The novel function of JADE1S in cytokinesis of epithelial cells

References

• Zhou MI, Wang H, Ross JJ, Kuzmin I, Xu C, Cohen HT. The von Hippel-Lindau tumor suppressor stabilizes novel plant homeodomain protein Jade-1. J Biol Chem 2002; 277:39887-98; PMID:12169691; http://dx.doi.org/10.1074/jbc.M205040200
   PubMed Web of Science ®Google Scholar
• Tzouanacou E, Tweedie S, Wilson V. Identification of Jade1, a gene encoding a PHD zinc finger protein, in a gene trap mutagenesis screen for genes involved in anteroposterior axis development. Mol Cell Biol 2003; 23:8553-2; PMID:14612400; http://dx.doi.org/10.1128/MCB.23.23.8553-8562.2003
   PubMed Web of Science ®Google Scholar
• Szelei J, Soto AM, Geck P, Desronvil M, Prechtl NV, Weill BC, Sonnenschein C. Identification of human estrogen-inducible transcripts that potentially mediate the apoptotic response in breast cancer. J Steroid Biochem Mol Biol 2000; 72:89-102; PMID:10775800; http://dx.doi.org/10.1016/S0960-0760(00)00025-X
   PubMed Web of Science ®Google Scholar
• Havasi A, Haegele JA, Gall JM, Blackmon S, Ichimura T, Bonegio RG, Panchenko MV. Histone acetyl transferase (HAT) HBO1 and JADE1 in epithelial cell regeneration. Am J Pathol 2013; 182:152-62; PMID:23159946; http://dx.doi.org/10.1016/j.ajpath.2012.09.017
   PubMed Web of Science ®Google Scholar
• Aasland R, Gibson TJ, Stewart AF. The PHD finger: implications for chromatin-mediated transcriptional regulation. Trends Biochem Sci 1995; 20:56-9; PMID:7701562; http://dx.doi.org/10.1016/S0968-0004(00)88957-4
   PubMed Web of Science ®Google Scholar
• Foy RL, Song IY, Chitalia VC, Cohen HT, Saksouk N, Cayrou C, Vaziri C, Côté J, Panchenko MV. Role of Jade-1 in the histone acetyltransferase (HAT) HBO1 complex. J Biol Chem 2008; 283:28817-26; PMID:18684714; http://dx.doi.org/10.1074/jbc.M801407200
   PubMed Web of Science ®Google Scholar
• Panchenko MV, Zhou MI, Cohen HT. von Hippel-Lindau partner Jade-1 is a transcriptional co-activator associated with histone acetyltransferase activity. J Biol Chem 2004; 279:56032-41; PMID:15502158; http://dx.doi.org/10.1074/jbc.M410487200
   PubMed Web of Science ®Google Scholar
• Siriwardana NS, Meyer R, Havasi A, Dominguez I, Panchenko MV. Cell cycle-dependent chromatin shuttling of HBO1-JADE1 histone acetyl transferase (HAT) complex. Cell Cycle 2014; 13:0-1; http://dx.doi.org/10.4161/cc.28759
   Web of Science ®Google Scholar
• Zhou MI, Foy RL, Chitalia VC, Zhao J, Panchenko MV, Wang H, Cohen HT. Jade-1, a candidate renal tumor suppressor that promotes apoptosis. Proc Natl Acad Sci U S A 2005; 102:11035-40; PMID:16046545; http://dx.doi.org/10.1073/pnas.0500757102
   PubMed Web of Science ®Google Scholar
• Doyon Y, Cayrou C, Ullah M, Landry AJ, Côté V, Selleck W, Lane WS, Tan S, Yang XJ, Côté J. ING tumor suppressor proteins are critical regulators of chromatin acetylation required for genome expression and perpetuation. Mol Cell 2006; 21:51-64; PMID:16387653; http://dx.doi.org/10.1016/j.molcel.2005.12.007
   PubMed Web of Science ®Google Scholar
