Bioinformatic analysis of the nucleolus.
Abstract
The nucleolus is a plurifunctional, nuclear organelle, which is responsible for ribosome biogenesis and many other functions in eukaryotes, including RNA processing, viral replication and tumour suppression. Our knowledge of the human nucleolar proteome has been expanded dramatically by the two recent MS studies on isolated nucleoli from HeLa cells [Andersen, Lyon, Fox, Leung, Lam, Steen, Mann and Lamond (2002) Curr. Biol. 12, 1-11; Scherl, Coute, Deon, Calle, Kindbeiter, Sanchez, Greco, Hochstrasser and Diaz (2002) Mol. Biol. Cell 13, 4100-4109]. Nearly 400 proteins were identified within the nucleolar proteome so far in humans. Approx. 12% of the identified proteins were previously shown to be nucleolar in human cells and, as expected, nearly all of the known housekeeping proteins required for ribosome biogenesis were identified in these analyses. Surprisingly, approx. 30% represented either novel or uncharacterized proteins. This review focuses on how to apply the derived knowledge of this newly recognized nucleolar proteome, such as their amino acid/peptide composition and their homologies across species, to explore the function and dynamics of the nucleolus, and suggests ways to identify, in silico, possible functions of the novel/uncharacterized proteins and potential interaction networks within the human nucleolus, or between the nucleolus and other nuclear organelles, by drawing resources from the public domain.
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- Franke WW. Matthias Jacob Schleiden and the definition of the cell nucleus. Eur J Cell Biol. 1988 Dec;47(2):145–156. [PubMed] [Google Scholar]
- Moss Tom, Stefanovsky Victor Y. At the center of eukaryotic life. Cell. 2002 May 31;109(5):545–548. [PubMed] [Google Scholar]
- Warner JR. The economics of ribosome biosynthesis in yeast. Trends Biochem Sci. 1999 Nov;24(11):437–440. [PubMed] [Google Scholar]
- Visintin R, Amon A. The nucleolus: the magician's hat for cell cycle tricks. Curr Opin Cell Biol. 2000 Jun;12(3):372–377. [PubMed] [Google Scholar]
- Hiscox JA. The nucleolus--a gateway to viral infection? Arch Virol. 2002 Jun;147(6):1077–1089.[PMC free article] [PubMed] [Google Scholar]
- Carmo-Fonseca M, Mendes-Soares L, Campos I. To be or not to be in the nucleolus. Nat Cell Biol. 2000 Jun;2(6):E107–E112. [PubMed] [Google Scholar]
- Andersen Jens S, Lyon Carol E, Fox Archa H, Leung Anthony K L, Lam Yun Wah, Steen Hanno, Mann Matthias, Lamond Angus I. Directed proteomic analysis of the human nucleolus. Curr Biol. 2002 Jan 8;12(1):1–11. [PubMed] [Google Scholar]
- Scherl Alexander, Couté Yohann, Déon Catherine, Callé Aleth, Kindbeiter Karine, Sanchez Jean-Charles, Greco Anna, Hochstrasser Denis, Diaz Jean-Jacques. Functional proteomic analysis of human nucleolus. Mol Biol Cell. 2002 Nov;13(11):4100–4109.[PMC free article] [PubMed] [Google Scholar]
- Aebersold Ruedi, Mann Matthias. Mass spectrometry-based proteomics. Nature. 2003 Mar 13;422(6928):198–207. [PubMed] [Google Scholar]
- Tyers Mike, Mann Matthias. From genomics to proteomics. Nature. 2003 Mar 13;422(6928):193–197. [PubMed] [Google Scholar]
- Andersen JS, Mann M. Functional genomics by mass spectrometry. FEBS Lett. 2000 Aug 25;480(1):25–31. [PubMed] [Google Scholar]
- Olson MO, Dundr M, Szebeni A. The nucleolus: an old factory with unexpected capabilities. Trends Cell Biol. 2000 May;10(5):189–196. [PubMed] [Google Scholar]
- Scheer U, Hock R. Structure and function of the nucleolus. Curr Opin Cell Biol. 1999 Jun;11(3):385–390. [PubMed] [Google Scholar]
- Pederson T, Politz JC. The nucleolus and the four ribonucleoproteins of translation. J Cell Biol. 2000 Mar 20;148(6):1091–1095.[PMC free article] [PubMed] [Google Scholar]
- Carmo-Fonseca Maria. The contribution of nuclear compartmentalization to gene regulation. Cell. 2002 Feb 22;108(4):513–521. [PubMed] [Google Scholar]
- Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. [PubMed] [Google Scholar]
- Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997 Sep 1;25(17):3389–3402.[PMC free article] [PubMed] [Google Scholar]
- Gerbi Susan A, Borovjagin Anton V, Lange Thilo Sascha. The nucleolus: a site of ribonucleoprotein maturation. Curr Opin Cell Biol. 2003 Jun;15(3):318–325. [PubMed] [Google Scholar]
- Politz JC, Yarovoi S, Kilroy SM, Gowda K, Zwieb C, Pederson T. Signal recognition particle components in the nucleolus. Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):55–60.[PMC free article] [PubMed] [Google Scholar]
- Politz Joan C, Lewandowski Laura B, Pederson Thoru. Signal recognition particle RNA localization within the nucleolus differs from the classical sites of ribosome synthesis. J Cell Biol. 2002 Nov 11;159(3):411–418.[PMC free article] [PubMed] [Google Scholar]
- Pederson T. Is the nucleus in need of translation? Trends Cell Biol. 2001 Oct;11(10):395–397. [PubMed] [Google Scholar]
- Iborra FJ, Jackson DA, Cook PR. Coupled transcription and translation within nuclei of mammalian cells. Science. 2001 Aug 10;293(5532):1139–1142. [PubMed] [Google Scholar]
- BIRNSTIEL ML, FLAMM WG. INTRANUCLEAR SITE OF HISTONE SYNTHESIS. Science. 1964 Sep 25;145(3639):1435–1437. [PubMed] [Google Scholar]
- BIRNSTIEL ML, HYDE BB. Protein synthesis by isolated pea nucleoli. J Cell Biol. 1963 Jul;18:41–50.[PMC free article] [PubMed] [Google Scholar]
- Maggio R. Progress report on the characterization of nucleoli from guinea pig liver. Natl Cancer Inst Monogr. 1966 Dec;23:213–222. [PubMed] [Google Scholar]
