Functional architecture in the cell nucleus.

The major functions of the cell nucleus, including transcription, pre-mRNA splicing and ribosome assembly, have been studied extensively by biochemical, genetic and molecular methods. An overwhelming amount of information about their molecular mechanisms is available. In stark contrast, very little is known about how these processes are integrated into the structural framework of the cell nucleus and how they are spatially and temporally co-ordinated within the three-dimensional confines of the nucleus. It is also largely unknown how nuclear architecture affects gene expression. In order to understand how genomes are organized, and how they function, the basic principles that govern nuclear architecture and function must be uncovered. Recent work combining molecular, biochemical and cell biological methods is beginning to shed light on how the nucleus functions and how genes are expressed in vivo. It has become clear that the nucleus contains distinct compartments and that many nuclear components are highly dynamic. Here we describe the major structural compartments of the cell nucleus and discuss their established and proposed functions. We summarize recent observations regarding the dynamic properties of chromatin, mRNA and nuclear proteins, and we consider the implications these findings have for the organization of nuclear processes and gene expression. Finally, we speculate that self-organization might play a substantial role in establishing and maintaining nuclear organization.

[1]  T. Pederson,et al.  Half a century of "the nuclear matrix". , 2000, Molecular biology of the cell.

[2]  A. F. Neuwald,et al.  Purification and biochemical characterization of interchromatin granule clusters , 1999, The EMBO journal.

[3]  E. Manders,et al.  The RNA 3′ cleavage factors CstF 64 kDa and CPSF 100 kDa are concentrated in nuclear domains closely associated with coiled bodies and newly synthesized RNA. , 1996, The EMBO journal.

[4]  A. Matera,et al.  Nuclear bodies: multifaceted subdomains of the interchromatin space. , 1999, Trends in cell biology.

[5]  A. Lamond,et al.  Structure and function in the nucleus. , 1998, Science.

[6]  T Misteli,et al.  Protein dynamics: implications for nuclear architecture and gene expression. , 2001, Science.

[7]  Jason R. Swedlow,et al.  In Vivo Analysis of Cajal Body Movement, Separation, and Joining in Live Human Cells , 2000, The Journal of cell biology.

[8]  Yunfeng Yang,et al.  Nopp140 Functions as a Molecular Link Between the Nucleolus and the Coiled Bodies , 1998, The Journal of cell biology.

[9]  Y. Nogi,et al.  Structural alterations of the nucleolus in mutants of Saccharomyces cerevisiae defective in RNA polymerase I , 1993, Molecular and cellular biology.

[10]  L. Manuelidis,et al.  Movement of the X chromosome in epilepsy. , 1988, Science.

[11]  M. Lyon Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.

[12]  P. Cook,et al.  Site of transcription of ribosomal RNA and intranucleolar structure in HeLa cells. , 1994, Journal of cell science.

[13]  D. Kioussis,et al.  Locus control regions and epigenetic chromatin modifiers. , 2000, Current opinion in genetics & development.

[14]  Ronald Berezney,et al.  Spatial and Temporal Dynamics of DNA Replication Sites in Mammalian Cells , 1998, The Journal of cell biology.

[15]  P. Pandolfi,et al.  The puzzling multiple lives of PML and its role in the genesis of cancer. , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.

[16]  J. Sobczak-Thépot,et al.  The PML growth-suppressor has an altered expression in human oncogenesis. , 1995, Oncogene.

[17]  D. Ish-Horowicz,et al.  Apical localization of pair-rule transcripts requires 3′ sequences and limits protein diffusion in the Drosophila blastoderm embryo , 1991, Cell.

[18]  D. Hernandez-Verdun,et al.  Initiation of nucleolar assembly is independent of RNA polymerase I transcription. , 2000, Molecular biology of the cell.

[19]  D. Spector,et al.  In vivo evidence that transcription and splicing are coordinated by a recruiting mechanism , 1993, Cell.

[20]  R. Evans,et al.  A novel macromolecular structure is a target of the promyelocyte-retinoic acid receptor oncoprotein , 1994, Cell.

[21]  Anne E Carpenter,et al.  Large-scale chromatin structure and function. , 1999, Current opinion in cell biology.

