The roles of tubulin-folding cofactors in neuronal morphogenesis and disease

The roles of tubulin-folding cofactors in neuronal morphogenesis and disease

Microtubules play important roles in neuronal morphogenesis, including cellular polarization, neurite growth, and branching. A microtubule is a polymer of α- and β-tubulin heterodimers that are formed by a multistep process assisted by at least fi ve tubulin-folding cofactors (TBCA–E) (Lopez-Fanarraga et al., 2001). Newly synthesized α- and β-tubulins associate with the cytosolic chaperonin complex (CCT), and then the quasi-native tubulins interact with fi ve tubulin-folding cofactors. The α- and β-tubulins fi rst interact with TBCB and TBCA, which are further transferred to TBCE and TBCD, respectively. The α- and β-tubulins, TBCC, TBCD, and TBCE form a supercomplex, and guanosine triphosphate (GTP) hydrolysis occurs within the supercomplex, releasing a tubulin heterodimer. In addition to their functions in tubulin folding and tubulin heterodimer formation, excess amounts of TBCD or TBCE may interact with tubulin heterodimers, leading to their degradation. Thus, tubulin-folding cofactors may play a role in both the synthesis and degradation of tubulin heterodimers.

Recently, the functions of tubulin-folding cofactors in the nervous system have been revealed. The human TBCE mutation is a known cause of the hypoparathyroidism-retardation-dysmorphism and Kenny-Caff ey syndromes (Parvari et al., 2002). The progressive motor neuronopathy (pmn) mouse, a model for a fast developing human motor neuron disorder, is caused by a missense mutation in TBCE (Martin et al., 2002). The axons of pmn mice possess a reduced number of microtubules and progressively degenerate; eventually, the pmn mice die approximately 4–6 weeks after birth (Martin et al., 2002). Drosophila TBCE has also been shown to regulate the development and function of neuromuscular synapses and promote microtubule formation (Jin et al., 2009). Giant axonal neuropathy (GAN) is caused by mutations in GAN, which encodes for the protein gigaxonin that controls the protein degradation of TBCB (Wang et al., 2005). TBCB is localized at the transition zones of the growth cones of growing neurites. Knockdown of TBCB promotes axon growth and TBCB overexpression leads to microtubule depolymerization, growth cone retraction, and axon degeneration (Lopez-Fanarraga et al., 2007). The accumulation of TBCB may be a causative factor of cytoskeletal pathology in GAN. However, the functions and regulations of the other tubulin-folding cofactors in neurons remain largely unknown.

We recently reported that one of the tubulin-folding cofactors, TBCD, regulates neuronal morphogenesis by mediating Down syndrome cell adhesion molecule (Dscam) functions (Okumura et al., 2015). We utilized Drosophila olfactory projection neurons as a model for understanding the molecular mechanisms of neuronal morphogenesis. Mosaic analysis with a repressible cell marker (MARCM) system enabled us to generate labeled, homozygous cells with single-cell resolution in vivo. Using the MARCM system, we found that TBCD is required for the dendrite and axon morphogenesis in projection neurons. Wild-type projection neurons sent their dendrites to a single glomerulus, out of approximately 50 glomeruli, in the antennal lobe (Figure 1A). In contrast, TBCD mutant projection neurons exhibited ectopic dendrite branching, that is, the dendrite targeted the correct glomerulus and additional glomeruli (Figure 1B). Axons of the wild-type projection neurons innervated the mushroom body and lateral horn with stereotypical terminal arborization (Figure 1A). Axons of the TBCD mutant projection neurons elongated to the mushroom body and lateral horn during development, but degenerated soon after eclosion (Figure 1B). The ectopic dendrite branching defect was also observed in the loss of other tubulin-folding cofactors, that is, TBCB and TBCE, suggesting that the dendrite defect in the TBCD mutant is likely caused by the loss of TBCD function in tubulin heterodimer formation. Consistent with these results, the tubulin levels were found to be signifi cantly reduced in the TBCD mutant projection neurons. Interestingly, the overexpression of TBCD in projection neurons also showed ectopic dendrite branching. Both the loss- and gain-of-function studies suggested that the amount and dynamics of tubulin heterodimers must be tightly regulated for correct dendrite morphogenesis.

We also set out to understand how the function of TBCD is regulated in neuronal morphogenesis. We identifi ed Dscam, an immunoglobulin family protein, as a binding partner of TBCD (Figure 1C). Drosophila Dscam possesses extraordinary diversity because of the alternative splicing of extracellular and transmembrane domains, which can generate 38,016 isoforms, and has been reported to function in several processes of neural development, such as axon guidance and dendrite self-avoidance (Hattori et al., 2008). These isoforms show isoform-specifi c binding, which mediates homophilic repulsion. Although the function of Dscam in the nervous system has been studied extensively, the link between Dscam and cytoskeletal proteins (especially microtubules) remains unclear.

