Requirement of the Cep57-Cep63 Interaction for Proper Cep152 Recruitment and Centriole Duplication

REFERENCES

• Woodruff JB, Wueseke O, Hyman AA. 2014. Pericentriolar material structure and dynamics. Philos Trans R Soc Lond B Biol Sci 369:20130459. https://doi.org/10.1098/rstb.2013.0459.
   PubMed Web of Science ®Google Scholar
• Conduit PT, Wainman A, Raff JW. 2015. Centrosome function and assembly in animal cells. Nat Rev Mol Cell Biol 16:611–624. https://doi.org/10.1038/nrm4062.
   PubMed Web of Science ®Google Scholar
• Vertii A, Hehnly H, Doxsey S. 2016. The centrosome, a multitalented renaissance organelle. Cold Spring Harb Perspect Biol 8:a025049. https://doi.org/10.1101/cshperspect.a025049.
   PubMed Web of Science ®Google Scholar
• Lawo S, Hasegan M, Gupta GD, Pelletier L. 2012. Subdiffraction imaging of centrosomes reveals higher-order organizational features of pericentriolar material. Nat Cell Biol 14:1148–1158. https://doi.org/10.1038/ncb2591.
   PubMed Web of Science ®Google Scholar
• Mennella VK, Eszthelyi B, McDonald KL, Chhun B, Kan F, Rogers GC, Huang B, Agard DA. 2012. Subdiffraction-resolution fluorescence microscopy reveals a domain of the centrosome critical for pericentriolar material organization. Nat Cell Biol 14:1159–1168. https://doi.org/10.1038/ncb2597.
   PubMed Web of Science ®Google Scholar
• Fu J, Glover DM. 2012. Structured illumination of the interface between centriole and peri-centriolar material. Open Biol 2:120104. https://doi.org/10.1098/rsob.120104.
   PubMed Web of Science ®Google Scholar
• Sonnen KF, Schermelleh L, Leonhardt H, Nigg EA. 2012. 3D-structured illumination microscopy provides novel insight into architecture of human centrosomes. Biol Open 1:965–976. https://doi.org/10.1242/bio.20122337.
   PubMed Web of Science ®Google Scholar
• Olivier N, Keller D, Gonczy P, Manley S. 2013. Resolution doubling in 3D-STORM imaging through improved buffers. PLoS One 8:e69004. https://doi.org/10.1371/journal.pone.0069004.
   PubMed Web of Science ®Google Scholar
• Kim TS, Zhang L, Il Ahn J, Meng L, Chen Y, Lee E, Bang JK, Lim JM, Ghirlando R, Fan L, Wang YX, Kim BY, Park JE, Lee KS. 2019. Molecular architecture of a cylindrical self-assembly at human centrosomes. Nat Commun 10:1151. https://doi.org/10.1038/s41467-019-08838-2.
   PubMed Web of Science ®Google Scholar
• van Breugel M, Hirono M, Andreeva A, Yanagisawa HA, Yamaguchi S, Nakazawa Y, Morgner N, Petrovich M, Ebong IO, Robinson CV, Johnson CM, Veprintsev D, Zuber B. 2011. Structures of SAS-6 suggest its organization in centrioles. Science 331:1196–1199. https://doi.org/10.1126/science.1199325.
   PubMed Web of Science ®Google Scholar
• Kitagawa D, Vakonakis I, Olieric N, Hilbert M, Keller D, Olieric V, Bortfeld M, Erat MC, Flückiger I, Gönczy P, Steinmetz MO. 2011. Structural basis of the 9-fold symmetry of centrioles. Cell 144:364–375. https://doi.org/10.1016/j.cell.2011.01.008.
   PubMed Web of Science ®Google Scholar
• Lukinavicius G, Lavogina D, Orpinell M, Umezawa K, Reymond L, Garin N, Gonczy P, Johnsson K. 2013. Selective chemical crosslinking reveals a Cep57-Cep63-Cep152 centrosomal complex. Curr Biol 23:265–270. https://doi.org/10.1016/j.cub.2012.12.030.
