Literature DB >> 2546684

Functional relationship among TATA sequences, gene induction and transcription initiation in the beta-galactosidase, LAC4, gene from Kluyveromyces lactis.

A G Ficca1, C P Hollenberg.   

Abstract

In the 5' non-coding region of the beta-galactosidase, LAC4, gene of Kluyveromyces lactis, three TATA-like sequences are present at -230, -170 and -142 from the ATG translation start site. By means of deletion mutations in the TATA region, at least two of these TATA sequences, those at -230 and -142, were shown to be required for normal gene expression. Evidence is presented for a functional hierarchy and cooperation between these TATA sequences. The deletion or a change in the position of the TATA sequences affects both beta-galactosidase induction and the location of RNA initiation sites. The TATA sequence at -230 alone is sufficient for correct gene induction when it is moved to a position 41 bp from the major RNA initiation sites located around -110; the -142 TATA alone contributes only partly to gene induction. We suggest a functional distinction between these two related regulatory sequences. This functional distinction might be established by sequence differences and/or targets of unlike specific DNA binding protein(s). A conformational analysis of the LAC4 promoter showed that under torsional stress the functional elements UAS, TATA boxes RNA initiation sites and ATG can be detected as P1-sensitive sites. Possible functions of DNA structural alterations on gene expression are discussed.

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Year:  1989        PMID: 2546684     DOI: 10.1007/BF00447041

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  38 in total

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Authors:  K Struhl
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4.  In vivo DNA-binding properties of a yeast transcription activator protein.

Authors:  S B Selleck; J E Majors
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

5.  Saccharomyces cerevisiae PHO5 promoter region: location and function of the upstream activation site.

Authors:  J Nakao; A Miyanohara; A Toh-e; K Matsubara
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6.  Purified Saccharomyces cerevisiae RNA polymerase II interacts homologously with two different promoters as revealed by P1 endonuclease analysis.

Authors:  G Camilloni; F Della Seta; A Grazia Ficca; E Di Mauro
Journal:  Mol Gen Genet       Date:  1986-08

7.  Each of three "TATA elements" specifies a subset of the transcription initiation sites at the CYC-1 promoter of Saccharomyces cerevisiae.

Authors:  S Hahn; E T Hoar; L Guarente
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205

8.  Analysis of a eukaryotic beta-galactosidase gene: the N-terminal end of the yeast Kluyveromyces lactis protein shows homology to the Escherichia coli lacZ gene product.

Authors:  K D Breunig; U Dahlems; S Das; C P Hollenberg
Journal:  Nucleic Acids Res       Date:  1984-03-12       Impact factor: 16.971

9.  A general method for polyethylene-glycol-induced genetic transformation of bacteria and yeast.

Authors:  R J Klebe; J V Harriss; Z D Sharp; M G Douglas
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

10.  Functional homology between the yeast regulatory proteins GAL4 and LAC9: LAC9-mediated transcriptional activation in Kluyveromyces lactis involves protein binding to a regulatory sequence homologous to the GAL4 protein-binding site.

Authors:  K D Breunig; P Kuger
Journal:  Mol Cell Biol       Date:  1987-12       Impact factor: 4.272

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  3 in total

1.  Kluyveromyces lactis LAC4 promoter variants that lack function in bacteria but retain full function in K. lactis.

Authors:  Paul A Colussi; Christopher H Taron
Journal:  Appl Environ Microbiol       Date:  2005-11       Impact factor: 4.792

2.  Two types of TATA elements for the CYC1 gene of the yeast Saccharomyces cerevisiae.

Authors:  W Z Li; F Sherman
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

3.  Coregulation of the Kluyveromyces lactis lactose permease and beta-galactosidase genes is achieved by interaction of multiple LAC9 binding sites in a 2.6 kbp divergent promoter.

Authors:  A Gödecke; W Zachariae; A Arvanitidis; K D Breunig
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

  3 in total

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