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盘基网柄菌中一个cAMP调节的前孢子细胞类型特异性基因的表达空间梯度。

A spatial gradient of expression of a cAMP-regulated prespore cell-type-specific gene in Dictyostelium.

作者信息

Haberstroh L, Firtel R A

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093.

出版信息

Genes Dev. 1990 Apr;4(4):596-612. doi: 10.1101/gad.4.4.596.

Abstract

Previously, we identified a class of genes in Dictyostelium that are prespore cell-type specific in their expression in the multicellular aggregate and are inducible by cAMP acting through cell-surface cAMP receptors. In this paper, we report the cloning and analysis of the regulatory regions controlling the expression of one such gene that encodes a spore coat protein, SP60. By use of a fusion of the firefly luciferase gene and Escherichia coli lacZ [expresses beta-galactosidase (beta-gal)], we have identified cis-acting regions required for proper spatial and temporal expression in multicellular aggregates and for cAMP induction in shaking cell culture. Deletion analysis suggests that a CA-rich element (CAE) and surrounding sequences present three times within the 5'-flanking sequence are required for proper regulation. SP60-lacZ fusions that include all three of these regions express lacZ only in the posterior approximately 85% of migrating slugs (prespore zone). Studies show that SP60 is expressed during mid to late aggregation, and SP60-lacZ-positive cells are spatially localized as a doughnut-shaped ring within the forming aggregate. Cells within the skirt that surrounds the aggregate and that are still migrating into the aggregate do not stain. Sequential 5' deletions of CAEs and surrounding regions affect the expression level of SP60-luciferase in response to developmental signals and cAMP, as well as the spatial pattern of SP60-lacZ. Deletion of the first (most 5') of these regions restricts the spatial expression of SP60-lacZ fusions to the anterior of the prespore zone. When both the first and second regions are removed, the expression level drops, and the staining is restricted to the prespore/prestalk boundary. Furthermore, the staining pattern that is seen with these two deletions is present as a gradient from anterior to posterior within the prespore zone. Deletion of all three regions results in a loss of both cAMP and developmentally induced expression. These results suggest the presence of a gradient within the prespore zone that differentially affects the activity of promoters containing different numbers of response elements.

摘要

此前,我们在盘基网柄菌中鉴定出一类基因,它们在多细胞聚集体中的表达具有前孢子细胞类型特异性,并且可被通过细胞表面cAMP受体起作用的cAMP诱导。在本文中,我们报告了对控制一个编码孢子壁蛋白SP60的此类基因表达的调控区域的克隆和分析。通过使用萤火虫荧光素酶基因与大肠杆菌lacZ(表达β-半乳糖苷酶(β-gal))的融合,我们确定了在多细胞聚集体中进行适当的时空表达以及在振荡细胞培养中进行cAMP诱导所需的顺式作用区域。缺失分析表明,5'侧翼序列中出现三次的富含CA的元件(CAE)及其周围序列对于正确调控是必需的。包含所有这三个区域的SP60-lacZ融合体仅在迁移蛞蝓后部约85%(前孢子区)表达lacZ。研究表明,SP60在聚集中期至后期表达,并且SP60-lacZ阳性细胞在形成的聚集体中呈甜甜圈状环在空间上定位。围绕聚集体且仍在迁移进入聚集体的裙边内的细胞不着色。CAE及其周围区域的连续5'缺失会影响SP60-荧光素酶响应发育信号和cAMP的表达水平,以及SP60-lacZ的空间模式。删除这些区域中的第一个(最5'端)会将SP60-lacZ融合体的空间表达限制在前孢子区的前部。当第一和第二个区域都被去除时,表达水平下降,并且染色仅限于前孢子/前柄边界。此外,这两个缺失所观察到的染色模式在前孢子区内从前到后呈梯度分布。删除所有三个区域会导致cAMP和发育诱导表达均丧失。这些结果表明在前孢子区内存在一个梯度,该梯度对含有不同数量响应元件的启动子的活性有不同影响。

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