- Pederson T. The plurifunctional nucleolus. Nucleic Acids Res. 1998 Sep 1;26(17):3871–3876.[PMC free article] [PubMed] [Google Scholar]
- Schneiter R, Kadowaki T, Tartakoff AM. mRNA transport in yeast: time to reinvestigate the functions of the nucleolus. Mol Biol Cell. 1995 Apr;6(4):357–370.[PMC free article] [PubMed] [Google Scholar]
- Fatica Alessandro, Tollervey David. Making ribosomes. Curr Opin Cell Biol. 2002 Jun;14(3):313–318. [PubMed] [Google Scholar]
- Tschochner Herbert, Hurt Ed. Pre-ribosomes on the road from the nucleolus to the cytoplasm. Trends Cell Biol. 2003 May;13(5):255–263. [PubMed] [Google Scholar]
- Nissan Tracy A, Bassler Jochen, Petfalski Elisabeth, Tollervey David, Hurt Ed. 60S pre-ribosome formation viewed from assembly in the nucleolus until export to the cytoplasm. EMBO J. 2002 Oct 15;21(20):5539–5547.[PMC free article] [PubMed] [Google Scholar]
- Gadal O, Strauss D, Kessl J, Trumpower B, Tollervey D, Hurt E. Nuclear export of 60s ribosomal subunits depends on Xpo1p and requires a nuclear export sequence-containing factor, Nmd3p, that associates with the large subunit protein Rpl10p. Mol Cell Biol. 2001 May;21(10):3405–3415.[PMC free article] [PubMed] [Google Scholar]
- Ho JH, Kallstrom G, Johnson AW. Nmd3p is a Crm1p-dependent adapter protein for nuclear export of the large ribosomal subunit. J Cell Biol. 2000 Nov 27;151(5):1057–1066.[PMC free article] [PubMed] [Google Scholar]
- Aitchison JD, Rout MP. The road to ribosomes. Filling potholes in the export pathway. J Cell Biol. 2000 Nov 27;151(5):F23–F26.[PMC free article] [PubMed] [Google Scholar]
- Kurdi-Haidar B, Hom DK, Flittner DE, Heath D, Fink L, Naredi P, Howell SB. Dual cytoplasmic and nuclear distribution of the novel arsenite-stimulated human ATPase (hASNA-I). J Cell Biochem. 1998 Oct 1;71(1):1–10. [PubMed] [Google Scholar]
- Hatanaka M. Discovery of the nucleolar targeting signal. Bioessays. 1990 Mar;12(3):143–148. [PubMed] [Google Scholar]
- Bailey TL, Elkan C. Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc Int Conf Intell Syst Mol Biol. 1994;2:28–36. [PubMed] [Google Scholar]
- Gall JG. Cajal bodies: the first 100 years. Annu Rev Cell Dev Biol. 2000;16:273–300. [PubMed] [Google Scholar]
- Sleeman JE, Lamond AI. Nuclear organization of pre-mRNA splicing factors. Curr Opin Cell Biol. 1999 Jun;11(3):372–377. [PubMed] [Google Scholar]
- Gary JD, Clarke S. RNA and protein interactions modulated by protein arginine methylation. Prog Nucleic Acid Res Mol Biol. 1998;61:65–131. [PubMed] [Google Scholar]
- Xu Chong, Henry Pamela A, Setya Amit, Henry Michael F. In vivo analysis of nucleolar proteins modified by the yeast arginine methyltransferase Hmt1/Rmt1p. RNA. 2003 Jun;9(6):746–759.[PMC free article] [PubMed] [Google Scholar]
- McBride AE, Silver PA. State of the arg: protein methylation at arginine comes of age. Cell. 2001 Jul 13;106(1):5–8. [PubMed] [Google Scholar]
- Pintucci G, Quarto N, Rifkin DB. Methylation of high molecular weight fibroblast growth factor-2 determines post-translational increases in molecular weight and affects its intracellular distribution. Mol Biol Cell. 1996 Aug;7(8):1249–1258.[PMC free article] [PubMed] [Google Scholar]
- Hebert Michael D, Shpargel Karl B, Ospina Jason K, Tucker Karen E, Matera A Gregory. Coilin methylation regulates nuclear body formation. Dev Cell. 2002 Sep;3(3):329–337. [PubMed] [Google Scholar]
- Boisvert Francois-Michel, Cote Jocelyn, Boulanger Marie-Chloe, Cleroux Patrick, Bachand Francois, Autexier Chantal, Richard Stephane. Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing. J Cell Biol. 2002 Dec 23;159(6):957–969.[PMC free article] [PubMed] [Google Scholar]
- Janicki Susan M, Spector David L. Nuclear choreography: interpretations from living cells. Curr Opin Cell Biol. 2003 Apr;15(2):149–157. [PubMed] [Google Scholar]
- Carmo-Fonseca Maria, Platani Melpomeni, Swedlow Jason R. Macromolecular mobility inside the cell nucleus. Trends Cell Biol. 2002 Nov;12(11):491–495. [PubMed] [Google Scholar]
- Malatesta M, Zancanaro C, Martin TE, Chan EK, Amalric F, Lührmann R, Vogel P, Fakan S. Is the coiled body involved in nucleolar functions? Exp Cell Res. 1994 Apr;211(2):415–419. [PubMed] [Google Scholar]
- Ochs RL, Stein TW, Jr, Tan EM. Coiled bodies in the nucleolus of breast cancer cells. J Cell Sci. 1994 Feb;107(Pt 2):385–399. [PubMed] [Google Scholar]
- Lyon CE, Bohmann K, Sleeman J, Lamond AI. Inhibition of protein dephosphorylation results in the accumulation of splicing snRNPs and coiled bodies within the nucleolus. Exp Cell Res. 1997 Jan 10;230(1):84–93. [PubMed] [Google Scholar]
- Sleeman J, Lyon CE, Platani M, Kreivi JP, Lamond AI. Dynamic interactions between splicing snRNPs, coiled bodies and nucleoli revealed using snRNP protein fusions to the green fluorescent protein. Exp Cell Res. 1998 Sep 15;243(2):290–304. [PubMed] [Google Scholar]
- Snaar S, Wiesmeijer K, Jochemsen AG, Tanke HJ, Dirks RW. Mutational analysis of fibrillarin and its mobility in living human cells. J Cell Biol. 2000 Oct 30;151(3):653–662.[PMC free article] [PubMed] [Google Scholar]
- Platani M, Goldberg I, Swedlow JR, Lamond AI. In vivo analysis of Cajal body movement, separation, and joining in live human cells. J Cell Biol. 2000 Dec 25;151(7):1561–1574.[PMC free article] [PubMed] [Google Scholar]
- Boudonck K, Dolan L, Shaw PJ. The movement of coiled bodies visualized in living plant cells by the green fluorescent protein. Mol Biol Cell. 1999 Jul;10(7):2297–2307.[PMC free article] [PubMed] [Google Scholar]
