Literature DB >> 2431292

Differential order of replication of Xenopus laevis 5S RNA genes.

D R Guinta, L J Korn.   

Abstract

In Xenopus laevis there are two multigene families of 5S RNA genes: the oocyte-type 5S RNA genes which are expressed only in oocytes and the somatic-type 5S RNA genes which are expressed throughout development. The Xenopus 5S RNA replication-expression model of Gottesfeld and Bloomer (Cell 28:781-791, 1982) and Wormington et al. (Cold Spring Harbor Symp. Quant. Biol. 47:879-884, 1983) predicts that the somatic-type 5S RNA genes replicate earlier in the cell cycle than do the oocyte-type genes. Hence, the somatic-type 5S RNA genes have a competitive advantage in binding the transcription factor TFIIIA in somatic cells and are thereby expressed to the exclusion of the oocyte-type genes. To test the replication-expression model, we determined the order of replication of the oocyte- and somatic-type 5S RNA genes. Xenopus cells were labeled with bromodeoxyuridine, stained for DNA content, and then sorted into fractions of S phase by using a fluorescence-activated cell sorter. The newly replicated DNA containing bromodeoxyuridine was separated from the lighter, unreplicated DNA by equilibrium centrifugation and was hybridized with DNA probes specific for the oocyte- and somatic-type 5S RNA genes. In this way we found that the somatic-type 5S RNA genes replicate early in S phase, whereas the oocyte-type 5S RNA genes replicate late in S phase, demonstrating a key aspect of the replication-expression model.

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Year:  1986        PMID: 2431292      PMCID: PMC367808          DOI: 10.1128/mcb.6.7.2536-2542.1986

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  52 in total

1.  Formation and stability of the 5 S RNA transcription complex.

Authors:  D R Setzer; D D Brown
Journal:  J Biol Chem       Date:  1985-02-25       Impact factor: 5.157

2.  Formation of a rate-limiting intermediate in 5S RNA gene transcription.

Authors:  J J Bieker; P L Martin; R G Roeder
Journal:  Cell       Date:  1985-01       Impact factor: 41.582

3.  Gene amplification in a single cell cycle in Chinese hamster ovary cells.

Authors:  B D Mariani; R T Schimke
Journal:  J Biol Chem       Date:  1984-02-10       Impact factor: 5.157

4.  The role of stable complexes that repress and activate eucaryotic genes.

Authors:  D D Brown
Journal:  Cell       Date:  1984-06       Impact factor: 41.582

5.  Transcription of Xenopus 5S ribosomal RNA genes.

Authors:  L J Korn
Journal:  Nature       Date:  1982-01-14       Impact factor: 49.962

6.  The transcriptional regulation of Xenopus 5s RNA genes in chromatin: the roles of active stable transcription complexes and histone H1.

Authors:  M S Schlissel; D D Brown
Journal:  Cell       Date:  1984-07       Impact factor: 41.582

7.  Chromosomal mapping of Xenopus 5S genes: somatic-type versus oocyte-type.

Authors:  M E Harper; J Price; L J Korn
Journal:  Nucleic Acids Res       Date:  1983-04-25       Impact factor: 16.971

8.  Transcription initiation of Xenopus 5S ribosomal RNA genes in vitro.

Authors:  L J Korn; E H Birkenmeier; D D Brown
Journal:  Nucleic Acids Res       Date:  1979-10-25       Impact factor: 16.971

9.  alpha-Globulin sequences are located in a region of early-replicating DNA in murine erythroleukemia cells.

Authors:  A Furst; E H Brown; J D Braunstein; C L Schildkraut
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

10.  Altered levels of a 5 S gene-specific transcription factor (TFIIIA) during oogenesis and embryonic development of Xenopus laevis.

Authors:  B S Shastry; B M Honda; R G Roeder
Journal:  J Biol Chem       Date:  1984-09-25       Impact factor: 5.157

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  11 in total

1.  Chromosomal footprinting of transcriptionally active and inactive oocyte-type 5S RNA genes of Xenopus laevis.

Authors:  D R Engelke; J M Gottesfeld
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

2.  The C-terminal domain of transcription factor IIIA interacts differently with different 5S RNA genes.

Authors:  Y Y Xing; A Worcel
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

3.  Activation and repression of a beta-globin gene in cell hybrids is accompanied by a shift in its temporal replication.

Authors:  V Dhar; A I Skoultchi; C L Schildkraut
Journal:  Mol Cell Biol       Date:  1989-08       Impact factor: 4.272

4.  Early replication and expression of oocyte-type 5S RNA genes in a Xenopus somatic cell line carrying a translocation.

Authors:  D R Guinta; J Y Tso; S Narayanswami; B A Hamkalo; L J Korn
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

5.  Upstream sequences required for transcription of the TFIIIA gene in Xenopus oocytes.

Authors:  Y Matsumoto; L J Korn
Journal:  Nucleic Acids Res       Date:  1988-05-11       Impact factor: 16.971

6.  Role for DNA replication in beta-globin gene activation.

Authors:  T Enver; A C Brewer; R K Patient
Journal:  Mol Cell Biol       Date:  1988-03       Impact factor: 4.272

7.  Cell-cycle regulation as a mechanism for targeting proteins to specific DNA sequences in Tetrahymena thermophila.

Authors:  M Wu; C D Allis; M A Gorovsky
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

8.  Silk gland-specific tRNA(Ala) genes are tightly clustered in the silkworm genome.

Authors:  D C Underwood; H Knickerbocker; G Gardner; D P Condliffe; K U Sprague
Journal:  Mol Cell Biol       Date:  1988-12       Impact factor: 4.272

9.  Transcriptionally inactive oocyte-type 5S RNA genes of Xenopus laevis are complexed with TFIIIA in vitro.

Authors:  L J Peck; L Millstein; P Eversole-Cire; J M Gottesfeld; A Varshavsky
Journal:  Mol Cell Biol       Date:  1987-10       Impact factor: 4.272

10.  Adenovirus DNA replication facilitates binding of the MLTF/USF transcription factor to the viral major late promoter within infected cells.

Authors:  M Toth; W Doerfler; T Shenk
Journal:  Nucleic Acids Res       Date:  1992-10-11       Impact factor: 16.971

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