Cargando…

The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus

Cilia are protrusions of the cell surface and composed of hundreds of proteins many of which are evolutionary and functionally well conserved. In cells assembling motile cilia the expression of numerous ciliary components is under the control of the transcription factor FOXJ1. Here, we analyse the e...

Descripción completa

Detalles Bibliográficos
Autores principales:	Beckers, Anja, Fuhl, Franziska, Ott, Tim, Boldt, Karsten, Brislinger, Magdalena Maria, Walentek, Peter, Schuster-Gossler, Karin, Hegermann, Jan, Alten, Leonie, Kremmer, Elisabeth, Przykopanski, Adina, Serth, Katrin, Ueffing, Marius, Blum, Martin, Gossler, Achim
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233316/ https://www.ncbi.nlm.nih.gov/pubmed/34172766 http://dx.doi.org/10.1038/s41598-021-92495-3

Ejemplares similares

The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice
por: Beckers, Anja, et al.
Publicado: (2018)

Ciliogenesis and cerebrospinal fluid flow in the developing Xenopus brain are regulated by foxj1
por: Hagenlocher, Cathrin, et al.
Publicado: (2013)

O-Fucosylation of DLL3 Is Required for Its Function during Somitogenesis
por: Serth, Katrin, et al.
Publicado: (2015)

Activity of the mouse Notch ligand DLL1 is sensitive to C-terminal tagging in vivo
por: Schuster-Gossler, Karin, et al.
Publicado: (2021)

O-fucosylation of the Notch Ligand mDLL1 by POFUT1 Is Dispensable for Ligand Function
por: Müller, Julia, et al.
Publicado: (2014)

Generation of an 870 kb deletion encompassing the Skt/Etl4 locus by combination of inter- and intra-chromosomal recombination
por: Serth, Katrin, et al.
Publicado: (2015)

Normal Development in Mice Over-Expressing the Intracellular Domain of DLL1 Argues against Reverse Signaling by DLL1 In Vivo
por: Redeker, Christian, et al.
Publicado: (2013)

Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development
por: Schuster-Gossler, Karin, et al.
Publicado: (2009)

Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium
por: Rudat, Carsten, et al.
Publicado: (2014)

Recessive Mutations in CFAP74 Cause Primary Ciliary Dyskinesia with Normal Ciliary Ultrastructure
por: Biebach, Luisa, et al.
Publicado: (2022)

CFAP300 mutation causing primary ciliary dyskinesia in Finland
por: Schultz, Rüdiger, et al.
Publicado: (2022)

Divergent functions and distinct localization of the Notch ligands DLL1 and DLL3 in vivo
por: Geffers, Insa, et al.
Publicado: (2007)

Genetic interaction between central pair apparatus genes CFAP221, CFAP54, and SPEF2 in mouse models of primary ciliary dyskinesia
por: McKenzie, Casey W., et al.
Publicado: (2020)

Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities
por: Morimoto, Yoshiro, et al.
Publicado: (2019)

Identification of Genetic Variants in CFAP221 as a Cause of Primary Ciliary Dyskinesia
por: Bustamante-Marin, Ximena M., et al.
Publicado: (2019)

A Novel Mammal-Specific Three Partite Enhancer Element Regulates Node and Notochord-Specific Noto Expression
por: Alten, Leonie, et al.
Publicado: (2012)

CFAP54 is required for proper ciliary motility and assembly of the central pair apparatus in mice
por: McKenzie, Casey W., et al.
Publicado: (2015)

Concurrent loss of ciliary genes WDR93 and CFAP46 in phylogenetically distant birds
por: Salve, Buddhabhushan Girish, et al.
Publicado: (2023)

Identification of Important Effector Proteins in the FOXJ1 Transcriptional Network Associated With Ciliogenesis and Ciliary Function
por: Mukherjee, Ishita, et al.
Publicado: (2019)

The Forkhead protein, FoxJ1, specifies node-like cilia in Xenopus and Zebrafish embryos
por: Stubbs, Jennifer, et al.
Publicado: (2008)

Both ciliary and non-ciliary functions of Foxj1a confer Wnt/β-catenin signaling in zebrafish left-right patterning
por: Zhu, Ping, et al.
Publicado: (2015)

Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalus
por: Shapiro, Adam J., et al.
Publicado: (2021)

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
por: Coutton, Charles, et al.
Publicado: (2018)

CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
por: Shamoto, Noritoshi, et al.
Publicado: (2018)

Sale of Professor Koch's Lymph
por: Gossler, Von
Publicado: (1891)

The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice
por: Wu, Bingbing, et al.
Publicado: (2023)

Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels
por: Jurisch-Yaksi, Nathalie, et al.
Publicado: (2013)

Scrutinizing ciliopathies by unravelling the ciliary interactome
por: van Reeuwijk, J, et al.
Publicado: (2012)

Compartmentalised expression of Delta-like 1 in epithelial somites is required for the formation of intervertebral joints
por: Teppner, Ingeborg, et al.
Publicado: (2007)

17th Library System Seminar on the Virtual Library
por: Böllmann, Elisabeth, et al.
Publicado: (1993)

Mutation of CFAP57, a protein required for the asymmetric targeting of a subset of inner dynein arms in Chlamydomonas, causes primary ciliary dyskinesia
por: Bustamante-Marin, Ximena M., et al.
Publicado: (2020)

A novel heterozygous variant of FOXJ1 in a Chinese female with primary ciliary dyskinesia and hydrocephalus: A case report and literature review
por: Gao, Shiyang, et al.
Publicado: (2023)

Essential Role of CFAP53 in Sperm Flagellum Biogenesis
por: Wu, Bingbing, et al.
Publicado: (2021)

Context-Dependent Functional Divergence of the Notch Ligands DLL1 and DLL4 In Vivo
por: Preuße, Kristina, et al.
Publicado: (2015)

The ectodomains determine ligand function in vivo and selectivity of DLL1 and DLL4 toward NOTCH1 and NOTCH2 in vitro
por: Tveriakhina, Lena, et al.
Publicado: (2018)

Ciliary transcription factors and miRNAs precisely regulate Cp110 levels required for ciliary adhesions and ciliogenesis
por: Walentek, Peter, et al.
Publicado: (2016)

From proteomic data to networks: statistics and methods reveal ciliary protein interaction landscape
por: Lu, Q, et al.
Publicado: (2015)

CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module
por: Dougherty, Gerard W., et al.
Publicado: (2020)

Arf4 Is Required for Mammalian Development but Dispensable for Ciliary Assembly
por: Follit, John A., et al.
Publicado: (2014)

Ciliary and extraciliary Gpr161 pools repress hedgehog signaling in a tissue-specific manner
por: Hwang, Sun-Hee, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_9sqbju9rkb7sv87tvsgnkqb8nq