Literature DB >> 6088064

Structural and functional analysis of the par region of the pSC 10 1 plasmid.

W T Tucker, C A Miller, S N Cohen.   

Abstract

Three distinct segments (the partition-related, or PR segments) within the 370 bp par region of pSC101 have been shown by deletion analysis to be involved in partitioning of the plasmid to daughter cells. The two lateral segments are direct repeats, each of which potentially can pair with an inverted repeat located between them to form a hairpin-loop structure. Deletion of either lateral segment, together with the middle segment, results in plasmid instability (the Par- phenotype). Deletion of one PR segment yields a stable plasmid that nevertheless shows reduced ability to compete with a coexisting wild-type derivative of the same replicon (the Cmp- phenotype). Deletion of all three segments results in a rate of plasmid loss far in excess of that predicted from the observed copy number of the plasmid. Analysis of the segregation properties of these mutants and of temperature-sensitive and high copy number derivatives of the pSC101 replicon suggests a model in which the par function allows the nonreplicating plasmids of the intracellular pool to be counted as individual molecules, and to be distributed evenly to daughter cells. In the absence of par, the multicopy pool of plasmids behaves as a single segregation unit.

Mesh:

Substances:

Year:  1984        PMID: 6088064     DOI: 10.1016/0092-8674(84)90540-3

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


  42 in total

1.  Mechanistic aspects of DnaA-RepA interaction as revealed by yeast forward and reverse two-hybrid analysis.

Authors:  R Sharma; A Kachroo; D Bastia
Journal:  EMBO J       Date:  2001-08-15       Impact factor: 11.598

2.  Random diffusion can account for topA-dependent suppression of partition defects in low-copy-number plasmids.

Authors:  S J Austin; B G Eichorn
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

Review 3.  High-expression of a target gene and high-stability of the plasmid.

Authors:  M Kobayashi; Y Kurusu; H Yukawa
Journal:  Appl Biochem Biotechnol       Date:  1991-02       Impact factor: 2.926

4.  Initiation of RNA decay in Escherichia coli by 5' pyrophosphate removal.

Authors:  Helena Celesnik; Atilio Deana; Joel G Belasco
Journal:  Mol Cell       Date:  2007-07-06       Impact factor: 17.970

5.  New pSC101-derivative cloning vectors with elevated copy numbers.

Authors:  James Peterson; Gregory J Phillips
Journal:  Plasmid       Date:  2008-03-04       Impact factor: 3.466

6.  RNAII transcribed by IPTG-induced T7 RNA polymerase is non-functional as a replication primer for ColE1-type plasmids in Escherichia coli.

Authors:  M Y Chao; M C Kan; S Lin-Chao
Journal:  Nucleic Acids Res       Date:  1995-05-25       Impact factor: 16.971

7.  Apparent and real recombination frequencies in multicopy plasmids: the need for a novel approach in frequency determination.

Authors:  F Chédin; R Dervyn; S D Ehrlich; P Noirot
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

8.  New quantitative methods for measuring plasmid loss rates reveal unexpected stability.

Authors:  Billy T C Lau; Per Malkus; Johan Paulsson
Journal:  Plasmid       Date:  2013-09-13       Impact factor: 3.466

9.  A DNA segment conferring stable maintenance on R6K gamma-origin core replicons.

Authors:  F Wu; I Levchenko; M Filutowicz
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

10.  Analysis of Agrobacterium tumefaciens plasmid pTiC58 replication region with a novel high-copy-number derivative.

Authors:  D R Gallie; M Hagiya; C I Kado
Journal:  J Bacteriol       Date:  1985-03       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.