   PubMed Web of Science ®Google Scholar
• Bossard C, Laurell H, Van den Berghe L, Meunier S, Zanibellato C, Prats H. 2003. Translokin is an intracellular mediator of FGF-2 trafficking. Nat Cell Biol 5:433–439. https://doi.org/10.1038/ncb979.
   PubMed Web of Science ®Google Scholar
• Park SY, Park JE, Kim TS, Kim JH, Kwak MJ, Ku B, Tian L, Murugan RN, Ahn M, Komiya S, Hojo H, Kim NH, Kim BY, Bang JK, Erikson RL, Lee KW, Kim SJ, Oh BH, Yang W, Lee KS. 2014. Molecular basis for unidirectional scaffold switching of human Plk4 in centriole biogenesis. Nat Struct Mol Biol 21:696–703. https://doi.org/10.1038/nsmb.2846.
   PubMed Web of Science ®Google Scholar
• Banterle N, Gonczy P. 2017. Centriole biogenesis: from identifying the characters to understanding the plot. Annu Rev Cell Dev Biol 33:23–49. https://doi.org/10.1146/annurev-cellbio-100616-060454.
   PubMed Web of Science ®Google Scholar
• Zitouni S, Nabais C, Jana SC, Guerrero A, Bettencourt-Dias M. 2014. Polo-like kinases: structural variations lead to multiple functions. Nat Rev Mol Cell Biol 15:433–452. https://doi.org/10.1038/nrm3819.
   PubMed Web of Science ®Google Scholar
• Aziz K, Sieben CJ, Jeganathan KB, Hamada M, Davies BA, Velasco ROF, Rahman N, Katzmann DJ, van Deursen JM. 2018. Mosaic-variegated aneuploidy syndrome mutation or haploinsufficiency in Cep57 impairs tumor suppression. J Clin Invest 128:3517–3534. https://doi.org/10.1172/JCI120316.
   PubMed Web of Science ®Google Scholar
• Watanabe K, Takao D, Ito KK, Takahashi M, Kitagawa D. 2019. The Cep57-pericentrin module organizes PCM expansion and centriole engagement. Nat Commun 10:931. https://doi.org/10.1038/s41467-019-08862-2.
   PubMed Web of Science ®Google Scholar
• Delaval B, Doxsey SJ. 2010. Pericentrin in cellular function and disease. J Cell Biol 188:181–190. https://doi.org/10.1083/jcb.200908114.
   PubMed Web of Science ®Google Scholar
• Wu Q, He R, Zhou H, Yu AC, Zhang B, Teng J, Chen J. 2012. Cep57, a NEDD1-binding pericentriolar material component, is essential for spindle pole integrity. Cell Res 22:1390–1401. https://doi.org/10.1038/cr.2012.61.
   PubMed Web of Science ®Google Scholar
• He R, Wu Q, Zhou H, Huang N, Chen J, Teng J. 2013. Cep57 protein is required for cytokinesis by facilitating central spindle microtubule organization. J Biol Chem 288:14384–14390. https://doi.org/10.1074/jbc.M112.441501.
   PubMed Web of Science ®Google Scholar
• Zhou H, Wang T, Zheng T, Teng J, Chen J. 2016. Cep57 is a Mis12-interacting kinetochore protein involved in kinetochore targeting of Mad1-Mad2. Nat Commun 7:10151. https://doi.org/10.1038/ncomms10151.
   PubMed Web of Science ®Google Scholar
• Snape K, Hanks S, Ruark E, Barros-Nunez P, Elliott A, Murray A, Lane AH, Shannon N, Callier P, Chitayat D, Clayton-Smith J, Fitzpatrick DR, Gisselsson D, Jacquemont S, Asakura-Hay K, Micale MA, Tolmie J, Turnpenny PD, Wright M, Douglas J, Rahman N. 2011. Mutations in CEP57 cause mosaic variegated aneuploidy syndrome. Nat Genet 43:527–529. https://doi.org/10.1038/ng.822.
