Haas C A, DeGennaro L J
Department of Neurochemistry, Max Planck Institute for Psychiatry, Martinsried, Federal Republic of Germany.
J Cell Biol. 1988 Jan;106(1):195-203. doi: 10.1083/jcb.106.1.195.
Synapsin I is a neuron-specific protein consisting of two isoforms Ia and Ib. It is thought to play a role in the regulation of neurotransmitter release. In this study the structure and expression of two classes of synapsin I mRNA have been examined. The two mRNA classes have molecular sizes of 3.4 and 4.5 kb, respectively. Both classes translate into synapsin I polypeptides and display a high degree of base sequence homology. Utilizing an oligonucleotide-directed RNase H assay we have shown that both mRNA classes have a common start site of transcription and differ from one another toward their 3' ends. The expression of the two synapsin I mRNA classes is differentially regulated during the development of the rat brain and cerebellum. In the cerebellum the 4.5-kb transcript is expressed until postnatal day 7, after which it decreases to an undetectable level. The 3.4-kb mRNA is found throughout cerebellar development and in the adult. This suggests that the 3.4-kb mRNA class consists of messages which can encode both synapsin I polypeptides. Using quantitative Northern blot analysis a peak in the expression of this mRNA was observed at postnatal day 20. The maximum expression of the 3.4-kb class coincides with the period of synaptogenesis in the cerebellum. In addition to the developmental time course of synapsin mRNA expression a description of its spatial distribution throughout the cerebellum was performed using in situ hybridization histochemistry. From postnatal day 15 onwards, with a maximum at postnatal day 20, synapsin mRNA was localized in the internal granule cell layer of the cerebellum. On a cellular level, the granule cells, but not the neighboring Purkinje cells, express high levels of synapsin mRNA. These observations implicate developmentally coordinated differential RNA splicing in the regulation of neuron-specific gene expression and substantiate the correlation of synapsin gene expression with the period of synaptogenic differentiation of neurons.
突触素I是一种神经元特异性蛋白,由两种亚型Ia和Ib组成。它被认为在神经递质释放的调节中起作用。在本研究中,对两类突触素I mRNA的结构和表达进行了检测。这两类mRNA的分子大小分别为3.4 kb和4.5 kb。两类mRNA均翻译成突触素I多肽,并显示出高度的碱基序列同源性。利用寡核苷酸定向RNase H分析,我们发现两类mRNA都有一个共同的转录起始位点,并且在其3'末端彼此不同。两类突触素I mRNA的表达在大鼠脑和小脑发育过程中受到不同的调节。在小脑中,4.5 kb的转录本在出生后第7天之前表达,之后降至无法检测的水平。3.4 kb的mRNA在整个小脑发育过程以及成年期都能检测到。这表明3.4 kb的mRNA类别包含能够编码突触素I多肽的信息。使用定量Northern印迹分析,在出生后第20天观察到该mRNA表达的峰值。3.4 kb类别的最大表达与小脑中突触形成的时期一致。除了突触素mRNA表达的发育时间进程外,还使用原位杂交组织化学对其在整个小脑中的空间分布进行了描述。从出生后第15天开始,在出生后第20天达到最大值,突触素mRNA定位于小脑的内颗粒细胞层。在细胞水平上,颗粒细胞而非相邻的浦肯野细胞表达高水平的突触素mRNA。这些观察结果表明,在神经元特异性基因表达的调节中存在发育协调的差异RNA剪接,并证实了突触素基因表达与神经元突触发生分化时期的相关性。