On was not contained in the 2 kb 59 flanking sequence (22045.Lpin1.Luc) that is sufficient to GBT-440 confer responsiveness to several other transcription factors [22,23,24,25]. However, PGC-1a overexpression activated a promoter driven by 393 nucleotides of the 59 flanking sequence, the first Lpin1 exon (53 nucleotides), and 2,240 bp of the first intron of the mouse lipin 1 gene (+2293-Lpin1.luc). This suggests that the PGC-1a-responsive 18325633 element in HepG2 cells is contained in the first intron of the Lpin1 gene (Figure 1A). Interestingly, PGC-1a overexpression did not affect Lpin1 promoter activity. To begin to narrow the transcription factor partners of lipin 1 that might be mediating this response, we overexpressed PGC-1a with a site directed mutations in a leucine-rich (LXXLL to LXXFF) motif that mediates interactions with nuclear receptor partners. Mutation of the L2 domain of PGC-1a [26] was sufficient tocompletely block the activation of Lpin1 promoter GDC-0853 activity (Figure 1B). These data indicate that the ability of PGC-1a to induce lipin 1 expression depended upon a transcription factor partner, likely a nuclear receptor, which interacted with the L2 domain. Based on these results, we hypothesized that HNF4a might be involved in this response since HNF4a requires the L2 motif of PGC-1a to interact with that coactivator [27] and interacts only weakly with PGC-1b [28]. Transfection of an expression construct for HNF4a led to a 2-fold increase in Lpin1 promoter activity and this was additively enhanced by cotransfection of PGC-1a (Figure 1C). Chromatin immunoprecipitation studies confirmed that HNF4a was interacting with chromatin at two previouslyidentified [13] nuclear 18297096 receptor response elements in the first intron of the Lpin1 gene (Figure 1D), which is consistent with the promoter mapping studies. Finally, knockdown of HNF4a protein content by using siRNA led to diminished expression of Lpin1 in HepG2 cells and abolished the induction in Lpin1 expression caused by PGC-1a overexpression (Figure 1E).Lipin 1 Enhances the Effects of HNF4a on Fatty Acid OxidationWe have previously demonstrated a direct protein-protein interaction between HNF4a and lipin 1 in GST pull-down assays [10]. To confirm the interaction between HNF4a and lipin 1, HNF4a was immunoprecipitated from isolated hepatocytes overexpressing lipin 1 protein that was either wild-type or harboring a mutation in the LXXIL domain of lipin 1 that mediates its interaction with PPARa [10]. Lipin 1 was found to be immuno-coprecipitated with HNF4a and the interaction required the LXXIL motif (Figure 2A). We next evaluated the functionalFigure 3. Lipin 1 deficiency impairs the ability of HNF4a to induce fatty acid oxidation. [A] Western blots inset above show the expression of HNF4a in hepatocytes from WT and fld mice infected with adenovirus to overexpress HNF4a (or GFP control). Graphs depict the expression of the indicated genes in hepatocytes from WT or fld hepatocytes infected with adenovirus to overexpress HNF4a or GFP (control) (n = 6). *p,0.05 versus GFP. **p,0.05 versus GFP control and WT cells expressing HNF4a. [B] The graphs depicts rates of palmitate oxidation in the experiment described in [A]. *p,0.05 versus WT GFP. **p,0.05 versus WT GFP and WT HNF4a. doi:10.1371/journal.pone.0051320.gLipin 1 and HNFLipin 1 and HNFFigure 4. Loss of lipin 1 enhances the effects of HNF4a on apoprotein gene expression. [A] Primary hepatocytes were isolated from 6 week old C57BL/6 mice and infec.On was not contained in the 2 kb 59 flanking sequence (22045.Lpin1.Luc) that is sufficient to confer responsiveness to several other transcription factors [22,23,24,25]. However, PGC-1a overexpression activated a promoter driven by 393 nucleotides of the 59 flanking sequence, the first Lpin1 exon (53 nucleotides), and 2,240 bp of the first intron of the mouse lipin 1 gene (+2293-Lpin1.luc). This suggests that the PGC-1a-responsive 18325633 element in HepG2 cells is contained in the first intron of the Lpin1 gene (Figure 1A). Interestingly, PGC-1a overexpression did not affect Lpin1 promoter activity. To begin to narrow the transcription factor partners of lipin 1 that might be mediating this response, we overexpressed PGC-1a with a site directed mutations in a leucine-rich (LXXLL to LXXFF) motif that mediates interactions with nuclear receptor partners. Mutation of the L2 domain of PGC-1a [26] was sufficient tocompletely block the activation of Lpin1 promoter activity (Figure 1B). These data indicate that the ability of PGC-1a to induce lipin 1 expression depended upon a transcription factor partner, likely a nuclear receptor, which interacted with the L2 domain. Based on these results, we hypothesized that HNF4a might be involved in this response since HNF4a requires the L2 motif of PGC-1a to interact with that coactivator [27] and interacts only weakly with PGC-1b [28]. Transfection of an expression construct for HNF4a led to a 2-fold increase in Lpin1 promoter activity and this was additively enhanced by cotransfection of PGC-1a (Figure 1C). Chromatin immunoprecipitation studies confirmed that HNF4a was interacting with chromatin at two previouslyidentified [13] nuclear 18297096 receptor response elements in the first intron of the Lpin1 gene (Figure 1D), which is consistent with the promoter mapping studies. Finally, knockdown of HNF4a protein content by using siRNA led to diminished expression of Lpin1 in HepG2 cells and abolished the induction in Lpin1 expression caused by PGC-1a overexpression (Figure 1E).Lipin 1 Enhances the Effects of HNF4a on Fatty Acid OxidationWe have previously demonstrated a direct protein-protein interaction between HNF4a and lipin 1 in GST pull-down assays [10]. To confirm the interaction between HNF4a and lipin 1, HNF4a was immunoprecipitated from isolated hepatocytes overexpressing lipin 1 protein that was either wild-type or harboring a mutation in the LXXIL domain of lipin 1 that mediates its interaction with PPARa [10]. Lipin 1 was found to be immuno-coprecipitated with HNF4a and the interaction required the LXXIL motif (Figure 2A). We next evaluated the functionalFigure 3. Lipin 1 deficiency impairs the ability of HNF4a to induce fatty acid oxidation. [A] Western blots inset above show the expression of HNF4a in hepatocytes from WT and fld mice infected with adenovirus to overexpress HNF4a (or GFP control). Graphs depict the expression of the indicated genes in hepatocytes from WT or fld hepatocytes infected with adenovirus to overexpress HNF4a or GFP (control) (n = 6). *p,0.05 versus GFP. **p,0.05 versus GFP control and WT cells expressing HNF4a. [B] The graphs depicts rates of palmitate oxidation in the experiment described in [A]. *p,0.05 versus WT GFP. **p,0.05 versus WT GFP and WT HNF4a. doi:10.1371/journal.pone.0051320.gLipin 1 and HNFLipin 1 and HNFFigure 4. Loss of lipin 1 enhances the effects of HNF4a on apoprotein gene expression. [A] Primary hepatocytes were isolated from 6 week old C57BL/6 mice and infec.
