Hanna Marley E, Bednářová Andrea, Rakshit Kuntol, Chaudhuri Anathbandhu, O'Donnell Janis M, Krishnan Natraj
Department of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS 39762, USA.
Department of Biochemistry, Molecular Biology, Entomology and Plant Pathology, Mississippi State University, Mississippi State, MS 39762, USA; Institute of Entomology, Biology Centre, Academy of Sciences and Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 České Budějovice, Czech Republic.
J Insect Physiol. 2015 Feb;73:11-9. doi: 10.1016/j.jinsphys.2015.01.001. Epub 2015 Jan 10.
The impact of mutations in four essential genes involved in dopamine (DA) synthesis and transport on longevity, motor behavior, and resistance to oxidative stress was monitored in Drosophila melanogaster. The fly lines used for this study were: (i) a loss of function mutation in Catecholamines up (Catsup(26)), which is a negative regulator of the rate limiting enzyme for DA synthesis, (ii) a mutant for the gene pale (ple(2)) that encodes for the rate limiting enzyme tyrosine hydroxylase (TH), (iii) a mutant for the gene Punch (Pu(Z22)) that encodes guanosine triphosphate cyclohydrolase, required for TH activity, and (iv) a mutant in the vesicular monoamine transporter (VMAT(Δ14)), which is required for packaging of DA as vesicles inside DA neurons. Median lifespans of ple(2), Pu(Z22) and VMAT(Δ14) mutants were significantly decreased compared to Catsup(26) and wild type controls that did not significantly differ between each other. Catsup(26) flies survived longer when exposed to hydrogen peroxide (80 μM) or paraquat (10mM) compared to ple(2), Pu(Z22) or VMAT(Δ14) and controls. These flies also exhibited significantly higher negative geotaxis activity compared to ple(2), Pu(Z22), VMAT(Δ14) and controls. All mutant flies demonstrated rhythmic circadian locomotor activity in general, albeit Catsup(26) and VMAT(Δ14) flies had slightly weaker rhythms. Expression analysis of some key antioxidant genes revealed that glutathione S-transferase Omega-1 (GSTO1) expression was significantly up-regulated in all DA synthesis pathway mutants and especially in Catsup(26) and VMAT(Δ14) flies at both mRNA and protein levels. Taken together, we hypothesize that DA could directly influence GSTO1 transcription and thus play a significant role in the regulation of response to oxidative stress. Additionally, perturbations in DA synthesis do not appear to have a significant impact on circadian locomotor activity rhythms per se, but do have an influence on general locomotor activity levels.
在黑腹果蝇中监测了参与多巴胺(DA)合成和转运的四个关键基因的突变对寿命、运动行为和抗氧化应激能力的影响。本研究使用的果蝇品系包括:(i)儿茶酚胺上调基因(Catsup(26))的功能缺失突变体,该基因是DA合成限速酶的负调节因子;(ii)编码限速酶酪氨酸羟化酶(TH)的基因苍白(ple(2))的突变体;(iii)编码TH活性所需的鸟苷三磷酸环化水解酶的基因打孔(Pu(Z22))的突变体;(iv)囊泡单胺转运体(VMAT(Δ14))的突变体,该转运体是DA神经元内将DA包装成囊泡所必需的。与Catsup(26)和彼此之间无显著差异的野生型对照相比,ple(2)、Pu(Z22)和VMAT(Δ14)突变体的平均寿命显著缩短。与ple(2)、Pu(Z22)、VMAT(Δ14)及对照相比,暴露于过氧化氢(80μM)或百草枯(10mM)时,Catsup(26)果蝇存活时间更长。与ple(2)、Pu(Z22)、VMAT(Δ14)及对照相比,这些果蝇还表现出显著更高的负趋地性活动。总体而言,所有突变果蝇均表现出有节律的昼夜运动活动,尽管Catsup(26)和VMAT(Δ14)果蝇的节律稍弱。一些关键抗氧化基因的表达分析表明,谷胱甘肽S-转移酶Omega-1(GSTO1)在所有DA合成途径突变体中,尤其是在Catsup(26)和VMAT(Δ14)果蝇的mRNA和蛋白质水平上均显著上调。综上所述,我们推测DA可能直接影响GSTO1转录,从而在氧化应激反应调节中发挥重要作用。此外,DA合成的扰动似乎本身对昼夜运动活动节律没有显著影响,但对一般运动活动水平有影响。