• Borgal L, Habbig S, Hatzold J, Liebau MC, Dafinger C, Sacarea I, Hammerschmidt M, Benzing T, Schermer B. The ciliary protein nephrocystin-4 translocates the canonical Wnt regulator Jade-1 to the nucleus to negatively regulate β-catenin signaling. J Biol Chem 2012; 287:25370-80; PMID:22654112; http://dx.doi.org/10.1074/jbc.M112.385658
   PubMed Web of Science ®Google Scholar
• Borgal L, Rinschen MM, Dafinger C, Hoff S, Reinert MJ, Lamkemeyer T, Lienkamp SS, Benzing T, Schermer B. Casein kinase 1 α phosphorylates the Wnt regulator Jade-1 and modulates its activity. J Biol Chem 2014; 289:26344-56; PMID:25100726; http://dx.doi.org/10.1074/jbc.M114.562165
   PubMed Web of Science ®Google Scholar
• Avvakumov N, Lalonde ME, Saksouk N, Paquet E, Glass KC, Landry AJ, Doyon Y, Cayrou C, Robitaille GA, Richard DE, et al. Conserved molecular interactions within the HBO1 acetyltransferase complexes regulate cell proliferation. Mol Cell Biol 2012; 32:689-703; PMID:22144582; http://dx.doi.org/10.1128/MCB.06455-11
   PubMed Web of Science ®Google Scholar
• Saksouk N, Avvakumov N, Champagne KS, Hung T, Doyon Y, Cayrou C, Paquet E, Ullah M, Landry AJ, Côté V, et al. HBO1 HAT complexes target chromatin throughout gene coding regions via multiple PHD finger interactions with histone H3 tail. Mol Cell 2009; 33:257-65; PMID:19187766; http://dx.doi.org/10.1016/j.molcel.2009.01.007
   PubMed Web of Science ®Google Scholar
• Lalonde ME, Avvakumov N, Glass KC, Joncas FH, Saksouk N, Holliday M, Paquet E, Yan K, Tong Q, Klein BJ, et al. Exchange of associated factors directs a switch in HBO1 acetyltransferase histone tail specificity. Genes Dev 2013; 27:2009-24; PMID:24065767; http://dx.doi.org/10.1101/gad.223396.113
   PubMed Web of Science ®Google Scholar
• Allis CD, Berger SL, Cote J, Dent S, Jenuwien T, Kouzarides T, Pillus L, Reinberg D, Shi Y, Shiekhattar R, et al. New nomenclature for chromatin-modifying enzymes. Cell 2007; 131:633-6; PMID:18022353; http://dx.doi.org/10.1016/j.cell.2007.10.039
   PubMed Web of Science ®Google Scholar
• Iizuka M, Matsui T, Takisawa H, Smith MM. Regulation of replication licensing by acetyltransferase Hbo1. Mol Cell Biol 2006; 26:1098-108; PMID:16428461; http://dx.doi.org/10.1128/MCB.26.3.1098-1108.2006
   PubMed Web of Science ®Google Scholar
• Iizuka M, Stillman B. Histone acetyltransferase HBO1 interacts with the ORC1 subunit of the human initiator protein. J Biol Chem 1999; 274:23027-34; PMID:10438470; http://dx.doi.org/10.1074/jbc.274.33.23027
   PubMed Web of Science ®Google Scholar
• Burke TW, Cook JG, Asano M, Nevins JR. Replication factors MCM2 and ORC1 interact with the histone acetyltransferase HBO1. J Biol Chem 2001; 276:15397-408; PMID:11278932; http://dx.doi.org/10.1074/jbc.M011556200
   PubMed Web of Science ®Google Scholar
• Georgiakaki M, Chabbert-Buffet N, Dasen B, Meduri G, Wenk S, Rajhi L, Amazit L, Chauchereau A, Burger CW, Blok LJ, et al. Ligand-controlled interaction of histone acetyltransferase binding to ORC-1 (HBO1) with the N-terminal transactivating domain of progesterone receptor induces steroid receptor coactivator 1-dependent coactivation of transcription. Mol Endocrinol 2006; 20:2122-40; PMID:16645042; http://dx.doi.org/10.1210/me.2005-0149
