Literature DB >> 1691791

Control of ColE1 plasmid replication. Interaction of Rom protein with an unstable complex formed by RNA I and RNA II.

J Tomizawa1.   

Abstract

A transcript (RNA I) from ColE1 inhibits initiation of replication of the plasmid DNA by binding to the precursor of the primer RNA (RNA II). The ability of RNA I to inhibit replication is altered by the presence of a plasmid-specified small protein, Rom. In vitro, RNA I binds to RNA II to form a very unstable complex, C*. Binding of a single molecule of Rom converts C* to a more stable complex, Cm*. Each of these complexes, C* or Cm*, transforms to a more stable complex, C** or Cm**, respectively. While formation of complex C* or Cm* is inferred from the inhibition of binding caused by a second RNA I species, that of complex C** or Cm** is detected by alteration of RNase sensitivity. Complex C* converts to complex Cm* very rapidly upon addition of Rom to the medium and complex Cm* converts to complex C* very rapidly by removal of Rom from the medium. On the other hand, complexes C** and Cm** do not rapidly interconvert, but can eventually transform to the same stable final product. Thus, Rom affects binding of RNA I to RNA II through conversion of a very unstable early intermediate to a more stable complex, creating a second pathway for their stable binding.

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Year:  1990        PMID: 1691791     DOI: 10.1016/0022-2836(90)90231-a

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  17 in total

1.  An unusual structure formed by antisense-target RNA binding involves an extended kissing complex with a four-way junction and a side-by-side helical alignment.

Authors:  F A Kolb; C Malmgren; E Westhof; C Ehresmann; B Ehresmann; E G Wagner; P Romby
Journal:  RNA       Date:  2000-03       Impact factor: 4.942

2.  Progression of a loop-loop complex to a four-way junction is crucial for the activity of a regulatory antisense RNA.

Authors:  F A Kolb; H M Engdahl; J G Slagter-Jäger; B Ehresmann; C Ehresmann; E Westhof; E G Wagner; P Romby
Journal:  EMBO J       Date:  2000-11-01       Impact factor: 11.598

3.  Association of an RNA kissing complex analyzed using 2-aminopurine fluorescence.

Authors:  M Rist; J Marino
Journal:  Nucleic Acids Res       Date:  2001-06-01       Impact factor: 16.971

4.  Unique plasmids generated via pUC replicon mutagenesis in an error-prone thermophile derived from Geobacillus kaustophilus HTA426.

Authors:  Jyumpei Kobayashi; Misaki Tanabiki; Shohei Doi; Akihiko Kondo; Takashi Ohshiro; Hirokazu Suzuki
Journal:  Appl Environ Microbiol       Date:  2015-08-28       Impact factor: 4.792

5.  Interaction between the antisense and target RNAs involved in the regulation of IncB plasmid replication.

Authors:  K R Siemering; J Praszkier; A J Pittard
Journal:  J Bacteriol       Date:  1993-05       Impact factor: 3.490

6.  The Escherichia coli OxyS regulatory RNA represses fhlA translation by blocking ribosome binding.

Authors:  S Altuvia; A Zhang; L Argaman; A Tiwari; G Storz
Journal:  EMBO J       Date:  1998-10-15       Impact factor: 11.598

7.  Interactions of cations with RNA loop-loop complexes.

Authors:  Abhishek Singh; Latsavongsakda Sethaphong; Yaroslava G Yingling
Journal:  Biophys J       Date:  2011-08-03       Impact factor: 4.033

8.  Self-assembling RNA nanorings based on RNAI/II inverse kissing complexes.

Authors:  Wade W Grabow; Paul Zakrevsky; Kirill A Afonin; Arkadiusz Chworos; Bruce A Shapiro; Luc Jaeger
Journal:  Nano Lett       Date:  2011-01-13       Impact factor: 11.189

Review 9.  Modulation of ColE1-like plasmid replication for recombinant gene expression.

Authors:  Manel Camps
Journal:  Recent Pat DNA Gene Seq       Date:  2010-01

Review 10.  Proteins That Chaperone RNA Regulation.

Authors:  Sarah A Woodson; Subrata Panja; Andrew Santiago-Frangos
Journal:  Microbiol Spectr       Date:  2018-07
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