Abstract

Cell wall formation and maintenance are crucial for hyphal morphogenesis. In many filamentous fungi, chitin is one of the main structural components of the cell wall. Aspergillus nidulans ChsB, a chitin synthase, and CsmA, a chitin synthase with a myosin motor-like domain (MMD) at its N-terminus, both localize predominantly at the hyphal tip regions and at forming septa. ChsB and CsmA play crucial roles in polarized hyphal growth in A. nidulans. In this study, we investigated the mechanism by which CsmA and ChsB accumulate at the hyphal tip in living hyphae. Deletion of kinA, a gene encoding conventional kinesin (kinesin-1), impaired the localization of GFP-CsmA and GFP-ChsB at the hyphal tips. The transport frequency of GFP-CsmA and GFP-ChsB in both anterograde and retrograde direction appeared lower in the kinA-deletion strain compared to wild type, although the velocities of the movements were comparable. Co-localization of GFP-ChsB and GFP-CsmA with mRFP1-KinArigor, a KinA mutant that binds to microtubules but does not move along them, was observed in the posterior of the hyphal tip regions. KinA co-immunoprecipitated with ChsB and CsmA. Co-localization and association of CsmA with KinA did not depend on the MMD. These findings indicate that ChsB and CsmA are transported along microtubules to the subapical region by KinA.

Highlights

  • Hyphae of filamentous fungi represent extremely polarized cells

  • We investigated the localization of class III and V chitin synthases in A. nidulans, ChsB and CsmA, respectively [24,25]

  • Our results suggest that these chitin synthases are delivered to hyphal tips along microtubules through the interaction with conventional kinesin

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Summary

Introduction

Hyphae of filamentous fungi represent extremely polarized cells. Since “polarized growth” is a general growth mechanism common in the elongation of cells as distinct as neurons or pollen tubes, as well as in the differentiation of embryos [1], the mechanism of hyphal tip growth in filamentous fungi may provide a helpful basic model. This mechanism is thought to be highly elaborate and is supported by the continuous delivery of vesicles containing proteins required.

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