Reference Report

Reference
Citation	Huang, X., Suyama, K., Buchanan, J.A., Zhu, A.J., Scott, M.P. (2005). A Drosophila model of the Niemann-Pick type C lysosome storage disease: dnpc1a is required for molting and sterol homeostasis. Development 132(22): 5115--5124. (Export to RIS)
FlyBase ID	FBrf0190297
Publication Type	Research paper
PubMed ID	16221727
PubMed Abstract	Niemann-Pick type C (NPC) disease is a fatal autosomal-recessive neurodegenerative disorder characterized by the inappropriate accumulation of unesterified cholesterol in aberrant organelles. The disease is due to mutations in either of two genes, NPC1, which encodes a transmembrane protein related to the Hedgehog receptor Patched, and NPC2, which encodes a secreted cholesterol-binding protein. Npc1 mutant mice can be partially rescued by treatment with specific steroids. We have created a Drosophila NPC model by mutating dnpc1a, one of two Drosophila genes related to mammalian NPC1. Cells throughout the bodies of dnpc1a mutants accumulated sterol in a punctate pattern, as in individuals with NPC1 mutations. The mutants developed only to the first larval stage and were unable to molt. Molting after the normal first instar period was restored to various degrees by feeding the mutants the steroid molting hormone 20-hydroxyecdysone, or the precursors of ecdysone biosynthesis, cholesterol and 7-dehydrocholesterol. dnpc1a is normally highly expressed in the ecdysone-producing ring gland. Ring gland-specific expression of dnpc1a in otherwise mutant flies allowed development to adulthood, suggesting that the lack of ecdysone in the mutants is the cause of death. We propose that dnpc1a mutants have sterols trapped in aberrant organelles, leading to a shortage of sterol in the endoplasmic reticulum and/or mitochondria of ring gland cells, and, consequently, inadequate ecdysone synthesis.
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Language of Publication	English
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Publication Type	Journal
Abbreviation	Development
Title	Development
Publication Year	1987-
ISBN/ISSN	0950-1991
Data from Reference
Alleles (14)
	Npc1a¹ Npc1a² Npc1a^dsRNA.cHa Npc1a^{Scer\UAS.T:Avic\GFP-EYFP} Scer\GAL4^2-286 Scer\GAL4^48Y Scer\GAL4^69B Scer\GAL4^Aug21 Scer\GAL4^elav-C155 Scer\GAL4^Feb36 Scer\GAL4^Mhc.PW Scer\GAL4^tub.PU T:Avic\GFP^EYFP w^+mC
Constructs (4)
	P{GAL4-Mhc.W} P{tub-GAL4.U} P{UAS-NPC1.dsRNA} P{UAS-NPC1.YFP}
Genes (5)
	Npc1a Npc1b Prosα6 Scer\GAL4 w
Insertions (7)
	P{GawB}2-286 P{GawB}48Y P{GawB}69B P{GawB}Aug21 P{GawB}elav^C155 P{GawB}Feb36 P{SUPor-P}KG05670
Natural transposons (1)
	P-element