Literature DB >> 8575878

The nuclear matrix: a structural milieu for genomic function.

R Berezney1, M J Mortillaro, H Ma, X Wei, J Samarabandu.   

Abstract

While significant progress has been made in elucidating molecular properties of specific genes and their regulation, our understanding of how the whole genome is coordinated has lagged behind. To understand how the genome functions as a coordinated whole, we must understand how the nucleus is put together and functions as a whole. An important step in that direction occurred with the isolation and characterization of the nuclear matrix. Aside from the plethora of functional properties associated with these isolated nuclear structures, they have enabled the first direct examination and molecular cloning of specific nuclear matrix proteins. The isolated nuclear matrix can be used for providing an in vitro model for understanding nuclear matrix organization in whole cells. Recent development of high-resolution and three-dimensional approaches for visualizing domains of genomic organization and function in situ has provided corroborative evidence for the nuclear matrix as the site of organization for replication, transcription, and post-transcriptional processing. As more is learned about these in situ functional sites, appropriate experiments could be designed to test molecular mechanisms with the in vitro nuclear matrix systems. This is illustrated in this chapter by the studies of nuclear matrix-associated DNA replication which have evolved from biochemical studies of in vitro nuclear matrix systems toward three-dimensional computer image analysis of replication sites for individual genes.

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Year:  1995        PMID: 8575878     DOI: 10.1016/s0074-7696(08)61228-0

Source DB:  PubMed          Journal:  Int Rev Cytol        ISSN: 0074-7696


  87 in total

1.  Flanking nuclear matrix attachment regions synergize with the T cell receptor delta enhancer to promote V(D)J recombination.

Authors:  X P Zhong; J Carabaña; M S Krangel
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

2.  Rearrangement of chromatin domains during development in Xenopus.

Authors:  Y Vassetzky; A Hair; M Méchali
Journal:  Genes Dev       Date:  2000-06-15       Impact factor: 11.361

3.  Quantitative motion analysis of subchromosomal foci in living cells using four-dimensional microscopy.

Authors:  H Bornfleth; P Edelmann; D Zink; T Cremer; C Cremer
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

4.  Dynamics of association of origins of DNA replication with the nuclear matrix during the cell cycle.

Authors:  V Djeliova; G Russev; B Anachkova
Journal:  Nucleic Acids Res       Date:  2001-08-01       Impact factor: 16.971

5.  Engineering gene expression and protein synthesis by modulation of nuclear shape.

Authors:  Carson H Thomas; Joel H Collier; Charles S Sfeir; Kevin E Healy
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-12       Impact factor: 11.205

6.  Gene positional changes relative to the nuclear substructure correlate with the proliferating status of hepatocytes during liver regeneration.

Authors:  Apolinar Maya-Mendoza; Rolando Hernández-Muñoz; Patricio Gariglio; Armando Aranda-Anzaldo
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

7.  Matrix attachment region (MAR) properties and abnormal expansion of AT island minisatellites in FRA16B fragile sites in leukemic CEM cells.

Authors:  Jennifer A Jackson; Alex V Trevino; Maryanne C Herzig; Terence S Herman; Jan M Woynarowski
Journal:  Nucleic Acids Res       Date:  2003-11-01       Impact factor: 16.971

8.  DNA-PK-dependent binding of DNA ends to plasmids containing nuclear matrix attachment region DNA sequences: evidence for assembly of a repair complex.

Authors:  Stanley K Mauldin; Robert C Getts; Wenjing Liu; Thomas D Stamato
Journal:  Nucleic Acids Res       Date:  2002-09-15       Impact factor: 16.971

Review 9.  Pioneer factors and their in vitro identification methods.

Authors:  Xinyang Yu; Michael J Buck
Journal:  Mol Genet Genomics       Date:  2020-04-15       Impact factor: 3.291

10.  Recombination and transcription of the endogenous Ig heavy chain locus is effected by the Ig heavy chain intronic enhancer core region in the absence of the matrix attachment regions.

Authors:  E Sakai; A Bottaro; L Davidson; B P Sleckman; F W Alt
Journal:  Proc Natl Acad Sci U S A       Date:  1999-02-16       Impact factor: 11.205

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