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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Differential expression of rat and human type I metabotropic glutamate receptor splice variant messenger RNAs.
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Differential expression of rat and human type I metabotropic glutamate receptor splice variant messenger RNAs.

机译:大鼠和人I型代谢型谷氨酸受体剪接变体信使RNA的差异表达。

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The type I metabotropic glutamate receptor (mGlu1) messenger RNA and protein are known to be widely expressed in rat brain, but knowledge of the regional expression of splice variants other than mGlu1a is limited. Probes were designed for in situ hybridization that specifically recognize each of the carboxy-terminal splice variants mGlu1a, -1b, -1c and -1d. The novel rat mGlu1d sequence was obtained by polymerase chain reaction and the predicted protein is highly homologous to the human sequence but contains both conservative and radical substitutions and is slightly longer (912 vs 908 amino acids). Each rat mGlu1 splice variant messenger RNA was found in a unique expression pattern. The messenger RNA encoding mGlu1a was abundant in cerebellar Purkinje cells and in mitral and tufted cells of the olfactory bulb. Strong expression was also detected in hippocampal interneurons, and neurons of the thalamus and substantia nigra, while moderate expression was found in colliculi and cerebellar granule cells. The mGlu1b messenger RNA was strongly expressed in Purkinje cells, hippocampal pyramidal neurons, dentate gyrus granule cells and lateral septum, and moderately expressed in striatal, superficial cortical and cerebellar granule neurons. The mGlu1d messenger RNA was expressed in all regions where mGlu1a and -1b were detected; abundant in Purkinje cells, mitral and tufted cells, and hippocampal principal neurons and interneurons, strong in thalamus and substantia nigra, and moderate in lateral septum, cortex, striatum and colliculi. Human mGlu1 splice variant expression in the cerebellum matched that found for the rat. No specific signal was found with a probe capable of hybridizing to the rat mGlu1c splice junction, although another probe designed against a more 3' sequence of mGlu1c gave strong signals in the cerebellum and hippocampus, and moderate signals in thalamus and colliculi. It is concluded that mGlu1d messenger RNA is widely expressed, that mGlu1a and -1b messenger RNAs are expressed in almost complementary patterns and that formation of the mGlu1c splice junction is a rare event.
机译:已知I型代谢型谷氨酸受体(mGlu1)信使RNA和蛋白在大鼠脑中广泛表达,但对mGlu1a以外的剪接变体的区域表达的了解有限。设计用于原位杂交的探针,可以特异性识别每个羧基末端剪接变体mGlu1a,-1b,-1c和-1d。通过聚合酶链反应获得了新的大鼠mGlu1d序列,预测的蛋白与人序列高度同源,但同时包含保守和自由基取代,并且略长(912对908个氨基酸)。发现每个大鼠mGlu1剪接变体信使RNA均具有独特的表达模式。编码mGlu1a的信使RNA在小脑浦肯野细胞以及嗅球的二尖瓣和簇状细胞中含量丰富。在海马中间神经元,丘脑和黑质神经元中也检测到强表达,而在丘脑和小脑颗粒细胞中发现中等表达。 mGlu1b信使RNA在浦肯野细胞,海马锥体神经元,齿状回颗粒细胞和外侧中隔中强烈表达,并在纹状体,浅层皮质和小脑颗粒神经元中中等表达。在检测到mGlu1a和-1b的所有区域均表达了mGlu1d信使RNA。在浦肯野细胞,二尖瓣和簇状细胞以及海马主要神经元和中间神经元中含量丰富,在丘脑和黑质中很强,在外侧中隔,皮层,纹状体和胶质中中等。小脑中的人mGlu1剪接变体表达与在大鼠中发现的相匹配。尽管能够与大鼠mGlu1c剪接点杂交的探针没有发现特异性信号,但是针对mGlu1c的3'序列设计的另一种探针在小脑和海马中发出强信号,在丘脑和结肠中发出中等信号。结论是,mGlu1d信使RNA广泛表达,mGlu1a和-1b信使RNA以几乎互补的模式表达,并且mGlu1c剪接点的形成是罕见的。

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