The AmAZI1ng Roles of Centriolar Satellites during Development

article has not abstract

Vyšlo v časopise: The AmAZI1ng Roles of Centriolar Satellites during Development. PLoS Genet 9(12): e32767. doi:10.1371/journal.pgen.1004070
Kategorie: Perspective
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1004070

Souhrn

article has not abstract

Zdroje

1. NiggEA, StearnsT (2011) The centrosome cycle: Centriole biogenesis, duplication and inherent asymmetries. Nat Cell Biol 13: 1154–1160.

2. NachuryMV, SeeleyES, JinH (2010) Trafficking to the ciliary membrane: how to get across the periciliary diffusion barrier? Annu Rev Cell Dev Biol 26: 59–87.

3. VincensiniL, BlisnickT, BastinP (2011) 1001 model organisms to study cilia and flagella. Biol Cell 103: 109–130.

4. Bettencourt-DiasM, HildebrandtF, PellmanD, WoodsG, GodinhoSA (2011) Centrosomes and cilia in human disease. Trends Genet 27: 307–315.

5. NiggEA, RaffJW (2009) Centrioles, centrosomes, and cilia in health and disease. Cell 139: 663–678.

6. BarenzF, MayiloD, GrussOJ (2011) Centriolar satellites: busy orbits around the centrosome. Eur J Cell Biol 90: 983–989.

7. BalczonR, BaoL, ZimmerWE (1994) PCM-1, A 228-kD centrosome autoantigen with a distinct cell cycle distribution. J Cell Biol 124: 783–793.

8. KuboA, SasakiH, Yuba-KuboA, TsukitaS, ShiinaN (1999) Centriolar satellites: molecular characterization, ATP-dependent movement toward centrioles and possible involvement in ciliogenesis. J Cell Biol 147: 969–980.

9. DammermannA, MerdesA (2002) Assembly of centrosomal proteins and microtubule organization depends on PCM-1. J Cell Biol 159: 255–266.

10. KimJ, KrishnaswamiSR, GleesonJG (2008) CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium. Hum Mol Genet 17: 3796–3805.

11. KimJC, BadanoJL, SiboldS, EsmailMA, HillJ, et al. (2004) The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nat Genet 36: 462–470.

12. KodaniA, TonthatV, WuB, SutterlinC (2010) Par6 alpha interacts with the dynactin subunit p150 Glued and is a critical regulator of centrosomal protein recruitment. Mol Biol Cell 21: 3376–3385.

13. LopesCA, ProsserSL, RomioL, HirstRA, O'CallaghanC, et al. (2011) Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1. J Cell Sci 124: 600–612.

14. StoweTR, WilkinsonCJ, IqbalA, StearnsT (2012) The centriolar satellite proteins Cep72 and Cep290 interact and are required for recruitment of BBS proteins to the cilium. Mol Biol Cell 23: 3322–3335.

15. HallEA, KeighrenM, FordMJ, DaveyT, JarmanAP, et al. (2013) Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes. PLoS Genet 9: e1003928 doi:10.1371/journal.pgen.1003928

16. AndersenJS, WilkinsonCJ, MayorT, MortensenP, NiggEA, et al. (2003) Proteomic characterization of the human centrosome by protein correlation profiling. Nature 426: 570–574.

17. StaplesCJ, MyersKN, BeveridgeRD, PatilAA, LeeAJ, et al. (2012) The centriolar satellite protein Cep131 is important for genome stability. J Cell Sci 125: 4770–4779.

18. CzarneckiPG, ShahJV (2012) The ciliary transition zone: from morphology and molecules to medicine. Trends Cell Biol 22: 201–210.

19. WilkinsonCJ, CarlM, HarrisWA (2009) Cep70 and Cep131 contribute to ciliogenesis in zebrafish embryos. BMC Cell Biol 10: 17.

20. MaL, JarmanAP (2011) Dilatory is a Drosophila protein related to AZI1 (CEP131) that is located at the ciliary base and required for cilium formation. J Cell Sci 124: 2622–2630.

21. GraserS, StierhofYD, LavoieSB, GassnerOS, LamlaS, et al. (2007) Cep164, a novel centriole appendage protein required for primary cilium formation. J Cell Biol 179: 321–330.

22. RauchA, ThielCT, SchindlerD, WickU, CrowYJ, et al. (2008) Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science 319: 816–819.

23. KumarA, GirimajiSC, DuvvariMR, BlantonSH (2009) Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly. Am J Hum Genet 84: 286–290.

24. GuernseyDL, JiangH, HussinJ, ArnoldM, BouyakdanK, et al. (2010) Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4. Am J Hum Genet 87: 40–51.

25. HussainMS, BaigSM, NeumannS, NurnbergG, FarooqM, et al. (2012) A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. Am J Hum Genet 90: 871–878.

26. MarthiensV, RujanoMA, PennetierC, TessierS, Paul-GilloteauxP, et al. (2013) Centrosome amplification causes microcephaly. Nat Cell Biol 15: 731–740.