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首页> 外文期刊>Thyroid: official journal of the American Thyroid Association >A GC box in the human sodium iodide symporter gene promoter is essential for full activity.
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A GC box in the human sodium iodide symporter gene promoter is essential for full activity.

机译:人碘化钠同向转运蛋白基因启动子中的GC盒对于充分发挥活性至关重要。

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摘要

We previously reported that the human sodium iodide symporter (hNIS) 5'-flanking region between -603 and -415 is essential for full expression. In this study, we further localized sequences within this region required for the basal expression of the hNIS promoter and identified a functional GC box. Activity of the hNIS promoter was assessed by transient transfection of luciferase reporter gene constructs with progressive 5' deletions into the human papillary thyroid cancer cell line BHP 2-7. Deletion from -603 to -535 enhanced promoter activity, further deletion to -469 decreased promoter activity, and deletion to -415 nearly abolished promoter activity. The DNA sequence within this critical 55 bp region from -469 to -415 contains a GC box. Introduction of mutations into the GC box of the deletion constructs -603, -535 and -469 decreased promoter activity in both thyroid cells (BHP 2-7 and rat thyroid cell FRTL-5) and nonthyroid cells (human prostate cancer cell LNCaP-2 and human breast cancer cell MCF-7). The magnitude of reduction for the -603 mutation construct was significantly greater than that for the -469 mutation construct in thyroid cells compared to non-thyroid cells. In vitro transcription using nuclear extracts isolated from HeLa cells was reduced from DNA templates with the GC box mutation and nearly abolished from templates with 5' deletion to -415. Identification of proteins interacting with the GC box was performed by gel retardation assays with or without Sp1 specific antibodies. Sp1 and an "Sp1-like" protein bound to the wild-type GC box sequence but not to the GC box mutant. In summary, the GC box is a positive regulatory element in the hNIS basal promoter.
机译:先前我们曾报道过-603和-415之间的人类碘化钠同向转运蛋白(hNIS)5'侧翼区对于完整表达至关重要。在这项研究中,我们进一步定位了hNIS启动子基础表达所需的该区域内的序列,并鉴定了功能性GC框。通过将具有进行性5'缺失的萤光素酶报道基因基因构建体瞬时转染到人乳头状甲状腺癌细胞系BHP 2-7中来评估hNIS启动子的活性。 -603至-535的缺失增强了启动子活性,进一步缺失至-469降低了启动子活性,而缺失至-415则几乎消除了启动子活性。从-469到-415的55 bp关键区域内的DNA序列包含一个GC盒。在缺失构建体-603,-535和-469的GC盒中引入突变会降低甲状腺细胞(BHP 2-7和大鼠甲状腺细胞FRTL-5)和非甲状腺细胞(人前列腺癌细胞LNCaP-2)中的启动子活性和人类乳腺癌细胞MCF-7)。与非甲状腺细胞相比,甲状腺细胞中-603突变构建体的还原幅度明显大于-469突变构建体的还原幅度。使用从HeLa细胞中分离出的核提取物进行的体外转录,从具有GC盒突变的DNA模板中减少,并从具有5'缺失的模板中消除到-415。与凝胶盒相互作用的蛋白质的鉴定是通过使用或不使用Sp1特异性抗体的凝胶阻滞测定法进行的。 Sp1和“ Sp1样”蛋白与野生型GC box序列结合,但不与GC box突变体结合。总之,GC盒是hNIS基础启动子中的阳性调控元件。

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