Sis of the in-frame cDNA library was performed on 198 representative plasmids isolated from random colonies of the library. doi:10.1371/journal.pone.0052290.gmost frequent Kozak sequences (CCCGCCGCCACCATGG; CCCGCCGCCGCCATGG) in the human genome were identified in 49 and 37 of the sequenced expression constructs. (Table S2). In order to identify the Tetracosactrin web proteins that interact with ARL11, we used yellow fluorescent protein fragment 1 (YFP1) as an Nterminal tag for proteins expressed by the in-frame library and ARL11 fused to yellow fluorescent protein fragment 2 (YFP2) at ARL11’s C-terminus as bait. We transiently co-transfected HEK293T cells with the prey cDNA library and ARL11-YFP2. After 24 hours, we harvested the transfected cells and used flow cytometry to collect fluorescent cells. We collected only the brightest cells (approximately 1 of the total) for plasmid isolation. Before performing sequencing and partner protein identification,we transiently co-transfected the HEK-293T cells again with plasmids from individual colonies and ARL11-YFP2 to confirm the bait and prey interactions by fluorescence. We identified 27 plasmids encoding candidate ARL11-binding partners, which we subjected to amplification using DH5a competent Escherichia coli followed by final DNA sequencing to identify interacting proteins (Tables S3 and S4). The data we obtained revealed sequences corresponding to five ribosomal binding proteins, most of which represented short fragments of coding sequences. In addition, there were three clones containing the full-length sequence of cellular retinoic acid binding protein 2 (CRABP2), a retinoic acid (RA) carrier protein that facilitates RA transfer from the cytosol to the nucleus and binding to its receptors [9,10].In-Frame cDNA LibraryA role for ARL11 in facilitating this transfer is consistent with the functions of other members of the ARF/ARL superfamily, which interact with intracellular membranes and facilitate protein and vesicular trafficking [11]. The idea that downregulation of ARL11 expression might promote early carcinogenesis via disruption of RA signaling is consistent with a very large body of work BI-78D3 biological activity demonstrating that exogenous retinoids have chemopreventative effects in preclinical models and in patients with bladder cancer [12,13,14,15,16,17]. The remaining clone contained the full-length sequence encoding phosphoglycerate mutase 1 (PGAM1), which catalyzes the reversible actions of 3-phosphoglycerate to 2-phosphoglycerate in the glycolytic pathway [18,19]. The potential biological significance of its binding to ARL11 is unknown. However, because phosphorylation of PGAM1 is considered to play a role in the activation of an alternative glycolytic pathway of rapidly proliferating cells and phosphorylated PGAM1 has been shown to be overexpressed in these cells, phosphorylated PGAM1 represents a potential novel therapeutic target in several solid human tumors [20,21,22,23,24]. Finally, we examined whether the removal of 59-UTRs from the constructs of CRABP2 and PGAM1 facilitated the identification of their interactions with ARL11. The presence of a 59-UTR in the CRABP2 insert construct caused a frame shift with a premature stop codon resulting in the expression of a 78-amino-acid artificial peptide (Fig. 2A). For PGAM1, the presence of a 59-UTR generated a stop codon within the 59-UTR sequence and resulted in the expression of an 18-amino-acid artificial peptide (Fig. 2B). Western blot analysis confirmed that.Sis of the in-frame cDNA library was performed on 198 representative plasmids isolated from random colonies of the library. doi:10.1371/journal.pone.0052290.gmost frequent Kozak sequences (CCCGCCGCCACCATGG; CCCGCCGCCGCCATGG) in the human genome were identified in 49 and 37 of the sequenced expression constructs. (Table S2). In order to identify the proteins that interact with ARL11, we used yellow fluorescent protein fragment 1 (YFP1) as an Nterminal tag for proteins expressed by the in-frame library and ARL11 fused to yellow fluorescent protein fragment 2 (YFP2) at ARL11’s C-terminus as bait. We transiently co-transfected HEK293T cells with the prey cDNA library and ARL11-YFP2. After 24 hours, we harvested the transfected cells and used flow cytometry to collect fluorescent cells. We collected only the brightest cells (approximately 1 of the total) for plasmid isolation. Before performing sequencing and partner protein identification,we transiently co-transfected the HEK-293T cells again with plasmids from individual colonies and ARL11-YFP2 to confirm the bait and prey interactions by fluorescence. We identified 27 plasmids encoding candidate ARL11-binding partners, which we subjected to amplification using DH5a competent Escherichia coli followed by final DNA sequencing to identify interacting proteins (Tables S3 and S4). The data we obtained revealed sequences corresponding to five ribosomal binding proteins, most of which represented short fragments of coding sequences. In addition, there were three clones containing the full-length sequence of cellular retinoic acid binding protein 2 (CRABP2), a retinoic acid (RA) carrier protein that facilitates RA transfer from the cytosol to the nucleus and binding to its receptors [9,10].In-Frame cDNA LibraryA role for ARL11 in facilitating this transfer is consistent with the functions of other members of the ARF/ARL superfamily, which interact with intracellular membranes and facilitate protein and vesicular trafficking [11]. The idea that downregulation of ARL11 expression might promote early carcinogenesis via disruption of RA signaling is consistent with a very large body of work demonstrating that exogenous retinoids have chemopreventative effects in preclinical models and in patients with bladder cancer [12,13,14,15,16,17]. The remaining clone contained the full-length sequence encoding phosphoglycerate mutase 1 (PGAM1), which catalyzes the reversible actions of 3-phosphoglycerate to 2-phosphoglycerate in the glycolytic pathway [18,19]. The potential biological significance of its binding to ARL11 is unknown. However, because phosphorylation of PGAM1 is considered to play a role in the activation of an alternative glycolytic pathway of rapidly proliferating cells and phosphorylated PGAM1 has been shown to be overexpressed in these cells, phosphorylated PGAM1 represents a potential novel therapeutic target in several solid human tumors [20,21,22,23,24]. Finally, we examined whether the removal of 59-UTRs from the constructs of CRABP2 and PGAM1 facilitated the identification of their interactions with ARL11. The presence of a 59-UTR in the CRABP2 insert construct caused a frame shift with a premature stop codon resulting in the expression of a 78-amino-acid artificial peptide (Fig. 2A). For PGAM1, the presence of a 59-UTR generated a stop codon within the 59-UTR sequence and resulted in the expression of an 18-amino-acid artificial peptide (Fig. 2B). Western blot analysis confirmed that.
