Keegan C E, Karolyi I J, Knapp L T, Bourbonais F J, Camper S A, Seasholtz A F
Department of Human Genetics, University of Michigan, Ann Arbor 48109-0720.
Mol Cell Neurosci. 1994 Dec;5(6):505-14. doi: 10.1006/mcne.1994.1062.
The DNA sequences important for cell-specific expression and developmental regulation of corticotropin-releasing hormone (CRH) were analyzed in transgenic mice. A construct containing 0.5 kb of CRH 5' flanking DNA linked to the chloramphenicol acetyltransferase reporter gene was expressed in many brain regions and in several ectopic peripheral sites, suggesting that this portion of the CRH gene contains basal promoter activity but lacks DNA elements necessary for appropriate tissue specificity. Cell specificity of transgene expression was examined with a CRH-beta-galactosidase reporter construct containing the same 0.5-kb CRH promoter fragment, but also including the CRH structural gene and 2 kb of CRH 3' flanking DNA. Transgene expression was observed in inappropriate regions of the brain, but no expression was detected in peripheral tissues, suggesting that these additional CRH sequences suppress inappropriately high levels of peripheral expression. Cell-specific expression improved significantly with the inclusion of 8.7 kb of CRH 5' flanking DNA. Individual transgenic lines exhibited expression in a number of the major CRH neuronal groups including the paraventricular nucleus, medial geniculate nucleus, inferior olivary nucleus, and Barrington's nucleus. Transgene expression was properly activated in Barrington's nucleus during development. This study demonstrates that the regulatory control of cell-specific and developmentally appropriate CRH expression is complex, utilizing multiple DNA sequence elements located upstream and downstream of the CRH transcription start site.
在转基因小鼠中分析了对促肾上腺皮质激素释放激素(CRH)细胞特异性表达和发育调控至关重要的DNA序列。一个包含0.5 kb CRH 5'侧翼DNA与氯霉素乙酰转移酶报告基因相连的构建体在许多脑区和几个异位外周位点表达,这表明CRH基因的这一部分含有基础启动子活性,但缺乏适当组织特异性所需的DNA元件。用一个CRH-β-半乳糖苷酶报告构建体检测转基因表达的细胞特异性,该构建体包含相同的0.5 kb CRH启动子片段,但也包括CRH结构基因和2 kb CRH 3'侧翼DNA。在大脑的不适当区域观察到转基因表达,但在外周组织中未检测到表达,这表明这些额外的CRH序列抑制了外周不适当的高水平表达。包含8.7 kb CRH 5'侧翼DNA后,细胞特异性表达显著改善。各个转基因品系在一些主要的CRH神经元群体中表现出表达,包括室旁核、内侧膝状体核、下橄榄核和巴林顿核。在发育过程中,转基因在巴林顿核中被正确激活。这项研究表明,细胞特异性和发育适当的CRH表达的调控控制是复杂的,利用了位于CRH转录起始位点上游和下游的多个DNA序列元件。