Mol Cell Biol. 1994 December; 14(12): 7899-7908
Functional and conserved domains of the Drosophila transcription factor encoded by the segmentation gene knirps.
N Gerwin,
A La Rosée,
F Sauer,
H P Halbritter,
M Neumann,
H Jäckle and
U Nauber
Max-Planck-Institut für biophysikalische Chemie, Abteilung Molekulare Entwicklungsbiologie, Göttingen, Germany.
ABSTRACT
The Drosophila gap gene knirps (kni) is required for abdominal segmentation. It encodes a steroid/thyroid orphan receptor-type transcription factor which is distributed in a broad band of nuclei in the posterior region of the blastoderm. To identify essential domains of the kni protein (KNI), we cloned and sequenced the DNA encompassing the coding region of nine kni mutant alleles of different strength and kni-homologous genes of related insect species. We also examined in vitro-modified versions of KNI in various assay systems both in vitro and in tissue culture. The results show that KNI contains several functional domains which are arranged in a modular fashion. The N-terminal 185-amino-acid region which includes the DNA-binding domain and a functional nuclear location signal fails to provide kni activity to the embryo. However, a truncated KNI protein that contains additional 47 amino acids exerts rather strong kni activity which is functionally defined by a weak kni mutant phenotype of the embryo. The additional 47-amino-acid stretch includes a transcriptional repressor domain which acts in the context of a heterologous DNA-binding domain of the yeast transcriptional activator GAL4. The different domains of KNI as defined by functional studies are conserved during insect evolution.
Mol Cell Biol. 1994 December; 14(12): 7899-7908
This article has been cited by other articles:
-
Struffi, P., Corado, M., Kulkarni, M., Arnosti, D. N.
(2004). Quantitative contributions of CtBP-dependent and -independent repression activities of Knirps. Development
131: 2419-2429
[Abstract]
[Full Text]
-
Ryu, J.-R., Olson, L. K., Arnosti, D. N.
(2001). Cell-type specificity of short-range transcriptional repressors. Proc. Natl. Acad. Sci. USA
10.1073/pnas.231394998v1
[Abstract]
[Full Text]
-
Keller, S. A., Mao, Y., Struffi, P., Margulies, C., Yurk, C. E., Anderson, A. R., Amey, R. L., Moore, S., Ebels, J. M., Foley, K., Corado, M., Arnosti, D. N.
(2000). dCtBP-Dependent and -Independent Repression Activities of the Drosophila Knirps Protein. Mol. Cell. Biol.
20: 7247-7258
[Abstract]
[Full Text]
-
Batchelder, C., Dunn, M. A., Choy, B., Suh, Y., Cassie, C., Shim, E. Y., Shin, T. H., Mello, C., Seydoux, G., Blackwell, T. K.
(1999). Transcriptional repression by the Caenorhabditis elegans germ-line protein PIE-1. Genes Dev.
13: 202-212
[Abstract]
[Full Text]
-
Ben-Shushan, E., Thompson, J. R., Gudas, L. J., Bergman, Y.
(1998). Rex-1, a Gene Encoding a Transcription Factor Expressed in the Early Embryo, Is Regulated via Oct-3/4 and Oct-6 Binding to an Octamer Site and a Novel Protein, Rox-1, Binding to an Adjacent Site. Mol. Cell. Biol.
18: 1866-1878
[Abstract]
[Full Text]
-
Jimenez, G., Paroush, Z.'e., Ish-Horowicz, D.
(1997). Groucho acts as a corepressor for a subset of negative regulators, including Hairy and Engrailed. Genes Dev.
11: 3072-3082
[Abstract]
[Full Text]
-
Gray, S, Levine, M
(1996). Short-range transcriptional repressors mediate both quenching and direct repression within complex loci in Drosophila.. Genes Dev.
10: 700-710
[Abstract]
-
Ryu, J.-R., Olson, L. K., Arnosti, D. N.
(2001). Cell-type specificity of short-range transcriptional repressors. Proc. Natl. Acad. Sci. USA
98: 12960-12965
[Abstract]
[Full Text]
Copyright © 1994 by the American Society for Microbiology. All rights reserved.