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大鼠促肾上腺皮质激素释放激素基因。

The rat corticotropin-releasing hormone gene.

作者信息

Thompson R C, Seasholtz A F, Douglass J O, Herbert E

机构信息

Vollum Institute for Advanced Biomedical Research, Oregon Health Sciences University, Portland 97201.

出版信息

Ann N Y Acad Sci. 1987;512:1-11. doi: 10.1111/j.1749-6632.1987.tb24947.x.

Abstract

In this paper we have described the isolation and characterization of the rat corticotropin releasing hormone gene. Nucleotide sequence comparisons with the human CRH gene have demonstrated several interesting regions of homology and suggest that the gene was highly conserved through evolution. Additionally we have demonstrated the tissue-specific expression of the rat CRH gene. The regional distribution of expression parallels previously documented immunocytochemical demonstrations and supports the hypothesis that CRH peptides have multiple roles in different tissues. In the peripheral tissues that express CRH mRNA it will be very interesting to document the specific cell type of synthesis by using combined immunocytochemical and in situ histochemical techniques. Additionally we have described initial studies using gene transfer techniques to examine the cAMP responsiveness of the rat CRH gene. We are presently constructing other fusion genes (CRHCAT plasmids) in order to more carefully localize the DNA sequence in the rat CRH gene which mediates this effect, and compare it to the previously reported cAMP-responsive "consensus sequence." Similarly, we also plan to utilize the CRHCAT constructs to examine regulation of the rat CRH gene by glucocorticoids and several other hormone-mediated regulatory pathways. Through these CAT fusion studies we hope to gain a better understanding of the role of certain conserved sequences in the 5' flanking DNA for transcriptional control of the rat (and human) CRH genes.

摘要

在本文中,我们描述了大鼠促肾上腺皮质激素释放激素基因的分离和特性。与人类CRH基因的核苷酸序列比较显示了几个有趣的同源区域,并表明该基因在进化过程中高度保守。此外,我们还证明了大鼠CRH基因的组织特异性表达。表达的区域分布与先前记录的免疫细胞化学结果相似,并支持CRH肽在不同组织中具有多种作用的假说。在表达CRH mRNA的外周组织中,使用免疫细胞化学和原位组织化学相结合的技术来确定合成的特定细胞类型将非常有趣。此外,我们还描述了使用基因转移技术来检测大鼠CRH基因对cAMP反应性的初步研究。我们目前正在构建其他融合基因(CRHCAT质粒),以便更精确地定位大鼠CRH基因中介导这种效应的DNA序列,并将其与先前报道的cAMP反应性“共有序列”进行比较。同样,我们还计划利用CRHCAT构建体来研究糖皮质激素和其他几种激素介导的调节途径对大鼠CRH基因的调控。通过这些CAT融合研究,我们希望更好地理解5'侧翼DNA中某些保守序列在大鼠(和人类)CRH基因转录控制中的作用。

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