- Sleeman JE, Ajuh P, Lamond AI. snRNP protein expression enhances the formation of Cajal bodies containing p80-coilin and SMN. J Cell Sci. 2001 Dec;114(Pt 24):4407–4419. [PubMed] [Google Scholar]
- Sleeman JE, Lamond AI. Newly assembled snRNPs associate with coiled bodies before speckles, suggesting a nuclear snRNP maturation pathway. Curr Biol. 1999 Oct 7;9(19):1065–1074. [PubMed] [Google Scholar]
- Leung Anthony K L, Lamond Angus I. In vivo analysis of NHPX reveals a novel nucleolar localization pathway involving a transient accumulation in splicing speckles. J Cell Biol. 2002 May 13;157(4):615–629.[PMC free article] [PubMed] [Google Scholar]
- Nicol SM, Causevic M, Prescott AR, Fuller-Pace FV. The nuclear DEAD box RNA helicase p68 interacts with the nucleolar protein fibrillarin and colocalizes specifically in nascent nucleoli during telophase. Exp Cell Res. 2000 Jun 15;257(2):272–280. [PubMed] [Google Scholar]
- Sanz MM, Proytcheva M, Ellis NA, Holloman WK, German J. BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins. Cytogenet Cell Genet. 2000;91(1-4):217–223. [PubMed] [Google Scholar]
- Yankiwski V, Marciniak RA, Guarente L, Neff NF. Nuclear structure in normal and Bloom syndrome cells. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5214–5219.[PMC free article] [PubMed] [Google Scholar]
- Mintz PJ, Patterson SD, Neuwald AF, Spahr CS, Spector DL. Purification and biochemical characterization of interchromatin granule clusters. EMBO J. 1999 Aug 2;18(15):4308–4320.[PMC free article] [PubMed] [Google Scholar]
- Zhou Zhaolan, Licklider Lawrence J, Gygi Steven P, Reed Robin. Comprehensive proteomic analysis of the human spliceosome. Nature. 2002 Sep 12;419(6903):182–185. [PubMed] [Google Scholar]
- Neubauer G, King A, Rappsilber J, Calvio C, Watson M, Ajuh P, Sleeman J, Lamond A, Mann M. Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex. Nat Genet. 1998 Sep;20(1):46–50. [PubMed] [Google Scholar]
- Rappsilber Juri, Ryder Ursula, Lamond Angus I, Mann Matthias. Large-scale proteomic analysis of the human spliceosome. Genome Res. 2002 Aug;12(8):1231–1245.[PMC free article] [PubMed] [Google Scholar]
- Makarov Evgeny M, Makarova Olga V, Urlaub Henning, Gentzel Marc, Will Cindy L, Wilm Matthias, Lührmann Reinhard. Small nuclear ribonucleoprotein remodeling during catalytic activation of the spliceosome. Science. 2002 Dec 13;298(5601):2205–2208. [PubMed] [Google Scholar]
- Wagner Stefan, Chiosea Simion, Nickerson Jeffrey A. The spatial targeting and nuclear matrix binding domains of SRm160. Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3269–3274.[PMC free article] [PubMed] [Google Scholar]
- Lai Ming-Chih, Kuo Hao-Wei, Chang Wen-Cheng, Tarn Woan-Yuh. A novel splicing regulator shares a nuclear import pathway with SR proteins. EMBO J. 2003 Mar 17;22(6):1359–1369.[PMC free article] [PubMed] [Google Scholar]
- Chen D, Huang S. Nucleolar components involved in ribosome biogenesis cycle between the nucleolus and nucleoplasm in interphase cells. J Cell Biol. 2001 Apr 2;153(1):169–176.[PMC free article] [PubMed] [Google Scholar]
- Reits EA, Neefjes JJ. From fixed to FRAP: measuring protein mobility and activity in living cells. Nat Cell Biol. 2001 Jun;3(6):E145–E147. [PubMed] [Google Scholar]
- Misteli T. Protein dynamics: implications for nuclear architecture and gene expression. Science. 2001 Feb 2;291(5505):843–847. [PubMed] [Google Scholar]
- Fox Archa H, Lam Yun Wah, Leung Anthony K L, Lyon Carol E, Andersen Jens, Mann Matthias, Lamond Angus I. Paraspeckles: a novel nuclear domain. Curr Biol. 2002 Jan 8;12(1):13–25. [PubMed] [Google Scholar]
- Pellegrini M, Marcotte EM, Thompson MJ, Eisenberg D, Yeates TO. Assigning protein functions by comparative genome analysis: protein phylogenetic profiles. Proc Natl Acad Sci U S A. 1999 Apr 13;96(8):4285–4288.[PMC free article] [PubMed] [Google Scholar]
- Boguski MS, Schuler GD. ESTablishing a human transcript map. Nat Genet. 1995 Aug;10(4):369–371. [PubMed] [Google Scholar]
- Lash AE, Tolstoshev CM, Wagner L, Schuler GD, Strausberg RL, Riggins GJ, Altschul SF. SAGEmap: a public gene expression resource. Genome Res. 2000 Jul;10(7):1051–1060.[PMC free article] [PubMed] [Google Scholar]
- Gavin Anne-Claude, Bösche Markus, Krause Roland, Grandi Paola, Marzioch Martina, Bauer Andreas, Schultz Jörg, Rick Jens M, Michon Anne-Marie, Cruciat Cristina-Maria, et al. Functional organization of the yeast proteome by systematic analysis of protein complexes. Nature. 2002 Jan 10;415(6868):141–147. [PubMed] [Google Scholar]
- Ho Yuen, Gruhler Albrecht, Heilbut Adrian, Bader Gary D, Moore Lynda, Adams Sally-Lin, Millar Anna, Taylor Paul, Bennett Keiryn, Boutilier Kelly, et al. Systematic identification of protein complexes in Saccharomyces cerevisiae by mass spectrometry. Nature. 2002 Jan 10;415(6868):180–183. [PubMed] [Google Scholar]
- Flory Mark R, Griffin Timothy J, Martin Daniel, Aebersold Ruedi. Advances in quantitative proteomics using stable isotope tags. Trends Biotechnol. 2002 Dec;20(12 Suppl):S23–S29. [PubMed] [Google Scholar]
- Hartwell LH, Hopfield JJ, Leibler S, Murray AW. From molecular to modular cell biology. Nature. 1999 Dec 2;402(6761 Suppl):C47–C52. [PubMed] [Google Scholar]
- Eisenberg D, Marcotte EM, Xenarios I, Yeates TO. Protein function in the post-genomic era. Nature. 2000 Jun 15;405(6788):823–826. [PubMed] [Google Scholar]
