Browsing by Subject "Transmembrane protein 67 (TMEM67)"

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    Hydrocephalus in a rat model of Meckel Gruber syndrome with a TMEM67 mutation
    (Springer Nature, 2019-01-31) Shim, Joon W.; Territo, Paul R.; Simpson, Stefanie; Watson, John C.; Jiang, Lei; Riley, Amanda A.; McCarthy, Brian; Persohn, Scott; Fulkerson, Daniel; Blazer-Yost, Bonnie L.; Biology, School of Science
    Transmembrane protein 67 (TMEM67) is mutated in Meckel Gruber Syndrome type 3 (MKS3) resulting in a pleiotropic phenotype with hydrocephalus and renal cystic disease in both humans and rodent models. The precise pathogenic mechanisms remain undetermined. Herein it is reported for the first time that a point mutation of TMEM67 leads to a gene dose-dependent hydrocephalic phenotype in the Wistar polycystic kidney (Wpk) rat. Animals with TMEM67 heterozygous mutations manifest slowly progressing hydrocephalus, observed during the postnatal period and continuing into adulthood. These animals have no overt renal phenotype. The TMEM67 homozygous mutant rats have severe ventriculomegaly as well as severe polycystic kidney disease and die during the neonatal period. Protein localization in choroid plexus epithelial cells indicates that aquaporin 1 and claudin-1 both remain normally polarized in all genotypes. The choroid plexus epithelial cells may have selectively enhanced permeability as evidenced by increased Na+, K+ and Cl- in the cerebrospinal fluid of the severely hydrocephalic animals. Collectively, these results suggest that TMEM67 is required for the regulation of choroid plexus epithelial cell fluid and electrolyte homeostasis. The Wpk rat model, orthologous to human MKS3, provides a unique platform to study the development of both severe and mild hydrocephalus.
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    Identification of elongated cilia and chiral malformation in TMEM67 mutant brains
    (Office of the Vice Chancellor for Research, 2015-04-17) Shim, Joon W.; Territo, Paul R.; Maue, Ellen; Ahmed, Shehab; Watson, John C.; Fulkerson, Dan; Blazer-Yost, Bonnie L.
    Transmembrane protein 67 (TMEM67) is encoded by one of four syndromic encephalocele genes. In humans a mutation in TMEM67 causes Meckel Gruber Syndrome, type 3 (MKS3) which is characterized by severe encephalocele and cystic kidneys and is usually fatal in the neonatal period. MKS3 is one of a spectrum of diseases known as ciliopathies because the proteins responsible for the disease are found in cells with the primary cilia. Primary cilia are a single, hair-like organelle that is found on the apical membrane of polarized cells and is thought to be involved in formation of left-right asymmetry during development as well as mechano- and chemo-reception. Here we characterize previously unreported details of cerebral phenotype in the Wistar polycystic kidney (Wpk) rats with a TMEM67 mutation. In choroid plexus (CP) epithelia of wild type animals, TMEM67 localizes to the plasma membrane and to a region close to the basal side of CP primary cilia. In a choroid plexus cell line that forms an epithelial sheet, the TMEM67 is found intracellularly but also localizes to the junctional complexes as evidenced by β catenin co-localization. Absence of normal TMEM67 leads to elongation of primary cilia in the ependymal cells lining the cerebral ventricles of the TMEM67-/- animals indicating that this protein is involved in the regulation of cilia length. Reduced aqueduct, bilateral dilatation with fusion of lateral ventricles, swelling of the hippocampus, and altered hindbrain histoarchitecture are noted in the TMEM67-/- rats. In the heterozygous animals mild asymmetric ventriculomegaly primarily on the left side is observed during early postnatal periods and continues into adulthood. These results suggest that TMEM67 is required for cilia length control and normal development of cerebral midline that maintains the symmetry of the left and right hemispheres. The Wpk rat model, orthologous to human MKS3, provides a unique model in which to study the development of both severe (TMEM67-/-) and mild (TMEM67+/-) hydrocephalus and other developmental abnormalities that are commonly found in human patients with ciliopathies.