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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.
Afiliación
  • Lee JA; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Hwang SJ; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Hong SC; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Myung CH; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Lee JE; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Park JI; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea.
  • Hwang JS; Department of Genetic Engineering & Graduate School of Biotechnology, Kyung Hee University, Yongin, Gyeonggi-do 446-701, Korea. jshwang@khu.ac.kr.
Biomolecules ; 9(7)2019 07 08.
Article en En | MEDLINE | ID: mdl-31288473
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Melanosomas / MicroARNs / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Biomolecules Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Melanosomas / MicroARNs / Proteínas Adaptadoras Transductoras de Señales Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Biomolecules Año: 2019 Tipo del documento: Article
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