A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4.
Nephronophthisis (NPHP) is a ciliopathy in which genetic modifiers may underlie the variable penetrance of clinical features. To identify modifiers, a screen was conducted on C. elegans nphp-4(tm925) mutants. Mutations in ten loci exacerbating nphp-4(tm925) ciliary defects were obtained. Four loci h...
Main Authors: | Svetlana V Masyukova, Dawn E Landis, Scott J Henke, Corey L Williams, Jay N Pieczynski, Kelly N Roszczynialski, Jannese E Covington, Erik B Malarkey, Bradley K Yoder |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2016-02-01
|
Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC4749664?pdf=render |
Similar Items
-
MKS-NPHP module proteins control ciliary shedding at the transition zone.
by: Delphine Gogendeau, et al.
Published: (2020-03-01) -
A complex of BBS1 and NPHP7 is required for cilia motility in zebrafish.
by: Yun Hee Kim, et al.
Published: (2013-01-01) -
Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome
by: Cheng Cui, et al.
Published: (2011-01-01) -
Many Genes—One Disease? Genetics of Nephronophthisis (NPHP) and NPHP-Associated Disorders
by: Shalabh Srivastava, et al.
Published: (2018-01-01) -
Role of MKS1 in epithelial homeostasis
by: Song, Yuxiang
Published: (2018)