Literature DB >> 2985284

The termination region for SV40 DNA replication directs the mode of separation for the two sibling molecules.

D T Weaver, S C Fields-Berry, M L DePamphilis.   

Abstract

Separation of the two newly replicated chromosomes in simian virus 40 late replicating intermediates (RI*) occurred by two pathways. The parental DNA strands were completely unwound, releasing circular DNA monomers with a gap in the nascent strand (Form II*), or duplex DNA in the termination region was not unwound, resulting in formation of catenated dimers. Under optimal conditions, both products were transient intermediates in replication, although Form II* was predominant. However, in hypertonic medium both RI* and catenated dimers accumulated, and Form II* was not observed. Hypertonic medium appeared to inhibit both DNA unwinding in the termination region and separation of catenated dimers. When the size of the genome or the position of the origin of replication was changed, termination occurred at sites other than that of wild-type SV40. Neither catenated dimers nor RI* DNA accumulated at these sites. Instead, RI* separated into Form II*. Unwinding parental DNA was more difficult at some termination regions than others. Therefore, although completion of DNA replication does not require a unique termination sequence, this sequence can determine the mode of separation for sibling molecules.

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Year:  1985        PMID: 2985284     DOI: 10.1016/s0092-8674(85)80029-5

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  31 in total

1.  Structure of the ColE1 DNA molecule before segregation to daughter molecules.

Authors:  S Nakasu; J Tomizawa
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-01       Impact factor: 11.205

2.  Dideoxynucleoside triphosphates inhibit a late stage of SV40 DNA replication in vitro.

Authors:  P Zahradka
Journal:  Mol Cell Biochem       Date:  1992-03-04       Impact factor: 3.396

3.  Induction and utilization of an ATM signaling pathway by polyomavirus.

Authors:  Jean Dahl; John You; Thomas L Benjamin
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

4.  T-antigen binding to site I facilitates initiation of SV40 DNA replication but does not affect bidirectionality.

Authors:  Z S Guo; U Heine; M L DePamphilis
Journal:  Nucleic Acids Res       Date:  1991-12       Impact factor: 16.971

5.  Inactivation of topoisomerase I or II may lead to recombination or to aberrant replication termination on both SV40 and yeast 2 micron DNA.

Authors:  P Levac; T Moss
Journal:  Chromosoma       Date:  1996-10       Impact factor: 4.316

6.  Sequences that promote formation of catenated intertwines during termination of DNA replication.

Authors:  S C Fields-Berry; M L DePamphilis
Journal:  Nucleic Acids Res       Date:  1989-04-25       Impact factor: 16.971

7.  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

8.  DNA topoisomerase II must act at mitosis to prevent nondisjunction and chromosome breakage.

Authors:  C Holm; T Stearns; D Botstein
Journal:  Mol Cell Biol       Date:  1989-01       Impact factor: 4.272

9.  Topoisomerase inhibitors can selectively interfere with different stages of simian virus 40 DNA replication.

Authors:  R M Snapka
Journal:  Mol Cell Biol       Date:  1986-12       Impact factor: 4.272

10.  Asynchronous DNA replication within the human beta-globin gene locus.

Authors:  E Epner; W C Forrester; M Groudine
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

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