Used to xPer 327?36. (E ) The reporter fused to xPer 317?36 sequences containing

Used to xPer 327?36. (E ) The reporter fused to xPer 317?36 sequences containing polyalanine amino acid substitutions indicated below the panels. Abbreviations are: OS ?outer segment, IS ?inner segment, N ?nuclei, ST ?synaptic termini. The nuclei (blue) are stained with Hoechst; scale bar: 5 mm. (H) A schematic of a frog rod photoreceptor illustrating its principle compartments. doi:10.1371/journal.pone.0054292.gwas shown to be delivered to rod outer segments of transgenic Xenopus [33]. We first demonstrated that the YFP-fused Htr1a construct was completely excluded 11967625 from rod outer segments of transgenic Xenopus, in agreement with observations in other ciliated cells (Figure 3A). This construct distributed throughout the plasma membrane of the inner ML-281 segment and synaptic terminal and was prominently present in the calycal processes, which are microvillarextensions of the inner segment plasma membrane surrounding the outer segment ([34] white arrowheads in Figures 3A and 3C). We next expressed the Htr1a-YFP construct fused to peripherin’s ten amino acid targeting sequence and found that it was localized exclusively to the outer segment (Figure 3B). This result shows that the Naringin chemical information Peripherin targeting signal is sorted in such a way that it overrides all other targeting information contained within Htr1a and redirects it to the outer segment, just as the rhodopsinA Single Valine Defines Peripherin TargetingFigure 2. Alanine scanning mutagenesis of the peripherin targeting sequence identifies V332 as the only residue essential for targeting. Panels A show confocal images of transgenic frog retinas expressing the YFP-xRhoCTD5-xPer317?36 (green) variations containing single alanine substitutions of individual residues. (J) Multiple sequence alignment of peripherin targeting sequences from different species; residues with over 90 identity are highlighted yellow and the 100 conserved valine is highlighted orange. Abbreviations are: OS ?outer segment, IS ?inner segment, N ?nuclei, ST ?synaptic termini. Nuclei (blue) are stained with Hoechst. Scale bar 5 mm. doi:10.1371/journal.pone.0054292.gtargeting sequence did [33]. We next demonstrated that Htr1a retargeting was completely abrogated when the critical valine residue within peripherin’s targeting sequence was substituted for an alanine (Figure 3C). This result confirms the critical role of V332 and conclusively demonstrates that the absence of spillage seen with the original reporter fused to peripherin’s targeting sequence was not a result of its very efficient degradation in the inner segment.Outer Segment Targeting of Full-length Peripherin is Dependent on VOur next task was to demonstrate that V332 is critical for targeting full-length peripherin. The challenge of these experiments was the property of peripherin to form high order oligomers [35?7]. Consequently, any exogenously expressed peripherin mutant may oligomerize with endogenous peripherin, making it difficult to distinguish whether its intracellular distribution is determined by its own targeting information or information contained within higher order oligomers. For example, Cterminally truncated peripherin was targeted to outer segments of transgenic Xenopus, presumably due to oligomerization with the endogenous protein [22]. Therefore, we switched from frogs to mice, taking advantage of the rds mouse model lacking endogenous peripherin. Photoreceptors of these mice do not form outersegments [18], a phenotype restored upon transgeni.Used to xPer 327?36. (E ) The reporter fused to xPer 317?36 sequences containing polyalanine amino acid substitutions indicated below the panels. Abbreviations are: OS ?outer segment, IS ?inner segment, N ?nuclei, ST ?synaptic termini. The nuclei (blue) are stained with Hoechst; scale bar: 5 mm. (H) A schematic of a frog rod photoreceptor illustrating its principle compartments. doi:10.1371/journal.pone.0054292.gwas shown to be delivered to rod outer segments of transgenic Xenopus [33]. We first demonstrated that the YFP-fused Htr1a construct was completely excluded 11967625 from rod outer segments of transgenic Xenopus, in agreement with observations in other ciliated cells (Figure 3A). This construct distributed throughout the plasma membrane of the inner segment and synaptic terminal and was prominently present in the calycal processes, which are microvillarextensions of the inner segment plasma membrane surrounding the outer segment ([34] white arrowheads in Figures 3A and 3C). We next expressed the Htr1a-YFP construct fused to peripherin’s ten amino acid targeting sequence and found that it was localized exclusively to the outer segment (Figure 3B). This result shows that the peripherin targeting signal is sorted in such a way that it overrides all other targeting information contained within Htr1a and redirects it to the outer segment, just as the rhodopsinA Single Valine Defines Peripherin TargetingFigure 2. Alanine scanning mutagenesis of the peripherin targeting sequence identifies V332 as the only residue essential for targeting. Panels A show confocal images of transgenic frog retinas expressing the YFP-xRhoCTD5-xPer317?36 (green) variations containing single alanine substitutions of individual residues. (J) Multiple sequence alignment of peripherin targeting sequences from different species; residues with over 90 identity are highlighted yellow and the 100 conserved valine is highlighted orange. Abbreviations are: OS ?outer segment, IS ?inner segment, N ?nuclei, ST ?synaptic termini. Nuclei (blue) are stained with Hoechst. Scale bar 5 mm. doi:10.1371/journal.pone.0054292.gtargeting sequence did [33]. We next demonstrated that Htr1a retargeting was completely abrogated when the critical valine residue within peripherin’s targeting sequence was substituted for an alanine (Figure 3C). This result confirms the critical role of V332 and conclusively demonstrates that the absence of spillage seen with the original reporter fused to peripherin’s targeting sequence was not a result of its very efficient degradation in the inner segment.Outer Segment Targeting of Full-length Peripherin is Dependent on VOur next task was to demonstrate that V332 is critical for targeting full-length peripherin. The challenge of these experiments was the property of peripherin to form high order oligomers [35?7]. Consequently, any exogenously expressed peripherin mutant may oligomerize with endogenous peripherin, making it difficult to distinguish whether its intracellular distribution is determined by its own targeting information or information contained within higher order oligomers. For example, Cterminally truncated peripherin was targeted to outer segments of transgenic Xenopus, presumably due to oligomerization with the endogenous protein [22]. Therefore, we switched from frogs to mice, taking advantage of the rds mouse model lacking endogenous peripherin. Photoreceptors of these mice do not form outersegments [18], a phenotype restored upon transgeni.