Literature DB >> 11245576

Establishment and maintenance of parasegmental compartments.

S C Hughes1, H M Krause.   

Abstract

Embryos of higher metazoans are divided into repeating units early in development. In Drosophila, the earliest segmental units to form are the parasegments. Parasegments are initially defined by alternating stripes of expression of the fushi-tarazu and even-skipped genes. How fushi-tarazu and even-skipped define the parasegment boundaries, and how parasegments are lost when fushi-tarazu or even-skipped fail to function correctly, have never been fully or properly explained. Here we show that parasegment widths are defined early by the relative levels of fushi-tarazu and even-skipped at stripe junctions. Changing these levels results in alternating wide and narrow parasegments. When shifted by 30% or more, the enlarged parasegments remain enlarged and the reduced parasegments are lost. Loss of the reduced parasegments occurs in three steps; delamination of cells from the epithelial layer, apoptosis of the delaminated cells and finally apoptosis of inappropriate cells remaining at the surface. The establishment and maintenance of vertebrate metameres may be governed by similar processes and properties.

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Year:  2001        PMID: 11245576     DOI: 10.1242/dev.128.7.1109

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


  16 in total

1.  Drawing lines in the sand: even skipped et al. and parasegment boundaries.

Authors:  James B Jaynes; Miki Fujioka
Journal:  Dev Biol       Date:  2004-05-15       Impact factor: 3.582

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.  Conservation and variation in pair-rule gene expression and function in the intermediate-germ beetle Dermestes maculatus.

Authors:  Jie Xiang; Katie Reding; Alison Heffer; Leslie Pick
Journal:  Development       Date:  2017-10-30       Impact factor: 6.868

4.  Sip1, the Drosophila orthologue of EBP50/NHERF1, functions with the sterile 20 family kinase Slik to regulate Moesin activity.

Authors:  Sarah C Hughes; Etienne Formstecher; Richard G Fehon
Journal:  J Cell Sci       Date:  2010-03-09       Impact factor: 5.285

5.  Mis-specified cells die by an active gene-directed process, and inhibition of this death results in cell fate transformation in Drosophila.

Authors:  Christian Werz; Tom V Lee; Peter L Lee; Melinda Lackey; Clare Bolduc; David S Stein; Andreas Bergmann
Journal:  Development       Date:  2005-11-09       Impact factor: 6.868

6.  Natural variation of the expression pattern of the segmentation gene even-skipped in melanogaster.

Authors:  Pengyao Jiang; Michael Z Ludwig; Martin Kreitman; John Reinitz
Journal:  Dev Biol       Date:  2015-06-27       Impact factor: 3.582

7.  How to make stripes: deciphering the transition from non-periodic to periodic patterns in Drosophila segmentation.

Authors:  Mark D Schroeder; Christina Greer; Ulrike Gaul
Journal:  Development       Date:  2011-07       Impact factor: 6.868

8.  A screen for genes that interact with the Drosophila pair-rule segmentation gene fushi tarazu.

Authors:  Mark W Kankel; Dianne M Duncan; Ian Duncan
Journal:  Genetics       Date:  2004-09       Impact factor: 4.562

9.  Stripy Ftz target genes are coordinately regulated by Ftz-F1.

Authors:  Hui Ying Hou; Alison Heffer; W Ray Anderson; Jingnan Liu; Timothy Bowler; Leslie Pick
Journal:  Dev Biol       Date:  2009-08-11       Impact factor: 3.582

10.  The repressor activity of Even-skipped is highly conserved, and is sufficient to activate engrailed and to regulate both the spacing and stability of parasegment boundaries.

Authors:  Miki Fujioka; Galina L Yusibova; Nipam H Patel; Susan J Brown; James B Jaynes
Journal:  Development       Date:  2002-10       Impact factor: 6.868

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