Shayan A J, Brodin L, Ottersen O P, Birinyi A, Hill C E, Govind C K, Atwood H L, Shupliakov O
Department of Physiology, Faculty of Medicine, Medical Science Building, University of Toronto, 1, King's College Circle, Toronto, ON, Canada M5S 1A8.
J Neurogenet. 2000 Sep;14(3):165-92. doi: 10.3109/01677060009083481.
The sluggish-A (slgA) gene of Drosophila melanogaster has been shown to encode for the enzyme proline oxidase, a mitochondrial enzyme which catalyzes the first step in the conversion of L-proline to L-glutamate. The slgA transcript is expressed in both larval and adult Drosophila melanogaster. Mutations in this gene lead to reduced proline oxidase activity and an elevation of free proline levels. Adult mutant flies show a striking reduction of motor activity. Since proline oxidase may contribute to the supply of the neurotransmitter glutamate in the nervous system, a reduction in proline oxidase activity could reduce neural glutamate pools and affect synaptic transmission in neurons utilizing glutamate as a transmitter, including peripheral motor neurons. We tested the hypothesis that glutamate, and synaptic transmission mediated by glutamate, are reduced at synapses of glutamatergic motor neurons in slgA mutants. Levels of glutamate and proline in different cell compartments, and functional properties of synaptic transmission were compared in slgA and control specimens. Proline is elevated in muscle cells of slgA mutants, indicating that the slgA gene regulates tissue proline levels. In nerve terminal varicosities, proline levels were low in both mutants and controls. Glutamate levels in nerve terminal varicosities of slgA mutants and controls were similar. In addition, we found that glutamatergic synaptic transmission at individual nerve endings and at the whole-cell level was similar in slgA mutants and controls. Thus, proline oxidase does not play a major role in generating neuronal glutamate pools at the Drosophila larval neuromuscular junction, and larval neuromuscular performance is not altered significantly in slgA mutants. Metabolic pathways other than that involving proline oxidase are able to sustain glutamatergic synaptic function in Drosophila larvae.
黑腹果蝇的迟缓-A(slgA)基因已被证明编码脯氨酸氧化酶,这是一种线粒体酶,催化L-脯氨酸转化为L-谷氨酸的第一步。slgA转录本在黑腹果蝇的幼虫和成虫中均有表达。该基因的突变导致脯氨酸氧化酶活性降低和游离脯氨酸水平升高。成年突变果蝇的运动活性显著降低。由于脯氨酸氧化酶可能有助于神经系统中神经递质谷氨酸的供应,脯氨酸氧化酶活性的降低可能会减少神经谷氨酸池,并影响利用谷氨酸作为递质的神经元中的突触传递,包括外周运动神经元。我们测试了这样一个假设,即slgA突变体中谷氨酸能运动神经元突触处的谷氨酸以及由谷氨酸介导的突触传递会减少。比较了slgA和对照样本中不同细胞区室的谷氨酸和脯氨酸水平以及突触传递的功能特性。slgA突变体的肌肉细胞中脯氨酸升高,表明slgA基因调节组织脯氨酸水平。在神经末梢膨体中,突变体和对照中的脯氨酸水平都很低。slgA突变体和对照的神经末梢膨体中的谷氨酸水平相似。此外,我们发现slgA突变体和对照在单个神经末梢和全细胞水平上的谷氨酸能突触传递相似。因此,脯氨酸氧化酶在果蝇幼虫神经肌肉接头处产生神经元谷氨酸池方面不起主要作用,并且slgA突变体中幼虫神经肌肉性能没有明显改变。除了涉及脯氨酸氧化酶的代谢途径外,其他代谢途径能够维持果蝇幼虫的谷氨酸能突触功能。