Cargando…
Spata7 is required for maintenance of the retinal connecting cilium
SPATA7, an early onset LCA3 retinal disease gene, encodes a putative scaffold protein that is essential for the proper assembly of the connecting cilium (CC) complex in photoreceptors. Previous studies have shown that SPATA7 interacts with other photoreceptor-specific ciliary proteins, such as RPGR...
Autores principales: | Lu, Jiaxiong, Xiong, Kaitlyn, Qian, Xinye, Choi, Jongsu, Shim, Yoon-Kyung, Burnett, Jacob, Mardon, Graeme, Chen, Rui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976851/ https://www.ncbi.nlm.nih.gov/pubmed/35368022 http://dx.doi.org/10.1038/s41598-022-09530-0 |
Ejemplares similares
-
SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium
por: Dharmat, Rachayata, et al.
Publicado: (2018) -
Genetic evidence suggests that Spata22 is required for the maintenance of Rad51 foci in mammalian meiosis
por: Ishishita, Satoshi, et al.
Publicado: (2014) -
Mutation of SPATA7 in a family with autosomal recessive early-onset retinitis pigmentosa
por: Kannabiran, Chitra, et al.
Publicado: (2012) -
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiency
por: Puusepp, Sanna, et al.
Publicado: (2018) -
Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22: Human SPATA22 assists MEIOB to enter the nucleus
por: Xu, Yating, et al.
Publicado: (2022)