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α2,8唾液酸转移酶基因在成年小鼠脑和视网膜中的位点限制及神经元优势表达。

Site restricted and neuron dominant expression of alpha 2,8sialyltransferase gene in the adult mouse brain and retina.

作者信息

Yamamoto A, Yamashiro S, Fukumoto S, Haraguchi M, Atsuta M, Shiku H, Furukawa K

机构信息

Department of Prosthodontology, Nagasaki University School of Dentistry, Japan.

出版信息

Glycoconj J. 1996 Jun;13(3):471-80. doi: 10.1007/BF00731480.

Abstract

Gene expression of the alpha 2,8sialyltransferase (alpha 2,8S-T) responsible for GD3 synthesis in the adult mouse brain and retina was analysed by reverse transcription-polymerase chain reaction/Southern blotting (RT-PCR/Southern) and in situ hybridization. Among various portions of the brain, high levels of 9.5 kb mRNA were observed in the retina and midbrain. Results of RT-PCR/Southern did not necessarily correlate with the enzyme activities in the individual sites. In situ hybridization analysis revealed that this gene was characteristically expressed in the inner segment of photoreceptor cells, some nuclei in the midbrain, cranial nerve nuclei in the pons-medulla, Purkinje cells in the cerebellum, pyramidal cells of the hippocampus and granular cells of the dentate gyrus. In the retina, the alpha 2,8S-T gene was broadly expressed over the layers during development, and retained high expression levels in the photoreceptor cells of adult mice consistent with high expression of GD3. Destruction of neurons in the hippocampus and dentate gyrus by injection of kainic acid and colchicine respectively resulted in the disappearance of the hybridization signal, suggesting that the alpha 2,8S-T gene was mainly expressed by neurons.

摘要

通过逆转录-聚合酶链反应/ Southern印迹法(RT-PCR / Southern)和原位杂交技术,分析了成年小鼠脑和视网膜中负责GD3合成的α2,8唾液酸转移酶(α2,8S-T)的基因表达。在脑的各个部位中,视网膜和中脑观察到高水平的9.5 kb mRNA。RT-PCR / Southern的结果不一定与各个部位的酶活性相关。原位杂交分析显示,该基因在光感受器细胞的内段、中脑的一些核、脑桥-延髓中的脑神经核、小脑的浦肯野细胞、海马的锥体细胞和齿状回的颗粒细胞中特异性表达。在视网膜中,α2,8S-T基因在发育过程中在各层广泛表达,并在成年小鼠的光感受器细胞中保持高表达水平,这与GD3的高表达一致。分别通过注射红藻氨酸和秋水仙碱破坏海马和齿状回中的神经元,导致杂交信号消失,表明α2,8S-T基因主要由神经元表达。

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