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Cajal body

From Wikipedia, the free encyclopedia
Structures in cell nuclei
Image of four oval-shaped blue nuclei containing small green dots representing Cajal bodies.
Nuclei of mouse cells (blue) containing Cajal bodies (green) visualized by fusion of p80/Coilin protein to GFP

Cajal bodies (CBs), alsocoiled bodies, are sphericalnuclear bodies of 0.3–1.0 μm in diameter found in thenucleus of proliferativecells likeembryonic cells andtumor cells, or metabolically active cells likeneurons. CBs are membrane-lessorganelles and largely consist ofproteins andRNA. They were first reported bySantiago Ramón y Cajal in 1903, who called themnucleolar accessory bodies due to their association with thenucleoli in neuronal cells.[1] They were rediscovered with the use of theelectron microscope (EM) and namedcoiled bodies, according to their appearance as coiled threads on EM images, and later renamed after their discoverer.[2] Research on CBs was accelerated after discovery andcloning of the marker proteinp80/Coilin.[3] CBs have been implicated in RNA-related metabolic processes such as the biogenesis, maturation and recycling ofsnRNPs,histone mRNA processing andtelomere maintenance. CBs assemble RNA which is used bytelomerase to addnucleotides to the ends of telomeres.[4]

History

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CBs were initially discovered by neurobiologistSantiago Ramón y Cajal in 1903 as smallargyrophilic (readily stained by silver salts, literally "silver loving") spots in the nuclei of silver-stained neuronal cells. Because of their close association with nucleoli, he named themnucleolar accessory bodies. Later on, they were forgotten and rediscovered multiple times independently which led to a state where scientists from different research fields used different names for the same structure. Names used for CBs included "sphere organelles", "Binnenkörper", "nucleolar bodies" or "coiled bodies". The name coiled bodies comes from observation of electron microscopists Monneron and Bernhard. They described bodies as aggregates composed of coiled threads with thickness of 400–600Å. When using higher magnification, they appear as tiny, 50 Å thick fibrils irregularly twisted along the axis of the threads. The bodies were even predicted to consist ofribonucleoproteins since treatment of cells withprotease andRNase together, but not alone, caused dramatic changes to the structure of CBs.[5]

Localization

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Cajal bodies are found in all eukaryotes that have been carefully studied.[6]The cells in which Cajal bodies are most apparent usually demonstrate high levels of transcriptional activity, and are often dividing rapidly.[7]

Cell cycle

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They are about 0.1–2.0micrometres and are found one to five per nucleus. The number varies in different types of cells and over the cell cycle. Maximum number is reached in mid G1 phase and towards G2 they become larger and their number decreases. CBs disassemble during the M phase and reappear again later in G1 phase. Cajal bodies are possibly sites of assembly or modification of thetranscription machinery of the nucleus.[8]

Functions

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CBs are bound to thenucleolus bycoilin proteins. P80-coilin is a specific marker for coiled bodies,[9] and demonstrates these bodies tend to be associated with the nucleolus when cells are not dividing. CBs are associated with telomerase assembly and recruitment via a CAB-RNA sequence common in both CB RNAs (scaRNAs) and theRNA component of telomerase (TERC). TCAB1 recognizes the CAB sequence in both and recruits telomerase to the CBs.[citation needed]

CBs contain high concentrations ofsplicing small nuclear ribonucleoproteins (snRNPs), possibly indicating that they function to modify RNA after it has beentranscribed from DNA.[10] Experimental evidence indicates that CBs contribute to the biogenesis of enzymetelomerase, and assist in subsequent transport of telomerase totelomeres.[11][12]

References

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  1. ^Cajal SR (1903). "Un sencillo metodo de coloracion selectiva del reticulo protoplasmico y sus efectos en los diversos organos nerviosos de vertebrados e invertebrados".Trab Lab Investig Biol Univ Madr.2:129–221.
  2. ^Gall JG, Bellini M, Wu Z, Murphy C (December 1999)."Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes".Molecular Biology of the Cell.10 (12):4385–4402.doi:10.1091/mbc.10.12.4385.PMC 25765.PMID 10588665.
  3. ^Andrade LE, Chan EK, Raska I, Peebles CL, Roos G, Tan EM (June 1991)."Human autoantibody to a novel protein of the nuclear coiled body: immunological characterization and cDNA cloning of p80-coilin".The Journal of Experimental Medicine.173 (6):1407–1419.doi:10.1084/jem.173.6.1407.PMC 2190846.PMID 2033369.
  4. ^Zhao Y, Abreu E, Kim J, Stadler G, Eskiocak U, Terns MP, et al. (May 2011)."Processive and distributive extension of human telomeres by telomerase under homeostatic and nonequilibrium conditions".Molecular Cell.42 (3):297–307.doi:10.1016/j.molcel.2011.03.020.PMC 3108241.PMID 21549308.
  5. ^Monneron A, Bernhard W (May 1969). "Fine structural organization of the interphase nucleus in some mammalian cells".Journal of Ultrastructure Research.27 (3):266–288.doi:10.1016/S0022-5320(69)80017-1.PMID 5813971.
  6. ^Nizami Z, Deryusheva S, Gall JG (July 2010)."The Cajal body and histone locus body".Cold Spring Harbor Perspectives in Biology.2 (7): a000653.doi:10.1101/cshperspect.a000653.PMC 2890199.PMID 20504965.
  7. ^Ogg SC, Lamond AI (October 2002)."Cajal bodies and coilin--moving towards function".The Journal of Cell Biology.159 (1):17–21.doi:10.1083/jcb.200206111.PMC 2173504.PMID 12379800.
  8. ^Cremer T, Cremer C (April 2001). "Chromosome territories, nuclear architecture and gene regulation in mammalian cells".Nature Reviews. Genetics.2 (4):292–301.doi:10.1038/35066075.PMID 11283701.S2CID 8547149.
  9. ^Raska I, Ochs RL, Andrade LE, Chan EK, Burlingame R, Peebles C, et al. (1990). "Association between the nucleolus and the coiled body".Journal of Structural Biology.104 (1–3):120–127.doi:10.1016/1047-8477(90)90066-L.PMID 2088441.
  10. ^Nizami Z, Deryusheva S, Gall JG (July 2010)."The Cajal body and histone locus body".Cold Spring Harbor Perspectives in Biology.2 (7): a000653.doi:10.1101/cshperspect.a000653.PMC 2890199.PMID 20504965.
  11. ^Jády BE, Richard P, Bertrand E, Kiss T (February 2006)."Cell cycle-dependent recruitment of telomerase RNA and Cajal bodies to human telomeres".Molecular Biology of the Cell.17 (2):944–954.doi:10.1091/mbc.E05-09-0904.PMC 1356602.PMID 16319170.
  12. ^Tomlinson RL, Ziegler TD, Supakorndej T, Terns RM, Terns MP (February 2006)."Cell cycle-regulated trafficking of human telomerase to telomeres".Molecular Biology of the Cell.17 (2):955–965.doi:10.1091/mbc.E05-09-0903.PMC 1356603.PMID 16339074.
Structures of thecell nucleus /nuclear protein
Envelope (membrane)/
nuclear lamina
Nucleolus
Other
SMC protein:
Transition nuclear protein:
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