Bunched sets a boundary for Notch signaling to pattern anterior eggshell structures during Drosophila oogenesis

被引:38
作者
Dobens, L
Jaeger, A
Peterson, JS
Raftery, LA
机构
[1] Massachusetts Gen Hosp, Cutaneous Biol Res Ctr, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[3] Univ Missouri, Sch Biol Sci, Div Biochem & Mol Biol, Kansas City, MO 64110 USA
关键词
Drosophila oogenesis; Notch signaling; TSC-22/DIP/BUN family;
D O I
10.1016/j.ydbio.2005.09.019
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organized boundaries between different cell fates are critical in patterning and organogenesis. In some tissues, long-range signals position a boundary, and local Notch signaling maintains it. How Notch activity is restricted to boundary regions is not well understood. During Drosophila oogenesis, the long-range signals EGF and Dpp regulate expression of bunched (bun), which encodes a homolog of mammalian transcription factors TSC-22 and GILZ. Here, we show that bun establishes a boundary for Notch signaling in the follicle cell epithelium. Notch signaling is active in anterior follicle cells and is required for concurrent follicle cell reorganizations including centripetal migration and operculum formation. bun is required in posterior columnar follicle cells to repress the centripetal migration fate, including gene expression, cell shape changes and accumulation of cytoskeletal components. bun mutant clones adjacent to the centripetally migrating follicle cells showed ectopic Notch responses. bun is necessary, but not sufficient, to down-regulate Serrate protein levels throughout the follicular epithelium. These data indicate that Notch signaling is necessary, but not sufficient, for centripetal migration and that bun regulates the level of Notch stimulation to position the boundary between centripetally migrating and stationary columnar follicle cells. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:425 / 437
页数:13
相关论文
共 102 条
[1]   A role for extra macrochaetae downstream of Notch in follicle cell differentiation [J].
Adam, JC ;
Montell, DJ .
DEVELOPMENT, 2004, 131 (23) :5971-5980
[2]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[3]   NOTCH SIGNALING [J].
ARTAVANISTSAKONAS, S ;
MATSUNO, K ;
FORTINI, ME .
SCIENCE, 1995, 268 (5208) :225-232
[4]   Modulation of T-cell activation by the glucocorticoid-induced leucine zipper factor via inhibition of nuclear factor κB [J].
Ayroldi, E ;
Migliorati, G ;
Bruscoli, S ;
Marchetti, C ;
Zollo, O ;
Cannarile, L ;
D'Adamio, F ;
Riccardi, C .
BLOOD, 2001, 98 (03) :743-753
[5]  
BENDER LB, 1993, GENETICS, V133, P967
[6]   Apoptosis-mediated cell death within the ovarian polar cell lineage of Drosophila melanogaster [J].
Besse, F ;
Pret, AM .
DEVELOPMENT, 2003, 130 (05) :1017-1027
[7]   Glycosyltransferase activity of fringe modulates notch-delta interactions [J].
Brückner, K ;
Perez, L ;
Clausen, H ;
Cohen, S .
NATURE, 2000, 406 (6794) :411-415
[8]   Frizzled regulation of Notch signalling polarizes cell fate in the Drosophila eye [J].
Cooper, MTD ;
Bray, SJ .
NATURE, 1999, 397 (6719) :526-530
[9]  
Crowe R, 1998, DEVELOPMENT, V125, P767
[10]   A new dexamethasone-induced gene of the leucine zipper family protects T lymphocytes from TCR/CD3-activated cell death [J].
D'Adamio, F ;
Zollo, O ;
Moraca, R ;
Ayroldi, E ;
Bruscoli, S ;
Bartoli, A ;
Cannarile, L ;
Migliorati, G ;
Riccardi, C .
IMMUNITY, 1997, 7 (06) :803-812