- Tong Amy Hin Yan, Drees Becky, Nardelli Giuliano, Bader Gary D, Brannetti Barbara, Castagnoli Luisa, Evangelista Marie, Ferracuti Silvia, Nelson Bryce, Paoluzi Serena, et al. A combined experimental and computational strategy to define protein interaction networks for peptide recognition modules. Science. 2002 Jan 11;295(5553):321–324. [PubMed] [Google Scholar]
- Stein Lincoln. Creating a bioinformatics nation. Nature. 2002 May 9;417(6885):119–120. [PubMed] [Google Scholar]
- Aebersold Ruedi, Watts Julian D. The need for national centers for proteomics. Nat Biotechnol. 2002 Jul;20(7):651–651. [PubMed] [Google Scholar]
- Swedlow Jason R, Goldberg Ilya, Brauner Erik, Sorger Peter K. Informatics and quantitative analysis in biological imaging. Science. 2003 Apr 4;300(5616):100–102.[PMC free article] [PubMed] [Google Scholar]
- Kaser A, Bogengruber E, Hallegger M, Doppler E, Lepperdinger G, Jantsch M, Breitenbach M, Kreil G. Brix from xenopus laevis and brx1p from yeast define a new family of proteins involved in the biogenesis of large ribosomal subunits. Biol Chem. 2001 Dec;382(12):1637–1647. [PubMed] [Google Scholar]
- Heese Klaus, Nakayama Takahiro, Hata Ryuji, Masumura Makoto, Akatsu Hiroyasu, Li Feng, Nagai Yasuo, Yamamoto Takayuki, Kosaka Kenji, Suemoto Takahiro, et al. Characterizing CGI-94 (comparative gene identification-94) which is down-regulated in the hippocampus of early stage Alzheimer's disease brain. Eur J Neurosci. 2002 Jan;15(1):79–86. [PubMed] [Google Scholar]
- Valdez BC, Henning D, Busch RK, Woods K, Flores-Rozas H, Hurwitz J, Perlaky L, Busch H. A nucleolar RNA helicase recognized by autoimmune antibodies from a patient with watermelon stomach disease. Nucleic Acids Res. 1996 Apr 1;24(7):1220–1224.[PMC free article] [PubMed] [Google Scholar]
- Iggo RD, Jamieson DJ, MacNeill SA, Southgate J, McPheat J, Lane DP. p68 RNA helicase: identification of a nucleolar form and cloning of related genes containing a conserved intron in yeasts. Mol Cell Biol. 1991 Mar;11(3):1326–1333.[PMC free article] [PubMed] [Google Scholar]
- Heiss NS, Knight SW, Vulliamy TJ, Klauck SM, Wiemann S, Mason PJ, Poustka A, Dokal I. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nat Genet. 1998 May;19(1):32–38. [PubMed] [Google Scholar]
- Busch H, Busch RK, Black A, Chan PK, Chatterjee A, Durban E, Freeman J, Ochs R, Reichlin M, Tan EM, et al. Novel nucleolar antigens in autoimmune disease. J Rheumatol Suppl. 1987 Jun;14 (Suppl 13):70–77. [PubMed] [Google Scholar]
- di Padua Mathieu D, Mura CV, Frado LL, Woodcock CL, Stollar BD. Differing accessibility in chromatin of the antigenic sites of regions 1-58 and 63-125 of histone H2B. J Cell Biol. 1981 Oct;91(1):135–141.[PMC free article] [PubMed] [Google Scholar]
- Pluk H, van Eenennaam H, Rutjes SA, Pruijn GJ, van Venrooij WJ. RNA-protein interactions in the human RNase MRP ribonucleoprotein complex. RNA. 1999 Apr;5(4):512–524.[PMC free article] [PubMed] [Google Scholar]
- Milarski KL, Welch WJ, Morimoto RI. Cell cycle-dependent association of HSP70 with specific cellular proteins. J Cell Biol. 1989 Feb;108(2):413–423.[PMC free article] [PubMed] [Google Scholar]
- Racevskis J, Dill A, Stockert R, Fineberg SA. Cloning of a novel nucleolar guanosine 5'-triphosphate binding protein autoantigen from a breast tumor. Cell Growth Differ. 1996 Feb;7(2):271–280. [PubMed] [Google Scholar]
- Francoeur AM, Peebles CL, Gompper PT, Tan EM. Identification of Ki (Ku, p70/p80) autoantigens and analysis of anti-Ki autoantibody reactivity. J Immunol. 1986 Mar 1;136(5):1648–1653. [PubMed] [Google Scholar]
- Schonk DM, Kuijpers HJ, van Drunen E, van Dalen CH, Geurts van Kessel AH, Verheijen R, Ramaekers FC. Assignment of the gene(s) involved in the expression of the proliferation-related Ki-67 antigen to human chromosome 10. Hum Genet. 1989 Oct;83(3):297–299. [PubMed] [Google Scholar]
- Takagi M, Sueishi M, Saiwaki T, Kametaka A, Yoneda Y. A novel nucleolar protein, NIFK, interacts with the forkhead associated domain of Ki-67 antigen in mitosis. J Biol Chem. 2001 Jul 6;276(27):25386–25391. [PubMed] [Google Scholar]
- Westendorf JM, Konstantinov KN, Wormsley S, Shu MD, Matsumoto-Taniura N, Pirollet F, Klier FG, Gerace L, Baserga SJ. M phase phosphoprotein 10 is a human U3 small nucleolar ribonucleoprotein component. Mol Biol Cell. 1998 Feb;9(2):437–449.[PMC free article] [PubMed] [Google Scholar]
- Peter M, Nakagawa J, Dorée M, Labbé JC, Nigg EA. Identification of major nucleolar proteins as candidate mitotic substrates of cdc2 kinase. Cell. 1990 Mar 9;60(5):791–801. [PubMed] [Google Scholar]
- Chang MS, Sasaki H, Campbell MS, Kraeft SK, Sutherland R, Yang CY, Liu Y, Auclair D, Hao L, Sonoda H, et al. HRad17 colocalizes with NHP2L1 in the nucleolus and redistributes after UV irradiation. J Biol Chem. 1999 Dec 17;274(51):36544–36549. [PubMed] [Google Scholar]
- Zirwes RF, Eilbracht J, Kneissel S, Schmidt-Zachmann MS. A novel helicase-type protein in the nucleolus: protein NOH61. Mol Biol Cell. 2000 Apr;11(4):1153–1167.[PMC free article] [PubMed] [Google Scholar]
- Busch H, Busch RK, Freeman JW, Perlaky L. Nucleolar protein P120 and its targeting for cancer chemotherapy. Boll Soc Ital Biol Sper. 1991 Aug;67(8):739–750. [PubMed] [Google Scholar]
- Gautier T, Bergès T, Tollervey D, Hurt E. Nucleolar KKE/D repeat proteins Nop56p and Nop58p interact with Nop1p and are required for ribosome biogenesis. Mol Cell Biol. 1997 Dec;17(12):7088–7098.[PMC free article] [PubMed] [Google Scholar]
