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CREB转录因子在中枢神经系统个体发育过程中的DNA结合活性。

DNA binding activity of CREB transcription factors during ontogeny of the central nervous system.

作者信息

Pennypacker K R, Hudson P M, Hong J S, McMillian M K

机构信息

Laboratory of Environmental Neuroscience, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Brain Res Dev Brain Res. 1995 May 26;86(1-2):242-9. doi: 10.1016/0165-3806(95)00033-a.

Abstract

During the early postnatal period, the rat brain contains high basal levels of AP-1 DNA binding activity which declines to the low levels found in the adult by the third postnatal week. Although the individual transcription factors that comprise this AP-1 DNA binding complex had not been identified, we discovered that these proteins were immunoreactive to the cAMP responsive element binding protein (CREB) and also recognized the CRE element. The 45 kDa CREB-immunoreactive protein was detected at high levels only during the first postnatal week. CRE and AP-1 DNA binding activities were studied in the olfactory bulb, striatum, hindbrain, hippocampus, hypothalamus and cerebellum. In general, the DNA binding activity correlated with the stage of maturation of the particular brain region. However, basal AP-1 DNA binding in the olfactory bulb from adults remained slightly elevated relative to other brain regions. Interestingly, the DNA binding complex in the olfactory bulb began to include fos-related antigen as well as CREB by the third postnatal week. The fra-containing complex only recognizes the AP-1 element, while the CREB complex can bind to either CRE or AP-1 sequences. Thus, there is crosstalk between the signal transduction systems that activate CREB and AP-1 transcription factors. This elevated CREB DNA binding activity may be a sensitive index for studying the development of the brain and could be involved in modulating the genomic program in differentiating cells.

摘要

在出生后的早期阶段,大鼠大脑中AP-1 DNA结合活性的基础水平很高,到出生后第三周时降至成年动物中发现的低水平。尽管构成这种AP-1 DNA结合复合物的各个转录因子尚未被鉴定出来,但我们发现这些蛋白质对环磷酸腺苷反应元件结合蛋白(CREB)具有免疫反应性,并且也能识别CRE元件。45 kDa的CREB免疫反应性蛋白仅在出生后的第一周高水平表达。对嗅球、纹状体、后脑、海马体、下丘脑和小脑中的CRE和AP-1 DNA结合活性进行了研究。一般来说,DNA结合活性与特定脑区的成熟阶段相关。然而,成年动物嗅球中的基础AP-1 DNA结合相对于其他脑区仍略有升高。有趣的是,到出生后第三周时,嗅球中的DNA结合复合物开始同时包含Fos相关抗原和CREB。含有Fos相关抗原的复合物仅识别AP-1元件,而CREB复合物既能结合CRE序列也能结合AP-1序列。因此,激活CREB和AP-1转录因子的信号转导系统之间存在相互作用。这种升高的CREB DNA结合活性可能是研究大脑发育的一个敏感指标,并且可能参与调节分化细胞中的基因组程序。

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