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两种具有不同细胞特异性的不同增强子共存于多瘤病毒的调控区域。

Two distinct enhancers with different cell specificities coexist in the regulatory region of polyoma.

作者信息

Herbomel P, Bourachot B, Yaniv M

出版信息

Cell. 1984 Dec;39(3 Pt 2):653-62. doi: 10.1016/0092-8674(84)90472-0.

Abstract

Two distinct nonoverlapping enhancer elements can be defined within the polyoma enhancer region. In mouse fibroblasts, element A provides a 3-fold higher enhancement of the alpha 2-collagen promoter than element B. In mouse embryonal carcinoma cells, element B shows the same efficiency as in fibroblasts, whereas that of element A decreases by a factor of 3.5. Moreover, a single point mutation (PyEC F9.1) increases the efficiency of element B in both cell types, making it superior to element A in embryonal carcinoma cells. The core of element A is located within a 35 bp region tandem duplicated in several wild-type strains, mostly homologous to a crucial repeated sequence of adenovirus E1a enhancer (Hearing and Shenk, 1983). Element B contains the consensus sequence of Weiher et al. (1982). These two homologies are precisely adjacent to the two DNAase l-hypersensitive sites present in viral chromatin.

摘要

在多瘤病毒增强子区域内可定义出两个不同且不重叠的增强子元件。在小鼠成纤维细胞中,元件A对α2 - 胶原蛋白启动子的增强作用比元件B高3倍。在小鼠胚胎癌细胞中,元件B的效率与在成纤维细胞中的相同,而元件A的效率降低了3.5倍。此外,一个单点突变(PyEC F9.1)在两种细胞类型中均提高了元件B的效率,使其在胚胎癌细胞中优于元件A。元件A的核心位于一个35 bp的区域内,该区域在几个野生型菌株中串联重复,大多与腺病毒E1a增强子的一个关键重复序列同源(Hearing和Shenk,1983)。元件B包含Weiher等人(1982)的共有序列。这两种同源性恰好与病毒染色质中存在的两个DNA酶I高敏位点相邻。

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