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斑马鱼fgfr1是fgf8共表达组的成员,是中脑-后脑边界处fgf8信号传导所必需的。

Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary.

作者信息

Scholpp Steffen, Groth Casper, Lohs Claudia, Lardelli Michael, Brand Michael

机构信息

Max-Planck Institute of Molecular Cell Biology and Genetics, Department of Genetics, University of Technology (TU), 01307, Dresden, Germany.

出版信息

Dev Genes Evol. 2004 Jun;214(6):285-95. doi: 10.1007/s00427-004-0409-1. Epub 2004 May 25.

Abstract

FGFR1 is an important signalling molecule during embryogenesis and in adulthood. FGFR1 mutations in human may lead to developmental defects and pathological conditions, including cancer and Alzheimer's disease. Here, we describe cloning and expression analysis of the zebrafish fibroblast growth factor receptor 1 ( fgfr1). Initially, fgfr1 is expressed in the adaxial mesoderm with transcripts distinctly localised to the anterior portion of each half-somite. Hereupon, fgfr1 is also strongly expressed in the otic vesicles, branchial arches and the brain, especially at the midbrain-hindbrain boundary (MHB). The expression patterns of fgfr1 and fgf8 are strikingly similar and knock-down of fgfr1 phenocopies many aspects observed in the fgf8 mutant acerebellar, suggesting that Fgf8 exerts its function mainly by binding to FgfR1.

摘要

FGFR1是胚胎发育过程中和成年期的重要信号分子。人类中的FGFR1突变可能导致发育缺陷和病理状况,包括癌症和阿尔茨海默病。在此,我们描述斑马鱼成纤维细胞生长因子受体1(fgfr1)的克隆和表达分析。最初,fgfr1在轴旁中胚层表达,转录本明显定位于每个半体节的前部。随后,fgfr1在耳泡、鳃弓和大脑中也强烈表达,尤其是在中脑-后脑边界(MHB)。fgfr1和fgf8的表达模式惊人地相似,敲低fgfr1会模拟在fgf8突变体小脑缺失中观察到的许多方面,表明Fgf8主要通过与FgfR1结合发挥其功能。

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