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小鼠威斯科特-奥尔德里奇综合征蛋白(WASP)家族成员Wave1/Scar的特性及表达分析

Characterization and expression analyses of the mouse Wiskott-Aldrich syndrome protein (WASP) family member Wave1/Scar.

作者信息

Benachenhou Nadia, Massy Isabelle, Vacher Jean

机构信息

Institut de Recherches Cliniques de Montréal, Faculté de Médecine de l'Université de Montréal, 110 Pine avenue West, Room 5690, Montréal, Québec H2W 1R7, Canada.

出版信息

Gene. 2002 May 15;290(1-2):131-40. doi: 10.1016/s0378-1119(02)00560-7.

Abstract

Characterization of multiprotein complexes involved in actin remodeling and cytoskeleton reorganization is essential to understand the basic mechanisms of cell motility and migration. To identify proteins implicated in these processes, we have isolated the mouse Wave1/Scar gene, a member of the Wiskott-Aldrich syndrome protein (WASP) family. The mouse Wave1 gene was physically localized on chromosome 10 and spans over 12 Kb comprising eight exons and seven introns. The mouse Wave1 complementary DNA encodes a predicted 559 amino acid protein, with a SCAR homology domain, a basic domain, a proline-rich region, a WASP homology domain and an acidic domain conserved in the orthologous proteins. The Wave1 transcription initiation site was mapped 210 base pairs upstream of the ATG translational start site. The presumptive proximal promoter contains putative consensus binding sites for E2 basic helix-loop-helix transcription factors, hepatocyte nuclear factor-3beta, S8 homeodomain protein, zinc finger transcription factor MZF-1, and an interferon-stimulated response element. Northern analysis demonstrated a strong expression of a unique approximately 2.6 Kb Wave1 transcript in brain tissue, and in situ hybridization showed restricted expression to Purkinje cells from the cerebellum and pyramidal cells from the hippocampus. Characterization and expression analyses of the murine Wave1 gene provide the basis toward functional studies in mouse models of the role of Wave1 in neuronal cytoskeleton organization.

摘要

对参与肌动蛋白重塑和细胞骨架重组的多蛋白复合物进行表征,对于理解细胞运动和迁移的基本机制至关重要。为了鉴定与这些过程相关的蛋白质,我们分离了小鼠Wave1/Scar基因,它是威斯科特-奥尔德里奇综合征蛋白(WASP)家族的成员。小鼠Wave1基因物理定位于10号染色体上,跨度超过12 kb,包含8个外显子和7个内含子。小鼠Wave1互补DNA编码一个预测的559个氨基酸的蛋白质,具有一个SCAR同源结构域、一个碱性结构域、一个富含脯氨酸的区域、一个WASP同源结构域和一个在直系同源蛋白中保守的酸性结构域。Wave1转录起始位点定位于ATG翻译起始位点上游210个碱基对处。推测的近端启动子包含E2碱性螺旋-环-螺旋转录因子、肝细胞核因子-3β、S8同源结构域蛋白、锌指转录因子MZF-1和干扰素刺激反应元件的假定共有结合位点。Northern分析表明,在脑组织中强烈表达一种独特的约2.6 kb的Wave1转录本,原位杂交显示其表达局限于小脑的浦肯野细胞和海马的锥体细胞。对小鼠Wave1基因的表征和表达分析为在小鼠模型中研究Wave1在神经元细胞骨架组织中的作用的功能研究提供了基础。

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