scholarly journals Ectopic expression of human p53 inhibits entry into S phase and induces apoptosis in the Drosophila eye imaginal disc

Oncogene ◽  
1999 ◽  
Vol 18 (48) ◽  
pp. 6767-6775 ◽  
Author(s):  
Masamitsu Yamaguchi ◽  
Fumiko Hirose ◽  
Yoshihiro H Inoue ◽  
Michina Shiraki ◽  
Yuko Hayashi ◽  
...  
Chromosoma ◽  
2001 ◽  
Vol 110 (5) ◽  
pp. 313-321 ◽  
Author(s):  
Masamitsu Yamaguchi ◽  
Hideki Yoshida ◽  
Fumiko Hirose ◽  
Yoshihiro H. Inoue ◽  
Yuko Hayashi ◽  
...  

Development ◽  
1995 ◽  
Vol 121 (10) ◽  
pp. 3371-3379 ◽  
Author(s):  
H. Richardson ◽  
L.V. O'Keefe ◽  
T. Marty ◽  
R. Saint

During animal development, cell proliferation is controlled in many cases by regulation of the G1 to S phase transition. Studies of mammalian tissue culture cells have shown that the G1-specific cyclin, cyclin E, can be rate limiting for progression from G1 to S phase. During Drosophila development, down-regulation of cyclin E is required for G1 arrest in terminally differentiating embryonic epidermal cells. Whether cyclin E expression limits progression into S phase in proliferating, as opposed to differentiating, cells during development has not been investigated. Here we show that Drosophila cyclin E (DmcycE) protein is absent in G1 phase cells but appears at the onset of S phase in proliferating cells of the larval optic lobe and eye imaginal disc. We have examined cells in the eye imaginal epithelium, where a clearly defined developmentally regulated G1 to S phase transition occurs. Ectopic expression of DmcycE induces premature entry of most of these G1 cells into S phase. Thus in these cells, control of DmcycE expression is required for regulated entry into S phase. Significantly, a band of eye imaginal disc cells in G1 phase was not induced to enter S phase by ectopic expression of DmcycE. This provides evidence for additional regulatory mechanisms that operate during G1 phase to limit cell proliferation during development. These results demonstrate that the role of cyclin E in regulating progression into S phase in mammalian tissue culture cells applies to some, but not all, cells during Drosophila development.(ABSTRACT TRUNCATED AT 250 WORDS)


Author(s):  
Patrick Cafferty ◽  
Xiaojun Xie ◽  
Kristen Browne ◽  
Vanessa J. Auld

2010 ◽  
Vol 342 (1-2) ◽  
pp. 223-232 ◽  
Author(s):  
Masaru Umehara ◽  
Akira Ichikawa ◽  
Harunobu Sakamoto ◽  
Ayako Yamada ◽  
Yasuhide Yoshioka ◽  
...  

Development ◽  
1997 ◽  
Vol 124 (17) ◽  
pp. 3233-3240 ◽  
Author(s):  
D.I. Strutt ◽  
M. Mlodzik

Pattern formation in the eye imaginal disc of Drosophila occurs in a wave that moves from posterior to anterior. The anterior edge of this wave is marked by a contracted band of cells known as the morphogenetic furrow, behind which photoreceptors differentiate. The movement of the furrow is dependent upon the secretion of the signalling protein Hedgehog (Hh) by more posterior cells, and it has been suggested that Hh acts as an inductive signal to induce cells to enter a furrow fate and begin differentiation. To further define the role of Hh in this process, we have analysed clones of cells lacking the function of the smoothened (smo) gene, which is required for transduction of the Hh signal and allows the investigation of the autonomous requirement for hh signalling. These experiments demonstrate that the function of hh in furrow progression is indirect. Cells that cannot receive/transduce the Hh signal are still capable of entering a furrow fate and differentiating normally. However, hh is required to promote furrow progression and regulate its rate of movement across the disc, since the furrow is significantly delayed in smo clones.


Development ◽  
1995 ◽  
Vol 121 (11) ◽  
pp. 3519-3527 ◽  
Author(s):  
J.E. Treisman ◽  
G.M. Rubin

Differentiation of the Drosophila eye imaginal disc is an asynchronous, repetitive process which proceeds across the disc from posterior to anterior. Its propagation correlates with the expression of decapentaplegic at the front of differentiation, in the morphogenetic furrow. Both differentiation and decapentaplegic expression are maintained by Hedgehog protein secreted by the differentiated cells posterior to the furrow. However, their initiation at the posterior margin occurs prior to hedgehog expression by an unknown mechanism. We show here that the wingless gene contributes to the correct spatial localization of initiation. Initiation of the morphogenetic furrow is restricted to the posterior margin by the presence of wingless at the lateral margins; removal of wingless allows lateral initiation. Ectopic expression of wingless at the posterior margin can also inhibit normal initiation. In addition, the presence of wingless in the center of the disc can prevent furrow progression. These effects of wingless are achieved without altering the expression of decapentaplegic.


Biosystems ◽  
2018 ◽  
Vol 173 ◽  
pp. 256-265 ◽  
Author(s):  
Bradly Alicea ◽  
Thomas E. Portegys ◽  
Diana Gordon ◽  
Richard Gordon

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