Literature DB >> 2824998

A nuclease-hypersensitive region forms de novo after chromosome replication.

M J Solomon1, A Varshavsky.   

Abstract

Regular nucleosome arrays in eucaryotic chromosomes are punctuated at specific locations, such as active promoters and replication origins, by apparently nucleosome-free sites, also called nuclease-hypersensitive, or exposed, regions. The -400-base pair-exposed region within simian virus 40 (SV40) chromosomes is present in approximately 20% of the chromosomes in lytically infected cells and encompasses the replication origin, transcriptional enhancer, and both late and early SV40 promoters. We report that nearly all SV40 chromosomes lacked the exposed region during replication and that newly formed chromosomes acquired the exposed region of the same degree as did bulk SV40 chromosomes within 1 h after replication. Furthermore, a much lower but significant level of exposure was detectable in late SV40 replication intermediates, indicating that formation of the exposed region could start within minutes after passage of the replication fork.

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Year:  1987        PMID: 2824998      PMCID: PMC368040          DOI: 10.1128/mcb.7.10.3822-3825.1987

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


  24 in total

1.  A stretch of "late" SV40 viral DNA about 400 bp long which includes the origin of replication is specifically exposed in SV40 minichromosomes.

Authors:  A J Varshavsky; O Sundin; M Bohn
Journal:  Cell       Date:  1979-02       Impact factor: 41.582

2.  Sites in simian virus 40 chromatin which are preferentially cleaved by endonucleases.

Authors:  W A Scott; D J Wigmore
Journal:  Cell       Date:  1978-12       Impact factor: 41.582

3.  Staphylococcal nuclease makes a single non-random cut in the simian virus 40 viral minichromosome.

Authors:  O Sundin; A Varshavsky
Journal:  J Mol Biol       Date:  1979-08-15       Impact factor: 5.469

Review 4.  Core particle, fiber, and transcriptionally active chromatin structure.

Authors:  D S Pederson; F Thoma; R T Simpson
Journal:  Annu Rev Cell Biol       Date:  1986

5.  Terminal stages of SV40 DNA replication proceed via multiply intertwined catenated dimers.

Authors:  O Sundin; A Varshavsky
Journal:  Cell       Date:  1980-08       Impact factor: 41.582

6.  Propagation of globin DNAase I-hypersensitive sites in absence of factors required for induction: a possible mechanism for determination.

Authors:  M Groudine; H Weintraub
Journal:  Cell       Date:  1982-08       Impact factor: 41.582

7.  A nucleosome-free region in SV40 minichromosomes.

Authors:  E B Jakobovits; S Bratosin; Y Aloni
Journal:  Nature       Date:  1980-05-22       Impact factor: 49.962

8.  Absence of nucleosomes in a fraction of SV40 chromatin between the origin of replication and the region coding for the late leader RNA.

Authors:  S Saragosti; G Moyne; M Yaniv
Journal:  Cell       Date:  1980-05       Impact factor: 41.582

9.  Bidirectional replication of Simian Virus 40 DNA.

Authors:  K J Danna; D Nathans
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

10.  Arrest of segregation leads to accumulation of highly intertwined catenated dimers: dissection of the final stages of SV40 DNA replication.

Authors:  O Sundin; A Varshavsky
Journal:  Cell       Date:  1981-09       Impact factor: 41.582

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  5 in total

1.  DNA polymerase epsilon, acetylases and remodellers cooperate to form a specialized chromatin structure at a tRNA insulator.

Authors:  Namrita Dhillon; Jesse Raab; Julie Guzzo; Shawn J Szyjka; Sunil Gangadharan; Oscar M Aparicio; Brenda Andrews; Rohinton T Kamakaka
Journal:  EMBO J       Date:  2009-07-23       Impact factor: 11.598

2.  Mapping in vivo topoisomerase I sites on simian virus 40 DNA: asymmetric distribution of sites on replicating molecules.

Authors:  S E Porter; J J Champoux
Journal:  Mol Cell Biol       Date:  1989-02       Impact factor: 4.272

Review 3.  DNA methylation and cell memory.

Authors:  A D Riggs
Journal:  Cell Biophys       Date:  1989 Aug-Oct

4.  Tissue-specific factors additively increase the probability of the all-or-none formation of a hypersensitive site.

Authors:  J Boyes; G Felsenfeld
Journal:  EMBO J       Date:  1996-05-15       Impact factor: 11.598

5.  Measuring the buffering capacity of gene silencing in Saccharomyces cerevisiae.

Authors:  Kenneth Wu; Namrita Dhillon; Kelvin Du; Rohinton T Kamakaka
Journal:  Proc Natl Acad Sci U S A       Date:  2021-12-07       Impact factor: 11.205

  5 in total

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