TY - JOUR
T1 - WDR72 models of structure and function
T2 - A stage-specific regulator of enamel mineralization
AU - Katsura, K. A.
AU - Horst, J. A.
AU - Chandra, D.
AU - Le, T. Q.
AU - Nakano, Y.
AU - Zhang, Y.
AU - Horst, O. V.
AU - Zhu, L.
AU - Le, M. H.
AU - DenBesten, P. K.
N1 - Funding Information:
Thank you to our AI patients and family members for contributing samples for this study. In addition, we would like to acknowledge Dr. Neil Katsura for providing the clinical evaluations of the AI patients' radiographs and Dr. Yuki Mochida for the comparative discussions of rodent Wdr72 knockout models. MicroCT imaging work was performed by Sabra Djomehri at the Division of Biomaterials and Bioengineering MicroCT Imaging Facility, UCSF, generously supported by the Department of Health and Human Services/NIH S10 Shared Instrumentation Grant ( S10RR026645 ), and Departments of Preventive and Restorative Dental Sciences and Orofacial Sciences, School of Dentistry, UCSF. This research was funded by the UCSF Department of Oral and Craniofacial Sciences , NIDCR 1R03 DE019682 and UCSF Start-up Fund to T.L., and NIDCR T32 DE007306 to P.D.
Publisher Copyright:
© 2014.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Amelogenesis Imperfecta (AI) is a clinical diagnosis that encompasses a group of genetic mutations, each affecting processes involved in tooth enamel formation and thus, result in various enamel defects. The hypomaturation enamel phenotype has been described for mutations involved in the later stage of enamel formation, including Klk4, Mmp20, C4orf26, and Wdr72. Using a candidate gene approach we discovered a novel Wdr72 human mutation in association with AI to be a 5-base pair deletion (c.806_810delGGCAG; p.G255VfsX294). To gain insight into the function of WDR72, we used computer modeling of the full-length human WDR72 protein structure and found that the predicted N-terminal sequence forms two beta-propeller folds with an alpha-solenoid tail at the C-terminus. This domain iteration is characteristic of vesicle coat proteins, such as beta'-COP, suggesting a role for WDR72 in the formation of membrane deformation complexes to regulate intracellular trafficking. Our Wdr72 knockout mouse model (Wdr72-/-), containing a LacZ reporter knock-in, exhibited hypomineralized enamel similar to the AI phenotype observed in humans with Wdr72 mutations. MicroCT scans of Wdr72-/- mandibles affirmed the hypomineralized enamel phenotype occurring at the onset of the maturation stage. H&E staining revealed a shortened height phenotype in the Wdr72-/- ameloblasts with retained proteins in the enamel matrix during maturation stage. H+/Cl- exchange transporter 5 (CLC5), an early endosome acidifier, was co-localized with WDR72 in maturation-stage ameloblasts and decreased in Wdr72-/- maturation-stage ameloblasts. There were no obvious differences in RAB4A and LAMP1 immunostaining of Wdr72-/- mice as compared to wildtype controls. Moreover, Wdr72-/- ameloblasts had reduced amelogenin immunoreactivity, suggesting defects in amelogenin fragment resorption from the matrix. These data demonstrate that WDR72 has a major role in enamel mineralization, most notably during the maturation stage, and suggest a function involving endocytic vesicle trafficking, possibly in the removal of amelogenin proteins.
AB - Amelogenesis Imperfecta (AI) is a clinical diagnosis that encompasses a group of genetic mutations, each affecting processes involved in tooth enamel formation and thus, result in various enamel defects. The hypomaturation enamel phenotype has been described for mutations involved in the later stage of enamel formation, including Klk4, Mmp20, C4orf26, and Wdr72. Using a candidate gene approach we discovered a novel Wdr72 human mutation in association with AI to be a 5-base pair deletion (c.806_810delGGCAG; p.G255VfsX294). To gain insight into the function of WDR72, we used computer modeling of the full-length human WDR72 protein structure and found that the predicted N-terminal sequence forms two beta-propeller folds with an alpha-solenoid tail at the C-terminus. This domain iteration is characteristic of vesicle coat proteins, such as beta'-COP, suggesting a role for WDR72 in the formation of membrane deformation complexes to regulate intracellular trafficking. Our Wdr72 knockout mouse model (Wdr72-/-), containing a LacZ reporter knock-in, exhibited hypomineralized enamel similar to the AI phenotype observed in humans with Wdr72 mutations. MicroCT scans of Wdr72-/- mandibles affirmed the hypomineralized enamel phenotype occurring at the onset of the maturation stage. H&E staining revealed a shortened height phenotype in the Wdr72-/- ameloblasts with retained proteins in the enamel matrix during maturation stage. H+/Cl- exchange transporter 5 (CLC5), an early endosome acidifier, was co-localized with WDR72 in maturation-stage ameloblasts and decreased in Wdr72-/- maturation-stage ameloblasts. There were no obvious differences in RAB4A and LAMP1 immunostaining of Wdr72-/- mice as compared to wildtype controls. Moreover, Wdr72-/- ameloblasts had reduced amelogenin immunoreactivity, suggesting defects in amelogenin fragment resorption from the matrix. These data demonstrate that WDR72 has a major role in enamel mineralization, most notably during the maturation stage, and suggest a function involving endocytic vesicle trafficking, possibly in the removal of amelogenin proteins.
KW - Amelogenesis imperfecta (AI)
KW - Hypomaturation
KW - Maturation-stage ameloblasts
KW - Protein modeling
KW - Vesicle trafficking
KW - Wdr72 knockout mouse
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U2 - 10.1016/j.matbio.2014.06.005
DO - 10.1016/j.matbio.2014.06.005
M3 - Article
C2 - 25008349
AN - SCOPUS:84908024612
SN - 0945-053X
VL - 38
SP - 48
EP - 58
JO - Collagen and Related Research
JF - Collagen and Related Research
ER -