   PubMed Web of Science ®Google Scholar
• Momotani K, Khromov AS, Miyake T, Stukenberg PT, Somlyo AV. 2008. Cep57, a multidomain protein with unique microtubule and centrosomal localization domains. Biochem J 412:265–273. https://doi.org/10.1042/BJ20071501.
   PubMed Web of Science ®Google Scholar
• Brown NJ, Marjanovic M, Luders J, Stracker TH, Costanzo V. 2013. Cep63 and Cep152 cooperate to ensure centriole duplication. PLoS One 8:e69986. https://doi.org/10.1371/journal.pone.0069986.
   PubMed Web of Science ®Google Scholar
• Gillingham AK, Munro S. 2000. The PACT domain, a conserved centrosomal targeting motif in the coiled-coil proteins AKAP450 and pericentrin. EMBO Rep 1:524–529. https://doi.org/10.1093/embo-reports/kvd105.
   PubMed Web of Science ®Google Scholar
• Pinson L, Mannini L, Willems M, Cucco F, Sirvent N, Frebourg T, Quarantotti V, Collet C, Schneider A, Sarda P, Genevieve D, Puechberty J, Lefort G, Musio A. 2014. CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome. Am J Med Genet A 164A:177–181. https://doi.org/10.1002/ajmg.a.36166.
   PubMedGoogle Scholar
• Brightman DS, Ejaz S, Dauber A. 2018. Mosaic variegated aneuploidy syndrome caused by a CEP57 mutation diagnosed by whole exome sequencing. Clin Case Rep 6:1531–1534. https://doi.org/10.1002/ccr3.1655.
   PubMed Web of Science ®Google Scholar
• Kim J, Kim J, Rhee K. 2019. PCNT is critical for the association and conversion of centrioles to centrosomes during mitosis. J Cell Sci 132:jcs225789. https://doi.org/10.1242/jcs.225789.
   PubMed Web of Science ®Google Scholar
• Sieben C, Banterle N, Douglass KM, Gonczy P, Manley S. 2018. Multicolor single-particle reconstruction of protein complexes. Nat Methods 15:777–780. https://doi.org/10.1038/s41592-018-0140-x.
   PubMed Web of Science ®Google Scholar
• Gonczy P. 2015. Centrosomes and cancer: revisiting a long-standing relationship. Nat Rev Cancer 15:639–652. https://doi.org/10.1038/nrc3995.
   PubMed Web of Science ®Google Scholar
• Nigg EA, Holland AJ. 2018. Once and only once: mechanisms of centriole duplication and their deregulation in disease. Nat Rev Mol Cell Biol 19:297–312. https://doi.org/10.1038/nrm.2017.127.
   PubMed Web of Science ®Google Scholar
• Lee KS, Yuan Y-L, Kuriyama R, Erikson RL. 1995. Plk is an M-phase-specific protein kinase and interacts with a kinesin-like protein, CHO1/MKLP-1. Mol Cell Biol 15:7143–7151. https://doi.org/10.1128/mcb.15.12.7143.
   PubMed Web of Science ®Google Scholar
• Park JE, Zhang L, Bang JK, Andresson T, DiMaio F, Lee KS. 2019. Phase separation of Polo-like kinase 4 by autoactivation and clustering drives centriole biogenesis. Nat Commun 10:4959. https://doi.org/10.1038/s41467-019-12619-2.
   PubMed Web of Science ®Google Scholar
• Arquint C, Nigg EA. 2016. The PLK4-STIL-SAS-6 module at the core of centriole duplication. Biochem Soc Trans 44:1253–1263. https://doi.org/10.1042/BST20160116.
   PubMed Web of Science ®Google Scholar
• Fu J, Hagan IM, Glover DM. 2015. The centrosome and its duplication cycle. Cold Spring Harb Perspect Biol 7:a015800. https://doi.org/10.1101/cshperspect.a015800.
   PubMed Web of Science ®Google Scholar