Previous Article | Next Article ![]()
Mol Cell Biol, May 1998, p. 2455-2461, Vol. 18, No. 5
Department of Genetics, The Graduate
University for Advanced Studies, and Department of Developmental
Genetics, National Institute of Genetics, Mishima, Shizuoka-ken 411, Japan
Received 30 December 1997/Returned for modification 6 February
1998/Accepted 24 February 1998
GAGA factor is known to remodel the chromatin structure in concert
with nucleosome-remodeling factor NURF in a Drosophila embryonic S150 extract. The promoter region of the Drosophila fushi tarazu (ftz) gene carries several binding sites
for GAGA factor. Both the GAGA factor-binding sites and GAGA factor per se are necessary for the proper expression of ftz in vivo.
We observed transcriptional activation of the ftz gene when
a preassembled chromatin template was incubated with GAGA factor and
the S150 extract. The chromatin structure within the ftz
promoter was specifically disrupted by incubation of the preassembled
chromatin with GAGA factor and the S150 extract. Both transcriptional
activation and chromatin disruption were blocked by an antiserum raised
against ISWI or by base substitutions in the GAGA factor-binding sites in the ftz promoter region. These results demonstrate that
GAGA factor- and ISWI-mediated disruption of the chromatin structure within the promoter region of ftz activates transcription
on the chromatin template.
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Chromatin Remodeling Mediated by Drosophila GAGA
Factor and ISWI Activates fushi tarazu Gene
Transcription In Vitro
*
Corresponding author. Mailing address: Department of
Developmental Genetics, National Institute of Genetics, Mishima,
Shizuoka-ken 411, Japan. Phone: 81-559-81-6771. Fax: 81-559-81-6776. E-mail: shirose{at}lab.nig.ac.jp.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»