首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Modulation of tyrosine hydroxylase gene expression in the central nervous system visualized by in situ hybridization.
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Modulation of tyrosine hydroxylase gene expression in the central nervous system visualized by in situ hybridization.

机译:通过原位杂交观察中枢神经系统中酪氨酸羟化酶基因表达的调节。

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摘要

A rat tyrosine hydroxylase [TyrOHase; tyrosine 3-monooxygenase; L-tyrosine, tetrahydropteridine:oxygen oxidoreductase (3-hydroxylating); EC 1.14.16.2] cDNA probe was used for in situ hybridization studies on histological sections through the locus coeruleus, substantia nigra, and the ventral tegmental area of the rat brain. Experimental conditions were established that yielded no background and no signal when pBR322 was used as a control probe. Using the tyrosine hydroxylase probe, we ascertained the specificity of the labeling over catecholaminergic cells by denervation experiments and comparison of the hybridization pattern with that of immunoreactivity. The use of 35S-labeled probe enabled the hybridization signal to be resolved at the cellular level. A single injection of reserpine into the rat led to an increase of the intensity of the autoradiographic signal over the locus coeruleus area, confirming an RNA gel blot analysis. The potential of in situ hybridization to analyze patterns of modulation of gene activity as a result of nervous activity is discussed.
机译:大鼠酪氨酸羟化酶[TyrOHase;酪氨酸3-单加氧酶; L-酪氨酸,四氢吡啶:氧氧化还原酶(3-羟基化); EC 1.14.16.2] cDNA探针用于通过大鼠蓝斑,黑质和大鼠腹侧被盖区的组织学切片进行原位杂交研究。建立了将pBR322用作对照探针时无背景且无信号的实验条件。使用酪氨酸羟化酶探针,我们通过去神经实验以及杂交模式与免疫反应性的比较,确定了对儿茶酚胺能细胞的标记特异性。使用35S标记的探针能够在细胞水平上分辨杂交信号。向大鼠单次注射利血平可导致在蓝斑区域的放射自显影信号强度增加,从而证实了RNA凝胶印迹分析。讨论了原位杂交分析神经活动导致基因活性调节模式的潜力。

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