Characteristic clusters at the abaxonal Schwann cell membrane [35]. Ezrin was found to be expressed in defined regions which sharpened during postnatal development. These regions represent Schwann cell microvilli at the nodes of Ranvier [45]. Caspr1/paranodin marked the paranodal axonal compartments [36,46] at early and later stages (Fig. 5). No differences in DRP2, ezrin, or Caspr1/paranodin staining were observed between wild-type and MAP1B deficient fibers during postnatal Autophagy development and in the adult. Moreover, no significant differences could be detected between wild-type and MAP1B deficient fibers in the distance between consecutive nodes of Ranvier (normalized to fiber diameter), in the number and spacing of Schmidt-Lantermann incisures, or in the distance from the nodes of Ranvier to the first SchmidtLantermann incisure in the internodal region (not shown).DiscussionOur results demonstrate that the light chains 1326631 of MAP1A and MAP1B interact with the modular adapter protein a1-syntrophin in the central and peripheral nervous system. We identified the conserved COOH termini of the light chains and the PH2 and PDZ domains of syntrophin as interacting domains. The light chains of MAP1A and MAP1B have previously been reported to bind to PDZ domains of glutamate receptor interacting protein 1 [47], PDZrhoGEF [42], and neuronal nitric oxide synthase [40]. Thus, interaction with PDZ domains of target proteins involved in signal transduction emerges as a characteristic function of the COOH-terminal domain of the light chains of MAP1 proteins. The direct comparison of MAP1B expression in sciatic nerve fibers of wild-type and MAP1B2/2 mice by immunohistochemistry allowed us to specifically detect MAP1B expression in myelinating Schwann cells of the adult, uninjured nerve and atFigure 4. MAP1B and syntrophin co-localize at the nodes of Ranvier and the abaxonal Schwann cell membrane. Sciatic nerves were prepared from 4-day (4d) or 14-day (14d) old or adult (adult) wild-type (WT) and MAP1B2/2 (KO) mice. Individual myelinated axons were isolated and stained for MAP1B (antibody anti-HC750) or syntrophin (pan syntrophin antibody anti-syn1351) as indicated. The pictures represent projections of confocal Z-stacks. The staining for MAP1B in postnatal and adult Schwann cells is specific as it is absent in Schwann cells of MAP1B2/2 mice. At all ages MAP1B was found to be concentrated at the nodes of Ranvier (inhibitor asterisks). It also localized at the abaxonal membrane (arrow heads), particularly strong at postnatal day 14. Syntrophin was also found at nodes of Ranvier and the abaxonal membrane. In the adult, it was found to be localized to Cajal bands (arrows) in agreement with previous results [44]. Co-localization of MAP1B and syntrophin was most prominent at the nodes of Ranvier and partial co-localization was found at the abaxonal membrane (arrow heads). Scale bar, 20 mm. doi:10.1371/journal.pone.0049722.gMAP1A and MAP1B Interact with a1-SyntrophinFigure 5. DRP2, ezrin and Caspr1/paranodin localization in peripheral nerve is not affected by MAP1B deficiency. Sciatic nerves were prepared from 4-day (4d) or 14-day (14d) old or adult (adult) wild-type (WT) and MAP1B2/2 (KO) mice. Individual myelinated axons were 
isolated and stained for DRP2, ezrin, or Caspr1/paranodin as indicated. The pictures represent projections of confocal Z-stacks. The nodes of Ranvier (asterisks) and the DRP2 clusters (arrows) are indicated where it was possible to define them. The.Characteristic clusters at the abaxonal Schwann cell membrane [35]. Ezrin was found to be expressed in defined regions which sharpened during postnatal development. These regions represent Schwann cell microvilli at the nodes of Ranvier [45]. Caspr1/paranodin marked the paranodal axonal compartments [36,46] at early and later stages (Fig. 5). No differences in DRP2, ezrin, or Caspr1/paranodin staining were observed between wild-type and MAP1B deficient fibers during postnatal development and in the adult. Moreover, no significant differences could be detected between wild-type and MAP1B deficient fibers in the distance between consecutive nodes of Ranvier (normalized to fiber diameter), in the number and spacing of Schmidt-Lantermann incisures, or in the distance from the nodes of Ranvier to the first SchmidtLantermann incisure in the internodal region (not shown).DiscussionOur results demonstrate that the light chains 1326631 of MAP1A and MAP1B interact with the modular adapter protein a1-syntrophin in the central and peripheral nervous system. We identified the conserved COOH termini of the light chains and the PH2 and PDZ domains of syntrophin as interacting domains. The light chains of MAP1A and MAP1B have previously been reported to bind to PDZ domains of glutamate receptor interacting protein 1 [47], PDZrhoGEF [42], and neuronal nitric oxide synthase [40]. Thus, interaction with PDZ domains of target proteins involved in signal transduction emerges as a characteristic function of the COOH-terminal domain of the light chains of MAP1 proteins. The direct comparison of MAP1B expression in sciatic nerve fibers of wild-type and MAP1B2/2 mice by immunohistochemistry allowed us to specifically detect MAP1B expression in myelinating Schwann cells of the adult, uninjured nerve and atFigure 4. MAP1B and syntrophin co-localize at the nodes of Ranvier and the abaxonal Schwann cell membrane. Sciatic nerves were prepared from 4-day (4d) or 14-day (14d) old or adult (adult) wild-type (WT) and MAP1B2/2 (KO) mice. Individual myelinated axons were isolated and stained for MAP1B (antibody anti-HC750) or syntrophin (pan syntrophin antibody anti-syn1351) as indicated. The pictures represent projections of confocal Z-stacks. The staining for 
MAP1B in postnatal and adult Schwann cells is specific as it is absent in Schwann cells of MAP1B2/2 mice. At all ages MAP1B was found to be concentrated at the nodes of Ranvier (asterisks). It also localized at the abaxonal membrane (arrow heads), particularly strong at postnatal day 14. Syntrophin was also found at nodes of Ranvier and the abaxonal membrane. In the adult, it was found to be localized to Cajal bands (arrows) in agreement with previous results [44]. Co-localization of MAP1B and syntrophin was most prominent at the nodes of Ranvier and partial co-localization was found at the abaxonal membrane (arrow heads). Scale bar, 20 mm. doi:10.1371/journal.pone.0049722.gMAP1A and MAP1B Interact with a1-SyntrophinFigure 5. DRP2, ezrin and Caspr1/paranodin localization in peripheral nerve is not affected by MAP1B deficiency. Sciatic nerves were prepared from 4-day (4d) or 14-day (14d) old or adult (adult) wild-type (WT) and MAP1B2/2 (KO) mice. Individual myelinated axons were isolated and stained for DRP2, ezrin, or Caspr1/paranodin as indicated. The pictures represent projections of confocal Z-stacks. The nodes of Ranvier (asterisks) and the DRP2 clusters (arrows) are indicated where it was possible to define them. The.
