Literature DB >> 17383627

Notch signaling links interactions between the C/EBP homolog slow border cells and the GILZ homolog bunched during cell migration.

Benjamin Levine1, Michelle Jean-Francois, Fabio Bernardi, Giuseppe Gargiulo, Leonard Dobens.   

Abstract

In the follicle cell (FC) epithelium that surrounds the Drosophila egg, a complex set of cell signals specifies two cell fates that pattern the eggshell: the anterior centripetal FC that produce the operculum and the posterior columnar FC that produce the main body eggshell structure. We have previously shown that the long-range morphogen DPP represses the expression of the bunched (bun) gene in the anterior-most centripetal FC. bun, which encodes a homolog of vertebrate TSC-22/GILZ, in turn represses anterior gene expression and antagonizes Notch signaling to restrict centripetal FC fates in posterior cells. From a screen for novel targets of bun repression we have identified the C/EBP homolog slow border cells (slbo). At stage 10A, slbo expression overlaps bun in anterior FC; by stage 10B they repress each other's expression to establish a sharp slbo/bun expression boundary. The precise position of the slbo/bun expression boundary is sensitive to Notch signaling, which is required for both slbo activation and bun repression. As centripetal migration proceeds from stages 10B-14, slbo represses its own expression and both slbo loss-of-function mutations and overexpression approaches reveal that slbo is required to coordinate centripetal migration with nurse cell dumping. We propose that in anterior FC exposed to a Dpp morphogen gradient, high and low levels of slbo and bun, respectively, are established by modulation of Notch signaling to direct threshold cell fates. Interactions among Notch, slbo and bun resemble a conserved signaling cassette that regulates mammalian adipocyte differentiation.

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Year:  2007        PMID: 17383627     DOI: 10.1016/j.ydbio.2007.02.013

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  7 in total

Review 1.  Drosophila follicle cells: morphogenesis in an eggshell.

Authors:  Xiaodong Wu; Pradeep Singh Tanwar; Laurel A Raftery
Journal:  Semin Cell Dev Biol       Date:  2008-01-20       Impact factor: 7.727

2.  The Drosophila homolog of human tumor suppressor TSC-22 promotes cellular growth, proliferation, and survival.

Authors:  Xiaodong Wu; Megumu Yamada-Mabuchi; Erick J Morris; Pradeep Singh Tanwar; Leonard Dobens; Silvia Gluderer; Sabina Khan; Jing Cao; Hugo Stocker; Ernst Hafen; Nick J Dyson; Laurel A Raftery
Journal:  Proc Natl Acad Sci U S A       Date:  2008-03-28       Impact factor: 11.205

3.  Notch Signaling during Oogenesis in Drosophila melanogaster.

Authors:  Jingxia Xu; Thomas Gridley
Journal:  Genet Res Int       Date:  2012-05-03

Review 4.  Post-Developmental Roles of Notch Signaling in the Nervous System.

Authors:  Jose L Salazar; Sheng-An Yang; Shinya Yamamoto
Journal:  Biomolecules       Date:  2020-07-01

5.  Characterisation of the fibroblast growth factor dependent transcriptome in early development.

Authors:  Peter A Branney; Laura Faas; Sarah E Steane; Mary Elizabeth Pownall; Harry V Isaacs
Journal:  PLoS One       Date:  2009-03-31       Impact factor: 3.240

6.  Transcriptome analysis of the painted lady butterfly, Vanessa cardui during wing color pattern development.

Authors:  Heidi Connahs; Turk Rhen; Rebecca B Simmons
Journal:  BMC Genomics       Date:  2016-03-31       Impact factor: 3.969

7.  GAGA Regulates Border Cell Migration in Drosophila.

Authors:  Anna A Ogienko; Lyubov A Yarinich; Elena V Fedorova; Natalya V Dorogova; Sergey I Bayborodin; Elina M Baricheva; Alexey V Pindyurin
Journal:  Int J Mol Sci       Date:  2020-10-10       Impact factor: 5.923

  7 in total

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