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腺病毒12S E1A基因抑制F9畸胎瘤细胞的分化。

Adenovirus 12S E1A gene represses differentiation of F9 teratocarcinoma cells.

作者信息

Weigel R J, Devoto S H, Nevins J R

机构信息

Department of Microbiology and Immunology, Duke University Medical Center, Durham, NC 27710.

出版信息

Proc Natl Acad Sci U S A. 1990 Dec;87(24):9878-82. doi: 10.1073/pnas.87.24.9878.

Abstract

The F9 teratocarcinoma cell line differentiates in vitro after treatment with retinoic acid and cAMP and has been a widely used model system for the study of the molecular events that are responsible for cellular commitment and differentiation during early development. Previous experiments have suggested intriguing parallels between the control of gene expression during F9 cell differentiation and the regulation of gene expression by adenovirus E1A. Transfection of a 12S E1A-expressing plasmid into terminally differentiated, nonproliferating F9 cells generates, at high frequency, colonies of dividing cells, each of which expresses E1A. Cell lines established from these colonies proliferate in the presence of retinoic acid and have lost the fully differentiated phenotype as characterized by the absence of expression of a series of differentiation-specific genes. We conclude that expression of the viral 12S E1A gene product interferes with retinoic acid-induced F9 cell differentiation. Moreover, the results suggest that the differentiation process, as defined by markers of terminal differentiation, may not be a permanent event but can be reversed by E1A expression.

摘要

F9畸胎瘤细胞系在用视黄酸和环磷酸腺苷处理后可在体外分化,并且一直是研究早期发育过程中负责细胞定向和分化的分子事件的广泛使用的模型系统。先前的实验表明,F9细胞分化过程中的基因表达控制与腺病毒E1A对基因表达的调控之间存在有趣的相似之处。将表达12S E1A的质粒转染到终末分化、不增殖的F9细胞中,可高频产生分裂细胞集落,每个集落都表达E1A。从这些集落建立的细胞系在视黄酸存在下增殖,并丧失了以一系列分化特异性基因不表达为特征的完全分化表型。我们得出结论,病毒12S E1A基因产物的表达会干扰视黄酸诱导的F9细胞分化。此外,结果表明,由终末分化标志物定义的分化过程可能不是一个永久性事件,而是可以被E1A表达逆转。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea9d/55277/578927ba14d7/pnas01049-0381-a.jpg

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