[22]  I. Raška,et al.  Immunological and ultrastructural studies of the nuclear coiled body with autoimmune antibodies. , 1991, Experimental cell research.

[23]  A. Lamond,et al.  Inhibition of protein dephosphorylation results in the accumulation of splicing snRNPs and coiled bodies within the nucleolus. , 1997, Experimental cell research.

[24]  D. Tollervey,et al.  The box H + ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthase. , 1998, Genes & development.

[25]  D. Bregman,et al.  Splicing Factors Associate with Hyperphosphorylated RNA Polymerase II in the Absence of Pre-mRNA , 1997, The Journal of cell biology.

[26]  A. Verkman,et al.  Translational Diffusion of Macromolecule-sized Solutes in Cytoplasm and Nucleus , 1997, The Journal of cell biology.

[27]  M. Dorée,et al.  Mitotic phosphorylation of the TBP-containing factor SL1 represses ribosomal gene transcription. , 1998, Journal of molecular biology.

[28]  B. Ganem RNA world , 1987, Nature.

[29]  A. Fisher,et al.  Dynamic repositioning of genes in the nucleus of lymphocytes preparing for cell division. , 1999, Molecular cell.

[30]  Y. Yang,et al.  Conserved composition of mammalian box H/ACA and box C/D small nucleolar ribonucleoprotein particles and their interaction with the common factor Nopp140. , 2000, Molecular biology of the cell.

[31]  D. Jackson,et al.  The balance sheet for transcription: an analysis of nuclear RNA metabolism in mammalian cells , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[32]  Charles J. Sherr,et al.  Nucleolar Arf sequesters Mdm2 and activates p53 , 1999, Nature Cell Biology.

[33]  T. Misteli,et al.  High mobility of proteins in the mammalian cell nucleus , 2000, Nature.

[34]  D. Tollervey,et al.  A Novel In Vivo Assay Reveals Inhibition of Ribosomal Nuclear Export in Ran-Cycle and Nucleoporin Mutants , 1999, The Journal of cell biology.

[35]  M. Nomura,et al.  Mutational Analysis of the Structure and Localization of the Nucleolus in the Yeast Saccharomyces cerevisiae , 1998, The Journal of cell biology.

[36]  D. Spector,et al.  Intron-dependent recruitment of pre-mRNA splicing factors to sites of transcription , 1996, The Journal of cell biology.

[37]  Daniel Axelrod,et al.  Chromatin Dynamics in Interphase Nuclei and Its Implications for Nuclear Structure , 1997, The Journal of cell biology.

[38]  I. Raška,et al.  Nonisotopic ultrastructural mapping of transcription sites within the nucleolus. , 1993, Experimental cell research.

[39]  Andrew S. Belmont,et al.  Interphase movements of a DNA chromosome region modulated by VP16 transcriptional activator , 2001, Nature Cell Biology.

[40]  C. Prives,et al.  The p53 pathway , 1999, The Journal of pathology.

[41]  F S Fay,et al.  A three-dimensional view of precursor messenger RNA metabolism within the mammalian nucleus. , 1993, Science.

[42]  F. Boisvert,et al.  The Transcription Coactivator Cbp Is a Dynamic Component of the Promyelocytic Leukemia Nuclear Body , 2001, The Journal of cell biology.

[43]  R. Morimoto,et al.  Rapid and reversible relocalization of heat shock factor 1 within seconds to nuclear stress granules. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[44]  B. Edgar,et al.  Repression and turnover pattern fushi tarazu RNA in the early Drosophila embryo , 1986, Cell.

[45]  H. Leonhardt,et al.  Dynamics of DNA Replication Factories in Living Cells , 2000, The Journal of cell biology.

[46]  S. Gasser,et al.  Nuclear compartments and gene regulation. , 1999, Current opinion in genetics & development.

[47]  W. Marzluff,et al.  Coiled bodies preferentially associate with U4, U11, and U12 small nuclear RNA genes in interphase HeLa cells but not with U6 and U7 genes. , 1999, Molecular biology of the cell.

[48]  P. Silver,et al.  Nuclear export of the small ribosomal subunit requires the ran-GTPase cycle and certain nucleoporins. , 1999, Genes & development.

