Suppr超能文献

腺病毒E1A介导的对F9细胞分化过程中激活基因的负调控。

Adenovirus E1A-mediated negative control of genes activated during F9 differentiation.

作者信息

Young K S, Weigel R, Hiebert S, Nevins J R

机构信息

Rockefeller University, New York, New York 10021.

出版信息

Mol Cell Biol. 1989 Jul;9(7):3109-13. doi: 10.1128/mcb.9.7.3109-3113.1989.

Abstract

The phenotype of a differentiated cell results from the expression of a unique set of genes in that cell. The differentiation of F9 teratocarcinoma cells in response to retinoic acid and cyclic AMP is an excellent example of this process, as the appearance of several gene products during the course of the differentiation process has been documented. In principle, the activation of gene expression could be due to the appearance of positive-acting factors, the loss of negative-acting factors, or a combination of both. Since F9 cells have been shown to express a cellular E1A analog whereas differentiated F9 cells do not, and it is known that the viral E1A gene exerts a negative effect on transcription of both viral and cellular genes, we determined whether the cellular genes activated during F9 cell differentiation are subject to E1A negative control. We found that infection of differentiated F9 cells with wild-type adenovirus resulted in a decline in the levels of collagen type IV mRNA and plasminogen activator mRNA, both of which are induced by differentiation. At least for the collagen gene, this phenomenon appears to involve a transcriptional repression.

摘要

分化细胞的表型源于该细胞中一组独特基因的表达。F9畸胎癌细胞在视黄酸和环磷酸腺苷作用下的分化就是这一过程的一个绝佳例子,因为在分化过程中几种基因产物的出现已被记录在案。原则上,基因表达的激活可能是由于正性作用因子的出现、负性作用因子的缺失,或者两者兼而有之。由于已证明F9细胞表达一种细胞E1A类似物,而分化的F9细胞则不表达,并且已知病毒E1A基因对病毒和细胞基因的转录均有负性作用,我们确定了F9细胞分化过程中被激活的细胞基因是否受到E1A的负性调控。我们发现,用野生型腺病毒感染分化的F9细胞会导致IV型胶原mRNA和纤溶酶原激活剂mRNA水平下降,这两种mRNA都是由分化诱导产生的。至少对于胶原基因来说,这种现象似乎涉及转录抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8713/362783/ff5b5ed48b39/molcellb00055-0350-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验