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多个顺式作用元件协同作用,指导髌骨胚胎中α-微管蛋白-4基因的滋养层细胞特异性表达。

Multiple cis-acting elements act cooperatively in directing trochoblast-specific expression of the alpha-tubulin-4 gene in Patella embryos.

作者信息

Damen W G, van Loon A E

机构信息

Department of Experimental Zoology, Ultrecht University, the Netherlands.

出版信息

Dev Biol. 1996 Jun 15;176(2):313-24. doi: 10.1006/dbio.1996.0136.

Abstract

During early embryogenesis of the mollusc Patella vulgata the alpha-tubulin-4 gene is specifically expressed in the differentiation process of a particular cell type, the trochoblasts. The 5' region of the gene has been analysed for elements that are required for the regulation of the cell-type-specific activation of the gene. In a functional assay, seven elements that play a role in the spatiotemporal activation of the gene were detected in the promoter sequence. They are not required all together at the same time. A core of two elements, together with two or three auxiliary elements, are sufficient in controlling trochoblast-specific expression of the gene in the Patella embryo. One of the core elements is always required, without it, the gene is not expressed at all. The other core element acts as a positive element in trochoblasts and as a negative element in non-trochoblasts and thus is involved in directing the cell-type specificity of expression. The seven elements act cooperatively, and at least some of them can substitute for each other. Sequence comparison revealed that six of the seven fragments contain the sequence element GTTAA, including one of the core elements. Both core elements seem to play a crucial role in the expression of the alpha-tubulin-4 gene during the differentiation process of trochoblasts in the Patella embryo. A model for the regulation of the cell-type specificity of the gene during trochoblast differentiation is proposed.

摘要

在帽贝(Patella vulgata)的早期胚胎发育过程中,α-微管蛋白-4基因在特定细胞类型——原肠胚细胞的分化过程中特异性表达。对该基因的5'区域进行了分析,以寻找调节该基因细胞类型特异性激活所需的元件。在一项功能测定中,在启动子序列中检测到七个在基因的时空激活中起作用的元件。它们并非同时都需要。两个元件组成的核心,再加上两到三个辅助元件,足以控制帽贝胚胎中该基因在原肠胚细胞中的特异性表达。其中一个核心元件始终是必需的,没有它,基因根本不表达。另一个核心元件在原肠胚细胞中作为正调控元件,在非原肠胚细胞中作为负调控元件,因此参与指导表达的细胞类型特异性。这七个元件协同作用,并且它们中的至少一些可以相互替代。序列比较显示,七个片段中的六个包含序列元件GTTAA,其中包括一个核心元件。这两个核心元件似乎在帽贝胚胎原肠胚细胞分化过程中α-微管蛋白-4基因的表达中起着关键作用。提出了一个在原肠胚细胞分化过程中该基因细胞类型特异性调控的模型。

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