[49]  C. Murphy,et al.  RNA polymerase II in Cajal bodies of amphibian oocytes. , 2000, Journal of structural biology.

[50]  P. Lichter,et al.  Identification of an interchromosomal compartment by polymerization of nuclear-targeted vimentin. , 1998, Journal of cell science.

[51]  M. Dundr,et al.  The nucleolus: an old factory with unexpected capabilities. , 2000, Trends in cell biology.

[52]  S. Wolin,et al.  The trials and travels of tRNA. , 1999, Genes & development.

[53]  B. Daneholt Transcription in polytene chromosomes , 1975, Cell.

[54]  Dirk Schübeler,et al.  Nuclear compartmentalization and gene activity , 2000, Nature Reviews Molecular Cell Biology.

[55]  S. Altman,et al.  Localization in the Nucleolus and Coiled Bodies of Protein Subunits of the Ribonucleoprotein Ribonuclease P , 1999, The Journal of cell biology.

[56]  A. Weiner,et al.  Association of snRNA genes with coiled bodies is mediated by nascent snRNA transcripts , 1999, Current Biology.

[57]  J. Gall,et al.  H3 uridine incorporation in lampbrush chromosomes. , 1962, Proceedings of the National Academy of Sciences of the United States of America.

[58]  K. Narayan,et al.  Isolation of nucleoli in a medium containing spermine and magnesium acetate. , 1967, Experimental cell research.

[59]  Barbara L. Billington,et al.  Position effect at S. cerevisiae telomeres: Reversible repression of Pol II transcription , 1990, Cell.

[60]  Eric Verdin,et al.  Reduced Mobility of the Alternate Splicing Factor (Asf) through the Nucleoplasm and Steady State Speckle Compartments , 2000, The Journal of cell biology.

[61]  A. Raap,et al.  RNAs radiate from gene to cytoplasm as revealed by fluorescence in situ hybridization. , 1995, Journal of cell science.

[62]  D. E. Wolf,et al.  Intranuclear diffusion and hybridization state of oligonucleotides measured by fluorescence correlation spectroscopy in living cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[63]  B. van Steensel,et al.  Fluorescent labeling of nascent RNA reveals transcription by RNA polymerase II in domains scattered throughout the nucleus , 1993, The Journal of cell biology.

[64]  B. O’Malley,et al.  FRAP reveals that mobility of oestrogen receptor-α is ligand- and proteasome-dependent , 2000, Nature Cell Biology.

[65]  T. Sternsdorf,et al.  Nuclear dots: actors on many stages. , 1997, Immunobiology.

[66]  D. Jackson,et al.  Visualization of focal sites of transcription within human nuclei. , 1993, The EMBO journal.

[67]  R. van Driel,et al.  Nuclear distribution of transcription factors in relation to sites of transcription and RNA polymerase II. , 1997, Journal of cell science.

[68]  I. Bozzoni,et al.  Inhibition of human immunodeficiency virus type 1 replication by nuclear chimeric anti-HIV ribozymes in a human T lymphoblastoid cell line. , 1998, Human gene therapy.

[69]  W. Chia,et al.  The EAST protein of Drosophila controls an expandable nuclear endoskeleton , 2000, Nature Cell Biology.

[70]  A. Lamond,et al.  Mutational analysis of p80 coilin indicates a functional interaction between coiled bodies and the nucleolus , 1995, The Journal of cell biology.

[71]  A S Belmont,et al.  In vivo localization of DNA sequences and visualization of large-scale chromatin organization using lac operator/repressor recognition , 1996, The Journal of cell biology.

[72]  J. Politz,et al.  Review: movement of mRNA from transcription site to nuclear pores. , 2000, Journal of structural biology.

[73]  R. Terns,et al.  Role of the box C/D motif in localization of small nucleolar RNAs to coiled bodies and nucleoli. , 1999, Molecular biology of the cell.

[74]  M. Dundr,et al.  Partially processed pre-rRNA is preserved in association with processing components in nucleolus-derived foci during mitosis. , 1998, Molecular biology of the cell.

[75]  A. Dejean,et al.  PML nuclear bodies are general targets for inflammation and cell proliferation. , 1995, Cancer research.

