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斑马鱼中枢神经系统髓磷脂的36K蛋白是一种短链脱氢酶。

The 36K protein of zebrafish CNS myelin is a short-chain dehydrogenase.

作者信息

Morris Jacqueline K, Willard Belinda B, Yin Xinghua, Jeserich Gunnar, Kinter Michael, Trapp Bruce D

机构信息

Department of Neurosciences, Cleveland Clinic Foundation, Lerner Research Institute, Cleveland, Ohio 44195, USA.

出版信息

Glia. 2004 Mar;45(4):378-91. doi: 10.1002/glia.10338.

Abstract

Previous studies identified homologues to mammalian myelin genes expressed in the teleost central nervous system (CNS), including myelin basic protein (MBP), protein zero (P0), and a member of the proteolipid protein family, DM20. In addition, an uncharacterized 36-kDa (36K) protein is a major component of teleost myelin, but is not a major component of myelin in other species. In the present study, we sought to better understand myelin proteins and myelination in one teleost, zebrafish, by molecular characterization of the zebrafish 36K protein. Purified zebrafish CNS myelin was isolated and the amino acid sequences of peptides present in the 36-kDa band were determined by mass spectrometry. These sequences matched a previously uncharacterized EST in The Institute for Genome Research (TIGR) zebrafish database that is related to the short-chain dehydrogenase/reductase (SDR) protein family. In vitro expression of the zebrafish 36K cDNA in Neuro 2a cells resulted in a protein product that was recognized by a 36K polyclonal antibody. The zebrafish 36K mRNA and protein expression patterns were determined and correlated to other known myelin gene expression profiles. In addition, we determined by in situ hybridization that a human 36K homologue (FLJ13639) is expressed in oligodendrocytes and neurons in the adult human cortex. This study identified a major myelin protein in zebrafish, 36K, as a member of the SDR superfamily; an expression pattern similar to other myelin genes was demonstrated.

摘要

以往的研究在硬骨鱼的中枢神经系统(CNS)中鉴定出了与哺乳动物髓鞘基因同源的基因,包括髓鞘碱性蛋白(MBP)、零蛋白(P0)以及蛋白脂蛋白家族的一个成员DM20。此外,一种未鉴定的36 kDa(36K)蛋白是硬骨鱼髓鞘的主要成分,但在其他物种的髓鞘中并非主要成分。在本研究中,我们试图通过对斑马鱼36K蛋白进行分子特征分析,更好地了解一种硬骨鱼——斑马鱼的髓鞘蛋白和髓鞘形成过程。分离出纯化的斑马鱼中枢神经系统髓鞘,通过质谱法测定36 kDa条带中存在的肽段的氨基酸序列。这些序列与基因组研究所(TIGR)斑马鱼数据库中一个先前未鉴定的EST匹配,该EST与短链脱氢酶/还原酶(SDR)蛋白家族相关。斑马鱼36K cDNA在Neuro 2a细胞中的体外表达产生了一种能被36K多克隆抗体识别的蛋白产物。确定了斑马鱼36K mRNA和蛋白的表达模式,并将其与其他已知的髓鞘基因表达谱相关联。此外,我们通过原位杂交确定,人类36K同源物(FLJ13639)在成人皮质的少突胶质细胞和神经元中表达。本研究鉴定出斑马鱼中的一种主要髓鞘蛋白36K属于SDR超家族;证明了其与其他髓鞘基因相似的表达模式。

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