wang, Yan
Li, Diyan
Zhang, Yao
Zhao, Xiaoling
Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title_full Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title_fullStr Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title_full_unstemmed Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title_short Circadian miR-449c-5p regulates uterine Ca(2+) transport during eggshell calcification in chickens
title_sort circadian mir-449c-5p regulates uterine ca(2+) transport during eggshell calcification in chickens
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547053/
https://www.ncbi.nlm.nih.gov/pubmed/34702171
http://dx.doi.org/10.1186/s12864-021-08074-3
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