[76]  Susan M. Kilroy,et al.  Signal recognition particle components in the nucleolus. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[77]  Patrick Linder,et al.  Protein trans-Acting Factors Involved in Ribosome Biogenesis in Saccharomyces cerevisiae , 1999, Molecular and Cellular Biology.

[78]  D L Spector,et al.  Dynamic organization of DNA replication in mammalian cell nuclei: spatially and temporally defined replication of chromosome-specific alpha-satellite DNA sequences , 1992, The Journal of cell biology.

[79]  G. Sudlow,et al.  Large-Scale Chromatin Unfolding and Remodeling Induced by VP16 Acidic Activation Domain , 1999, The Journal of cell biology.

[80]  M. Koken,et al.  PML induces a novel caspase-independent death process , 1998, Nature Genetics.

[81]  P. Bingham,et al.  Evidence for channeled diffusion of pre-mRNAs during nuclear RNA transport in metazoans , 1993, The Journal of cell biology.

[82]  D. Ward,et al.  Association of RNase mitochondrial RNA processing enzyme with ribonuclease P in higher ordered structures in the nucleolus: a possible coordinate role in ribosome biogenesis. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[83]  A. Houtsmuller,et al.  Action of DNA repair endonuclease ERCC1/XPF in living cells. , 1999, Science.

[84]  L. Du,et al.  A Functional Interaction between the Carboxy-Terminal Domain of RNA Polymerase II and Pre-mRNA Splicing , 1997, The Journal of cell biology.

[85]  D. Tollervey,et al.  Function and synthesis of small nucleolar RNAs. , 1997, Current opinion in cell biology.

[86]  E. Yeh,et al.  Pml Is Critical for Nd10 Formation and Recruits the Pml-Interacting Protein Daxx to This Nuclear Structure When Modified by Sumo-1 , 1999, The Journal of cell biology.

[87]  G. Sinclair,et al.  The reversible action of alpha-amanitin on nuclear structure and molecular composition. , 1978, Experimental Cell Research.

[88]  X. Darzacq,et al.  Nucleolar Factors Direct the 2′-O-Ribose Methylation and Pseudouridylation of U6 Spliceosomal RNA , 1999, Molecular and Cellular Biology.

[89]  L. Wieslander,et al.  Splicing of Balbiani ring 1 gene pre-mRNA occurs simultaneously with transcription , 1994, Cell.

[90]  A. Matera,et al.  Cell cycle-dependent localization of the CDK2-cyclin E complex in Cajal (coiled) bodies. , 2000, Journal of cell science.

[91]  J. Lawrence,et al.  Discrete nuclear domains of poly(A) RNA and their relationship to the functional organization of the nucleus , 1991, The Journal of cell biology.

[92]  P. Cook The organization of replication and transcription. , 1999, Science.

[93]  A. Dajani,et al.  Effect of Bactericidal Substance from Staphylococcus aureus on Group A Streptococci II. Structural Alterations , 1970, Infection and immunity.

[94]  L. Dolan,et al.  The movement of coiled bodies visualized in living plant cells by the green fluorescent protein. , 1999, Molecular biology of the cell.

[95]  D. Spector,et al.  Visualization of gene activity in living cells , 2000, Nature Cell Biology.

[96]  Laurie Smith,et al.  The RNA World of the Nucleolus: Two Major Families of Small RNAs Defined by Different Box Elements with Related Functions , 1996, Cell.

[97]  R. Sternglanz,et al.  Perinuclear localization of chromatin facilitates transcriptional silencing , 1998, Nature.

[98]  J. Lawrence,et al.  Higher level organization of individual gene transcription and RNA splicing. , 1993, Science.

[99]  A. Zolotukhin,et al.  Nucleoporins Nup98 and Nup214 Participate in Nuclear Export of Human Immunodeficiency Virus Type 1 Rev , 1999, Journal of Virology.

[100]  D. Agard,et al.  Perturbation of Nuclear Architecture by Long-Distance Chromosome Interactions , 1996, Cell.

[101]  Maria Carmo-Fonseca,et al.  To be or not to be in the nucleolus , 2000, Nature Cell Biology.

[102]  E M Manders,et al.  Numbers and organization of RNA polymerases, nascent transcripts, and transcription units in HeLa nuclei. , 1998, Molecular biology of the cell.

