Literature DB >> 1773662

Histone genes are located at the sphere loci of Xenopus lampbrush chromosomes.

H G Callan1, J G Gall, C Murphy.   

Abstract

In the anuran Xenopus, as has been demonstrated previously in several species of urodele Amphibia, histone genes lie at the sphere organizer loci of the lampbrush chromosomes. They were located by in situ hybridization of a 3H-labelled histone H4 anti-sense cRNA probe applied to lampbrush preparations in which transcript RNA had been retained, and likewise to preparations in which transcripts were absent but whose DNA had been denatured prior to hybridization. In Xenopus the histone genes lie in intimate association with the spheres that are attached to the lampbrush chromosomes, but they are absent from spheres that lie free in the germinal vesicle. The Anura separated from the Urodela several hundred million years ago, so the sphere organizer/histone gene association is of great antiquity. This suggests that the association has a functional significance, though it is one that has yet to be discovered.

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Year:  1991        PMID: 1773662     DOI: 10.1007/bf00365156

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  16 in total

1.  Giant readthrough transcription units at the histone loci on lampbrush chromosomes of the newt Notophthalmus.

Authors:  M O Diaz; J G Gall
Journal:  Chromosoma       Date:  1985       Impact factor: 4.316

2.  Ecdysone-stimulated RNA synthesis in imaginal discs of Drosophila melanogaster. Assay by in situ hybridization.

Authors:  J J Bonner; M L Pardue
Journal:  Chromosoma       Date:  1976-10-12       Impact factor: 4.316

Review 3.  The organization and expression of histone gene families.

Authors:  C C Hentschel; M L Birnstiel
Journal:  Cell       Date:  1981-08       Impact factor: 41.582

4.  Histone genes are located at the sphere loci of newt lampbrush chromosomes.

Authors:  J G Gall; E C Stephenson; H P Erba; M O Diaz; G Barsacchi-Pilone
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

5.  Histone gene number in relation to C-value in amphibians.

Authors:  V A Hilder; R N Livesey; P C Turner; M T Vlad
Journal:  Nucleic Acids Res       Date:  1981-11-11       Impact factor: 16.971

6.  The lampbrush chromosomes of Xenopus laevis: preparation, identification, and distribution of 5S DNA sequences.

Authors:  H G Callan; J G Gall; C A Berg
Journal:  Chromosoma       Date:  1987       Impact factor: 4.316

7.  Histone gene clusters of the newt notophthalmus are separated by long tracts of satellite DNA.

Authors:  E C Stephenson; H P Erba; J G Gall
Journal:  Cell       Date:  1981-06       Impact factor: 41.582

8.  Genomic organization and nucleotide sequence of two distinct histone gene clusters from Xenopus laevis. Identification of novel conserved upstream sequence elements.

Authors:  M Perry; G H Thomsen; R G Roeder
Journal:  J Mol Biol       Date:  1985-10-05       Impact factor: 5.469

9.  Reiteration frequency of the histone genes in the genome of the amphibian, Xenopus laevis.

Authors:  E Jacob; G Malacinski; M L Birnstiel
Journal:  Eur J Biochem       Date:  1976-10-01

10.  Small nuclear ribonucleoproteins and heterogeneous nuclear ribonucleoproteins in the amphibian germinal vesicle: loops, spheres, and snurposomes.

Authors:  Z A Wu; C Murphy; H G Callan; J G Gall
Journal:  J Cell Biol       Date:  1991-05       Impact factor: 10.539

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  31 in total

1.  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

2.  Replication-dependent histone gene expression is related to Cajal body (CB) association but does not require sustained CB contact.

Authors:  L S Shopland; M Byron; J L Stein; J B Lian; G S Stein; J B Lawrence
Journal:  Mol Biol Cell       Date:  2001-03       Impact factor: 4.138

3.  Coiled bodies preferentially associate with U4, U11, and U12 small nuclear RNA genes in interphase HeLa cells but not with U6 and U7 genes.

Authors:  E Y Jacobs; M R Frey; W Wu; T C Ingledue; T C Gebuhr; L Gao; W F Marzluff; A G Matera
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

4.  Interactions of U2 gene loci and their nuclear transcripts with Cajal (coiled) bodies: evidence for PreU2 within Cajal bodies.

Authors:  K P Smith; J B Lawrence
Journal:  Mol Biol Cell       Date:  2000-09       Impact factor: 4.138

Review 5.  Lampbrush chromosomes and associated bodies: new insights into principles of nuclear structure and function.

Authors:  Garry T Morgan
Journal:  Chromosome Res       Date:  2002       Impact factor: 5.239

6.  Non-canonical Cajal bodies form in the nucleus of late stage avian oocytes lacking functional nucleolus.

Authors:  Tatiana Khodyuchenko; Elena Gaginskaya; Alla Krasikova
Journal:  Histochem Cell Biol       Date:  2012-03-02       Impact factor: 4.304

Review 7.  The Cajal body and histone locus body.

Authors:  Zehra Nizami; Svetlana Deryusheva; Joseph G Gall
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-05-26       Impact factor: 10.005

Review 8.  Mobility of multi-subunit complexes in the nucleus: accessibility and dynamics of chromatin subcompartments.

Authors:  Sabine M Görisch; Peter Lichter; Karsten Rippe
Journal:  Histochem Cell Biol       Date:  2005-04-14       Impact factor: 4.304

9.  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

10.  Nuclear body movement is determined by chromatin accessibility and dynamics.

Authors:  Sabine M Görisch; Malte Wachsmuth; Carina Ittrich; Christian P Bacher; Karsten Rippe; Peter Lichter
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-26       Impact factor: 11.205

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