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小鼠神经粘蛋白基因的结构与染色体定位

Structure and chromosomal localization of the mouse neurocan gene.

作者信息

Rauch U, Grimpe B, Kulbe G, Arnold-Ammer I, Beier D R, Fässler R

机构信息

Max-Planck-Institut für Biochemie, Martinsried, Germany.

出版信息

Genomics. 1995 Aug 10;28(3):405-10. doi: 10.1006/geno.1995.1168.

Abstract

Cosmid clones containing the mouse neurocan gene were isolated from a genomic library using rat neurocan cDNA fragments as probe. The murine gene has a size of approximately 25 kb and contains the coding sequence for the mRNA on 15 exons. The exon-intron structure reflected the structural organization of neurocan, which is a multidomain protein belonging to the aggrecan/versican proteoglycan family. All introns between conserved modular protein domains are phase I introns. Primer extension experiments indicate a transcriptional start point 28 bases downstream of a consensus TATA sequence. Further analysis of 1 kb of 5' flanking sequence revealed in addition to AP1, AP2, and SP1 consensus binding sites multiple E-box elements and a glucocorticoid responsive element. Single-strand conformation polymorphism was used to map neurocan to chromosome 8 between the microsatellite markers D8Mit29 and D8Mit78. Among mouse mutants that have been mapped around this region are the three allelic neurological diseases tottering, leaner, and rolling. The multidomain structure and the preferential expression of neurocan in the brain suggest a potential involvement in these diseases.

摘要

使用大鼠神经粘蛋白cDNA片段作为探针,从基因组文库中分离出含有小鼠神经粘蛋白基因的黏粒克隆。该小鼠基因大小约为25 kb,其编码序列分布在15个外显子上。外显子-内含子结构反映了神经粘蛋白的结构组织,神经粘蛋白是一种属于聚集蛋白聚糖/多功能蛋白聚糖蛋白聚糖家族的多结构域蛋白。保守模块蛋白结构域之间的所有内含子均为I型内含子。引物延伸实验表明转录起始点位于共有TATA序列下游28个碱基处。对1 kb的5'侧翼序列进行进一步分析发现,除了AP1、AP2和SP1共有结合位点外,还有多个E盒元件和一个糖皮质激素反应元件。利用单链构象多态性将神经粘蛋白定位到8号染色体上微卫星标记D8Mit29和D8Mit78之间。在已定位到该区域附近的小鼠突变体中,有三种等位基因神经疾病,即蹒跚症、消瘦症和翻滚症。神经粘蛋白的多结构域结构及其在大脑中的优先表达表明它可能与这些疾病有关。

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