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在欧洲滨螺早期发育过程中,分化的原肠胚细胞中微管蛋白基因表达的转录调控。

Transcriptional regulation of tubulin gene expression in differentiating trochoblasts during early development of Patella vulgata.

作者信息

Damen W G, van Grunsven L A, van Loon A E

机构信息

Department of Experimental Zoology, Utrecht University, The Netherlands.

出版信息

Development. 1994 Oct;120(10):2835-45. doi: 10.1242/dev.120.10.2835.

Abstract

The expression of alpha- and beta-tubulin genes during the early development of the marine mollusk Patella vulgata has been investigated. From the 32-cell stage onwards, an enhanced expression of both alpha- and beta-tubulin mRNAs was detected in the primary trochoblasts. After one additional cleavage, these cells become cleavage-arrested and then form cilia. They are the first cells to differentiate during Patella development. Later, alpha- and beta-tubulin mRNA is also found in the accessory and secondary trochoblasts. Together these three cell-lines form the prototroch, the ciliated locomotory organ of the trochophore larva. The early and abundant expression of tubulin genes precede and accompany cilia formation in the trochoblasts and provides us with an excellent molecular differentiation marker for these cells. Apart from the trochoblasts, tubulin gene expression was also found in other cells at some stages. At the 88-cell stage, elevated tubulin mRNA levels were found around the large nucleus of the mesodermal stem cell 4d. In later stages, tubulin gene expression was detected in the cells that form the flagella of the apical tuft and in the refractive bodies. An alpha-tubulin gene was isolated and characterized. A lacZ fusion gene under control of the 5' upstream region of this tubulin gene was microinjected into embryos at the two-cell stage. The reporter gene product was only detected in the three trochoblast cell-lines at the same time as tubulin genes were expressed in these cells. Reporter gene product was not detected in any other cells. Thus, this 5' upstream region of this alpha-tubulin gene contains all the elements required for the correct spatiotemporal pattern of expression.

摘要

对海洋软体动物笠贝早期发育过程中α-微管蛋白和β-微管蛋白基因的表达进行了研究。从32细胞期开始,在初级原肠胚母细胞中检测到α-和β-微管蛋白mRNA的表达增强。再经过一次卵裂后,这些细胞停止分裂,然后形成纤毛。它们是笠贝发育过程中最早分化的细胞。后来,在辅助原肠胚母细胞和次级原肠胚母细胞中也发现了α-和β-微管蛋白mRNA。这三种细胞系共同形成了原纤毛轮,即担轮幼虫的纤毛运动器官。微管蛋白基因的早期大量表达先于原肠胚母细胞中纤毛的形成并与之相伴,为这些细胞提供了一个极好的分子分化标记。除了原肠胚母细胞外,在某些阶段其他细胞中也发现了微管蛋白基因的表达。在88细胞期,在中胚层干细胞4d的大核周围发现微管蛋白mRNA水平升高。在后期阶段,在形成顶簇鞭毛的细胞和折射体中检测到微管蛋白基因的表达。分离并鉴定了一个α-微管蛋白基因。将一个受该微管蛋白基因5'上游区域控制的lacZ融合基因在二细胞期显微注射到胚胎中。报告基因产物仅在与微管蛋白基因在这些细胞中表达的同时在三种原肠胚母细胞系中检测到。在任何其他细胞中均未检测到报告基因产物。因此,该α-微管蛋白基因的这个5'上游区域包含了正确的时空表达模式所需的所有元件。

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