DSpace
 

KNUSTSpace >
Conference Proceedings >
College of Science >

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/12884

Title: Missense pathogenic variants in KIF4A affect dental morphogenesis resulting in X-linked taurodontism, microdontia and dens-invaginatus
Authors: Gowans, Lord J.J.
Cameron-Christie, Sophia
Slayton, Rebecca L.
Busch, Tamara
Romero-Bustillos, Miguel
et. al
Keywords: exome sequencing
X-linked recessive
microdontia
taurodontism
dens invaginatus
Issue Date: 20-Sep-2019
Publisher: Frontiers in Genetics
Citation: Gowans LJJ, Cameron-Christie S, Slayton RL, Busch T, RomeroBustillos M, Eliason S, Sweat M, Sobreira N, Yu W, Kantaputra PN, Wohler E, Adeyemo WL, Lachke SA, Anand D, Campbell C, Drummond BK, Markie DM, van Vuuren WJ, van Vuuren LJ, Casamassimo PS, Ettinger R, Owais A, van Staden I, Amendt BA, Adeyemo AA, Murray JC, Robertson SP and Butali A (2019) Missense Pathogenic variants in KIF4A Affect Dental Morphogenesis Resulting in X-linked Taurodontism, Microdontia and Dens-Invaginatus. Front. Genet. 10:800. doi: 10.3389/fgene.2019.00800
Abstract: The etiology of dental anomalies is multifactorial; and genetic and environmental factors that affect the dental lamina have been implicated. We investigated two families of European ancestry in which males were affected by taurodontism, microdontia and dens invaginatus. In both families, males were related to each other via unaffected females. A linkage analysis was conducted in a New Zealand family, followed by exome sequencing and focused analysis of the X-chromosome. In a US family, exome sequencing of the X-chromosome was followed by Sanger sequencing to conduct segregation analyses. We identified two independent missense variants in KIF4A that segregate in affected males and female carriers. The variant in a New Zealand family (p.Asp371His) predicts the substitution of a residue in the motor domain of the protein while the one in a US family (p.Arg771Lys) predicts the substitution of a residue in the domain that interacts with Protein Regulator of Cytokinesis 1 (PRC1). We demonstrated that the gene is expressed in the developing tooth bud during development, and that the p.Arg771Lys variant influences cell migration in an in vitro assay. These data implicate missense variations in KIF4A in a pathogenic mechanism that causes taurodontism, microdontia and dens invaginatus phenotypes.
Description: An article published in Frontiers in Genetics and also available at
URI: http://hdl.handle.net/123456789/12884
Appears in Collections:College of Science

Files in This Item:

File Description SizeFormat
fgene-10-00800.pdf1.51 MBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback