Literature DB >> 7544413

Use of flow cytometry to identify a Caulobacter 4.5 S RNA temperature-sensitive mutant defective in the cell cycle.

E Winzeler1, L Shapiro.   

Abstract

Flow cytometry was used to screen a collection of temperature-sensitive mutants for those blocked at discrete points in the cell cycle with respect to the replicative status of the chromosome. At the non-permissive temperature, one such mutant, LS439, could not initiate new rounds of DNA replication and arrested primarily as cells with two completed chromosomes Extended incubation at the restrictive temperature resulted in filament formation. Following the shift to the restrictive temperature protein synthesis continued, but at a reduced rate. A 0.2 kb fragment of DNA located immediately upstream of the Caulobacter homolog of the Escherichia coli dnaX gene was able to completely rescue the temperature-sensitive phenotype of LS439. The 0.2 kb fragment contained a homolog of the bacterial gene encoding 4.5 S RNA. The original point mutation is predicted to disrupt the stem structure in the 4.5 S RNA thus providing a rationale for the genetic basis of the LS439 phenotype.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7544413     DOI: 10.1006/jmbi.1995.0439

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


  25 in total

1.  Dynamic localization of a cytoplasmic signal transduction response regulator controls morphogenesis during the Caulobacter cell cycle.

Authors:  C Jacobs; D Hung; L Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

2.  TmRNA is required for correct timing of DNA replication in Caulobacter crescentus.

Authors:  Kenneth C Keiler; Lucy Shapiro
Journal:  J Bacteriol       Date:  2003-01       Impact factor: 3.490

3.  Recruitment of a cytoplasmic response regulator to the cell pole is linked to its cell cycle-regulated proteolysis.

Authors:  Kathleen R Ryan; Sarah Huntwork; Lucy Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-29       Impact factor: 11.205

4.  The CcrM DNA methyltransferase of Agrobacterium tumefaciens is essential, and its activity is cell cycle regulated.

Authors:  L S Kahng; L Shapiro
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

5.  Correct timing of dnaA transcription and initiation of DNA replication requires trans translation.

Authors:  Lin Cheng; Kenneth C Keiler
Journal:  J Bacteriol       Date:  2009-05-08       Impact factor: 3.490

Review 6.  Flow cytometry and cell sorting of heterogeneous microbial populations: the importance of single-cell analyses.

Authors:  H M Davey; D B Kell
Journal:  Microbiol Rev       Date:  1996-12

7.  Isolation and characterization of a xylose-dependent promoter from Caulobacter crescentus.

Authors:  A C Meisenzahl; L Shapiro; U Jenal
Journal:  J Bacteriol       Date:  1997-02       Impact factor: 3.490

8.  The CcrM DNA methyltransferase is widespread in the alpha subdivision of proteobacteria, and its essential functions are conserved in Rhizobium meliloti and Caulobacter crescentus.

Authors:  R Wright; C Stephens; L Shapiro
Journal:  J Bacteriol       Date:  1997-09       Impact factor: 3.490

9.  Identification of ZipA, a signal recognition particle-dependent protein from Neisseria gonorrhoeae.

Authors:  Ying Du; Cindy Grove Arvidson
Journal:  J Bacteriol       Date:  2003-04       Impact factor: 3.490

10.  The Caulobacter crescentus Homolog of DnaA (HdaA) Also Regulates the Proteolysis of the Replication Initiator Protein DnaA.

Authors:  Richard Wargachuk; Gregory T Marczynski
Journal:  J Bacteriol       Date:  2015-08-31       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.