   PubMed Web of Science ®Google Scholar
• Johmura Y, Osada S, Nishizuka M, Imagawa M. FAD24 acts in concert with histone acetyltransferase HBO1 to promote adipogenesis by controlling DNA replication. J Biol Chem 2008; 283:2265-74; PMID:18029353; http://dx.doi.org/10.1074/jbc.M707880200
   PubMed Web of Science ®Google Scholar
• Sharma M, Zarnegar M, Li X, Lim B, Sun Z. Androgen receptor interacts with a novel MYST protein, HBO1. J Biol Chem 2000; 275:35200-8; PMID:10930412; http://dx.doi.org/10.1074/jbc.M004838200
   PubMed Web of Science ®Google Scholar
• Stedman W, Deng Z, Lu F, Lieberman PM. ORC, MCM, and histone hyperacetylation at the Kaposi's sarcoma-associated herpesvirus latent replication origin. J Virol 2004; 78:12566-75; PMID:15507644; http://dx.doi.org/10.1128/JVI.78.22.12566-12575.2004
   PubMed Web of Science ®Google Scholar
• Iizuka M, Takahashi Y, Mizzen CA, Cook RG, Fujita M, Allis CD, Frierson HF Jr, Fukusato T, Smith MM. Histone acetyltransferase Hbo1: catalytic activity, cellular abundance, and links to primary cancers. Gene 2009; 436:108-14; PMID:19393168; http://dx.doi.org/10.1016/j.gene.2009.01.020
   PubMed Web of Science ®Google Scholar
• Wang WZ, Liu HO, Wu YH, Hong Y, Yang JW, Liu YH, Wu WB, Zhou L, Sun LL, Xu JJ, et al. Estrogen receptor α (ERalpha) mediates 17beta-estradiol (E2)-activated expression of HBO1. J Exp Clin Cancer Res 2010; 29:140; http://dx.doi.org/10.1186/1756-9966-29-140
   PubMed Web of Science ®Google Scholar
• Mishima Y, Miyagi S, Saraya A, Negishi M, Endoh M, Endo TA, Toyoda T, Shinga J, Katsumoto T, Chiba T, et al. The Hbo1-Brd1/Brpf2 complex is responsible for global acetylation of H3K14 and required for fetal liver erythropoiesis. Blood 2011; 118:2443-53; PMID:21753189; http://dx.doi.org/10.1182/blood-2011-01-331892
   PubMed Web of Science ®Google Scholar
• Chitalia VC, Foy RL, Bachschmid MM, Zeng L, Panchenko MV, Zhou MI, Bharti A, Seldin DC, Lecker SH, Dominguez I, et al. Jade-1 inhibits Wnt signalling by ubiquitylating β-catenin and mediates Wnt pathway inhibition by pVHL. Nat Cell Biol 2008; 10:1208-16; PMID:18806787; http://dx.doi.org/10.1038/ncb1781
   PubMed Web of Science ®Google Scholar
• Wan G, Hu X, Liu Y, Han C, Sood AK, Calin GA, Zhang X, Lu X. A novel non-coding RNA lncRNA-JADE connects DNA damage signalling to histone H4 acetylation. Embo J 2013; 32:2833-47; PMID:24097061; http://dx.doi.org/10.1038/emboj.2013.221
   PubMed Web of Science ®Google Scholar
• Agromayor M, Martin-Serrano J. Knowing when to cut and run: mechanisms that control cytokinetic abscission. Trends Cell Biol 2013; 23:433-41; PMID:23706391; http://dx.doi.org/10.1016/j.tcb.2013.04.006
   PubMed Web of Science ®Google Scholar
• Schiel JA, Prekeris R. Membrane dynamics during cytokinesis. Curr Opin Cell Biol 2013; 25:92-8; PMID:23177492; http://dx.doi.org/10.1016/j.ceb.2012.10.012
   PubMed Web of Science ®Google Scholar
