Skip Navigation

This Article
Right arrow Print PDF (1340K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Legrain, M.
Right arrow Articles by Hilger, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Legrain, M.
Right arrow Articles by Hilger, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1986, Vol. 14, No. 7 3059-3073
© 1986


Articles

Isolation, physical characterization and expression analysis of the Saccharomyces cerevisiae positive regulatory gene PH04

M. Legrain, M. De Wilde1 and F. Hilger*

Laboratoire de Microbiologie, Facultè des Sciences Agronomiques B 5800 Gembloux 1Molecular Genetics, Smith Kline–RIT B 1330 Rixensart, Belgium

*To whom reprint requests should be sent

Received January 29, 1986. Accepted March 11, 1986.

The Saccharomyces cerevisiae PH04 gene, which positively controls the expression of phosphatase genes, has been isolated by complementation of a PH04 mutation. The Isolated DNA directed integration at the chromosomal PH04 locus. The nucleotide sequence of PH04 has a coding region of 930 nucleotides, flanked by sequences with typical transcription initiation and termination signals. The 5' region has characteristics of low–expression promoters and carries several uncommon elements, whose significance is not known. The predicted primary structure of the PH04 protein, of 309 residues, does not show sequence elements typical of DNA–binding proteins. The transcription of PH04 is independent of inorganic phosphate. Like other regulatory genes, PH04 is transcribed at a very low level and the translation of its message uses preferentially several codons which are not employed for highly expressed genes.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
A. Dhasarathy and M. P. Kladde
Promoter Occupancy Is a Major Determinant of Chromatin Remodeling Enzyme Requirements
Mol. Cell. Biol., April 1, 2005; 25(7): 2698 - 2707.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
C. D. Carvin, A. Dhasarathy, L. B. Friesenhahn, W. J. Jessen, and M. P. Kladde
Targeted cytosine methylation for in vivo detection of protein-DNA interactions
PNAS, June 24, 2003; 100(13): 7743 - 7748.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
V. Rubio, F. Linhares, R. Solano, A. C. Martin, J. Iglesias, A. Leyva, and J. Paz-Ares
A conserved MYB transcription factor involved in phosphate starvation signaling both in vascular plants and in unicellular algae
Genes & Dev., August 15, 2001; 15(16): 2122 - 2133.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
A Kaffman, I Herskowitz, R Tjian, and E. O'Shea
Phosphorylation of the transcription factor PHO4 by a cyclin-CDK complex, PHO80-PHO85
Science, February 25, 1994; 263(5150): 1153 - 1156.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.