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Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes

α-MSH is known for melanogenesis stimulation, and ceRNA is a new method involved in physiological regulation. However, whether ceRNA participates in α-MSH-induced melanogenesis remains unknown. We used ceRNA array to detect the expression profiles of lncRNAs, circRNAs, and mRNAs in melanocytes after...

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Autores principales: Jiang, Ling, Huang, Jinhua, Hu, Yibo, Lei, Li, Ouyang, Yujie, Long, Yan, Li, Hui, Li, Si, Yang, Lun, Yang, Yan, Huang, Lihua, Xiang, Hong, Xiao, Rong, Chen, Jing, Zeng, Qinghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880406/
https://www.ncbi.nlm.nih.gov/pubmed/33318297
http://dx.doi.org/10.18632/aging.202320
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author Jiang, Ling
Huang, Jinhua
Hu, Yibo
Lei, Li
Ouyang, Yujie
Long, Yan
Li, Hui
Li, Si
Yang, Lun
Yang, Yan
Huang, Lihua
Xiang, Hong
Xiao, Rong
Chen, Jing
Zeng, Qinghai
author_facet Jiang, Ling
Huang, Jinhua
Hu, Yibo
Lei, Li
Ouyang, Yujie
Long, Yan
Li, Hui
Li, Si
Yang, Lun
Yang, Yan
Huang, Lihua
Xiang, Hong
Xiao, Rong
Chen, Jing
Zeng, Qinghai
author_sort Jiang, Ling
collection PubMed
description α-MSH is known for melanogenesis stimulation, and ceRNA is a new method involved in physiological regulation. However, whether ceRNA participates in α-MSH-induced melanogenesis remains unknown. We used ceRNA array to detect the expression profiles of lncRNAs, circRNAs, and mRNAs in melanocytes after α-MSH treatment. Moreover, the melanogenesis-related ceRNA regulatory networks were screened and validated. The expression profile analysis showed that 20 lncRNAs and 49 circRNAs changed five-fold after α-MSH treatment, while 933 mRNAs changed two-fold. Based on differentially expressed genes, GO and KEGG analysis were conducted and revealed that 14 genes were enriched in melanogenesis. Then, multiple lncRNA or circRNA-miRNA-mRNA ceRNA networks and lncRNA/circRNA-miRNA-mRNA quaternary ceRNA networks were identified. Thereinto, ENST00000606533, circ_0091223, and TYR expression were upregulated in α-MSH-treated melanocytes, while their complementary miR-1291 was decreased. Dual-luciferase reporter assay further verified that ENST00000606533 and circ_0091223 could bind to miR-1291. ENST00000606533 and circ_0091223 siRNAs decreased circ_0091223, ENST00000606533, and TYR expression, but increased miR-1291 expression. Conversely, miR-1291 mimics inhibited ENST00000606533, circ_0091223, and TYR expression. Moreover, miR-1291 inhibitor could reverse the inhibitory effect of the two siRNAs on TYR expression. Hence, the “ENST00000606533/circ_0091223-miR-1291-TYR” ceRNA network is involved in α-MSH-induced melanogenesis, and ceRNA networks may be potential therapeutic targets for skin pigmentation disorders.
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spelling pubmed-78804062021-02-22 Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes Jiang, Ling Huang, Jinhua Hu, Yibo Lei, Li Ouyang, Yujie Long, Yan Li, Hui Li, Si Yang, Lun Yang, Yan Huang, Lihua Xiang, Hong Xiao, Rong Chen, Jing Zeng, Qinghai Aging (Albany NY) Research Paper α-MSH is known for melanogenesis stimulation, and ceRNA is a new method involved in physiological regulation. However, whether ceRNA participates in α-MSH-induced melanogenesis remains unknown. We used ceRNA array to detect the expression profiles of lncRNAs, circRNAs, and mRNAs in melanocytes after α-MSH treatment. Moreover, the melanogenesis-related ceRNA regulatory networks were screened and validated. The expression profile analysis showed that 20 lncRNAs and 49 circRNAs changed five-fold after α-MSH treatment, while 933 mRNAs changed two-fold. Based on differentially expressed genes, GO and KEGG analysis were conducted and revealed that 14 genes were enriched in melanogenesis. Then, multiple lncRNA or circRNA-miRNA-mRNA ceRNA networks and lncRNA/circRNA-miRNA-mRNA quaternary ceRNA networks were identified. Thereinto, ENST00000606533, circ_0091223, and TYR expression were upregulated in α-MSH-treated melanocytes, while their complementary miR-1291 was decreased. Dual-luciferase reporter assay further verified that ENST00000606533 and circ_0091223 could bind to miR-1291. ENST00000606533 and circ_0091223 siRNAs decreased circ_0091223, ENST00000606533, and TYR expression, but increased miR-1291 expression. Conversely, miR-1291 mimics inhibited ENST00000606533, circ_0091223, and TYR expression. Moreover, miR-1291 inhibitor could reverse the inhibitory effect of the two siRNAs on TYR expression. Hence, the “ENST00000606533/circ_0091223-miR-1291-TYR” ceRNA network is involved in α-MSH-induced melanogenesis, and ceRNA networks may be potential therapeutic targets for skin pigmentation disorders. Impact Journals 2020-12-14 /pmc/articles/PMC7880406/ /pubmed/33318297 http://dx.doi.org/10.18632/aging.202320 Text en Copyright: © 2020 Jiang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Jiang, Ling
Huang, Jinhua
Hu, Yibo
Lei, Li
Ouyang, Yujie
Long, Yan
Li, Hui
Li, Si
Yang, Lun
Yang, Yan
Huang, Lihua
Xiang, Hong
Xiao, Rong
Chen, Jing
Zeng, Qinghai
Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title_full Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title_fullStr Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title_full_unstemmed Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title_short Identification of the ceRNA networks in α-MSH-induced melanogenesis of melanocytes
title_sort identification of the cerna networks in α-msh-induced melanogenesis of melanocytes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880406/
https://www.ncbi.nlm.nih.gov/pubmed/33318297
http://dx.doi.org/10.18632/aging.202320
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