• Schiel JA, Childs C, Prekeris R. Endocytic transport and cytokinesis: from regulation of the cytoskeleton to midbody inheritance. Trends Cell Biol 2013; 23:319-27; PMID:23522622; http://dx.doi.org/10.1016/j.tcb.2013.02.003
   PubMed Web of Science ®Google Scholar
• Green RA, Paluch E, Oegema K. Cytokinesis in animal cells. Annu Rev Cell Dev Biol 2012; 28:29-58; PMID:22804577; http://dx.doi.org/10.1146/annurev-cellbio-101011-155718
   PubMed Web of Science ®Google Scholar
• Steigemann P, Gerlich DW. Cytokinetic abscission: cellular dynamics at the midbody. Trends Cell Biol 2009; 19:606-16; PMID:19733077; http://dx.doi.org/10.1016/j.tcb.2009.07.008
   PubMed Web of Science ®Google Scholar
• Elia N, Sougrat R, Spurlin TA, Hurley JH, Lippincott-Schwartz J. Dynamics of endosomal sorting complex required for transport (ESCRT) machinery during cytokinesis and its role in abscission. Proc Natl Acad Sci U S A 2011; 108:4846-51; PMID:21383202; http://dx.doi.org/10.1073/pnas.1102714108
   PubMed Web of Science ®Google Scholar
• Fabbro M, Zhou BB, Takahashi M, Sarcevic B, Lal P, Graham ME, Gabrielli BG, Robinson PJ, Nigg EA, Ono Y, et al. Cdk1/Erk2- and Plk1-dependent phosphorylation of a centrosome protein, Cep55, is required for its recruitment to midbody and cytokinesis. Dev Cell 2005; 9:477-88; PMID:16198290; http://dx.doi.org/10.1016/j.devcel.2005.09.003
   PubMed Web of Science ®Google Scholar
• Hu CK, Coughlin M, Mitchison TJ. Midbody assembly and its regulation during cytokinesis. Mol Biol Cell 2012; 23:1024-34; PMID:22278743; http://dx.doi.org/10.1091/mbc.E11-08-0721
   PubMed Web of Science ®Google Scholar
• Gromley A, Jurczyk A, Sillibourne J, Halilovic E, Mogensen M, Groisman I, Blomberg M, Doxsey S. A novel human protein of the maternal centriole is required for the final stages of cytokinesis and entry into S phase. J Cell Biol 2003; 161:535-45; PMID:12732615; http://dx.doi.org/10.1083/jcb.200301105
   PubMed Web of Science ®Google Scholar
• Thoresen SB, Campsteijn C, Vietri M, Schink KO, Liestøl K, Andersen JS, Raiborg C, Stenmark H. ANCHR mediates Aurora-B-dependent abscission checkpoint control through retention of VPS4. Nat Cell Biol 2014; 16:550-60; PMID:24814515; http://dx.doi.org/10.1038/ncb2959
   PubMed Web of Science ®Google Scholar
• Steigemann P, Wurzenberger C, Schmitz MH, Held M, Guizetti J, Maar S, Gerlich DW. Aurora B-mediated abscission checkpoint protects against tetraploidization. Cell 2009; 136:473-84; PMID:19203582; http://dx.doi.org/10.1016/j.cell.2008.12.020
   PubMed Web of Science ®Google Scholar
• Carlton JG, Caballe A, Agromayor M, Kloc M, Martin-Serrano J. ESCRT-III governs the Aurora B-mediated abscission checkpoint through CHMP4C. Science 2012; 336:220-5; PMID:22422861; http://dx.doi.org/10.1126/science.1217180
   PubMed Web of Science ®Google Scholar
• Mackay DR, Makise M, Ullman KS. Defects in nuclear pore assembly lead to activation of an Aurora B-mediated abscission checkpoint. J Cell Biol 2010; 191:923-31; PMID:21098116; http://dx.doi.org/10.1083/jcb.201007124
   PubMed Web of Science ®Google Scholar
