Rare autosomal recessive phenotype characterized by mild to severe lactic acidemia associated with delayed psychomotor development and death within the first year of life in about one-half the cases [12]. PC is allosterically activated by acetyl-CoA, a signaling molecule that is produced by increased fatty acid oxidation during prolonged starvation. In mammals, the PC gene is transcriptionally regulated by alternate promoters which mediate the production of multiple mRNA isoforms which differ in their 59-untranslated regions. The PC genes from rat and mouse arewell characterized and they are controlled by 1531364 two promoters namely the proximal and the distal promoters [13?5]. The proximal promoter is responsible for production of PC mRNA in the gluconeogenic tissues including liver and kidney, as well as the lipogenic tissues including liver and adipose tissues. The presence of a cAMP-responsive element (CRE) [16]) and a peroxisome proliferator activated receptor response element (PPRE) [17] in the proximal promoter allows liver and adipose tissue, respectively, to produce more PC during prolonged fasting. In contrast, the distal promoter is linked to anaplerosis especially in pancreatic b-cells. The structural region of the human PC gene has been cloned and characterized [18]. However, the regulatory JW-74 web regions of the PC gene that confer tissue-specific expression of PC in humans are not known. Recently, Wang et al [19] reported that unlike the rat and mouse PC genes, the human PC gene is transcribed from three promoters. Herein, we present evidence that similar to the rodent PC genes, the human PC gene is transcribed from two promoters. In ��-Sitosterol ��-D-glucoside web addition, we identified some of the important cisacting elements of the distal human PC promoter that direct transcription of PC in beta cells.Distal Promoter of the Human Pyruvate CarboxylaseDistal Promoter of the Human Pyruvate CarboxylaseFigure 1. RT-PCR analysis of PC mRNA variants in human liver and human pancreatic islets. (A) Schematic diagram showing alignment of 3 variants of human PC mRNA (GenBank NM_000920.3, NM_022172.2, BC011617.2). (B) Schematic diagram showing the structure of the human PC gene. Two isoforms of human PC mRNA are initiated by two alternative promoters, the proximal (P1) promoter and the distal (P2) promoter. All PC mRNA variants contain the same coding sequences but differ in their 59-untranslated regions (UTR) produced from different 59-UTR exons (UE1/UE2, UE3 and UE4) (C) Examination of human PC mRNA 1662274 in liver and pancreatic islets using RT-PCR. Two sets of primers were used to amplify two different isoforms of human PC mRNA both in human liver and human islets. The 173 bp fragment PCR product of variant 2 and the 200 bp fragment PCR product of variant 1 were amplified by using Primers set no. 1 and primer set no.2, respectively, Lane 1; 1 kb marker, Lane 2; Negative control for primer set no.1, Lane 3; Negative control for primer set no.2, Lane 4; PCR using primer set no.1 and cDNA prepared from human liver, Lane 5; PCR using primer set no.2 and cDNA prepared from human liver, Lane 6; PCR using primer set no.1 and cDNA prepared from human islets, Lane 7; PCR using primer set no.2 and cDNA prepared from human islets. doi:10.1371/journal.pone.0055139.gResults and Discussion The Human PC Gene is Regulated by Two Promoters and the Distal Promoter is Functional in Pancreatic b-cellsWe have previously reported two PC mRNA isoforms with distinct 59-untranslated regions (UTR) that.Rare autosomal recessive phenotype characterized by mild to severe lactic acidemia associated with delayed psychomotor development and death within the first year of life in about one-half the cases [12]. PC is allosterically activated by acetyl-CoA, a signaling molecule that is produced by increased fatty acid oxidation during prolonged starvation. In mammals, the PC gene is transcriptionally regulated by alternate promoters which mediate the production of multiple mRNA isoforms which differ in their 59-untranslated regions. The PC genes from rat and mouse arewell characterized and they are controlled by 1531364 two promoters namely the proximal and the distal promoters [13?5]. The proximal promoter is responsible for production of PC mRNA in the gluconeogenic tissues including liver and kidney, as well as the lipogenic tissues including liver and adipose tissues. The presence of a cAMP-responsive element (CRE) [16]) and a peroxisome proliferator activated receptor response element (PPRE) [17] in the proximal promoter allows liver and adipose tissue, respectively, to produce more PC during prolonged fasting. In contrast, the distal promoter is linked to anaplerosis especially in pancreatic b-cells. The structural region of the human PC gene has been cloned and characterized [18]. However, the regulatory regions of the PC gene that confer tissue-specific expression of PC in humans are not known. Recently, Wang et al [19] reported that unlike the rat and mouse PC genes, the human PC gene is transcribed from three promoters. Herein, we present evidence that similar to the rodent PC genes, the human PC gene is transcribed from two promoters. In addition, we identified some of the important cisacting elements of the distal human PC promoter that direct transcription of PC in beta cells.Distal Promoter of the Human Pyruvate CarboxylaseDistal Promoter of the Human Pyruvate CarboxylaseFigure 1. RT-PCR analysis of PC mRNA variants in human liver and human pancreatic islets. (A) Schematic diagram showing alignment of 3 variants of human PC mRNA (GenBank NM_000920.3, NM_022172.2, BC011617.2). (B) Schematic diagram showing the structure of the human PC gene. Two isoforms of human PC mRNA are initiated by two alternative promoters, the proximal (P1) promoter and the distal (P2) promoter. All PC mRNA variants contain the same coding sequences but differ in their 59-untranslated regions (UTR) produced from different 59-UTR exons (UE1/UE2, UE3 and UE4) (C) Examination of human PC mRNA 1662274 in liver and pancreatic islets using RT-PCR. Two sets of primers were used to amplify two different isoforms of human PC mRNA both in human liver and human islets. The 173 bp fragment PCR product of variant 2 and the 200 bp fragment PCR product of variant 1 were amplified by using Primers set no. 1 and primer set no.2, respectively, Lane 1; 1 kb marker, Lane 2; Negative control for primer set no.1, Lane 3; Negative control for primer set no.2, Lane 4; PCR using primer set no.1 and cDNA prepared from human liver, Lane 5; PCR using primer set no.2 and cDNA prepared from human liver, Lane 6; PCR using primer set no.1 and cDNA prepared from human islets, Lane 7; PCR using primer set no.2 and cDNA prepared from human islets. doi:10.1371/journal.pone.0055139.gResults and Discussion The Human PC Gene is Regulated by Two Promoters and the Distal Promoter is Functional in Pancreatic b-cellsWe have previously reported two PC mRNA isoforms with distinct 59-untranslated regions (UTR) that.
