Structure of two genes at the gooseberry locus related to the paired gene and their spatial expression during Drosophila embryogenesis.

The gooseberry (gsb) locus contains two closely linked genes, BSH9 and BSH4, which are structurally related to each other and to the paired (prd) gene. Sequence analysis of genomic DNA and cDNA shows that BSH9 and BSH4 can encode proteins of 427 and 452 amino acids, respectively. The structural homology between these two putative proteins and the prd protein consists essentially of two domains forming most of the amino-terminal halves of the proteins: the prd domain of 128 amino acids and a prd-type homeo domain of 60 amino acids, which is extended by 18 amino acids at its amino-terminal end. The temporal profiles of BSH9 and BSH4 transcripts, as characterized by Northern analysis, show a peak shortly after the peak of prd transcripts. The spatial distributions of BSH9 and BSH4 transcripts have been analyzed by in situ hybridization to whole-mount and sectioned embryos. BSH9 transcripts appear in the posterior ventrolateral part of each primordial segment throughout the embryo, including head and tail segments. Transcripts are initially restricted to the ectoderm, in which they arise as two spatially shifted and temporally delayed waves exhibiting double-segment periodicity and anteroposterior polarity. During germ-band extension, BSH9 is induced in the mesoderm in register with the ectoderm and neurectoderm and in the tail segments A9-A11. In contrast, BSH4 transcripts appear with a single-segment repeat, first, in the neurectoderm during germ-band extension and, later, in single neurons during neuronal differentiation. BSH9, BSH4, and prd are activated in cells that are in register along the anteroposterior axis of the embryo in the posterior parts of primordial segments comprising the posterior compartments of engrailed expression.

[1]  A. Garcı́a-Bellido Genetic control of wing disc development in Drosophila. , 2008, Ciba Foundation symposium.

[2]  N. Patel,et al.  Characterization and cloning of fasciclin III: A glycoprotein expressed on a subset of neurons and axon pathways in Drosophila , 1987, Cell.

[3]  M. Bastiani,et al.  Expression of fasciclin I and II glycoproteins on subsets of axon pathways during neuronal development in the grasshopper , 1987, Cell.

[4]  K. G. Coleman,et al.  The invected gene of Drosophila: sequence analysis and expression studies reveal a close kinship to the engrailed gene. , 1987, Genes & development.

[5]  M. Frasch,et al.  Characterization and localization of the even‐skipped protein of Drosophila. , 1987, The EMBO journal.

[6]  M. Noll,et al.  Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila , 1986, Cell.

[7]  M. Noll,et al.  Structure of the segmentation gene paired and the Drosophila PRD gene set as part of a gene network , 1986, Cell.

[8]  P. Ingham,et al.  Isolation, structure, and expression of even-skipped: A second pair-rule gene of Drosophila containing a homeo box , 1986, Cell.

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

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

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

[13]  M. Levine,et al.  Cross-regulatory interactions among pair-rule genes in Drosophila. , 1986, Science.

[14]  N. Perrimon,et al.  Developmental analysis of the torso-like phenotype in Drosophila produced by a maternal-effect locus. , 1986, Developmental Biology.

[15]  M. Noll,et al.  Isolation of the paired gene of Drosophila and its spatial expression during early embryogenesis , 1986, Nature.

[16]  S. Carroll,et al.  Zygotically active genes that affect the spatial expression of the fushi tarazu segmentation gene during early Drosophila embryogenesis , 1986, Cell.

[17]  P. Ingham,et al.  Regulatory interactions between the segmentation genes fushi tarazu, hairy, and engrailed in the Drosophila blastoderm , 1986, Cell.

[18]  M. Levine,et al.  Homeotic gene expression in Drosophila , 1985, Trends in Neurosciences.

[19]  T. Kornberg,et al.  Patterns of engrailed and fushi tarazu transcripts reveal novel intermediate stages in Drosophila segmentation , 1985, Nature.

[20]  Walter J. Gehring,et al.  Control elements of the Drosophila segmentation gene fushi tarazu , 1985, Cell.

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

[22]  S. Carroll,et al.  Localization of the fushi tarazu protein during Drosophila embryogenesis , 1985, Cell.

[23]  P. O’Farrell,et al.  Development of embryonic pattern in D. melanogaster as revealed by accumulation of the nuclear engrailed protein , 1985, Cell.

[24]  P. Lawrence,et al.  Expression of engrailed in the parasegment of Drosophila , 1985, Nature.

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

[26]  L. Kauvar,et al.  The engrailed locus of drosophila: Structural analysis of an embryonic transcript , 1985, Cell.

[27]  P. O’Farrell,et al.  The engrailed locus of drosophila: In situ localization of transcripts reveals compartment-specific expression , 1985, Cell.

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

[29]  S. Henikoff Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing. , 1984, Gene.

[30]  A. Poustka,et al.  Lambda replacement vectors carrying polylinker sequences. , 1983, Journal of molecular biology.

[31]  J. Sedat,et al.  Localization of antigenic determinants in whole Drosophila embryos. , 1983, Developmental biology.

[32]  B. Alberts,et al.  Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis. , 1983, Journal of cell science.

[33]  E. Hafen,et al.  An improved in situ hybridization method for the detection of cellular RNAs in Drosophila tissue sections and its application for localizing transcripts of the homeotic Antennapedia gene complex , 1983, The EMBO journal.

[34]  P. Lawrence,et al.  Further studies of the engrailed phenotype in Drosophila. , 1982, The EMBO journal.

[35]  T. Kornberg Compartments in the abdomen of Drosophila and the role of the engrailed locus. , 1981, Developmental biology.

[36]  G. Struhl A blastoderm fate map of compartments and segments of the Drosophila head. , 1981, Developmental biology.

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

[38]  F. Sanger,et al.  DNA sequencing with chain-terminating inhibitors. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[39]  H. Boedtker,et al.  RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination. , 1977, Biochemistry.

[40]  P. Lawrence,et al.  Control of compartment development by the engrailed gene in Drosophila , 1975, Nature.

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

[42]  W. McGinnis,et al.  Isolation of a homoeo box-containing gene from the engrailed region of Drosophila and the spatial distribution of its transcripts , 1985, Nature.

[43]  P. H. Son,et al.  Kilo-sequencing: creation of an ordered nest of asymmetric deletions across a large target sequence carried on phage M13. , 1983, Methods in enzymology.

[44]  F. Turner,et al.  Scanning electron microscopy of Drosophila melanogaster embryogenesis. III. Formation of the head and caudal segments. , 1979, Developmental biology.