Literature DB >> 28850540

Maintaining protein composition in cilia.

Louise A Stephen1, Yasmin Elmaghloob1, Shehab Ismail1.   

Abstract

The primary cilium is a sensory organelle that is vital in regulating several signalling pathways. Unlike most organelles cilia are open to the rest of the cell, not enclosed by membranes. The distinct protein composition is crucial to the function of cilia and many signalling proteins and receptors are specifically concentrated within distinct compartments. To maintain this composition, a mechanism is required to deliver proteins to the cilium whilst another must counter the entropic tendency of proteins to distribute throughout the cell. The combination of the two mechanisms should result in the concentration of ciliary proteins to the cilium. In this review we will look at different cellular mechanisms that play a role in maintaining the distinct composition of cilia, including regulation of ciliary access and trafficking of ciliary proteins to, from and within the cilium.

Keywords:  Arl13b; Arl2; Arl3; IFT; cilia; protein trafficking

Mesh:

Substances:

Year:  2017        PMID: 28850540     DOI: 10.1515/hsz-2017-0168

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  4 in total

Review 1.  Primary cilia in the postnatal brain: Subcellular compartments for organizing neuromodulatory signaling.

Authors:  Lauren Tereshko; Gina G Turrigiano; Piali Sengupta
Journal:  Curr Opin Neurobiol       Date:  2022-04-08       Impact factor: 7.070

2.  Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.

Authors:  Wu Li; Yong Feng; Anhai Chen; Taoxi Li; Sida Huang; Jing Liu; Xianlin Liu; Yalan Liu; Jiangang Gao; Denise Yan; Jie Sun; Lingyun Mei; Xuezhong Liu; Jie Ling
Journal:  Hum Mol Genet       Date:  2019-12-15       Impact factor: 6.150

3.  Phylogenetic profiling and cellular analyses of ARL16 reveal roles in traffic of IFT140 and INPP5E.

Authors:  Skylar I Dewees; Romana Vargová; Katherine R Hardin; Rachel E Turn; Saroja Devi; Joshua Linnert; Uwe Wolfrum; Tamara Caspary; Marek Eliáš; Richard A Kahn
Journal:  Mol Biol Cell       Date:  2022-02-23       Impact factor: 3.612

4.  Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy.

Authors:  Shakeel A Sheikh; Robert A Sisk; Cara R Schiavon; Yar M Waryah; Muhammad A Usmani; David H Steel; John A Sayer; Ashok K Narsani; Robert B Hufnagel; Saima Riazuddin; Richard A Kahn; Ali M Waryah; Zubair M Ahmed
Journal:  Invest Ophthalmol Vis Sci       Date:  2019-11-01       Impact factor: 4.799

  4 in total

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