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独特的NCAM VASE外显子的表达在发育过程中在不同组织中受到独立调控。

Expression of the unique NCAM VASE exon is independently regulated in distinct tissues during development.

作者信息

Small S J, Akeson R

机构信息

Division of Basic Research, Children's Hospital Research Foundation, Cincinnati, Ohio 45229.

出版信息

J Cell Biol. 1990 Nov;111(5 Pt 1):2089-96. doi: 10.1083/jcb.111.5.2089.

Abstract

During development of the rat central nervous system, neural cell adhesion molecule (NCAM) mRNAs containing in the extracellular domain a 30-bp alternative exon, here named VASE, replace RNAs that lack this exon. The presence of this alternative exon between previously described exons 7 and 8 changes the predicted loop structure of the derived polypeptide from one resembling an immunoglobulin constant region domain to one resembling an immunoglobulin variable domain. This change could have significant effects on NCAM polypeptide function and cell-cell interaction. In this report we test multiple rat tissues for the presence of additional alternative exons at this position and also examine the regulation of splicing of the previously described exon. To sensitively examine alternative splicing, polymerase chain reactions (PCRs) with primers flanking the exon 7/exon 8 alternative splicing site were performed. Four categories of RNA samples were tested for new exons: whole brain from embryonic day 11 to adult, specific brain regions dissected from adult brain, clonal lines of neural cells in vitro, and muscle cells and tissues cultured in vitro and obtained by dissection. Within the limits of the PCR methodology, no evidence for any alternative exon other than the previously identified VASE was obtained. The regulation of expression of this exon was found to be complex and tissue specific. Expression of the 30-bp exon in the heart and nervous system was found to be regulated independently; a significant proportion of embryonic day 15 heart NCAM mRNAs contain VASE while only a very small amount of day 15 nervous system mRNAs contain VASE. Some adult central nervous system regions, notably the olfactory bulb and the peripheral nervous system structures adrenal gland and dorsal root ganglia, express NCAM which contains very little VASE. VASE is undetectable in NCAM PCR products from the olfactory epithelium. Other nervous system regions express significant quantities of NCAM both with and without VASE. Clonal cell lines in culture generally expressed very little VASE. These results indicate that a single alternative exon, VASE, is found in NCAM immunoglobulin-like loop 4 and that distinct tissues and nervous system regions regulate expression of VASE independently both during development and in adult animals.

摘要

在大鼠中枢神经系统发育过程中,神经细胞黏附分子(NCAM)的信使核糖核酸(mRNA)在细胞外结构域含有一个30个碱基对的可变外显子,此处命名为VASE,它取代了缺乏该外显子的RNA。这个可变外显子位于先前描述的外显子7和8之间,它的存在将推导多肽的预测环结构从类似于免疫球蛋白恒定区结构域的结构改变为类似于免疫球蛋白可变区结构域的结构。这种变化可能对NCAM多肽功能和细胞间相互作用产生重大影响。在本报告中,我们检测了多个大鼠组织中该位置是否存在其他可变外显子,并研究了先前描述的外显子的剪接调控。为了灵敏地检测可变剪接,我们使用位于外显子7/外显子8可变剪接位点两侧的引物进行了聚合酶链反应(PCR)。我们检测了四类RNA样本中是否存在新的外显子:从胚胎第11天到成年期的全脑、从成年大脑中分离出的特定脑区、体外培养的神经细胞克隆系以及体外培养并通过解剖获得的肌肉细胞和组织。在PCR方法的检测范围内,除了先前鉴定的VASE外,未获得任何其他可变外显子的证据。发现该外显子的表达调控是复杂且具有组织特异性的。发现心脏和神经系统中30个碱基对外显子的表达是独立调控的;胚胎第15天心脏的NCAM mRNA中有很大一部分含有VASE,而第15天神经系统的mRNA中只有极少量含有VASE。一些成年中枢神经系统区域,特别是嗅球以及外周神经系统结构肾上腺和背根神经节,表达的NCAM含有很少的VASE。在嗅上皮的NCAM PCR产物中未检测到VASE。其他神经系统区域表达大量含有和不含有VASE的NCAM。培养中的克隆细胞系通常表达很少的VASE。这些结果表明,在NCAM免疫球蛋白样环4中发现了一个单一的可变外显子VASE,并且不同的组织和神经系统区域在发育过程中和成年动物中都独立地调控VASE的表达。

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