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小鼠瘙痒病反应基因1(Scrg1):基因组结构、与Sap30的物理连锁、在8号染色体上的基因定位以及在神经元原代细胞培养中的表达

Mouse scrapie responsive gene 1 (Scrg1): genomic organization, physical linkage to sap30, genetic mapping on chromosome 8, and expression in neuronal primary cell cultures.

作者信息

Dron M, Tartare X, Guillo F, Haik S, Barbin G, Maury C, Tovey M, Dandoy-Dron F

机构信息

Laboratory of Viral Oncology, CNRS UPR 9045, Villejuif Cedex, 94801, France.

出版信息

Genomics. 2000 Nov 15;70(1):140-9. doi: 10.1006/geno.2000.6358.

DOI:10.1006/geno.2000.6358
PMID:11087671
Abstract

We have previously reported a transcript of a novel mouse gene (Scrg1) with increased expression in transmissible spongiform encephalopathies and the cloning of the human mRNA analogue. In this paper, we present the genomic organization of the mouse and human SCRG1 loci, which exhibit a high degree of conservation. The genes are composed of three exons; the two downstream exons contain the protein coding region. The mouse gene is expressed in brain tissue essentially as a 0.7-kb message but also as a minor 2.6-kb mRNA. We have sequenced 20 kb of DNA at the mouse Scrg1 locus and found that the longer transcript is the prolongation of the 0.7-kb mRNA to a polyadenylation site located about 2 kb further downstream. Sequencing revealed that the mouse Scrg1 gene is physically linked to Sap30, a gene that encodes a protein of the histone deacetylase complex, and genetic linkage mapping assigned the localization of Scrg1 to chromosome 8 between Ant1 and Hmg2. Northern blot analysis showed that Scrg1 is under strict developmental control in mouse embryo and is expressed by cells of neuronal origin in vitro. Comparison of the rat, mouse, and human SCRG1 proteins identified a box of 35 identical contiguous amino acids and a characteristic cysteine distribution pattern defining a new protein signature.

摘要

我们之前报道过一种新的小鼠基因(Scrg1)的转录本,其在传染性海绵状脑病中表达增加,并且克隆了人类mRNA类似物。在本文中,我们展示了小鼠和人类SCRG1基因座的基因组结构,它们表现出高度的保守性。这些基因由三个外显子组成;下游的两个外显子包含蛋白质编码区。小鼠基因在脑组织中主要以0.7kb的信使RNA形式表达,但也有少量2.6kb的mRNA。我们对小鼠Scrg1基因座的20kb DNA进行了测序,发现较长的转录本是0.7kb mRNA延伸至下游约2kb处的一个聚腺苷酸化位点。测序显示,小鼠Scrg1基因与Sap30在物理上相连,Sap30是一个编码组蛋白去乙酰化酶复合体中一种蛋白质的基因,遗传连锁图谱将Scrg1定位到8号染色体上Ant1和Hmg2之间。Northern印迹分析表明,Scrg1在小鼠胚胎中受到严格的发育调控,并且在体外由神经源性细胞表达。对大鼠、小鼠和人类SCRG1蛋白的比较鉴定出一个由35个连续相同氨基酸组成的区域以及一种特征性的半胱氨酸分布模式,定义了一种新的蛋白质特征。

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