[103]  C. Lorson,et al.  SMN oligomerization defect correlates with spinal muscular atrophy severity , 1998, Nature Genetics.

[104]  E. Tan,et al.  Coiled bodies in the nucleolus of breast cancer cells. , 1994, Journal of cell science.

[105]  D. Hernandez-Verdun,et al.  The chromosome periphery during mitosis , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[106]  D. Spector,et al.  Macromolecular domains within the cell nucleus. , 1993, Annual review of cell biology.

[107]  A. Monneron,et al.  Fine structural organization of the interphase nucleus in some mammalian cells. , 1969, Journal of ultrastructure research.

[108]  A. Imbalzano,et al.  Human SWI/SNF nucleosome remodeling activity is partially inhibited by linker histone H1. , 2000, Biochemistry.

[109]  R. van Driel,et al.  Coiled bodies and U2 snRNA genes adjacent to coiled bodies are enriched in factors required for snRNA transcription. , 1998, Molecular biology of the cell.

[110]  G. Almouzni,et al.  The Ribosomal RNA Processing Machinery Is Recruited to the Nucleolar Domain before RNA Polymerase I during Xenopus laevis Development , 2000, The Journal of cell biology.

[111]  A. Pombo,et al.  Regional and temporal specialization in the nucleus: a transcriptionally‐active nuclear domain rich in PTF, Oct1 and PIKA antigens associates with specific chromosomes early in the cell cycle , 1998, The EMBO journal.

[112]  T. Deerinck,et al.  The Perinucleolar Compartment and Transcription , 1998, The Journal of cell biology.

[113]  D. Hernandez-Verdun,et al.  In Vivo Release of Mitotic Silencing of Ribosomal Gene Transcription Does Not Give Rise to Precursor Ribosomal RNA Processing , 2000, The Journal of cell biology.

[114]  A. Matera,et al.  Erratum: Coiled bodies contain U7 small nuclear RNA and associate with specific DNA sequences in interphase human cells (Proceedings of the National Academy of Sciences of United States of America (June 20, 1995) 92:13 (5915- 5919)) , 1995 .

[115]  J. Lawrence,et al.  Replication-dependent histone gene expression is related to Cajal body (CB) association but does not require sustained CB contact. , 2001, Molecular biology of the cell.

[116]  M. Rout,et al.  The Road to Ribosomes , 2000, The Journal of cell biology.

[117]  N. Stuurman,et al.  The t(15;17) translocation alters a nuclear body in a retinoic acid‐reversible fashion. , 1994, The EMBO journal.

[118]  H. Tanke,et al.  Mutational Analysis of Fibrillarin and Its Mobility in Living Human Cells , 2000, The Journal of cell biology.

[119]  J. Nickerson,et al.  Experimental observations of a nuclear matrix. , 2001, Journal of cell science.

[120]  T. Deerinck,et al.  The Dynamic Organization of the Perinucleolar Compartment in the Cell Nucleus , 1997, The Journal of cell biology.

[121]  Tom Misteli,et al.  Dynamic binding of histone H1 to chromatin in living cells , 2000, Nature.

[122]  J. Workman,et al.  Alteration of nucleosome structure as a mechanism of transcriptional regulation. , 1998, Annual review of biochemistry.

[123]  G. Maul Nuclear domain 10, the site of DNA virus transcription and replication , 1998, BioEssays : news and reviews in molecular, cellular and developmental biology.

[124]  J. Gall,et al.  Cajal bodies: the first 100 years. , 2000, Annual review of cell and developmental biology.

[125]  J. Bachellerie,et al.  Alterations of nucleolar ultrastructure and ribosome biogenesis by actinomycin D. Implications for U3 snRNP function. , 1992, European journal of cell biology.

[126]  T. Kanda,et al.  Histone–GFP fusion protein enables sensitive analysis of chromosome dynamics in living mammalian cells , 1998, Current Biology.

[127]  A. Budde,et al.  Mitotic silencing of human rRNA synthesis: inactivation of the promoter selectivity factor SL1 by cdc2/cyclin B‐mediated phosphorylation , 1998, The EMBO journal.

