A Drosophila Genome-Wide Screen Identifies Regulators of Steroid Hormone Production and Developmental Timing

被引:67
作者
Danielsen, E. Thomas [1 ]
Moeller, Morten E. [1 ]
Yamanaka, Naoki [2 ,7 ]
Ou, Qiuxiang [3 ]
Laursen, Janne M. [4 ]
Soenderholm, Caecilie [1 ]
Zhuo, Ran [3 ]
Phelps, Brian [3 ]
Tang, Kevin [3 ]
Zeng, Jie [3 ]
Kondo, Shu [5 ]
Nielsen, Christian H. [6 ]
Harvald, Eva B. [6 ]
Faergeman, Nils J. [6 ]
Haley, Macy J. [7 ]
O'Connor, Kyle A. [7 ]
King-Jones, Kirst [3 ]
O'Connor, Michael B. [7 ]
Rewitz, Kim F. [1 ]
机构
[1] Univ Copenhagen, Dept Biol, DK-2100 Copenhagen, Denmark
[2] Univ Calif Riverside, Dept Entomol, Riverside, CA 92521 USA
[3] Univ Alberta, Dept Biol Sci, Edmonton, AB T6G 2E9, Canada
[4] Tech Univ Denmark, DTU Syst Biol, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[5] Res Org Informat & Syst, Genet Strains Res Ctr, Natl Inst Genet, Mishima, Shizuoka 4118540, Japan
[6] Univ Southern Denmark, Dept Biochem & Mol Biol, Villum Ctr Bioanalyt Sci, DK-5230 Odense, Denmark
[7] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
关键词
ECDYSTEROID BIOSYNTHESIS; LIPID TRAFFICKING; PROTHORACIC GLAND; TRANSGENIC RNAI; PROSTATE-CANCER; CELL-GROWTH; CHOLESTEROL; AUTOPHAGY; RECEPTOR; ECDYSONE;
D O I
10.1016/j.devcel.2016.05.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Steroid hormones control important developmental processes and are linked to many diseases. To systematically identify genes and pathways required for steroid production, we performed a Drosophila genome-wide in vivo RNAi screen and identified 1,906 genes with potential roles in steroidogenesis and developmental timing. Here, we use our screen as a resource to identify mechanisms regulating intracellular levels of cholesterol, a substrate for steroidogenesis. We identify a conserved fatty acid elongase that underlies a mechanism that adjusts cholesterol trafficking and steroidogenesis with nutrition and developmental programs. In addition, we demonstrate the existence of an autophagosomal cholesterol mobilization mechanism and show that activation of this system rescues Niemann-Pick type C1 deficiency that causes a disorder characterized by cholesterol accumulation. These cholesterol-trafficking mechanisms are regulated by TOR and feedback signaling that couples steroidogenesis with growth and ensures proper maturation timing. These results reveal genes regulating steroidogenesis during development that likely modulate disease mechanisms.
引用
收藏
页码:558 / 570
页数:13
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