- Pai CY, Chen HK, Sheu HL, Yeh NH. Cell-cycle-dependent alterations of a highly phosphorylated nucleolar protein p130 are associated with nucleologenesis. J Cell Sci. 1995 May;108(Pt 5):1911–1920. [PubMed] [Google Scholar]
- Lyman SK, Gerace L, Baserga SJ. Human Nop5/Nop58 is a component common to the box C/D small nucleolar ribonucleoproteins. RNA. 1999 Dec;5(12):1597–1604.[PMC free article] [PubMed] [Google Scholar]
- Savino TM, Bastos R, Jansen E, Hernandez-Verdun D. The nucleolar antigen Nop52, the human homologue of the yeast ribosomal RNA processing RRP1, is recruited at late stages of nucleologenesis. J Cell Sci. 1999 Jun;112(Pt 12):1889–1900. [PubMed] [Google Scholar]
- Yung BY, Bor AM, Yang YH. Immunolocalization of phosphoprotein B23 in proliferating and non-proliferating HeLa cells. Int J Cancer. 1990 Aug 15;46(2):272–275. [PubMed] [Google Scholar]
- Utama Budi, Kennedy Derek, Ru Kelin, Mattick John S. Isolation and characterization of a new nucleolar protein, Nrap, that is conserved from yeast to humans. Genes Cells. 2002 Feb;7(2):115–132. [PubMed] [Google Scholar]
- Gelpi C, Algueró A, Angeles Martinez M, Vidal S, Juarez C, Rodriguez-Sanchez JL. Identification of protein components reactive with anti-PM/Scl autoantibodies. Clin Exp Immunol. 1990 Jul;81(1):59–64.[PMC free article] [PubMed] [Google Scholar]
- Blüthner M, Bautz FA. Cloning and characterization of the cDNA coding for a polymyositis-scleroderma overlap syndrome-related nucleolar 100-kD protein. J Exp Med. 1992 Oct 1;176(4):973–980.[PMC free article] [PubMed] [Google Scholar]
- Trinkle-Mulcahy L, Sleeman JE, Lamond AI. Dynamic targeting of protein phosphatase 1 within the nuclei of living mammalian cells. J Cell Sci. 2001 Dec;114(Pt 23):4219–4228. [PubMed] [Google Scholar]
- Huang S, Deerinck TJ, Ellisman MH, Spector DL. The dynamic organization of the perinucleolar compartment in the cell nucleus. J Cell Biol. 1997 Jun 2;137(5):965–974.[PMC free article] [PubMed] [Google Scholar]
- Le S, Sternglanz R, Greider CW. Identification of two RNA-binding proteins associated with human telomerase RNA. Mol Biol Cell. 2000 Mar;11(3):999–1010.[PMC free article] [PubMed] [Google Scholar]
- Michael WM, Dreyfuss G. Distinct domains in ribosomal protein L5 mediate 5 S rRNA binding and nucleolar localization. J Biol Chem. 1996 May 10;271(19):11571–11574. [PubMed] [Google Scholar]
- Thomson SR, Johnson SE. Isolation and characterization of chicken TaxREB107, a putative DNA binding protein abundantly expressed in muscle. Gene. 2001 Oct 31;278(1-2):81–88. [PubMed] [Google Scholar]
- Vater CA, Bartle LM, Leszyk JD, Lambert JM, Goldmacher VS. Ricin A chain can be chemically cross-linked to the mammalian ribosomal proteins L9 and L10e. J Biol Chem. 1995 May 26;270(21):12933–12940. [PubMed] [Google Scholar]
- Franco R, Rosenfeld MG. Hormonally inducible phosphorylation of a nuclear pool of ribosomal protein S6. J Biol Chem. 1990 Mar 15;265(8):4321–4325. [PubMed] [Google Scholar]
- Magoulas C, Fried M. Isolation and genomic analysis of the human surf-6 gene: a member of the Surfeit locus. Gene. 2000 Feb 8;243(1-2):115–123. [PubMed] [Google Scholar]
- Winokur ST, Shiang R. The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus. Hum Mol Genet. 1998 Nov;7(12):1947–1952. [PubMed] [Google Scholar]
- Zini N, Santi S, Ognibene A, Bavelloni A, Neri LM, Valmori A, Mariani E, Negri C, Astaldi-Ricotti GC, Maraldi NM. Discrete localization of different DNA topoisomerases in HeLa and K562 cell nuclei and subnuclear fractions. Exp Cell Res. 1994 Feb;210(2):336–348. [PubMed] [Google Scholar]
- Pluk H, Soffner J, Lührmann R, van Venrooij WJ. cDNA cloning and characterization of the human U3 small nucleolar ribonucleoprotein complex-associated 55-kilodalton protein. Mol Cell Biol. 1998 Jan;18(1):488–498.[PMC free article] [PubMed] [Google Scholar]
- Jantzen HM, Admon A, Bell SP, Tjian R. Nucleolar transcription factor hUBF contains a DNA-binding motif with homology to HMG proteins. Nature. 1990 Apr 26;344(6269):830–836. [PubMed] [Google Scholar]
- Pluta AF, Earnshaw WC. Specific interaction between human kinetochore protein CENP-C and a nucleolar transcriptional regulator. J Biol Chem. 1996 Aug 2;271(31):18767–18774. [PubMed] [Google Scholar]
- Hudson JW, Kozarova A, Cheung P, Macmillan JC, Swallow CJ, Cross JC, Dennis JW. Late mitotic failure in mice lacking Sak, a polo-like kinase. Curr Biol. 2001 Mar 20;11(6):441–446. [PubMed] [Google Scholar]
- Stegh AH, Schickling O, Ehret A, Scaffidi C, Peterhänsel C, Hofmann TG, Grummt I, Krammer PH, Peter ME. DEDD, a novel death effector domain-containing protein, targeted to the nucleolus. EMBO J. 1998 Oct 15;17(20):5974–5986.[PMC free article] [PubMed] [Google Scholar]
- Kaul SC, Kawai R, Nomura H, Mitsui Y, Reddel RR, Wadhwa R. Identification of a 55-kDa ezrin-related protein that induces cytoskeletal changes and localizes to the nucleolus. Exp Cell Res. 1999 Jul 10;250(1):51–61. [PubMed] [Google Scholar]
- Moroianu J, Riordan JF. Identification of the nucleolar targeting signal of human angiogenin. Biochem Biophys Res Commun. 1994 Sep 30;203(3):1765–1772. [PubMed] [Google Scholar]
- Modrell B, McDonald VL, Shoyab M. The interaction of amphiregulin with nuclei and putative nuclear localization sequence binding proteins. Growth Factors. 1992;7(4):305–314. [PubMed] [Google Scholar]
- Gualandris A, Arese M, Shen B, Rifkin DB. Modulation of cell growth and transformation by doxycycline-regulated FGF-2 expression in NIH-3T3 cells. J Cell Physiol. 1999 Nov;181(2):273–284. [PubMed] [Google Scholar]
