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发育中小鼠大脑中的腱生蛋白mRNA亚型。

Tenascin mRNA isoforms in the developing mouse brain.

作者信息

Dörries U, Schachner M

机构信息

Department of Neurobiology, Swiss Federal Institute of Technology, Zürich.

出版信息

J Neurosci Res. 1994 Feb 15;37(3):336-47. doi: 10.1002/jnr.490370306.

Abstract

The extracellular matrix glycoprotein tenascin is expressed in the developing mouse cerebellum as a group of four protein species of different molecular weights. The difference is most likely due to alternative splicing which is known to occur in tenascin mRNA within the region of the fibronectin type III repeats. In order to systematically analyze tenascin mRNA isoforms that would account for this heterogeneity, tenascin splice variants were isolated from mouse brain by the polymerase chain reaction (PCR). In agreement with Northern blot analysis, amplification by PCR revealed a general decrease in tenascin mRNA expression during development from embryonic and early postnatal to adult stages. This decrease was more pronounced for isoforms of high molecular weight compared to those of low molecular weight. In accord with the observations at the protein level, four splice variants were found to be predominantly expressed, containing insertions of either six, five, or one fibronectin type III repeat, or comprising no insertion. In addition, a minor splice variant with an insertion of four fibronectin type III repeats was isolated. Three of the isolated mRNA splice variants have not yet been described for mouse tenascin. Among them, an isoform containing six alternatively spliced repeats was found to include a novel fibronectin type III repeat. The sequence of this repeat displays 96.7% similarity to a corresponding type III repeat in human tenascin, revealing a strict evolutionary conservation between tenascin molecules from different species in the region of alternative splicing. Southern blot analysis of the amplified mRNA isoforms showed that the novel mouse type III repeat is confined to splice variants with an insertion of six fibronectin type III repeats. Furthermore, in situ hybridization on sections from mouse embryos indicated that tenascin-specific mRNAs containing the novel type III repeat are predominantly expressed in the central nervous system.

摘要

细胞外基质糖蛋白腱生蛋白在发育中的小鼠小脑中以一组四种不同分子量的蛋白质形式表达。这种差异很可能是由于选择性剪接造成的,已知这种剪接发生在腱生蛋白mRNA中纤连蛋白III型重复序列区域内。为了系统地分析导致这种异质性的腱生蛋白mRNA异构体,通过聚合酶链反应(PCR)从小鼠脑中分离出腱生蛋白剪接变体。与Northern印迹分析一致,PCR扩增显示从胚胎期、出生后早期到成年期发育过程中腱生蛋白mRNA表达普遍下降。与低分子量异构体相比,高分子量异构体的这种下降更为明显。与蛋白质水平的观察结果一致,发现四种剪接变体占主导表达,分别含有六个、五个或一个纤连蛋白III型重复序列的插入,或不包含插入序列。此外,还分离出一种含有四个纤连蛋白III型重复序列插入的次要剪接变体。所分离的mRNA剪接变体中有三种尚未在小鼠腱生蛋白中被描述。其中,一种含有六个选择性剪接重复序列的异构体被发现包含一个新的纤连蛋白III型重复序列。该重复序列的序列与人腱生蛋白中相应的III型重复序列显示出96.7%的相似性,揭示了不同物种的腱生蛋白分子在选择性剪接区域存在严格的进化保守性。对扩增的mRNA异构体进行Southern印迹分析表明,新的小鼠III型重复序列仅限于含有六个纤连蛋白III型重复序列插入的剪接变体。此外,对小鼠胚胎切片进行原位杂交表明,含有新型III型重复序列的腱生蛋白特异性mRNA主要在中枢神经系统中表达。

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