• Carmena M, Ruchaud S, Earnshaw WC. Making the Auroras glow: regulation of Aurora A and B kinase function by interacting proteins. Curr Opin Cell Biol 2009; 21:796-805; PMID:19836940; http://dx.doi.org/10.1016/j.ceb.2009.09.008
   PubMed Web of Science ®Google Scholar
• Kettenbach AN, Schweppe DK, Faherty BK, Pechenick D, Pletnev AA, Gerber SA. Quantitative phosphoproteomics identifies substrates and functional modules of Aurora and Polo-like kinase activities in mitotic cells. Sci Signal 2011; 4:rs5; PMID:21712546; http://dx.doi.org/10.1126/scisignal.2001497
   PubMed Web of Science ®Google Scholar
• Norden C, Mendoza M, Dobbelaere J, Kotwaliwale CV, Biggins S, Barral Y. The NoCut pathway links completion of cytokinesis to spindle midzone function to prevent chromosome breakage. Cell 2006; 125:85-98; PMID:16615892; http://dx.doi.org/10.1016/j.cell.2006.01.045
   PubMed Web of Science ®Google Scholar
• Mendoza M, Norden C, Durrer K, Rauter H, Uhlmann F, Barral Y. A mechanism for chromosome segregation sensing by the NoCut checkpoint. Nat Cell Biol 2009; 11:477-83; PMID:19270692; http://dx.doi.org/10.1038/ncb1855
   PubMed Web of Science ®Google Scholar
• Capalbo L, Montembault E, Takeda T, Bassi ZI, Glover DM, D'Avino PP. The chromosomal passenger complex controls the function of endosomal sorting complex required for transport-III Snf7 proteins during cytokinesis. Open Biol 2012; 2:120070; PMID:22724069; http://dx.doi.org/10.1098/rsob.120070
   PubMed Web of Science ®Google Scholar
• Chen CT, Hehnly H, Doxsey SJ. Orchestrating vesicle transport, ESCRTs and kinase surveillance during abscission. Nat Rev Mol Cell Biol 2012; 13:483-8; PMID:22781903; http://dx.doi.org/10.1038/nrm3395
   PubMed Web of Science ®Google Scholar
• Fadri-Moskwik M, Weiderhold KN, Deeraksa A, Chuang C, Pan J, Lin SH, Yu-Lee LY. Aurora B is regulated by acetylation/deacetylation during mitosis in prostate cancer cells. FASEB J 2012; 26:4057-67; PMID:22751009; http://dx.doi.org/10.1096/fj.12-206656
   PubMed Web of Science ®Google Scholar
• You J, Li Q, Wu C, Kim J, Ottinger M, Howley PM. Regulation of aurora B expression by the bromodomain protein Brd4. Mol Cell Biol 2009; 29:5094-103; PMID:19596781; http://dx.doi.org/10.1128/MCB.00299-09
   PubMed Web of Science ®Google Scholar
• Bailey JK, Fields AT, Cheng K, Lee A, Wagenaar E, Lagrois R, Schmidt B, Xia B, Ma D. WD repeat-containing protein 5 (WDR5) localizes to the midbody and regulates abscission. J Biol Chem 2015; 290:8987-9001; PMID:25666610; http://dx.doi.org/10.1074/jbc.M114.623611
   PubMed Web of Science ®Google Scholar
• Shi X, Hong T, Walter KL, Ewalt M, Michishita E, Hung T, Carney D, Peña P, Lan F, Kaadige MR, et al. ING2 PHD domain links histone H3 lysine 4 methylation to active gene repression. Nature 2006; 442:96-9; PMID:16728974; http://dx.doi.org/10.1038/nature05140
   PubMed Web of Science ®Google Scholar
• Ochoa CD, Alexeyev M, Pastukh V, Balczon R, Stevens T. Pseudomonas aeruginosa exotoxin Y is a promiscuous cyclase that increases endothelial tau phosphorylation and permeability. J Biol Chem 2012; 287:25407-18; PMID:22637478; http://dx.doi.org/10.1074/jbc.M111.301440
   PubMed Web of Science ®Google Scholar