Pole region-dependent repression of the Drosophila gap gene Krüppel by maternal gene products

We examined the protein domain of the gap gene Krüppel (Kr) in mutants that affect the establishment of different regions of the segment pattern along the longitudinal axis of the Drosophila embryo. Our data suggest that Kr provides cues for establishing the "central" pattern elements at the blastoderm stage, and that Kr activity is controlled by maternal effect genes acting at the poles. The formation of the Kr protein domain may involve ubiquitous activation of Kr gene expression which, however, is limited by region-specific repression through the action of the maternal anterior and posterior pattern organizer genes. In addition, the formation of the Kr protein domain depends on the activity of gap genes acting adjacent to the Kr domain, but it is independent of subordinate pair-rule gene activities.

[1]  P. Ingham,et al.  The correct activation of Antennapedia and bithorax complex genes requires the fushi tarazu gene , 1986, Nature.

[2]  H. Jäckle,et al.  Molecular genetics of Krüppel, a gene required for segmentation of the Drosophila embryo , 1985, Nature.

[3]  C. Nusslein-Volhard Maternal Effect Mutations that Alter the Spatial Coordinates of the Embryo of Drosophila melanogaste , 1979 .

[4]  N. Perrimon,et al.  Region-specific defects in l(1)giant embryos of Drosophila melanogaster. , 1987, Developmental biology.

[5]  C. Nüsslein-Volhard,et al.  Organization of anterior pattern in the Drosophila embryo by the maternal gene bicoid , 1986, Nature.

[6]  Alice Louise Bull,et al.  Bicaudal, a genetic factor which affects the polarity of the embryo in Drosophila melanogaster , 1966 .

[7]  C. Nüsslein-Volhard,et al.  Krüppel, a gene whose activity is required early in the zygotic genome for normal embryonic segmentation. , 1984, Developmental biology.

[8]  P. O’Farrell,et al.  Spatial programming of gene expression in early Drosophila embryogenesis. , 1986, Annual review of cell biology.

[9]  R. Lehmann,et al.  A gap gene, hunchback, regulates the spatial expression of Ultrabithorax , 1986, Cell.

[10]  A. Mahowald,et al.  tudor, a gene required for assembly of the germ plasm in Drosophila melanogaster , 1985, Cell.

[11]  Ruth Lehmann,et al.  Abdominal segmentation, pole cell formation, and embryonic polarity require the localized activity of oskar, a maternal gene in drosophila , 1986, Cell.

[12]  C. Nüsslein-Volhard,et al.  Maternal genes required for the anterior localization of bicoid activity in the embryo of Drosophila , 1987 .

[13]  H. Meinhardt,et al.  Hierarchical Inductions of Cell States: A Model for Segmentation in Drosophila , 1986, Journal of Cell Science.

[14]  Diethard Tautz,et al.  Finger protein of novel structure encoded by hunchback, a second member of the gap class of Drosophila segmentation genes , 1987, Nature.

[15]  C. Nüsslein-Volhard,et al.  Mutations affecting segment number and polarity in Drosophila , 1980, Nature.

[16]  J. Lengyel,et al.  The zygotic mutant tailless affects the anterior and posterior ectodermal regions of the Drosophila embryo. , 1986, Developmental biology.

[17]  P. Lawrence,et al.  Parasegments and compartments in the Drosophila embryo , 1985, Nature.

[18]  S. Carroll,et al.  Maternal control of Drosophila segmentation gene expression , 1986, Nature.

[19]  C Cremer,et al.  A fate map for the larval epidermis of Drosophila melanogaster: localized cuticle defects following irradiation of the blastoderm with an ultraviolet laser microbeam. , 1979, Developmental biology.

[20]  R. Lehmann,et al.  Cross-regulatory interactions among the gap genes of Drosophila , 1986, Nature.

[21]  E. Wieschaus,et al.  Dominant maternal-effect mutations of Drosophila melanogaster causing the production of double-abdomen embryos. , 1986, Genetics.

[22]  E. Lewis A gene complex controlling segmentation in Drosophila , 1978, Nature.

[23]  E Seifert,et al.  Analysis of Krüppel protein distribution during early Drosophila development reveals posttranscriptional regulation , 1987, Cell.