Literature DB >> 9367430

Integration of the head and trunk segmentation systems controls cephalic furrow formation in Drosophila.

A Vincent1, J T Blankenship, E Wieschaus.   

Abstract

Genetic and molecular analyses of patterning of the Drosophila embryo have shown that the process of segmentation of the head is fundamentally different from the process of segmentation of the trunk. The cephalic furrow (CF), one of the first morphological manifestations of the patterning process, forms at the juxtaposition of these two patterning systems. We report here that the initial step in CF formation is a change in shape and apical positioning of a single row of cells. The anteroposterior position of these initiator cells may be defined by the overlapping expression of the head gap gene buttonhead (btd) and the primary pair-rule gene even-skipped (eve). Re-examination of the btd and eve phenotypes in live embryos indicated that both genes are required for CF formation. Further, Eve expression in initiator cells was found to be dependent upon btd activity. The control of eve expression by btd in these cells is the first indication of a new level of integrated regulation that interfaces the head and trunk segmentation systems. In conjunction with previous data on the btd and eve embryonic phenotypes, our results suggest that interaction between these two genes both controls initiation of a specific morphogenetic movement that separates two morphogenetic fields and contributes to patterning the hinge region that demarcates the procephalon from the segmented germ band.

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Year:  1997        PMID: 9367430     DOI: 10.1242/dev.124.19.3747

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  19 in total

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Journal:  Eur Phys J E Soft Matter       Date:  2010-09-29       Impact factor: 1.890

2.  Characterization of the Drosophila segment determination morphome.

Authors:  Svetlana Surkova; David Kosman; Konstantin Kozlov; Ekaterina Myasnikova; Anastasia A Samsonova; Alexander Spirov; Carlos E Vanario-Alonso; Maria Samsonova; John Reinitz
Journal:  Dev Biol       Date:  2007-11-04       Impact factor: 3.582

3.  Cell shape changes indicate a role for extrinsic tensile forces in Drosophila germ-band extension.

Authors:  Lucy C Butler; Guy B Blanchard; Alexandre J Kabla; Nicola J Lawrence; David P Welchman; L Mahadevan; Richard J Adams; Benedicte Sanson
Journal:  Nat Cell Biol       Date:  2009-06-07       Impact factor: 28.824

4.  Maternal origins of developmental reproducibility.

Authors:  Mariela D Petkova; Shawn C Little; Feng Liu; Thomas Gregor
Journal:  Curr Biol       Date:  2014-05-22       Impact factor: 10.834

Review 5.  From morphogen to morphogenesis and back.

Authors:  Darren Gilmour; Martina Rembold; Maria Leptin
Journal:  Nature       Date:  2017-01-18       Impact factor: 49.962

6.  A model of epithelial invagination driven by collective mechanics of identical cells.

Authors:  Ana Hočevar Brezavšček; Matteo Rauzi; Maria Leptin; Primož Ziherl
Journal:  Biophys J       Date:  2012-09-05       Impact factor: 4.033

7.  Dynamic interpretation of maternal inputs by the Drosophila segmentation gene network.

Authors:  Feng Liu; Alexander H Morrison; Thomas Gregor
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-11       Impact factor: 11.205

8.  Transcriptional Timers Regulating Mitosis in Early Drosophila Embryos.

Authors:  Amir Momen-Roknabadi; Stefano Di Talia; Eric Wieschaus
Journal:  Cell Rep       Date:  2016-09-13       Impact factor: 9.423

9.  Mitotic cell rounding accelerates epithelial invagination.

Authors:  Takefumi Kondo; Shigeo Hayashi
Journal:  Nature       Date:  2013-01-13       Impact factor: 49.962

Review 10.  Setting up for gastrulation: D. melanogaster.

Authors:  Angelike Stathopoulos; Susan Newcomb
Journal:  Curr Top Dev Biol       Date:  2019-12-12       Impact factor: 4.897

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