Literature DB >> 7841523

Nucleologenesis: U3 snRNA-containing prenucleolar bodies move to sites of active pre-rRNA transcription after mitosis.

L F Jiménez-García1, M L Segura-Valdez, R L Ochs, L I Rothblum, R Hannan, D L Spector.   

Abstract

We have investigated the distribution of U3 snRNA and rRNA in HeLa cells and normal rat kidney cells during interphase and mitosis. U3 snRNA, known to be involved in pre-rRNA processing, was detected in nucleoli and coiled bodies during interphase, whereas rRNA was distributed in the nucleoli and throughout the cytoplasm. By comparison, ribosomal protein S6 was detected in nucleoli, coiled bodies, and in the cytoplasm. During nucleologenesis, pre-rRNA was observed in newly forming nucleoli during late telophase but not in prenucleolar bodies (PNBs), whereas U3 snRNA was detected in forming nucleoli and PNBs. Similar findings to those reported here for the localization of U3 snRNA have been reported previously for the U3 small nuclear ribonucleoprotein fibrillarin. These results suggest that components involved in pre-rRNA processing localize to discrete PNBs at the end of mitosis. The nucleolus is formed at specific telophase domains (nucleolar organizing regions) and the PNBs, containing factors essential for pre-rRNA processing, are recruited to these sites of rRNA transcription and processing.

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Year:  1994        PMID: 7841523      PMCID: PMC301119          DOI: 10.1091/mbc.5.9.955

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  69 in total

1.  Identification of the human U7 snRNP as one of several factors involved in the 3' end maturation of histone premessenger RNA's.

Authors:  K L Mowry; J A Steitz
Journal:  Science       Date:  1987-12-18       Impact factor: 47.728

Review 2.  Functional and dynamic aspects of the mammalian nucleolus.

Authors:  U Scheer; R Benavente
Journal:  Bioessays       Date:  1990-01       Impact factor: 4.345

3.  The U3 small nucleolar ribonucleoprotein functions in the first step of preribosomal RNA processing.

Authors:  S Kass; K Tyc; J A Steitz; B Sollner-Webb
Journal:  Cell       Date:  1990-03-23       Impact factor: 41.582

4.  Genes for human U3 small nucleolar RNA contain highly conserved flanking sequences.

Authors:  Y Yuan; R Reddy
Journal:  Biochim Biophys Acta       Date:  1989-06-01

5.  Nucleologenesis: use of non-isotopic in situ hybridization and immunocytochemistry to compare the localization of rDNA and nucleolar proteins during mitosis.

Authors:  L F Jiménez-García; L I Rothblum; H Busch; R L Ochs
Journal:  Biol Cell       Date:  1989       Impact factor: 4.458

6.  The paranucleolar structure, accessory body of Cajal, sex chromatin, and related structures in nuclei of rat trigeminal neurons: a cytochemical and ultrastructural study.

Authors:  J H Hardin; S S Spicer; W B Greene
Journal:  Anat Rec       Date:  1969-08

7.  The primary structure of rat ribosomal protein S6.

Authors:  Y L Chan; I G Wool
Journal:  J Biol Chem       Date:  1988-02-25       Impact factor: 5.157

8.  In vivo disruption of Xenopus U3 snRNA affects ribosomal RNA processing.

Authors:  R Savino; S A Gerbi
Journal:  EMBO J       Date:  1990-07       Impact factor: 11.598

9.  U3, U8 and U13 comprise a new class of mammalian snRNPs localized in the cell nucleolus.

Authors:  K Tyc; J A Steitz
Journal:  EMBO J       Date:  1989-10       Impact factor: 11.598

10.  Inhibition of nucleolar reformation after microinjection of antibodies to RNA polymerase I into mitotic cells.

Authors:  R Benavente; K M Rose; G Reimer; B Hügle-Dörr; U Scheer
Journal:  J Cell Biol       Date:  1987-10       Impact factor: 10.539

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  72 in total

1.  Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes.

Authors:  J G Gall; M Bellini; Z Wu; C Murphy
Journal:  Mol Biol Cell       Date:  1999-12       Impact factor: 4.138

2.  Nuclear domains enriched in RNA 3'-processing factors associate with coiled bodies and histone genes in a cell cycle-dependent manner.

Authors:  W Schul; I van Der Kraan; A G Matera; R van Driel; L de Jong
Journal:  Mol Biol Cell       Date:  1999-11       Impact factor: 4.138

3.  Nuclear retention elements of U3 small nucleolar RNA.

Authors:  W Speckmann; A Narayanan; R Terns; M P Terns
Journal:  Mol Cell Biol       Date:  1999-12       Impact factor: 4.272

4.  Role of the box C/D motif in localization of small nucleolar RNAs to coiled bodies and nucleoli.

Authors:  A Narayanan; W Speckmann; R Terns; M P Terns
Journal:  Mol Biol Cell       Date:  1999-07       Impact factor: 4.138

5.  snoRNA nuclear import and potential for cotranscriptional function in pre-rRNA processing.

Authors:  B A Peculis
Journal:  RNA       Date:  2001-02       Impact factor: 4.942

6.  Initiation of nucleolar assembly is independent of RNA polymerase I transcription.

Authors:  T Dousset; C Wang; C Verheggen; D Chen; D Hernandez-Verdun; S Huang
Journal:  Mol Biol Cell       Date:  2000-08       Impact factor: 4.138

Review 7.  Small nucleolar RNAs: versatile trans-acting molecules of ancient evolutionary origin.

Authors:  Michael P Terns; Rebecca M Terns
Journal:  Gene Expr       Date:  2002

8.  Components of U3 snoRNA-containing complexes shuttle between nuclei and the cytoplasm and differentially localize in nucleoli: implications for assembly and function.

Authors:  Daniel J Leary; Michael P Terns; Sui Huang
Journal:  Mol Biol Cell       Date:  2003-10-17       Impact factor: 4.138

9.  Partially processed pre-rRNA is preserved in association with processing components in nucleolus-derived foci during mitosis.

Authors:  M Dundr; M O Olson
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

10.  Coiled bodies contain U7 small nuclear RNA and associate with specific DNA sequences in interphase human cells.

Authors:  M R Frey; A G Matera
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-20       Impact factor: 11.205

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