School of Biological Sciences, Monash University, Clayton, Victoria, Australia.
PLoS One. 2010 Dec 20;5(12):e14303. doi: 10.1371/journal.pone.0014303.
Copper is essential for aerobic life, but many aspects of its cellular uptake and distribution remain to be fully elucidated. A genome-wide screen for copper homeostasis genes in Drosophila melanogaster identified the SNARE gene Syntaxin 5 (Syx5) as playing an important role in copper regulation; flies heterozygous for a null mutation in Syx5 display increased tolerance to high dietary copper. The phenotype is shown here to be due to a decrease in copper accumulation, a mechanism also observed in both Drosophila and human cell lines. Studies in adult Drosophila tissue suggest that very low levels of Syx5 result in neuronal defects and lethality, and increased levels also generate neuronal defects. In contrast, mild suppression generates a phenotype typical of copper-deficiency in viable, fertile flies and is exacerbated by co-suppression of the copper uptake gene Ctr1A. Reduced copper uptake appears to be due to reduced levels at the plasma membrane of the copper uptake transporter, Ctr1. Thus Syx5 plays an essential role in copper homeostasis and is a candidate gene for copper-related disease in humans.
铜对于需氧生命是必不可少的,但铜的细胞摄取和分布的许多方面仍有待充分阐明。在黑腹果蝇中进行的全基因组筛选铜稳态基因的研究,确定了 SNARE 基因 Syntaxin 5(Syx5)在铜调节中起着重要作用;Syx5 基因杂合缺失突变的果蝇对高膳食铜的耐受性增加。这里显示的表型是由于铜积累减少所致,这一机制也在果蝇和人类细胞系中观察到。在成年果蝇组织中的研究表明,Syx5 的极低水平会导致神经元缺陷和致死,而高水平也会产生神经元缺陷。相比之下,轻度抑制会产生一种类似于在有活力、可育的果蝇中铜缺乏的表型,并且与铜摄取基因 Ctr1A 的共抑制作用加剧。铜摄取的减少似乎是由于铜摄取转运蛋白 Ctr1 的质膜水平降低所致。因此,Syx5 在铜稳态中起着至关重要的作用,是人类铜相关疾病的候选基因。