[128]  A. Matera,et al.  Human genes encoding U3 snRNA associate with coiled bodies in interphase cells and are clustered on chromosome 17p11.2 in a complex inverted repeat structure. , 1997, Nucleic acids research.

[129]  L. Manuelidis Different central nervous system cell types display distinct and nonrandom arrangements of satellite DNA sequences. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[130]  P. Thuriaux,et al.  Cross Talk between tRNA and rRNA Synthesis inSaccharomyces cerevisiae , 2001, Molecular and Cellular Biology.

[131]  J. McNally,et al.  The glucocorticoid receptor: rapid exchange with regulatory sites in living cells. , 2000, Science.

[132]  M. Mann,et al.  A Functional Interaction between the Survival Motor Neuron Complex and RNA Polymerase II , 2001, The Journal of cell biology.

[133]  T. Kiss,et al.  A small nucleolar guide RNA functions both in 2′‐O‐ribose methylation and pseudouridylation of the U5 spliceosomal RNA , 2001, The EMBO journal.

[134]  Christine Chomienne,et al.  The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus , 1990, Nature.

[135]  R. van Driel,et al.  Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjection. , 1999, Molecular biology of the cell.

[136]  G. Karpen,et al.  A Drosophila rRNA gene located in euchromatin is active in transcription and nucleolus formation. , 1988, Genes & development.

[137]  Y. Xiong,et al.  Mutations in human ARF exon 2 disrupt its nucleolar localization and impair its ability to block nuclear export of MDM2 and p53. , 1999, Molecular cell.

[138]  S. Masich,et al.  The intranuclear movement of Balbiani ring premessenger ribonucleoprotein particles. , 1999, Experimental cell research.

[139]  J. Gall,et al.  Coiled bodies without coilin. , 1997, Molecular biology of the cell.

[140]  A. Murray,et al.  Interphase chromosomes undergo constrained diffusional motion in living cells , 1997, Current Biology.

[141]  S. Lall,et al.  Squid hnRNP Protein Promotes Apical Cytoplasmic Transport and Localization of Drosophila Pair-Rule Transcripts , 1999, Cell.

[142]  G. Blobel,et al.  NAP57, a mammalian nucleolar protein with a putative homolog in yeast and bacteria [published erratum appears in J Cell Biol 1998 Jan 26;140(2):447] , 1994, The Journal of cell biology.

[143]  R. Hock,et al.  Structure and function of the nucleolus. , 1999, Current opinion in cell biology.

[144]  T Misteli,et al.  Cell biology of transcription and pre-mRNA splicing: nuclear architecture meets nuclear function. , 2000, Journal of cell science.

[145]  C. Zancanaro,et al.  Cytochemical and immunocytochemical characterization of nuclear bodies during hibernation. , 1994, European journal of cell biology.

[146]  A. Lamond,et al.  Newly assembled snRNPs associate with coiled bodies before speckles, suggesting a nuclear snRNP maturation pathway , 1999, Current Biology.

[147]  R. van Driel,et al.  Nuclear domains enriched in RNA 3'-processing factors associate with coiled bodies and histone genes in a cell cycle-dependent manner. , 1999, Molecular biology of the cell.

[148]  Maria Carmo-Fonseca,et al.  The Spinal Muscular Atrophy Disease Gene Product, Smn , 1999, The Journal of cell biology.

[149]  Pier Paolo Pandolfi,et al.  The transcriptional role of PML and the nuclear body , 2000, Nature Cell Biology.

[150]  Tom Misteli,et al.  The dynamics of a pre-mRNA splicing factor in living cells , 1997, Nature.

[151]  P. Park,et al.  Changes in Morphology and Spatial Position of Coiled Bodies during NGF-induced Neuronal Differentiation of PC12 Cells , 1997, Journal of Histochemistry and Cytochemistry.

[152]  D. Tollervey,et al.  Temperature-sensitive mutations demonstrate roles for yeast fibrillarin in pre-rRNA processing, pre-rRNA methylation, and ribosome assembly , 1993, Cell.

[153]  R. Pictet,et al.  In vivo footprinting of rat TAT gene: Dynamic interplay between the glucocorticoid receptor and a liver-specific factor , 1991, Cell.

