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Article Publish Status: FREE
Abstract Title:

Mulberry Leaf Regulates Differentially Expressed Genes in Diabetic Mice Liver Based on RNA-Seq Analysis.

Abstract Source:

Front Physiol. 2018 ;9:1051. Epub 2018 Aug 7. PMID: 30131712

Abstract Author(s):

Qi Ge, Shu Zhang, Liang Chen, Min Tang, Lanlan Liu, Mengna Kang, Lu Gao, Shangshang Ma, Yanhua Yang, Peng Lv, Ming Kong, Qin Yao, Fan Feng, Keping Chen

Article Affiliation:

Qi Ge

Abstract:

The pathogenesis of diabetes mellitus is a complicated process involving much gene regulation. The molecular mechanism of mulberry (L.) leaf in the treatment of diabetes is not fully understood. In this study, we used the Illumina HiSeq™ 2,500 platform to explore the liver transcriptome of normal mice, STZ-induced diabetic mice, and mulberry leaf-treated diabetic mice, and we obtained 52,542,956, 52,626,414, and 52,780,196 clean reads, respectively. We identified differentially expressed genes (DEGs) during the pathogenesis of diabetes in mice. The functional properties of DEGs were characterized by comparison with the GO and KEGG databases, and the results show that DEGs are mainly involved in the metabolic pathway. qRT-PCR was used to analyse 27 differential genes involved in liver expression in different groups of diabetic mice. Among the DEGs, the expression of, and other genes between the control (C) and diabetic control (DC) groups was significantly upregulated; the expression of, andwas significantly downregulated; the expression of the, andgenes between the C group and diabetic group treated with mulberry (DD) was significantly upregulated; the expression of, andwas significantly downregulated; and the expression ofandwas significantly upregulated in the DC and DD groups, but, andwere significantly downregulated. The results of Western blot validation showed that dynamic changes in proteins, such as IGF2, Ly6a, Grb10, and UBD, occurred to regulate the incidence of diabetes by influencing the insulin receptor substrate (IRS) signaling pathway.

Study Type : Animal Study

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