Literature DB >> 2493136

The Drosophila fushi tarazu polypeptide is a DNA-binding transcriptional activator in yeast cells.

V D Fitzpatrick1, C J Ingles.   

Abstract

Many of the regulatory genes controlling the developmental pattern of segmentation during embryonic development in Drosophila melanogaster encode nuclear proteins containing either homoeobox or 'zinc-finger' domains with putative or demonstrated sequence-specific DNA-binding properties. One of these Drosophila homoeobox-containing proteins is encoded by the fushi tarazu (ftz) gene. The expression of ftz is spatially restricted during embryogenesis and the ftz polypeptide has an important role in different stages of development. To determine whether the ftz polypeptide is a sequence-specific DNA-binding activator of transcription, we expressed portions of ftz as fusions with the yeast transcription factor GAL4 in yeast cells. Chimaeric GAL4/ftz proteins, like GAL4 itself, activated the transcription of a GAL4-dependent reporter gene. With reporter constructs containing Drosophila-derived chromosomal DNA sequences as transcriptional elements, the ftz polypeptide acted as a sequence-specific DNA-binding transcriptional activator. In Drosophila, the ftz product may therefore be a positive regulator of transcription.

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Year:  1989        PMID: 2493136     DOI: 10.1038/337666a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  14 in total

1.  Oncogenic transformation by vrel requires an amino-terminal activation domain.

Authors:  J Kamens; P Richardson; G Mosialos; R Brent; T Gilmore
Journal:  Mol Cell Biol       Date:  1990-06       Impact factor: 4.272

2.  Role of the TATA binding protein-transcription factor IIB interaction in supporting basal and activated transcription in plant cells.

Authors:  S Pan; E Czarnecka-Verner; W B Gurley
Journal:  Plant Cell       Date:  2000-01       Impact factor: 11.277

3.  A nucleosome-positioning sequence is required for GCN4 to activate transcription in the absence of a TATA element.

Authors:  C J Brandl; K Struhl
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

4.  SWI-SNF complex participation in transcriptional activation at a step subsequent to activator binding.

Authors:  M P Ryan; R Jones; R H Morse
Journal:  Mol Cell Biol       Date:  1998-04       Impact factor: 4.272

5.  Mutations in RNA polymerase II enhance or suppress mutations in GAL4.

Authors:  L A Allison; C J Ingles
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

6.  Artificially recruited TATA-binding protein fails to remodel chromatin and does not activate three promoters that require chromatin remodeling.

Authors:  M P Ryan; G A Stafford; L Yu; R H Morse
Journal:  Mol Cell Biol       Date:  2000-08       Impact factor: 4.272

7.  Synergistic activation of transcription is mediated by the N-terminal domain of Drosophila fushi tarazu homeoprotein and can occur without DNA binding by the protein.

Authors:  J Ananthan; R Baler; D Morrissey; J Zuo; Y Lan; M Weir; R Voellmy
Journal:  Mol Cell Biol       Date:  1993-03       Impact factor: 4.272

8.  A screen for genes that interact with the Drosophila pair-rule segmentation gene fushi tarazu.

Authors:  Mark W Kankel; Dianne M Duncan; Ian Duncan
Journal:  Genetics       Date:  2004-09       Impact factor: 4.562

9.  Functional analysis of mouse Hoxa-7 in Saccharomyces cerevisiae: sequences outside the homeodomain base contact zone influence binding and activation.

Authors:  M K Gross; P Gruss
Journal:  Mol Cell Biol       Date:  1994-01       Impact factor: 4.272

10.  Fusion with E2A converts the Pbx1 homeodomain protein into a constitutive transcriptional activator in human leukemias carrying the t(1;19) translocation.

Authors:  Q Lu; D D Wright; M P Kamps
Journal:  Mol Cell Biol       Date:  1994-06       Impact factor: 4.272

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