Literature DB >> 8609158

The rDNA transcription machinery is assembled during mitosis in active NORs and absent in inactive NORs.

P Roussel1, C André, L Comai, D Hernandez-Verdun.   

Abstract

In cycling cells, the rDNAs are expressed from telophase to the end of G2 phase. The early resumption of rDNA transcription at telophase raises the question of the fate of the rDNA transcription machinery during mitosis. At the beginning of mitosis, rDNA transcription is arrested, and the rDNAs are clustered in specific chromosomal sites, the nucleolar organizer regions (NOR). In human cells, we demonstrate that the rDNA transcription machinery, as defined in vitro, is colocalized in some NORs and absent from others whatever the mitotic phase: RNA polymerase I and the RNA polymerase I transcription factors, upstream binding factor and promoter selectivity factor (as verified for TATA-binding protein and TATA-binding protein-associated factor for RNA polymerase I [110]), were colocalized in the same NORs. The RNA polymerase I complex was localized using two different antibodies recognizing the two largest subunits or only the third largest subunit, respectively. These two antibodies immunoprecipitated the RNA polymerase I complex in interphase cells as well as in mitotic cells. These results clearly indicated that the RNA polymerase I complex remained assembled during mitosis. In addition, RNA polymerase I and the transcription factors varied in the same proportions in the positive NORs, suggesting stoichiometric association of these components. The fact that the rDNA transcription machinery is not equally distributed among NORs most likely reflects the implication of the different NORs during the subsequent interphase. Indeed, we demonstrate that only positive NORs exhibit transcription activity at telophase and that the level of transcription activity is related to the amount of rDNA transcription machinery present in the NOR. We propose that assembly of rDNA transcription machinery preceding mitosis determines expression of the rDNAs at the beginning of the next cell cycle. Consequently, the association of rDNAs with the rDNA transcription machinery defines the "active" NORs and the level of activity at the transition telophase/interphase.

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Year:  1996        PMID: 8609158      PMCID: PMC2120807          DOI: 10.1083/jcb.133.2.235

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  50 in total

1.  Nucleolin is an Ag-NOR protein; this property is determined by its amino-terminal domain independently of its phosphorylation state.

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3.  Characterization and immunolocalization of a nucleolar antigen with anti-NOR serum in HeLa cells.

Authors:  M C Rendón; R M Rodrigo; L G Goenechea; G García-Herdugo; M M Valdivia; F J Moreno
Journal:  Exp Cell Res       Date:  1992-06       Impact factor: 3.905

Review 4.  The nucleolus and ribosome formation.

Authors:  J R Warner
Journal:  Curr Opin Cell Biol       Date:  1990-06       Impact factor: 8.382

5.  Molecular mechanisms governing species-specific transcription of ribosomal RNA.

Authors:  S P Bell; C S Pikaard; R H Reeder; R Tjian
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6.  The TATA-binding protein and associated factors are integral components of the RNA polymerase I transcription factor, SL1.

Authors:  L Comai; N Tanese; R Tjian
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7.  Nucleolar transcription factor hUBF contains a DNA-binding motif with homology to HMG proteins.

Authors:  H M Jantzen; A Admon; S P Bell; R Tjian
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8.  Quantitative determination of rDNA transcription units in vertebrate cells.

Authors:  T Haaf; D L Hayman; M Schmid
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9.  A growth-dependent transcription initiation factor (TIF-IA) interacting with RNA polymerase I regulates mouse ribosomal RNA synthesis.

Authors:  A Schnapp; C Pfleiderer; H Rosenbauer; I Grummt
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10.  Human autoantibody to RNA polymerase I transcription factor hUBF. Molecular identity of nucleolus organizer region autoantigen NOR-90 and ribosomal RNA transcription upstream binding factor.

Authors:  E K Chan; H Imai; J C Hamel; E M Tan
Journal:  J Exp Med       Date:  1991-11-01       Impact factor: 14.307

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  96 in total

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Authors:  T Dousset; C Wang; C Verheggen; D Chen; D Hernandez-Verdun; S Huang
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3.  Putative involvement of the histone acetyltransferase Tip60 in ribosomal gene transcription.

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4.  Oncogenesis by sequestration of CBP/p300 in transcriptionally inactive hyperacetylated chromatin domains.

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5.  Chromatin association and regulation of rDNA transcription by the Ras-family protein RasL11a.

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Review 6.  Nucleolar DNA: the host and the guests.

Authors:  E Smirnov; D Cmarko; T Mazel; M Hornáček; I Raška
Journal:  Histochem Cell Biol       Date:  2016-02-04       Impact factor: 4.304

7.  Tracking the interactions of rRNA processing proteins during nucleolar assembly in living cells.

Authors:  Nicole Angelier; Marc Tramier; Emilie Louvet; Maïté Coppey-Moisan; Tula M Savino; Jan R De Mey; Danièle Hernandez-Verdun
Journal:  Mol Biol Cell       Date:  2005-04-06       Impact factor: 4.138

8.  Involvement of SIRT7 in resumption of rDNA transcription at the exit from mitosis.

Authors:  Alice Grob; Pascal Roussel; Jane E Wright; Brian McStay; Danièle Hernandez-Verdun; Valentina Sirri
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9.  TFIIIB is phosphorylated, disrupted and selectively released from tRNA promoters during mitosis in vivo.

Authors:  Jennifer A Fairley; Pamela H Scott; Robert J White
Journal:  EMBO J       Date:  2003-11-03       Impact factor: 11.598

10.  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

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