- Kiefer P, Dickson C. Nucleolar association of fibroblast growth factor 3 via specific sequence motifs has inhibitory effects on cell growth. Mol Cell Biol. 1995 Aug;15(8):4364–4374.[PMC free article] [PubMed] [Google Scholar]
- Henderson JE, Amizuka N, Warshawsky H, Biasotto D, Lanske BM, Goltzman D, Karaplis AC. Nucleolar localization of parathyroid hormone-related peptide enhances survival of chondrocytes under conditions that promote apoptotic cell death. Mol Cell Biol. 1995 Aug;15(8):4064–4075.[PMC free article] [PubMed] [Google Scholar]
- Parsell DA, Sanchez Y, Stitzel JD, Lindquist S. Hsp104 is a highly conserved protein with two essential nucleotide-binding sites. Nature. 1991 Sep 19;353(6341):270–273. [PubMed] [Google Scholar]
- Biggiogera M, Tanguay RM, Marin R, Wu Y, Martin TE, Fakan S. Localization of heat shock proteins in mouse male germ cells: an immunoelectron microscopical study. Exp Cell Res. 1996 Nov 25;229(1):77–85. [PubMed] [Google Scholar]
- Owens-Grillo JK, Czar MJ, Hutchison KA, Hoffmann K, Perdew GH, Pratt WB. A model of protein targeting mediated by immunophilins and other proteins that bind to hsp90 via tetratricopeptide repeat domains. J Biol Chem. 1996 Jun 7;271(23):13468–13475. [PubMed] [Google Scholar]
- Jeffrey IW, Kadereit S, Meurs EF, Metzger T, Bachmann M, Schwemmle M, Hovanessian AG, Clemens MJ. Nuclear localization of the interferon-inducible protein kinase PKR in human cells and transfected mouse cells. Exp Cell Res. 1995 May;218(1):17–27. [PubMed] [Google Scholar]
- Welsh GI, Kadereit S, Coccia EM, Hovanessian AG, Meurs EF. Colocalization within the nucleolus of two highly related IFN-induced human nuclear phosphoproteins with nucleolin. Exp Cell Res. 1999 Jul 10;250(1):62–74. [PubMed] [Google Scholar]
- Scott M, Boisvert FM, Vieyra D, Johnston RN, Bazett-Jones DP, Riabowol K. UV induces nucleolar translocation of ING1 through two distinct nucleolar targeting sequences. Nucleic Acids Res. 2001 May 15;29(10):2052–2058.[PMC free article] [PubMed] [Google Scholar]
- Lin CY, Huang PH, Liao WL, Cheng HJ, Huang CF, Kuo JC, Patton WA, Massenburg D, Moss J, Lee FJ. ARL4, an ARF-like protein that is developmentally regulated and localized to nuclei and nucleoli. J Biol Chem. 2000 Dec 1;275(48):37815–37823. [PubMed] [Google Scholar]
- Opas M, Dziak E, Fliegel L, Michalak M. Regulation of expression and intracellular distribution of calreticulin, a major calcium binding protein of nonmuscle cells. J Cell Physiol. 1991 Oct;149(1):160–171. [PubMed] [Google Scholar]
- Hoogeveen André T, Rossetti Stefano, Stoyanova Violeta, Schonkeren Joris, Fenaroli Angelia, Schiaffonati Luisa, van Unen Leontine, Sacchi Nicoletta. The transcriptional corepressor MTG16a contains a novel nucleolar targeting sequence deranged in t (16; 21)-positive myeloid malignancies. Oncogene. 2002 Sep 26;21(43):6703–6712. [PubMed] [Google Scholar]
- Hattori H, Liu YC, Tohnai I, Ueda M, Kaneda T, Kobayashi T, Tanabe K, Ohtsuka K. Intracellular localization and partial amino acid sequence of a stress-inducible 40-kDa protein in HeLa cells. Cell Struct Funct. 1992 Feb;17(1):77–86. [PubMed] [Google Scholar]
- Munnia A, Schütz N, Romeike BF, Maldener E, Glass B, Maas R, Nastainczyk W, Feiden W, Fischer U, Meese E. Expression, cellular distribution and protein binding of the glioma amplified sequence (GAS41), a highly conserved putative transcription factor. Oncogene. 2001 Aug 9;20(35):4853–4863. [PubMed] [Google Scholar]
- Rizos H, Darmanian AP, Mann GJ, Kefford RF. Two arginine rich domains in the p14ARF tumour suppressor mediate nucleolar localization. Oncogene. 2000 Jun 15;19(26):2978–2985. [PubMed] [Google Scholar]
- Fischer H, Zhang XU, O'Brien KP, Kylsten P, Engvall E. C7, a novel nucleolar protein, is the mouse homologue of the Drosophila late puff product L82 and an isoform of human OXR1. Biochem Biophys Res Commun. 2001 Mar 2;281(3):795–803. [PubMed] [Google Scholar]
- Lindström MS, Klangby U, Inoue R, Pisa P, Wiman KG, Asker CE. Immunolocalization of human p14(ARF) to the granular component of the interphase nucleolus. Exp Cell Res. 2000 May 1;256(2):400–410. [PubMed] [Google Scholar]
- Dalmau J, Gultekin SH, Voltz R, Hoard R, DesChamps T, Balmaceda C, Batchelor T, Gerstner E, Eichen J, Frennier J, et al. Ma1, a novel neuron- and testis-specific protein, is recognized by the serum of patients with paraneoplastic neurological disorders. Brain. 1999 Jan;122(Pt 1):27–39. [PubMed] [Google Scholar]
- Chai Z, Sarcevic B, Mawson A, Toh BH. SET-related cell division autoantigen-1 (CDA1) arrests cell growth. J Biol Chem. 2001 Sep 7;276(36):33665–33674. [PubMed] [Google Scholar]
- Benninghoff J, Kartarius S, Teleb Z, Selter H, Unteregger G, Zwergel T, Wullich B, Montenarh M. Two different forms of p53 localized differently within cells of urogenital tumours. Cancer Lett. 1999 Sep 20;144(1):55–64. [PubMed] [Google Scholar]
- McNeil S, Guo B, Stein JL, Lian JB, Bushmeyer S, Seto E, Atchison ML, Penman S, van Wijnen AJ, Stein GS. Targeting of the YY1 transcription factor to the nucleolus and the nuclear matrix in situ: the C-terminus is a principal determinant for nuclear trafficking. J Cell Biochem. 1998 Mar 15;68(4):500–510. [PubMed] [Google Scholar]
- Payen E, Verkerk T, Michalovich D, Dreyer SD, Winterpacht A, Lee B, De Zeeuw CI, Grosveld F, Galjart N. The centromeric/nucleolar chromatin protein ZFP-37 may function to specify neuronal nuclear domains. J Biol Chem. 1998 Apr 10;273(15):9099–9109. [PubMed] [Google Scholar]
