GONUTS has been updated to MW1.31 Most things seem to be working but be sure to report problems.

Have any questions? Please email us at ecoliwiki@gmail.com

TableEdit

Jump to: navigation, search

PMID:1496003

You don't have sufficient rights on this wiki to edit tables. Perhaps you need to log in. Changes you make in the Table editor will not be saved back to the wiki

See Help for Help on this wiki. See the documentation for how to use the table editor

Citation

Prakash, K, Fang, XD, Engelberg, D, Behal, A and Parker, CS (1992) dOct2, a Drosophila Oct transcription factor that functions in yeast. Proc. Natl. Acad. Sci. U.S.A. 89:7080-4

Abstract

Oct factors are members of the POU family of transcription factors that are shown to play important roles during development in mammals. Here we report the cDNA cloning and expression of a Drosophila Oct transcription factor. Whole mount in situ hybridization experiments revealed that the spatial expression patterns of this gene during embryonic development have not yet been observed for any other gene. In early embryogenesis, its transcripts are transiently expressed as a wide uniform band from 20% to 40% of the egg length, very similar to that of gap genes. This pattern progressively resolves into a series of narrower stripes followed by expression in 14 stripes. Subsequently, transcripts from this gene are expressed in the central nervous system and the brain. When expressed in the yeast Saccharomyces cerevisiae, this Drosophila factor functions as a strong, octamer-dependent activator of transcription. Our data strongly suggest possible functions for the Oct factor in pattern formation in Drosophila that might transcend the boundaries of genetically defined segmentation genes.

Links

PubMed PMC49649

Keywords

Amino Acid Sequence; Animals; Base Sequence; Cloning, Molecular; DNA/genetics; DNA-Binding Proteins/metabolism; Drosophila/genetics; Drosophila/metabolism; Embryo, Nonmammalian; Gene Library; Humans; Molecular Sequence Data; Octamer Transcription Factor-2; Plasmids; Protein Conformation; Recombinant Fusion Proteins/isolation & purification; Recombinant Fusion Proteins/metabolism; Saccharomyces cerevisiae/genetics; Sequence Homology, Nucleic Acid; Transcription Factors/genetics; Transcription Factors/isolation & purification; Transcription Factors/metabolism; beta-Galactosidase/genetics; beta-Galactosidase/isolation & purification; beta-Galactosidase/metabolism

public



Cancel