Tyrosinase Small Interfering RNA Effectively Suppresses Tyrosinase Gene Expression In Vitro and In Vivo
Author(s) -
Xiuhua Jia,
Shaochun Lin,
Huang Bing,
Xiang Zhu,
Jing Zhuang,
Weihua Li,
Qian Liu,
Ting Luo,
XU Xiao-ping,
Chen Xi-gu
Publication year - 2010
Publication title -
molecular biology international
Language(s) - English
Resource type - Journals
eISSN - 2090-2190
pISSN - 2090-2182
DOI - 10.4061/2010/240472
Subject(s) - tyrosinase , small interfering rna , transfection , melanin , messenger rna , in vitro , gene expression , microbiology and biotechnology , rna , gene , tyrosine , in vivo , biochemistry , enzyme , chemistry , biology , genetics
Tyrosinase is a bifunctional enzyme which oxidizes the initial step of melanin biosynthesis, that is, conversion of tyrosine to dopa and subsequently dopa to dopaquinone. It is a glycosylated protein and a major regulator of melanogenesis. To date, many approaches have been tried to regulate tyrosinase activity and melanin content. To that end, we screened small interfering RNA sequences for sequence-inhibited tyrosinase expression in B16 cells and in C57BL/6 mice. We analyzed tyrosinase mRNA levels by quantitative real-time PCR and determined tyrosinase activity and melanin content at 24, 48, and 72 hours after transfection. Results showed that siNM_011661_001 was the most efficient small interfering RNA sequence in suppressing tyrosinase mRNA expression, and cells transfected with this sequence showed lower tyrosinase activity. Moreover, intravitreous injection of siNM_011661_001 in C57BL/6 mice induced an efficient and stable gene-specific inhibition of expression at the posttranscriptional level.
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