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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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Detalles Bibliográficos
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
Descripción
Sumario: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.