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Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport

Melanosomes undergo a complex maturation process and migrate into keratinocytes. Melanophilin (Mlph), a protein complex involving myosin Va (MyoVa) and Rab27a, enables the movement of melanosomes in melanocytes. In this study, we found six miRNAs targeting Mlph in mouse using two programs (http://ta...

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Autores principales: Lee, Jeong Ah, Hwang, Seok Joon, Hong, Sung Chan, Myung, Cheol Hwan, Lee, Ji Eun, Park, Jong Il, Hwang, Jae Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681522/
https://www.ncbi.nlm.nih.gov/pubmed/31288473
http://dx.doi.org/10.3390/biom9070265
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author Lee, Jeong Ah
Hwang, Seok Joon
Hong, Sung Chan
Myung, Cheol Hwan
Lee, Ji Eun
Park, Jong Il
Hwang, Jae Sung
author_facet Lee, Jeong Ah
Hwang, Seok Joon
Hong, Sung Chan
Myung, Cheol Hwan
Lee, Ji Eun
Park, Jong Il
Hwang, Jae Sung
author_sort Lee, Jeong Ah
collection PubMed
description Melanosomes undergo a complex maturation process and migrate into keratinocytes. Melanophilin (Mlph), a protein complex involving myosin Va (MyoVa) and Rab27a, enables the movement of melanosomes in melanocytes. In this study, we found six miRNAs targeting Mlph in mouse using two programs (http://targetscan.org and DianaTools). When melan-a melanocytes were treated with six synthesized microRNAs, miR-342-5p, miR-1839-5p, and miR-3082-5p inhibited melanosome transport and induced melanosome aggregation around the nucleus. The other microRNAs, miR-5110, miR-3090-3p, and miR-186-5p, did not inhibit melanosome transport. Further, miR-342-5p, miR-1839-5p, and miR-3082-5p decreased Mlph expression. The effect of miR-342-5p was the strongest among the six synthesized miRNAs. It inhibited melanosome transport in melan-a melanocytes and reduced Mlph expression in mRNA and protein levels in a dose-dependent manner; however, it did not affect Rab27a and MyoVa expressions, which are associated with melanosome transport. To examine miR-342-5p specificity, we performed luciferase assays in a mouse melanocyte-transfected reporter vector including Mlph at the 3′-UTR (untranslated region). When treated with miR-342-5p, luciferase activity that had been reduced by approximately 50% was restored after inhibitor treatment. Therefore, we identified a novel miRNA affecting Mlph and melanosome transport, and these results can be used for understanding Mlph expression and skin pigmentation regulation.
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spelling pubmed-66815222019-08-09 Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport Lee, Jeong Ah Hwang, Seok Joon Hong, Sung Chan Myung, Cheol Hwan Lee, Ji Eun Park, Jong Il Hwang, Jae Sung Biomolecules Article Melanosomes undergo a complex maturation process and migrate into keratinocytes. Melanophilin (Mlph), a protein complex involving myosin Va (MyoVa) and Rab27a, enables the movement of melanosomes in melanocytes. In this study, we found six miRNAs targeting Mlph in mouse using two programs (http://targetscan.org and DianaTools). When melan-a melanocytes were treated with six synthesized microRNAs, miR-342-5p, miR-1839-5p, and miR-3082-5p inhibited melanosome transport and induced melanosome aggregation around the nucleus. The other microRNAs, miR-5110, miR-3090-3p, and miR-186-5p, did not inhibit melanosome transport. Further, miR-342-5p, miR-1839-5p, and miR-3082-5p decreased Mlph expression. The effect of miR-342-5p was the strongest among the six synthesized miRNAs. It inhibited melanosome transport in melan-a melanocytes and reduced Mlph expression in mRNA and protein levels in a dose-dependent manner; however, it did not affect Rab27a and MyoVa expressions, which are associated with melanosome transport. To examine miR-342-5p specificity, we performed luciferase assays in a mouse melanocyte-transfected reporter vector including Mlph at the 3′-UTR (untranslated region). When treated with miR-342-5p, luciferase activity that had been reduced by approximately 50% was restored after inhibitor treatment. Therefore, we identified a novel miRNA affecting Mlph and melanosome transport, and these results can be used for understanding Mlph expression and skin pigmentation regulation. MDPI 2019-07-08 /pmc/articles/PMC6681522/ /pubmed/31288473 http://dx.doi.org/10.3390/biom9070265 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Jeong Ah
Hwang, Seok Joon
Hong, Sung Chan
Myung, Cheol Hwan
Lee, Ji Eun
Park, Jong Il
Hwang, Jae Sung
Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title_full Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title_fullStr Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title_full_unstemmed Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title_short Identification of MicroRNA Targeting Mlph and Affecting Melanosome Transport
title_sort identification of microrna targeting mlph and affecting melanosome transport
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6681522/
https://www.ncbi.nlm.nih.gov/pubmed/31288473
http://dx.doi.org/10.3390/biom9070265
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