Pericentrin in health and disease

References

• Doxsey SJ, Stein P, Evans L, Calarco PD, Kirschner M. Pericentrin, a highly conserved centrosome protein involved in microtubule organization. Cell 1994; 76:639 - 50; http://dx.doi.org/10.1016/0092-8674(94)90504-5; PMID: 8124707
   PubMed Web of Science ®Google Scholar
• Takahashi M, Yamagiwa A, Nishimura T, Mukai H, Ono Y. Centrosomal proteins CG-NAP and kendrin provide microtubule nucleation sites by anchoring gamma-tubulin ring complex. Mol Biol Cell 2002; 13:3235 - 45; http://dx.doi.org/10.1091/mbc.E02-02-0112; PMID: 12221128
   PubMed Web of Science ®Google Scholar
• Zimmerman WC, Sillibourne J, Rosa J, Doxsey SJ. Mitosis-specific anchoring of gamma tubulin complexes by pericentrin controls spindle organization and mitotic entry. Mol Biol Cell 2004; 15:3642 - 57; http://dx.doi.org/10.1091/mbc.E03-11-0796; PMID: 15146056
   PubMed Web of Science ®Google Scholar
• Delaval B, Doxsey SJ. Pericentrin in cellular function and disease. J Cell Biol 2010; 188:181 - 90; http://dx.doi.org/10.1083/jcb.200908114; PMID: 19951897
   PubMed Web of Science ®Google Scholar
• Rauch A, Thiel CT, Schindler D, Wick U, Crow YJ, Ekici AB, et al. Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science 2008; 319:816 - 9; http://dx.doi.org/10.1126/science.1151174; PMID: 18174396
   PubMed Web of Science ®Google Scholar
• Willems M, Geneviève D, Borck G, Baumann C, Baujat G, Bieth E, et al. Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families. J Med Genet 2010; 47:797 - 802; http://dx.doi.org/10.1136/jmg.2009.067298; PMID: 19643772
   PubMed Web of Science ®Google Scholar
• Jurczyk A, Gromley A, Redick S, San Agustin J, Witman G, Pazour GJ, et al. Pericentrin forms a complex with intraflagellar transport proteins and polycystin-2 and is required for primary cilia assembly. J Cell Biol 2004; 166:637 - 43; http://dx.doi.org/10.1083/jcb.200405023; PMID: 15337773
   PubMed Web of Science ®Google Scholar
• Miyoshi K, Onishi K, Asanuma MP, Miyazaki I, Diaz-Corrales FJ, Ogawa N. Embryonic expression of pericentrin suggests universal roles in ciliogenesis. Dev Genes Evol 2006; 216:537 - 42; http://dx.doi.org/10.1007/s00427-006-0065-8; PMID: 16534625
   PubMed Web of Science ®Google Scholar
• Martinez-Campos M, Basto R, Baker J, Kernan M, Raff JW. The Drosophila pericentrin-like protein is essential for cilia/flagella function, but appears to be dispensable for mitosis. J Cell Biol 2004; 165:673 - 83; http://dx.doi.org/10.1083/jcb.200402130; PMID: 15184400
   PubMed Web of Science ®Google Scholar
• Miyoshi K, Kasahara K, Miyazaki I, Shimizu S, Taniguchi M, Matsuzaki S, et al. Pericentrin, a centrosomal protein related to microcephalic primordial dwarfism, is required for olfactory cilia assembly in mice. FASEB J 2009; 23:3289 - 97; http://dx.doi.org/10.1096/fj.08-124420; PMID: 19470799
   PubMed Web of Science ®Google Scholar
• Mühlhans J, Brandstätter JH, Gießl A. The centrosomal protein pericentrin identified at the basal body complex of the connecting cilium in mouse photoreceptors. PLoS One 2011; 6:e26496; http://dx.doi.org/10.1371/journal.pone.0026496; PMID: 22031837
   PubMedGoogle Scholar
