Literature DB >> 2959840

Direction of transcription affects the replication mode of lambda in an in vitro system.

H Kouhara1, T Tsurimoto, K Matsubara.   

Abstract

A set of artificial circular plasmids, named plasmoids, was constructed. They are about 1 kb in size and consist of a 178 bp lambda dv minimal DNA replication origin (ori) which has four direct repeats and the A + T-rich region conferring polarity to the ori fragment, a 775 bp DNA segment that codes for the CAT amino acid sequence and the 99 bp lac promoter (plac). They carry no other functional genes or genetic sites. The constructions involved various combinations of relative orientations of these components. These molecules do not replicate in vivo because they lack genes coding for initiation proteins, but they do replicate in an in vitro system (Fuller et al. 1981), and can be used for studies of interactions between transcription and replication. In these plasmids, major transcription starts from the strong plac, and some weak unscheduled transcription starts from several other initiation sites. The major RNA synthesis was found to interfere with the unscheduled RNA synthesis, which was occurring on the opposite strand. The most active replication took place when the major RNA synthesis went through the lambda origin region in the direction which occurs naturally in the lambda genome. Under these conditions, DNA synthesis going against such transcription was less than that going along with the major transcription. When RNA synthesis through the lambda origin region was in the opposite direction, DNA synthesis in the same direction was about half of that observed in the above case, whereas that going against transcription was very weak.

Mesh:

Year:  1987        PMID: 2959840     DOI: 10.1007/bf00328134

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  25 in total

1.  Genetic regulation: the Lac control region.

Authors:  R C Dickson; J Abelson; W M Barnes; W S Reznikoff
Journal:  Science       Date:  1975-01-10       Impact factor: 47.728

2.  ON THE CONTROL OF THE REPLICATION OF TEMPERATE BACTERIOPHAGES SUPERINFECTING IMMUNE HOSTS.

Authors:  R THOMAS; L E BERTANI
Journal:  Virology       Date:  1964-11       Impact factor: 3.616

3.  Nucleotide sequence analysis of the chloramphenicol resistance transposon Tn9.

Authors:  N K Alton; D Vapnek
Journal:  Nature       Date:  1979 Dec 20-27       Impact factor: 49.962

4.  Replication of lambda dv plasmid in vitro promoted by purified lambda O and P proteins.

Authors:  T Tsurimoto; K Matsubara
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

5.  Enzymatic replication of the origin of the Escherichia coli chromosome.

Authors:  R S Fuller; J M Kaguni; A Kornberg
Journal:  Proc Natl Acad Sci U S A       Date:  1981-12       Impact factor: 11.205

6.  Nitrocellulose filter binding studies of the interactions of Escherichia coli RNA polymerase holoenzyme with deoxyribonucleic acid restriction fragments: evidence for multiple classes of nonpromoter interactions, some of which display promoter-like properties.

Authors:  P Melançon; R R Burgess; M T Record
Journal:  Biochemistry       Date:  1982-08-31       Impact factor: 3.162

7.  Replication of bacteriophage lambda DNA.

Authors:  T Tsurimoto; K Matsubara
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1983

8.  A model for transcription termination suggested by studies on the trp attenuator in vitro using base analogs.

Authors:  P J Farnham; T Platt
Journal:  Cell       Date:  1980-07       Impact factor: 41.582

9.  A membrane-filter technique for the detection of complementary DNA.

Authors:  D T Denhardt
Journal:  Biochem Biophys Res Commun       Date:  1966-06-13       Impact factor: 3.575

10.  Bacteriophage SP6-specific RNA polymerase. I. Isolation and characterization of the enzyme.

Authors:  E T Butler; M J Chamberlin
Journal:  J Biol Chem       Date:  1982-05-25       Impact factor: 5.157

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  3 in total

1.  Restriction analysis of lambda EMBL3 background recombinants: occurrence of lambda phages carrying a head to tail oriented left arm DNA sequence.

Authors:  H Tröster; W Kissel; M F Trendelenburg; A Hofmann
Journal:  Mol Gen Genet       Date:  1989-06

2.  Transcription of a region downstream from lambda ori is required for replication of plasmids derived from coliphage lambda.

Authors:  T Hase; M Nakai; Y Masamune
Journal:  Mol Gen Genet       Date:  1989-03

3.  Coupling of transcription and replication machineries in λ DNA replication initiation: evidence for direct interaction of Escherichia coli RNA polymerase and the λO protein.

Authors:  Anna Szambowska; Marcin Pierechod; Grzegorz Wegrzyn; Monika Glinkowska
Journal:  Nucleic Acids Res       Date:  2010-09-09       Impact factor: 16.971

  3 in total

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