<P>Our previous work has identified <I>miR-125b</I> as a negative regulator of melanogenesis. However, the specific melanogenesis-related genes targeted by this miRNA had not been identified. In this study, we established a screening...
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https://www.riss.kr/link?id=A107651114
2017
-
SCOPUS,KCI등재,SCIE
학술저널
e367
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
<P>Our previous work has identified <I>miR-125b</I> as a negative regulator of melanogenesis. However, the specific melanogenesis-related genes targeted by this miRNA had not been identified. In this study, we established a screening...
<P>Our previous work has identified <I>miR-125b</I> as a negative regulator of melanogenesis. However, the specific melanogenesis-related genes targeted by this miRNA had not been identified. In this study, we established a screening strategy involving three consecutive analytical approaches—analysis of target genes of <I>miR-125b</I>, expression correlation analysis between each target gene and representative pigmentary genes, and functional analysis of candidate genes related to melanogenesis—to discover melanogenesis-related genes targeted by <I>miR-125b</I>. Through these analyses, we identified SRC homology 3 domain-binding protein 4 (<I>SH3BP4</I>) as a novel pigmentation gene. In addition, by combining bioinformatics analysis and experimental validation, we demonstrated that <I>SH3BP4</I> is a direct target of <I>miR-125b</I>. Finally, we found that <I>SH3BP4</I> is transcriptionally regulated by microphthalmia-associated transcription factor as its direct target. These findings provide important insights into the roles of miRNAs and their targets in melanogenesis.</P>
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