We hypothesized that TBCD functions downstream of Dscam in neuronal morphogenesis, which was supported by the following results: First, Dscam overexpression caused ectopic dendrite branching, similar to that seen for TBCD mutant and TBCD overexpression. Second, the overexpression of Dscam in cultured Drosophila S2 cells led to a decrease in microtubules projecting radially from the cell center. Third, the overexpression of Dscam in cultured Drosophila primary neurons reduced α-tubulin staining locally at the site where Dscam accumulated. Fourth, the Dscam gain-of-function phenotype in mushroom body neurons was suppressed by the reduction of TBCD levels. Additionally, the reduction in TBCD levels did not aff ect the expression and localization of Dscam. These results suggest that TBCD is essential for Dscam function during neuronal morphogenesis.

We also examined how TBCD regulates dendrite morphogenesis. Phenotypic analysis of TBCD mutant projection neurons during their development showed that their dendrites fi rst targeted only the correct glomerulus; however, ectopic dendrite branches were observed at a later stage, suggesting that TBCD is required for the maintenance of correct dendrite morphology. Additional dendrite arborization in TBCD mutant projection neurons was seen between the cell body and the correct glomerulus (Figure 1B), implying that, in wild-type projection neurons, dendrite arborization within the dendrite stalk region (between the cell body and the correct glomerulus) is suppressed by the regulation of microtubule stabilization. In TBCD mutant, microtubule destabilization disrupts cellular transport; therefore, factors that inhibit the ectopic branching may not be transported to their proper sites. It is also possible that the disruption of cellular transport may cause proximal localization of factors regulating dendrite branching in the distal site (Sekine et al., 2009). A possible cargo to be transported is the Golgi outpost. In Drosophila dendrite arborization (da) neurons, Golgi outposts are localized at the dendrite branching point. The disruption of microtubule-dependent transport may result in the proximal accumulation of Golgi outposts, which induces ectopic dendrite branching. Another candidate cargo is the endosome. In da neurons, mutants of motor proteins, such as dynein, decrease the distal dendrite branches and increase the proximal branches. In this situation, Rab5, an early endosome marker, is proximally localized. Consistent with these results, we previously reported that the loss of strip, a regulator of early endosome organization, causes ectopic dendrite branching in projection neurons (Sakuma et al., 2014). Thus, tubulin-folding cofactors could aff ect dendrite branching by regulating microtubule-dependent endosome transport.

Figure 1 Tubulin folding cofactor D (TBCD) cooperates with Dscam during neuronal morphogenesis.

We have found that TBCD cooperates with Dscam during neuronal morphogenesis and that TBCD may function downstream of Dscam. The pathways acting downstream of Dscam, especially their eff ects on microtubules, are not fully understood, and only the Dock/Pak signaling pathway is known to function downstream of Dscam. Dscam forms a complex with Dock, DSH3PX (a sorting nexin), and Wasp (a protein component of the actin polymerization machinery) that may aff ect the actin cytoskeleton (Figure 1C, Worby et al., 2001). In Drosophila projection neurons, Dock and Pak mutants do not show obvious dendrite and axon morphological defects; therefore, TBCD may function downstream of Dscam, independently of the Dock/Pak signaling pathway in projection neurons. However, it is still possible that the tubulin-folding pathway coordinates with the Dock/Pak signaling pathway. For example, PAK1 (a human ortholog of Pak) phosphorylates human TBCB, and the knockdown of TBCB or PAK1 reduces microtubule polymerization (Figure 1C, Vadlamudi et al., 2005). Further studies are required in order to understand how the tubulin-folding pathway is regulated by Dscam and how the tubulin-folding pathway and other signaling pathways coordinate the dynamics of actin and microtubules under stimulus from the other guidance receptors.

Microtubule dynamics regulated by microtubule-associated proteins are important for neural development. Growing evidence suggests that regulation of the amount of free tubulins helps modulate microtubule dynamics. As we have described here, TBCD is an essential factor for neuronal morphogenesis. Although specifi c human disorders caused by TBCD mutation have not been identifi ed, human DSCAM is located in the Down syndrome critical region and is implicated in the cognitive disabilities seen in Down syndrome. We found that the gain-of-function phenotype of Dscam was suppressed by reduction of TBCD. Therefore, TBCD may contribute to structural alterations, functional alterations, or both of neural circuits in Down syndrome and other neurological disorders.

This work was supported by grants from the Ministry of Education, Culture, Sports, Science and Technology in Japan to MM and TC, the Japan Society for the Promotion of Science to MO, MM, and TC, and the Japan Science and Technology Agency to M.M. and TC.

Misako Okumura, Masayuki Miura, Takahiro Chihara*

Department of Genetics, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, Japan (Okumura M, Miura M, Chihara T)

Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Tokyo, Japan (Miura M, Chihara T)

*Correspondence to: Takahiro Chihara, Ph.D.,

tchihara@mol.f.u-tokyo.ac.jp.

Accepted: 2015-06-04

orcid: 0000-0001-9989-3619 (Takahiro Chihara)

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10.4103/1673-5374.165226 http://www.nrronline.org/

Okumura M, Miura M, Chihara T (2015) The roles of tubulin-folding cofactors in neuronal morphogenesis and disease. Neural Regen Res 10(9):1388-1389.