ALS基因的结构与调控

Guck T. Ooi , Fredric J. Cohen , Susan Hsieh , Donald Seto , Matthew M. Rechler , Yves R. Boisclair
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引用次数: 3

摘要

小鼠ALS基因长度至少为6kb。它含有2个外显子,编码一个与人类和大鼠ALS高度同源的蛋白质。通过荧光原位杂交将其定位在小鼠17号染色体上。5 '侧区缺少TATA盒,但包含可能被Sp1等转录因子识别的GC盒。大鼠肝肌萎缩侧索硬化酶mRNA在垂体切除术后下降,并通过重组人生长激素全身治疗恢复。在瞬时转染实验中,生长激素在大鼠肝癌细胞系中刺激ALS启动子活性,但在3T3-F442A小鼠前脂肪细胞成纤维细胞中没有,这表明ALS启动子的利用是细胞类型特异性的。大鼠肝癌系统是研究ALS基因表达调控和CH调控信号通路的一个有前景的系统。
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Structure and regulation of the ALS gene

The mouse ALS gene spans at least 6 kb. It contains 2 exons which encode a protein highly homologous to human and rat ALS. It was localized to mouse chromosome 17 by fluorescent in situ hybridization. The 5′ flanking region lacks a TATA box but contains GC boxes that may be recognised by transcription factors such as Sp1. Hepatic ALS mRNA is decreased in rats following hypophysectomy, and restored by systemic treatment with recombinant human GH. In transient transfection assays, GH stimulated ALS promoter activity in a rat hepatoma cell line, but not in 3T3-F442A mouse preadipocyte fibroblasts, suggesting that utilisation of the ALS promoter is cell-type specific. The rat hepatoma system is a promising system to study the regulation of ALS gene expression, and the signalling pathways of CH regulation.

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Author index Contents Subject word index Editorial Board Biochemical and mitogenic properties of the heparin-binding growth factor HARP
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