• Flory MR, Davis TN. The centrosomal proteins pericentrin and kendrin are encoded by alternatively spliced products of one gene. Genomics 2003; 82:401 - 5; http://dx.doi.org/10.1016/S0888-7543(03)00119-8; PMID: 12906865
   PubMed Web of Science ®Google Scholar
• Miyoshi K, Asanuma M, Miyazaki I, Matsuzaki S, Tohyama M, Ogawa N. Characterization of pericentrin isoforms in vivo. Biochem Biophys Res Commun 2006; 351:745 - 9; http://dx.doi.org/10.1016/j.bbrc.2006.10.101; PMID: 17084386
   PubMed Web of Science ®Google Scholar
• Piane M, Della Monica M, Piatelli G, Lulli P, Lonardo F, Chessa L, et al. Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: report of a novel mutation of the PCNT gene. Am J Med Genet A 2009; 149A:2452 - 6; http://dx.doi.org/10.1002/ajmg.a.33035; PMID: 19839044
   PubMed Web of Science ®Google Scholar
• Endoh-Yamagami S, Karkar KM, May SR, Cobos I, Thwin MT, Long JE, et al. A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice. Dev Biol 2010; 340:41 - 53; http://dx.doi.org/10.1016/j.ydbio.2010.01.017; PMID: 20096683
   PubMed Web of Science ®Google Scholar
• Kubo A, Tsukita S. Non-membranous granular organelle consisting of PCM-1: subcellular distribution and cell-cycle-dependent assembly/disassembly. J Cell Sci 2003; 116:919 - 28; http://dx.doi.org/10.1242/jcs.00282; PMID: 12571289
   PubMed Web of Science ®Google Scholar
• Jurczyk A, Pino SC, O’Sullivan-Murphy B, Addorio M, Lidstone EA, Diiorio P, et al. A novel role for the centrosomal protein, pericentrin, in regulation of insulin secretory vesicle docking in mouse pancreatic beta-cells. PLoS One 2010; 5:e11812; http://dx.doi.org/10.1371/journal.pone.0011812; PMID: 20676397
   PubMedGoogle Scholar
• Charters GA, Stones CJ, Shelling AN, Baguley BC, Finlay GJ. Centrosomal dysregulation in human metastatic melanoma cell lines. Cancer Genet 2011; 204:477 - 85; http://dx.doi.org/10.1016/j.cancergen.2011.07.001; PMID: 22018269
   PubMed Web of Science ®Google Scholar
• Flory MR, Moser MJ, Monnat RJ Jr., Davis TN. Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin. Proc Natl Acad Sci U S A 2000; 97:5919 - 23; http://dx.doi.org/10.1073/pnas.97.11.5919; PMID: 10823944
   PubMed Web of Science ®Google Scholar
• Griffith E, Walker S, Martin CA, Vagnarelli P, Stiff T, Vernay B, et al. Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling. Nat Genet 2008; 40:232 - 6; http://dx.doi.org/10.1038/ng.2007.80; PMID: 18157127
   PubMed Web of Science ®Google Scholar
• Hall JG, Flora C, Scott CI Jr., Pauli RM, Tanaka KI. Majewski osteodysplastic primordial dwarfism type II (MOPD II): natural history and clinical findings. Am J Med Genet A 2004; 130A:55 - 72; http://dx.doi.org/10.1002/ajmg.a.30203; PMID: 15368497
   PubMed Web of Science ®Google Scholar
• Brancati F, Castori M, Mingarelli R, Dallapiccola B. Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: clinical report and review of cerebral vascular anomalies. Am J Med Genet A 2005; 139:212 - 5; http://dx.doi.org/10.1002/ajmg.a.31009; PMID: 16278902
   PubMed Web of Science ®Google Scholar
• Delaval B, Doxsey S. Genetics. Dwarfism, where pericentrin gains stature. Science 2008; 319:732 - 3; http://dx.doi.org/10.1126/science.1154513; PMID: 18258883
   PubMed Web of Science ®Google Scholar