Expression pattern and preliminary functional analysis of human CREB4 gene.

Yong-Juan Gao, Gen-Tao Cao, Gang Yin, Xin Wang, Chao-Neng Ji, Shao-Hua Gu, Xiao-Hua Ni
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Abstract

cAMP response element-binding (CREB) proteins are a family of mammalian transcription activators that mediate cAMP and calcium-dependent gene expression through the cAMP response element (CRE). CREB4 is a novel member of the human CREB family. RT-PCR showed CREB4 transcripts were found in lung carcinoma LX-1, colon adenocarcinoma CX-1, prastatic adenocarcinoma PC-3, colon carcinoma G1-112, and pancreatic adenocarcinoma G1-103. Constructing CREB4 and CREB(215-395aa) fusion protein with the entire prokaryotic LexA protein respectively disclosed that CREB4 protein functioned as a transcription activator and its N-terminal accounted for the activation ability. Furthermore,a fusion protein of GFP and full-length CREB4 was localized in cytoplasm,whereas the fusion protein of GFP and a deletion mutant lacking the C-terminal putative transmembrane domain was translocated in nucleus. Our results suggested that putative transmembrane domain of CREB4 protein was associated with modulation of its function for the transcriptional activation.

人CREB4基因表达模式及初步功能分析。
cAMP反应元件结合蛋白(CREB)是一个哺乳动物转录激活因子家族,通过cAMP反应元件(CRE)介导cAMP和钙依赖性基因的表达。CREB4是人类CREB家族的新成员。RT-PCR结果显示,在肺癌LX-1、结肠癌CX-1、前列腺癌PC-3、结肠癌G1-112、胰腺腺癌G1-103中均发现了CREB4转录物。分别与整个原核生物LexA蛋白构建CREB4和CREB(215-395aa)融合蛋白,发现CREB4蛋白具有转录激活因子的功能,其n端具有激活能力。此外,GFP与全长CREB4的融合蛋白定位在细胞质中,而GFP与缺乏c端跨膜结构域的缺失突变体的融合蛋白在细胞核中易位。我们的研究结果表明,CREB4蛋白的跨膜结构域与其转录激活功能的调节有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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