首页> 美国卫生研究院文献>Molecular and Cellular Biology >The NGFI-B gene a transcriptionally inducible member of the steroid receptor gene superfamily: genomic structure and expression in rat brain after seizure induction.
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The NGFI-B gene a transcriptionally inducible member of the steroid receptor gene superfamily: genomic structure and expression in rat brain after seizure induction.

机译:NGFI-B基因是类固醇受体基因超家族的转录诱导成员:癫痫发作诱导后大鼠脑中的基因组结构和表达。

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摘要

The NGFI-B cDNA was previously isolated by virtue of its induction by nerve growth factor (NGF) in PC12 cells. It encodes a 61-kilodalton protein that has two regions of extensive homology with members of the steroid/thyroid hormone receptor gene family. The rat NGFI-B gene is approximately 7.6 kilobases long and is interrupted by six introns. Although the exon-intron structure of the gene is similar to those of several other members of the steroid/thyroid hormone receptor gene family, there is a novel splice site within the DNA-binding domain which suggests that NGFI-B constitutes yet another evolutionary digression from a postulated common ancestral receptor gene. Primer extension and S1 nuclease protection assays were used to determine the transcription initiation site, which displayed the heterogeneity typical of genes that lack a TATA box. Sequence analysis of the 5' flanking region revealed several GC boxes but no identifiable TATA box. Four potential AP1 binding sites were identified at nucleotides -49, -78, -222, and -242. Neither the serum response element nor the CArG box element, two sequences found in other growth factor-inducible genes, was detected in this region of the growth factor-inducible NGFI-B gene. Nevertheless, results of nuclear runoff experiments demonstrated that the NGFI-B gene was transcriptionally activated by nerve growth factor in PC12 cells. In vivo, a rapid, dramatic increase in NGFI-B mRNA was observed in the cerebral cortex, midbrain, and cerebellum of animals that experienced a convulsant-induced seizure.
机译:NGFI-B cDNA先前已通过神经生长因子(NGF)在PC12细胞中的诱导而被分离。它编码一个61公斤的蛋白质,与类固醇/甲状腺激素受体基因家族的成员具有两个广泛的同源性区域。大鼠NGFI-B基因长约7.6千碱基,被6个内含子打断。尽管该基因的外显子-内含子结构与类固醇/甲状腺激素受体基因家族的其他几个成员相似,但在DNA结合域中有一个新的剪接位点,这表明NGFI-B构成了另一个进化论题。来自假定的共同祖先受体基因。引物延伸和S1核酸酶保护试验用于确定转录起始位点,该位点显示了缺乏TATA框的基因的典型异质性。 5'侧翼区域的序列分析显示了几个GC盒,但是没有可识别的TATA盒。在核苷酸-49,-78,-222和-242处鉴定出四个潜在的AP1结合位点。在生长因子诱导的NGFI-B基因的这一区域中未检测到血清应答元件或CArG盒元件,这是在其他生长因子诱导的基因中发现的两个序列。尽管如此,核径流实验的结果表明,NGFI-B基因在PC12细胞中被神经生长因子转录激活。在体内,在惊厥诱导的癫痫发作的动物的大脑皮层,中脑和小脑中观察到NGFI-B mRNA的急剧增加。

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