- Galcheva-Gargova Z, Gangwani L, Konstantinov KN, Mikrut M, Theroux SJ, Enoch T, Davis RJ. The cytoplasmic zinc finger protein ZPR1 accumulates in the nucleolus of proliferating cells. Mol Biol Cell. 1998 Oct;9(10):2963–2971.[PMC free article] [PubMed] [Google Scholar]
- Ou JH, Yen TS, Wang YF, Kam WK, Rutter WJ. Cloning and characterization of a human ribosomal protein gene with enhanced expression in fetal and neoplastic cells. Nucleic Acids Res. 1987 Nov 11;15(21):8919–8934.[PMC free article] [PubMed] [Google Scholar]
- Annilo T, Karis A, Hoth S, Rikk T, Kruppa J, Metspalu A. Nuclear import and nucleolar accumulation of the human ribosomal protein S7 depends on both a minimal nuclear localization sequence and an adjacent basic region. Biochem Biophys Res Commun. 1998 Aug 28;249(3):759–766. [PubMed] [Google Scholar]
- Wu H, Xu H, Miraglia LJ, Crooke ST. Human RNase III is a 160-kDa protein involved in preribosomal RNA processing. J Biol Chem. 2000 Nov 24;275(47):36957–36965. [PubMed] [Google Scholar]
- Jarrous N, Wolenski JS, Wesolowski D, Lee C, Altman S. Localization in the nucleolus and coiled bodies of protein subunits of the ribonucleoprotein ribonuclease P. J Cell Biol. 1999 Aug 9;146(3):559–572.[PMC free article] [PubMed] [Google Scholar]
- Lee SG, Lee I, Park SH, Kang C, Song K. Identification and characterization of a human cDNA homologous to yeast SKI2. Genomics. 1995 Feb 10;25(3):660–666. [PubMed] [Google Scholar]
- Jarrous N, Reiner R, Wesolowski D, Mann H, Guerrier-Takada C, Altman S. Function and subnuclear distribution of Rpp21, a protein subunit of the human ribonucleoprotein ribonuclease P. RNA. 2001 Aug;7(8):1153–1164.[PMC free article] [PubMed] [Google Scholar]
- Ching Yick-Pang, Zhou Hai-Jun, Yuan Jian-Gang, Qiang Bo-Qin, Kung Hf Hsiang-fu, Jin Dong-Yan. Identification and characterization of FTSJ2, a novel human nucleolar protein homologous to bacterial ribosomal RNA methyltransferase. Genomics. 2002 Jan;79(1):2–6. [PubMed] [Google Scholar]
- Charroux B, Pellizzoni L, Perkinson RA, Yong J, Shevchenko A, Mann M, Dreyfuss G. Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli. J Cell Biol. 2000 Mar 20;148(6):1177–1186.[PMC free article] [PubMed] [Google Scholar]
- Jacobson MR, Pederson T. Localization of signal recognition particle RNA in the nucleolus of mammalian cells. Proc Natl Acad Sci U S A. 1998 Jul 7;95(14):7981–7986.[PMC free article] [PubMed] [Google Scholar]
- Amann J, Kidd VJ, Lahti JM. Characterization of putative human homologues of the yeast chromosome transmission fidelity gene, CHL1. J Biol Chem. 1997 Feb 7;272(6):3823–3832. [PubMed] [Google Scholar]
- Cabello OA, Eliseeva E, He WG, Youssoufian H, Plon SE, Brinkley BR, Belmont JW. Cell cycle-dependent expression and nucleolar localization of hCAP-H. Mol Biol Cell. 2001 Nov;12(11):3527–3537.[PMC free article] [PubMed] [Google Scholar]
- Knauf JA, Pendergrass SH, Marrone BL, Strniste GF, MacInnes MA, Park MS. Multiple nuclear localization signals in XPG nuclease. Mutat Res. 1996 May 15;363(1):67–75. [PubMed] [Google Scholar]
- Willemsen R, Bontekoe C, Tamanini F, Galjaard H, Hoogeveen A, Oostra B. Association of FMRP with ribosomal precursor particles in the nucleolus. Biochem Biophys Res Commun. 1996 Aug 5;225(1):27–33. [PubMed] [Google Scholar]
- Tamanini F, Kirkpatrick LL, Schonkeren J, van Unen L, Bontekoe C, Bakker C, Nelson DL, Galjaard H, Oostra BA, Hoogeveen AT. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins. Hum Mol Genet. 2000 Jun 12;9(10):1487–1493. [PubMed] [Google Scholar]
- Marciniak RA, Lombard DB, Johnson FB, Guarente L. Nucleolar localization of the Werner syndrome protein in human cells. Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6887–6892.[PMC free article] [PubMed] [Google Scholar]
- Zhu L, Perlaky L, Henning D, Valdez BC. Cloning and characterization of a new silver-stainable protein SSP29, a member of the LRR family. Biochem Mol Biol Int. 1997 Aug;42(5):927–935. [PubMed] [Google Scholar]
- Yang M, May WS, Ito T. JAZ requires the double-stranded RNA-binding zinc finger motifs for nuclear localization. J Biol Chem. 1999 Sep 24;274(39):27399–27406. [PubMed] [Google Scholar]
- Venables JP, Vernet C, Chew SL, Elliott DJ, Cowmeadow RB, Wu J, Cooke HJ, Artzt K, Eperon IC. T-STAR/ETOILE: a novel relative of SAM68 that interacts with an RNA-binding protein implicated in spermatogenesis. Hum Mol Genet. 1999 Jun;8(6):959–969. [PubMed] [Google Scholar]
- Williams JB, Lanahan AA. A mammalian delayed-early response gene encodes HNP36, a novel, conserved nucleolar protein. Biochem Biophys Res Commun. 1995 Aug 4;213(1):325–333. [PubMed] [Google Scholar]
- Eckmann CR, Jantsch MF. Xlrbpa, a double-stranded RNA-binding protein associated with ribosomes and heterogeneous nuclear RNPs. J Cell Biol. 1997 Jul 28;138(2):239–253.[PMC free article] [PubMed] [Google Scholar]
- Yang Yinhua, Chen Yaohui, Zhang Chunyu, Huang Hai, Weissman Sherman M. Nucleolar localization of hTERT protein is associated with telomerase function. Exp Cell Res. 2002 Jul 15;277(2):201–209. [PubMed] [Google Scholar]
- Lin CW, Darzynkiewicz Z, Li X, Traganos F, Bedner E, Tse-Dinh YC. Differential expression of human topoisomerase IIIalpha during the cell cycle progression in HL-60 leukemia cells and human peripheral blood lymphocytes. Exp Cell Res. 2000 Apr 10;256(1):225–236. [PubMed] [Google Scholar]
