Literature DB >> 3327750

A Saccharomyces cerevisiae genomic plasmid bank based on a centromere-containing shuttle vector.

M D Rose1, P Novick, J H Thomas, D Botstein, G R Fink.   

Abstract

A set of genomic plasmid banks was constructed using the centromere-containing yeast shuttle vector YCp50. The centromere-containing vector is useful for the isolation of genes that are toxic to yeast when present in high copy number. Fourteen independent banks were prepared each with an average representation of two to three times the yeast genome. Any individual plasmid from a given bank is guaranteed to be of independent origin from plasmids obtained from each of the other banks. The banks were constructed from three different size classes of DNA fragments that resulted from varying conditions of partial digestion with Sau3A. This avoided the bias caused by differential sensitivity of sites to cleavage with Sau3A. Insert DNA is sufficiently large that most genes will be present in the set of plasmid banks at a frequency of about 0.1%.

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Year:  1987        PMID: 3327750     DOI: 10.1016/0378-1119(87)90232-0

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  630 in total

1.  The morphogenesis checkpoint in Saccharomyces cerevisiae: cell cycle control of Swe1p degradation by Hsl1p and Hsl7p.

Authors:  J N McMillan; M S Longtine; R A Sia; C L Theesfeld; E S Bardes; J R Pringle; D J Lew
Journal:  Mol Cell Biol       Date:  1999-10       Impact factor: 4.272

2.  Coupling of Saccharomyces cerevisiae early meiotic gene expression to DNA replication depends upon RPD3 and SIN3.

Authors:  T M Lamb; A P Mitchell
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

3.  Dependence and independence of [PSI(+)] and [PIN(+)]: a two-prion system in yeast?

Authors:  I L Derkatch; M E Bradley; S V Masse; S P Zadorsky; G V Polozkov; S G Inge-Vechtomov; S W Liebman
Journal:  EMBO J       Date:  2000-05-02       Impact factor: 11.598

4.  Apg7p/Cvt2p is required for the cytoplasm-to-vacuole targeting, macroautophagy, and peroxisome degradation pathways.

Authors:  J Kim; V M Dalton; K P Eggerton; S V Scott; D J Klionsky
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

5.  Asg7p-Ste3p inhibition of pheromone signaling: regulation of the zygotic transition to vegetative growth.

Authors:  A F Roth; B Nelson; C Boone; N G Davis
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

6.  Rap1p requires Gcr1p and Gcr2p homodimers to activate ribosomal protein and glycolytic genes, respectively.

Authors:  S J Deminoff; G M Santangelo
Journal:  Genetics       Date:  2001-05       Impact factor: 4.562

7.  BUR1 and BUR2 encode a divergent cyclin-dependent kinase-cyclin complex important for transcription in vivo.

Authors:  S Yao; A Neiman; G Prelich
Journal:  Mol Cell Biol       Date:  2000-10       Impact factor: 4.272

8.  RADH, a gene of Saccharomyces cerevisiae encoding a putative DNA helicase involved in DNA repair. Characteristics of radH mutants and sequence of the gene.

Authors:  A Aboussekhra; R Chanet; Z Zgaga; C Cassier-Chauvat; M Heude; F Fabre
Journal:  Nucleic Acids Res       Date:  1989-09-25       Impact factor: 16.971

9.  Cloning and characterization of the SKI3 gene of Saccharomyces cerevisiae demonstrates allelism to SKI5.

Authors:  L Hougan; D Y Thomas; M Whiteway
Journal:  Curr Genet       Date:  1989-09       Impact factor: 3.886

10.  Binding and activation by the zinc cluster transcription factors of Saccharomyces cerevisiae. Redefining the UASGABA and its interaction with Uga3p.

Authors:  Anu M Idicula; Gregory L Blatch; Terrance G Cooper; Rosemary A Dorrington
Journal:  J Biol Chem       Date:  2002-09-13       Impact factor: 5.157

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