The Steroid Hormone Ecdysone Controls Systemic Growth by Repressing dMyc Function in Drosophila Fat Cells

被引:153
作者
Delanoue, Renald [1 ]
Slaidina, Maija [1 ]
Leopold, Pierre [1 ]
机构
[1] Univ Nice Sophia Antipolis, Inst Dev Biol & Canc, CNRS, F-06108 Nice, France
关键词
PROTHORACIC GLAND; EYE DEVELOPMENT; BODY-SIZE; MELANOGASTER; PATHWAY; INSULIN; MYC; METABOLISM; GENE; ENDOREPLICATION;
D O I
10.1016/j.devcel.2010.05.007
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
How steroid hormones shape animal growth remains poorly understood. In Drosophila, the main steroid hormone, ecdysone, limits systemic growth during juvenile development. Here we show that ecdysone controls animal growth rate by specifically acting on the fat body, an organ that retains endocrine and storage functions of the vertebrate liver and fat. We demonstrate that fat body-targeted loss of function of the Ecdysone receptor (EcR) increases dMyc expression and its cellular functions such as ribosome biogenesis. Moreover, changing dMyc levels in this tissue is sufficient to affect animal growth rate. Finally, the growth increase induced by silencing EcR in the fat body is suppressed by cosilencing dMyc. In conclusion, the present work reveals an unexpected function of dMyc in the systemic control of growth in response to steroid hormone signaling.
引用
收藏
页码:1012 / 1021
页数:10
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