- Huang Z, Philippin B, O'Leary E, Bonventre JV, Kriz W, Witzgall R. Expression of the transcriptional repressor protein Kid-1 leads to the disintegration of the nucleolus. J Biol Chem. 1999 Mar 19;274(12):7640–7648. [PubMed] [Google Scholar]
- Bukovský A, Caudle MR, Keenan JA, Wimalasena J, Foster JS, Van Meter SE. Quantitative evaluation of the cell cycle-related retinoblastoma protein and localization of Thy-1 differentiation protein and macrophages during follicular development and atresia, and in human corpora lutea. Biol Reprod. 1995 Apr;52(4):776–792. [PubMed] [Google Scholar]
- Ino H, Mochizuki T, Yanaihara N, Chiba T. p34cdc2 homologue is located in nucleoli of the nervous and endocrine systems. Brain Res. 1993 Jun 18;614(1-2):131–136. [PubMed] [Google Scholar]
- Kotani H, Ito M, Hamaguchi T, Ichikawa K, Nakano T, Shima H, Nagao M, Ohta N, Furuichi Y, Takahashi T, et al. The delta isoform of protein phosphatase type 1 is localized in nucleolus and dephosphorylates nucleolar phosphoproteins. Biochem Biophys Res Commun. 1998 Aug 10;249(1):292–296. [PubMed] [Google Scholar]
- Kreivi JP, Trinkle-Mulcahy L, Lyon CE, Morrice NA, Cohen P, Lamond AI. Purification and characterisation of p99, a nuclear modulator of protein phosphatase 1 activity. FEBS Lett. 1997 Dec 22;420(1):57–62. [PubMed] [Google Scholar]
- Whitehead CM, Winkfein RJ, Fritzler MJ, Rattner JB. ASE-1: a novel protein of the fibrillar centres of the nucleolus and nucleolus organizer region of mitotic chromosomes. Chromosoma. 1997 Dec;106(8):493–502. [PubMed] [Google Scholar]
- Bohmann K, Ferreira JA, Lamond AI. Mutational analysis of p80 coilin indicates a functional interaction between coiled bodies and the nucleolus. J Cell Biol. 1995 Nov;131(4):817–831.[PMC free article] [PubMed] [Google Scholar]
- Thébault S, Basbous J, Gay B, Devaux C, Mesnard JM. Sequence requirement for the nucleolar localization of human I-mfa domain-containing protein (HIC p40). Eur J Cell Biol. 2000 Nov;79(11):834–838. [PubMed] [Google Scholar]
- Bolívar J, Díaz I, Iglesias C, Valdivia MM. Molecular cloning of a zinc finger autoantigen transiently associated with interphase nucleolus and mitotic centromeres and midbodies. Orthologous proteins with nine CXXC motifs highly conserved from nematodes to humans. J Biol Chem. 1999 Dec 17;274(51):36456–36464. [PubMed] [Google Scholar]
- Ren Y, Busch RK, Perlaky L, Busch H. The 58-kDa microspherule protein (MSP58), a nucleolar protein, interacts with nucleolar protein p120. Eur J Biochem. 1998 May 1;253(3):734–742. [PubMed] [Google Scholar]
- Stoss O, Schwaiger FW, Cooper TA, Stamm S. Alternative splicing determines the intracellular localization of the novel nuclear protein Nop30 and its interaction with the splicing factor SRp30c. J Biol Chem. 1999 Apr 16;274(16):10951–10962. [PubMed] [Google Scholar]
- Ueki N, Kondo M, Seki N, Yano K, Oda T, Masuho Y, Muramatsu M. NOLP: identification of a novel human nucleolar protein and determination of sequence requirements for its nucleolar localization. Biochem Biophys Res Commun. 1998 Nov 9;252(1):97–102. [PubMed] [Google Scholar]
- Ochs RL, Stein TW, Jr, Chan EK, Ruutu M, Tan EM. cDNA cloning and characterization of a novel nucleolar protein. Mol Biol Cell. 1996 Jul;7(7):1015–1024.[PMC free article] [PubMed] [Google Scholar]
- Nishida T, Tanaka H, Yasuda H. A novel mammalian Smt3-specific isopeptidase 1 (SMT3IP1) localized in the nucleolus at interphase. Eur J Biochem. 2000 Nov;267(21):6423–6427. [PubMed] [Google Scholar]
- Carmo-Fonseca M, Pfeifer K, Schröder HC, Vaz MF, Fonseca JE, Müller WE, Bachmann M. Identification of La ribonucleoproteins as a component of interchromatin granules. Exp Cell Res. 1989 Nov;185(1):73–85. [PubMed] [Google Scholar]
- Hsu T, King DL, LaBonne C, Kafatos FC. A Drosophila single-strand DNA/RNA-binding factor contains a high-mobility-group box and is enriched in the nucleolus. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6488–6492.[PMC free article] [PubMed] [Google Scholar]
Abstract
The nucleolus is a plurifunctional, nuclear organelle, which is responsible for ribosome biogenesis and many other functions in eukaryotes, including RNA processing, viral replication and tumour suppression. Our knowledge of the human nucleolar proteome has been expanded dramatically by the two recent MS studies on isolated nucleoli from HeLa cells [Andersen, Lyon, Fox, Leung, Lam, Steen, Mann and Lamond (2002) Curr. Biol. 12, 1-11; Scherl, Coute, Deon, Calle, Kindbeiter, Sanchez, Greco, Hochstrasser and Diaz (2002) Mol. Biol. Cell 13, 4100-4109]. Nearly 400 proteins were identified within the nucleolar proteome so far in humans. Approx. 12% of the identified proteins were previously shown to be nucleolar in human cells and, as expected, nearly all of the known housekeeping proteins required for ribosome biogenesis were identified in these analyses. Surprisingly, approx. 30% represented either novel or uncharacterized proteins. This review focuses on how to apply the derived knowledge of this newly recognized nucleolar proteome, such as their amino acid/peptide composition and their homologies across species, to explore the function and dynamics of the nucleolus, and suggests ways to identify, in silico, possible functions of the novel/uncharacterized proteins and potential interaction networks within the human nucleolus, or between the nucleolus and other nuclear organelles, by drawing resources from the public domain.