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转基因动物中巨细胞病毒增强子的发育分析

Developmental analysis of the cytomegalovirus enhancer in transgenic animals.

作者信息

Baskar J F, Smith P P, Ciment G S, Hoffmann S, Tucker C, Tenney D J, Colberg-Poley A M, Nelson J A, Ghazal P

机构信息

Department of Immunology, Division of Virology R307B, Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Virol. 1996 May;70(5):3215-26. doi: 10.1128/JVI.70.5.3215-3226.1996.

Abstract

The major immediate-early promoter (MIEP) of human, cytomegalovirus (HCMV) constitutes a primary genetic switch for viral activation. In this study, regulation of the enhancer-containing segment (nucleotides -670 to +54) of the HCMV MIEP attached to the 1acZ reporter gene was examined in the developing embryos of transgenic mice to identify temporal and tissue-specific expression. We find that the transgene reporter is first detected as a dorsal stripe of expression in the neural folds of embryos at day 8.5 postcoitum (p.c.). A broad expression pattern is exhibited in embryos at day 9.5 p.c. This pattern becomes more restricted by day 10.5 p.c. as organogenesis progresses. By day 14.5 p.c., prominent expression is observed in a subpopulation of central nervous system cells and spinal ganglia, endothelial cells, muscle, skin, thyroid, parathyroid, kidney, lung, liver, and gut cells, and the pancreas and submandibular and pituitary glands. This distribution pattern is discussed in relation to human congenital HCMV infection. These results suggest that the transcriptional activity of the HCMV MIEP may determine in part, the ability of the virus to specifically target developing fetal tissues in utero.

摘要

人类巨细胞病毒(HCMV)的主要立即早期启动子(MIEP)构成病毒激活的主要基因开关。在本研究中,将与1acZ报告基因相连的HCMV MIEP的含增强子片段(核苷酸-670至+54)在转基因小鼠的发育胚胎中进行检测,以确定其时间和组织特异性表达。我们发现,转基因报告基因在受精后第8.5天(p.c.)胚胎的神经褶中首次检测为一条背侧表达带。在受精后第9.5天的胚胎中呈现广泛的表达模式。随着器官发生的进展,这种模式在受精后第10.5天变得更加局限。到受精后第14.5天,在中枢神经系统细胞和脊髓神经节、内皮细胞、肌肉、皮肤、甲状腺、甲状旁腺、肾脏、肺、肝脏和肠道细胞以及胰腺、下颌下腺和垂体的亚群中观察到显著表达。结合人类先天性HCMV感染对这种分布模式进行了讨论。这些结果表明,HCMV MIEP的转录活性可能部分决定病毒在子宫内特异性靶向发育中的胎儿组织的能力。

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Microgyria and cytomegalic inclusion disease in infancy.
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