Cajal bodies: A long history of discovery

被引:277
作者
Cioce, M [1 ]
Lamond, AI
机构
[1] IRBM, Merck Res Lab Rome, Rome, Italy
[2] Univ Dundee, Wellcome Trust Bioctr, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
coilin; snRNP; stress; nucleus; disease;
D O I
10.1146/annurev.cellbio.20.010403.103738
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This review surveys what is known about the structure and function of the subnuclear domains called Cajal bodies (CBs). The major focus is on CBs in mammalian cells but we provide an overview of homologous CB structures in other organisms. We discuss the protein and RNA components of Us, including factors recently found to associate in a cell cycle-dependent fashion or under specific metabolic or stress conditions. We also consider the dynamic properties of both Us and their molecular components, based largely on recent data obtained thanks to the advent of improved in vivo detection and imaging methods. We discuss how these data contribute to an understanding of CB functions and highlight major questions that remain to be answered. Finally, we consider the interesting links that have emerged between Us and alterations in nuclear structure apparent in a range of human pathologies, including cancer and inherited neurodegenerative diseases. We speculate on the relationship between CB function and molecular disease.
引用
收藏
页码:105 / 131
页数:27
相关论文
共 133 条
  • [21] TRANSCRIPTION-DEPENDENT COLOCALIZATION OF THE U1, U2, U4/U6, AND U5 SNRNPS IN COILED BODIES
    CARMOFONSECA, M
    PEPPERKOK, R
    CARVALHO, MT
    LAMOND, AI
    [J]. JOURNAL OF CELL BIOLOGY, 1992, 117 (01) : 1 - 14
  • [22] ASSEMBLY OF SNRNP-CONTAINING COILED BODIES IS REGULATED IN INTERPHASE AND MITOSIS - EVIDENCE THAT THE COILED BODY IS A KINETIC NUCLEAR-STRUCTURE
    CARMOFONSECA, M
    FERREIRA, J
    LAMOND, AI
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 120 (04) : 841 - 852
  • [23] Differential intranuclear localization of fibroblast growth factor-2 isoforms and specific interaction with the survival of motoneuron protein
    Claus, P
    Döring, F
    Gringel, S
    Müller-Ostermeyer, F
    Fuhlrott, J
    Kraft, T
    Grothe, C
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (01) : 479 - 485
  • [24] Ultrastructural analysis of transcription and splicing in the cell nucleus after bromo-UTP microinjection
    Cmarko, D
    Verschure, PJ
    Martin, TE
    Dahmus, ME
    Krause, S
    Fu, XD
    van Driel, R
    Fakan, S
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (01) : 211 - 223
  • [25] The double-stranded RNA activated protein kinase PKR physically associates with the tumor suppressor p53 protein and phosphorylates human p53 on serine 392 in vitro
    Cuddihy, AR
    Wong, AHT
    Tam, NWN
    Li, SY
    Koromilas, AE
    [J]. ONCOGENE, 1999, 18 (17) : 2690 - 2702
  • [26] Cajal body-specific small nuclear RNAs:: a novel class of 2′-O-methylation and pseudouridylation guide RNAs
    Darzacq, X
    Jády, BE
    Verheggen, C
    Kiss, AM
    Bertrand, E
    Kiss, T
    [J]. EMBO JOURNAL, 2002, 21 (11) : 2746 - 2756
  • [27] In vivo kinetics of Cajal body components
    Dundr, M
    Hebert, MD
    Karpova, TS
    Stanek, D
    Xu, HZ
    Shpargel, KB
    Meier, UT
    Neugebauer, KM
    Matera, AG
    Misteli, T
    [J]. JOURNAL OF CELL BIOLOGY, 2004, 164 (06) : 831 - 842
  • [28] A NOVEL MACROMOLECULAR STRUCTURE IS A TARGET OF THE PROMYELOCYTE-RETINOIC ACID RECEPTOR ONCOPROTEIN
    DYCK, JA
    MAUL, GG
    MILLER, WH
    CHEN, JD
    KAKIZUKA, A
    EVANS, RM
    [J]. CELL, 1994, 76 (02) : 333 - 343
  • [29] Cooperation between the RING+B1-B2 and coiled-coil domains of PML is necessary for its effects on cell survival
    Fagioli, M
    Alcalay, M
    Tomassoni, L
    Ferrucci, PF
    Mencarelli, A
    Riganelli, D
    Grignani, F
    Pozzan, T
    Nicoletti, I
    Grignani, F
    Pelicci, PG
    [J]. ONCOGENE, 1998, 16 (22) : 2905 - 2913
  • [30] Molecular phylogenetics of the RrmJ/fibrillarin superfamily of ribose 2′-O-methyltransferases
    Feder, M
    Pas, J
    Wyrwicz, LS
    Bujnicki, JM
    [J]. GENE, 2003, 302 (1-2) : 129 - 138