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Detection of subtle phenotypes: the case of the cell adhesion molecule csA in Dictyostelium.细微表型的检测:以盘基网柄菌中的细胞黏附分子csA为例。
Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9360-5. doi: 10.1073/pnas.95.16.9360.
2
Overexpression of the csA cell adhesion molecule under its own cAMP-regulated promoter impairs morphogenesis in Dictyostelium.在其自身cAMP调节启动子作用下,csA细胞黏附分子的过表达会损害盘基网柄菌的形态发生。
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Cell-cell signaling and adhesion in phagocytosis and early development of Dictyostelium.盘基网柄菌吞噬作用和早期发育中的细胞间信号传导与黏附
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Discrete interactions in cell adhesion measured by single-molecule force spectroscopy.通过单分子力谱法测量细胞黏附中的离散相互作用。
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Rapid antagonistic coevolution between strains of the social amoeba Dictyostelium discoideum.社会变形虫(Dictyostelium discoideum)菌株之间的快速拮抗协同进化。
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本文引用的文献

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Complete sequence and transcript regulation of a cell adhesion protein from aggregating Dictyostelium cells.完整的细胞黏附蛋白序列及其在聚集型 Dictyostelium 细胞中的转录调控。
EMBO J. 1986 Jul;5(7):1473-6. doi: 10.1002/j.1460-2075.1986.tb04384.x.
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Genetic redundancy.遗传冗余
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Evolution of genetic redundancy.遗传冗余的进化。
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Genetic networks that regulate development in Dictyostelium cells.调控盘基网柄菌细胞发育的遗传网络。
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Redundant control of Ultrabithorax by zeste involves functional levels of zeste protein binding at the Ultrabithorax promoter.zeste对超双胸的冗余控制涉及zeste蛋白在超双胸启动子上结合的功能水平。
Development. 1996 Jul;122(7):2303-11. doi: 10.1242/dev.122.7.2303.
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Cell adhesion in the life cycle of Dictyostelium.盘基网柄菌生命周期中的细胞黏附
Experientia. 1995 Dec 18;51(12):1175-88. doi: 10.1007/BF01944735.
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Thinking about genetic redundancy.思考基因冗余。
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8
Redundant genes?冗余基因?
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9
Mice lacking glial fibrillary acidic protein display astrocytes devoid of intermediate filaments but develop and reproduce normally.缺乏胶质纤维酸性蛋白的小鼠,其星形胶质细胞缺乏中间丝,但发育和繁殖正常。
EMBO J. 1995 Apr 18;14(8):1590-8. doi: 10.1002/j.1460-2075.1995.tb07147.x.
10
Metabolism of the cellular slime mould Dictyostelium discoideum grown in axenic culture.在无菌培养条件下生长的细胞黏菌盘基网柄菌的代谢。
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细微表型的检测:以盘基网柄菌中的细胞黏附分子csA为例。

Detection of subtle phenotypes: the case of the cell adhesion molecule csA in Dictyostelium.

作者信息

Ponte E, Bracco E, Faix J, Bozzaro S

机构信息

Dipartimento di Scienze Cliniche e Biologiche, Università di Torino, Ospedale S. Luigi, 10043-Orbassano, Italy.

出版信息

Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9360-5. doi: 10.1073/pnas.95.16.9360.

DOI:10.1073/pnas.95.16.9360
PMID:9689085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC21343/
Abstract

Dictyostelium amoebae aggregate into a multicellular organism by cAMP-driven chemotaxis and cell-cell adhesion. Cell adhesion is mediated by an EDTA-sensitive and an EDTA-resistant adhesion system. The latter is developmentally regulated and triggered by homophilic interactions of the membrane glycoprotein csA; on disruption of the encoding gene, EDTA-resistant contacts fail to form. Nevertheless, csA-null cells under usual laboratory conditions aggregate normally and complete development. By using experimental conditions that reproduce more closely the habitat of Dictyostelium amoebae, evidence is provided that csA is required for development and that its expression confers a selective advantage to populations of wild-type cells over csA-null mutants. The latter display reduced cell-cell adhesion, increased adhesiveness to the substratum, and slower motility, which lead to their sorting out from aggregating wild-type cells. It is proposed that the experimental conditions commonly used in the laboratory are not stringent enough to assess the developmental role of csA and other proteins. The assay described can be used to detect subtle phenotypes, to reexamine the developmental role of apparently nonessential genes, and to test the validity of recent models on emergence and maintenance of apparent genetic redundancy.

摘要

盘基网柄菌变形虫通过cAMP驱动的趋化作用和细胞间黏附聚集成多细胞生物体。细胞黏附由一个对EDTA敏感的黏附系统和一个对EDTA抗性的黏附系统介导。后者受发育调控,并由膜糖蛋白csA的同源相互作用触发;编码基因破坏后,对EDTA抗性的接触无法形成。然而,在通常的实验室条件下,缺失csA的细胞能正常聚集并完成发育。通过使用更接近盘基网柄菌变形虫栖息地的实验条件,有证据表明csA对发育是必需的,并且其表达赋予野生型细胞群体相对于缺失csA的突变体的选择性优势。后者表现出细胞间黏附减少、对底物的黏附性增加和运动性减慢,这导致它们从聚集的野生型细胞中被分选出来。有人提出,实验室中常用的实验条件不够严格,不足以评估csA和其他蛋白质的发育作用。所描述的检测方法可用于检测细微表型,重新审视明显非必需基因的发育作用,并检验最近关于明显遗传冗余的出现和维持模型的有效性。