首页> 美国卫生研究院文献>The Journal of Neuroscience >Identification of a New Exon in the Myelin Proteolipid Protein Gene Encoding Novel Protein Isoforms That Are Restricted to the Somata of Oligodendrocytes and Neurons
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Identification of a New Exon in the Myelin Proteolipid Protein Gene Encoding Novel Protein Isoforms That Are Restricted to the Somata of Oligodendrocytes and Neurons

机译:髓鞘蛋白脂蛋白基因编码的新蛋白同工型限制到少突胶质细胞和神经元的气孔的新外显子的鉴定。

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摘要

The myelin proteolipid protein (PLP) gene (i.e., the PLP/DM20 gene) has been of some interest because of its role in certain human demyelinating diseases, such as Pelizaeus-Merzbacher disease. A substantial amount of evidence, including neuronal pathology in knock-out and transgenic animals, suggests the gene also has functions unrelated to myelin structure, but the products of the gene responsible for these putative functions have not yet been identified. Here we report the identification of a new exon of the PLP/DM20 gene and at least two new products of the gene that contain this exon. The new exon, located between exons 1 and 2, is spliced into PLP and DM20 mRNAs creating a new translation initiation site that generates PLP and DM20 proteins with a 12 amino acid leader sequence. This leader sequence appears to target these proteins to a different cellular compartment within the cell bodies of oligodendrocytes and away from the myelin membranes. Furthermore, these new products are also expressed in a number of neuronal populations within the postnatal mouse brain, including the cerebellum, hippocampus, and olfactory system. We term these products somal-restricted PLP and DM20 proteins to distinguish them from the classic PLP and DM20 proteolipids. They represent putative candidates for some of the nonmyelin-related functions of the PLP/DM20 gene.
机译:髓磷脂蛋白脂蛋白(PLP)基因(即,PLP / DM20基因)因其在某些人类脱髓鞘疾病例如Pelizaeus-Merzbacher病中的作用而受到关注。大量证据,包括基因敲除动物和转基因动物的神经元病理,表明该基因还具有与髓磷脂结构无关的功能,但尚未鉴定出负责这些假定功能的基因产物。在这里,我们报告了P​​LP / DM20基因新外显子的鉴定以及该基因至少有两个新产物。位于第1外显子和第2外显子之间的新外显子被剪接成PLP和DM20 mRNA,从而创建了一个新的翻译起始位点,该位点产生了具有12个氨基酸前导序列的PLP和DM20蛋白。该前导序列似乎将这些蛋白质靶向少突胶质细胞的细胞体内的不同细胞区室,并远离髓磷脂膜。此外,这些新产品还在产后小鼠大脑内的许多神经元群体中表达,包括小脑,海马和嗅觉系统。我们称这些产品为受体细胞限制的PLP和DM20蛋白,以区别于经典的PLP和DM20蛋白脂。它们代表了PLP / DM20基因的一些非髓鞘相关功能的假定候选对象。

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