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成年及发育中大鼠大脑中Kv3.1钾通道基因的mRNA表达

Expression of the mRNAs for the Kv3.1 potassium channel gene in the adult and developing rat brain.

作者信息

Perney T M, Marshall J, Martin K A, Hockfield S, Kaczmarek L K

机构信息

Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

J Neurophysiol. 1992 Sep;68(3):756-66. doi: 10.1152/jn.1992.68.3.756.

Abstract
  1. The gene for a mammalian Shaw K+ channel has recently been cloned and has been shown, by alternative splicing, to give rise to two different transcripts, Kv3.1 alpha and Kv3.1 beta. To determine whether these channels are associated with specific types of neurons and to determine whether or not the alternately spliced K+ channel variants are differentially expressed, we used ribonuclease (RNase) protection assays and in situ hybridization histochemistry to localize the specific subsets of neurons containing Kv3.1 alpha and Kv3.1 beta mRNAs in the adult and developing rat brain. 2. In situ hybridization histochemistry revealed a heterogeneous expression pattern of Kv3.1 alpha mRNA in the adult rat brain. Highest Kv3.1 alpha mRNA levels were expressed in the cerebellum. High levels of hybridization were also detected in the globus pallidus, subthalamus, and substantia nigra reticulata. Many thalamic nuclei, but in particular the reticular thalamic nucleus, hybridized well to Kv3.1 alpha-specific probes. A subpopulation of cells in the cortex and hippocampus, which by their distribution and number may represent interneurons, were also found to contain high levels of Kv3.1 alpha mRNA. In the brain stem, many nuclei, including the inferior colliculus and the cochlear and vestibular nuclei, also express Kv3.1 alpha mRNA. Low or undetectable levels of Kv3.1 alpha mRNA were found in the caudate-putamen, olfactory tubercle, amygdala, and hypothalamus. 3. Kv3.1 beta mRNA was also detected in the adult rat brain by both RNase protection assays and by in situ hybridization experiments. Although the beta splice variant is expressed at lower levels than the alpha species, the overall expression pattern for both mRNAs is similar, indicating that both splice variants co-expressed in the same neurons. 4. The expression of Kv3.1 alpha and Kv3.1 beta transcripts was examined throughout development. Kv3.1 alpha mRNA is detected as early as embryonic day 17 and then increases gradually until approximately postnatal day 10, when there is a large increase in the amount of Kv3.1 alpha mRNA. Interestingly, the expression of Kv3.1 beta mRNA only increases gradually during the developmental time frame examined. Densitometric measurements indicated that Kv3.1 alpha is the predominant splice variant found in neurons of the adult brain, whereas Kv3.1 beta appears to be the predominant species in embryonic and perinatal neurons. 5. Most of the neurons that express the Kv3.1 transcripts have been characterized electrophysiologically to have narrow action potentials and display high-frequency firing rates with little or no spike adaptation.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 哺乳动物肖氏钾离子通道基因最近已被克隆,并且通过可变剪接产生了两种不同的转录本,即Kv3.1α和Kv3.1β。为了确定这些通道是否与特定类型的神经元相关联,以及确定可变剪接的钾离子通道变体是否存在差异表达,我们使用核糖核酸酶(RNase)保护分析和原位杂交组织化学来定位成年和发育中大鼠脑中含有Kv3.1α和Kv3.1β mRNA的特定神经元亚群。2. 原位杂交组织化学显示成年大鼠脑中Kv3.1α mRNA的表达模式具有异质性。小脑表达的Kv3.1α mRNA水平最高。在苍白球、丘脑底核和黑质网状部也检测到高水平的杂交信号。许多丘脑核团,特别是丘脑网状核,与Kv3.1α特异性探针杂交良好。皮层和海马中的一群细胞,根据其分布和数量可能代表中间神经元,也被发现含有高水平的Kv3.1α mRNA。在脑干中,许多核团,包括下丘以及耳蜗核和前庭核,也表达Kv3.1α mRNA。在尾状核 - 壳核、嗅结节、杏仁核和下丘脑中发现Kv3.1α mRNA水平较低或检测不到。3. 通过RNase保护分析和原位杂交实验在成年大鼠脑中也检测到了Kv3.1β mRNA。尽管β剪接变体的表达水平低于α变体,但两种mRNA的总体表达模式相似,表明两种剪接变体在同一神经元中共表达。4. 在整个发育过程中检查了Kv3.1α和Kv3.1β转录本的表达。早在胚胎第17天就检测到Kv3.1α mRNA,然后逐渐增加,直到出生后约第10天,此时Kv3.1α mRNA的量大幅增加。有趣的是,在检查的发育时间范围内,Kv3.1β mRNA的表达仅逐渐增加。密度测定表明,Kv3.1α是成年脑神经元中发现的主要剪接变体,而Kv3.1β似乎是胚胎和围产期神经元中的主要变体。5. 大多数表达Kv3.1转录本的神经元在电生理上已被表征为具有窄动作电位,并显示出高频放电率,几乎没有或没有峰适应。(摘要截短至400字)

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