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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.1004070Souhrn
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.
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