[154]  Y. Osheim,et al.  Splice site selection, rate of splicing, and alternative splicing on nascent transcripts. , 1988, Genes & development.

[155]  Matthias Merkenschlager,et al.  Association of Transcriptionally Silent Genes with Ikaros Complexes at Centromeric Heterochromatin , 1997, Cell.

[156]  D. Bentley,et al.  Coupling RNA polymerase II transcription with pre-mRNA processing. , 1999, Current opinion in cell biology.

[157]  D. Boisvert,et al.  Crystal structure of a fibrillarin homologue from Methanococcus jannaschii, a hyperthermophile, at 1.6 Å resolution , 2000, The EMBO journal.

[158]  H. Fried,et al.  Cytoplasmic transport of ribosomal subunits microinjected into the Xenopus laevis oocyte nucleus: a generalized, facilitated process , 1990, The Journal of cell biology.

[159]  P. Park,et al.  Transposition of DNase hypersensitive chromatin to the nuclear periphery coincides temporally with nerve growth factor-induced up-regulation of gene expression in PC12 cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[160]  C. Murphy,et al.  Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes. , 1999, Molecular biology of the cell.

[161]  M. Hendzel,et al.  Rapid exchange of histone H1.1 on chromatin in living human cells , 2000, Nature.

[162]  A Benner,et al.  Active and inactive genes localize preferentially in the periphery of chromosome territories , 1996, The Journal of cell biology.

[163]  E. Manders,et al.  Spatial Relationship between Transcription Sites and Chromosome Territories , 1999, The Journal of cell biology.

[164]  J. Lawrence,et al.  Nuclear RNA tracks: structural basis for transcription and splicing? , 1993, Trends in cell biology.

[165]  J. Manley,et al.  RNA polymerase II and the integration of nuclear events. , 2000, Genes & development.

[166]  G. Blobel,et al.  Gene gating: a hypothesis. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[167]  C. Souchier,et al.  Higher concentrations of histone macroH2A in the Barr body are correlated with higher nucleosome density , 2000, Current Biology.

[168]  A. Levine,et al.  P19(ARF) stabilizes p53 by blocking nucleo-cytoplasmic shuttling of Mdm2. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[169]  S. Gerbi,et al.  Transient nucleolar localization Of U6 small nuclear RNA in Xenopus Laevis oocytes. , 2000, Molecular biology of the cell.

[170]  Arlen W. Johnson,et al.  Nmd3p Is a Crm1p-Dependent Adapter Protein for Nuclear Export of the Large Ribosomal Subunit , 2000, The Journal of cell biology.

[171]  L. Manuelidis A view of interphase chromosomes , 1990, Science.

[172]  I. Raška,et al.  Nuclear pre-mRNA compartmentalization: trafficking of released transcripts to splicing factor reservoirs. , 2000, Molecular biology of the cell.

[173]  C Cremer,et al.  Chromosome territories, interchromatin domain compartment, and nuclear matrix: an integrated view of the functional nuclear architecture. , 2000, Critical reviews in eukaryotic gene expression.

[174]  S. Wolin,et al.  A perinucleolar compartment contains several RNA polymerase III transcripts as well as the polypyrimidine tract-binding protein, hnRNP I [published erratum appears in J Cell Biol 1995 Jul;130(2):497-500] , 1995, The Journal of cell biology.

[175]  L. Phan,et al.  Control of transfer RNA maturation by phosphorylation of the human La antigen on serine 366. , 2000, Molecular cell.

[176]  Tom Misteli,et al.  The Dynamics of Postmitotic Reassembly of the Nucleolus , 2000, The Journal of cell biology.

[177]  T. Misteli,et al.  RNA polymerase II targets pre-mRNA splicing factors to transcription sites in vivo. , 1999, Molecular cell.

[178]  J. Politz,et al.  The Nucleolus and the Four Ribonucleoproteins of Translation , 2000, The Journal of cell biology.

[179]  R. Singer,et al.  Movement of nuclear poly(A) RNA throughout the interchromatin space in living cells , 1999, Current Biology.

[180]  Z. Xue,et al.  The nucleolus: an organelle formed by the act of building a ribosome. , 1995, Current opinion in cell biology.