The Drosophila body plan is composed of a linear array of cephalic, thoracic, and abdominal segments along the anterior posterior axis. The number and positions of individual segments are established by a transcriptional network comprised of maternal effect, gap, pair-rule, and segment polarity genes. The sloppy-paired (slp) locus contains two genes (slp1 and slp2) that are expressed in overlapping striped patterns in the presumptive thorax and abdomen. Previous studies suggest that these genes function at the pair-rule and segment polarity levels to establish the spacing and polarity of thoracic and abdominal segments. One of these genes (slp1) is also expressed in a broad anterior domain that appears before the striped patterns. There are severe cephalic defects in slp1 mutants, including the complete loss of the mandibular segment, but the molecular roles played by Slp1 in anterior patterning are not clear. Here, we present evidence that the anterior Slp1 domain acts as a gradient to differentially repress the anteriormost stripes of several different pair-rule genes. This repressive gradient contributes to the precise spatial arrangement of anterior pair-rule stripe borders required for expression of the first engrailed stripe and the formation of the mandibular segment. These results suggest that Slp1 functions as a gap gene-like repressor, in addition to its roles at the pair-rule and segment polarity levels of the hierarchy. The Slp1 protein contains a protein motif (EH1) which mediates binding to the transcriptional corepressor Groucho (Gro). We show that this domain is required for Slp1-mediated repression in vivo.
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http://dx.doi.org/10.1016/j.ydbio.2004.09.025 | DOI Listing |
Establishing the anterior-posterior body axis is a fundamental process during embryogenesis, and the fruit fly, , provides one of the best-known case studies of this process. In Drosophila, localized mRNA of serves as anterior determinant (AD). Bicoid engages in a concentration-dependent competition with nucleosomes and initiates symmetry-breaking along the AP axis by promoting chromatin accessibility at the loci of transcription factor (TF) genes that are expressed in the anterior of the embryo.
View Article and Find Full Text PDFCurr Opin Insect Sci
December 2024
Department of Entomology, University of Maryland, 4291 Fieldhouse Drive, College Park, MD 20742, USA. Electronic address:
The division of the insect embryo into repeated units - segments - is a fundamental feature of the body plan. The genes controlling this process in Drosophila melanogaster were identified in genetic screens and characterized in that species in numerous studies in the 1980s and 1990s. These genes form a well-established hierarchy and have been leveraged to examine gene regulation, transcriptional machinery, chromatin structure, and more.
View Article and Find Full Text PDFSci Adv
November 2024
Department of Entomology, University of Maryland, 4291 Fieldhouse Dr., College Park, MD 20742, USA.
Morphological features of organismal body plans are often highly conserved within large taxa. For example, segmentation is a shared and defining feature of all insects. Screens in identified genes responsible for the development of body segments, including the "pair-rule" genes (PRGs), which subdivide embryos into double-segment units in a previously unexpected pre-patterning step.
View Article and Find Full Text PDFDev Biol
January 2025
University of Lisbon, IST, Dep. of Physics, Nonlinear Dynamics Group, Av. Rovisco Pais, 1049-001, Lisbon, Portugal. Electronic address:
We modelled and calibrated the distributions of the seven-stripe patterns of Even-skipped (Eve) and Fushi-tarazu (Ftz) pair-rule proteins along the anteroposterior axis of the Drosphila embryo, established during early development. We have identified the putative repressive combinations for five Eve enhancers, and we have explored the relationship between Eve and Ftz for complementary patterns. The regulators of Eve and Ftz are stripe-specific DNA enhancers with embryo position-dependent activation rates and are regulated by the gap family of proteins.
View Article and Find Full Text PDFJ Bioinform Comput Biol
June 2024
Mathematics Department, British Columbia Institute of Technology, 3700 Willingdon Ave., Burnaby, B.C. V5G 3H2, Canada.
Recent computational modeling of early fruit fly () development has characterized the degree to which gene regulation networks can be robust to natural variability. In the first few hours of development, broad spatial gradients of maternally derived transcription factors activate embryonic gap genes. These gap patterns determine the subsequent segmented insect body plan through pair-rule gene expression.
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