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. 2010 Jul 1;24(13):1403–1417. doi: 10.1101/gad.1901210

Figure 3.

Figure 3.

SIRT1 regulation of SREBP target gene expression during fasting in the mouse liver. qRT–PCR was used to analyze the mRNA levels of SREBP target genes FASN](A), ELOVL6 (B), and SREBP-1c (C) in the mouse liver. The fasting-dependent changes of gene expression are compared between livers of mice subjected to tail-vein injection of adenoviruses programmed to express control shRNA (C; n = 7) and SIRT1 shRNA (shSIRT1; n = 7) (fasted for 20 h). All data are normalized to 18s rRNA expression. Error bars represent SEM. (*) P < 0.05; (**) P < 0.01. (D) Hierarchical clustering of mouse liver transcriptomes with or without SIRT1 knockout. The heat map demonstrates that SREBP target genes are among the most significantly up-regulated genes in SIRT1 knockout livers.