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编码细胞黏附分子DdCAD-1的基因发生破坏,会导致盘基网柄菌发育过程中细胞分选异常和细胞类型比例失调。

Disruption of the gene encoding the cell adhesion molecule DdCAD-1 leads to aberrant cell sorting and cell-type proportioning during Dictyostelium development.

作者信息

Wong Estella, Yang Chunzhong, Wang Jun, Fuller Danny, Loomis William F, Siu Chi-Hung

机构信息

Banting and Best Department of Medical Research and Department of Biochemistry, University of Toronto, Toronto, Ontario M5G 1L6, Canada.

出版信息

Development. 2002 Aug;129(16):3839-50. doi: 10.1242/dev.129.16.3839.

Abstract

The cadA gene in Dictyostelium encodes the Ca2+-dependent cell adhesion molecule DdCAD-1, which is expressed soon after the initiation of development. To investigate the biological role of DdCAD-1, the cadA gene was disrupted by homologous recombination. The cadA-null cells showed a 50% reduction in EDTA-sensitive cell adhesion. The remaining EDTA-sensitive adhesion sites were resistant to dissociation by anti-DdCAD-1 antibody, suggesting that they were distinct adhesion sites. Cells that lacked DdCAD-1 were able to complete development and form fruiting bodies. However, they displayed abnormal slug morphology and culmination was delayed by approximately 6 hours. The yield of spores was reduced by approximately 50%. The proportion of prestalk cells in cadA(-) slugs showed a 2.5-fold increase over the parental strain. When cadA(-) cells were transfected with pcotB::GFP to label prespore cells, aberrant cell-sorting patterns in slugs became apparent. When mutant prestalk cells were mixed with wild-type prespore cells, mutant prestalk cells were unable to return to the anterior position of chimeric slugs, suggesting defects in the sorting mechanism. The wild-type phenotype was restored when cadA(-) cells were transfected with a cadA-expression vector. These results indicate that, in addition to cell-cell adhesion, DdCAD-1 plays a role in cell type proportioning and pattern formation.

摘要

盘基网柄菌中的cadA基因编码Ca2+依赖性细胞粘附分子DdCAD-1,该分子在发育开始后不久就会表达。为了研究DdCAD-1的生物学作用,通过同源重组破坏了cadA基因。cadA基因缺失的细胞对EDTA敏感的细胞粘附减少了50%。其余对EDTA敏感的粘附位点对抗DdCAD-1抗体的解离具有抗性,这表明它们是不同的粘附位点。缺乏DdCAD-1的细胞能够完成发育并形成子实体。然而,它们表现出异常的蛞蝓形态,发育顶峰延迟了约6小时。孢子产量降低了约50%。在cadA(-)蛞蝓中,前柄细胞的比例比亲本菌株增加了2.5倍。当用pcotB::GFP转染cadA(-)细胞以标记前孢子细胞时,蛞蝓中异常的细胞分选模式变得明显。当突变的前柄细胞与野生型前孢子细胞混合时,突变的前柄细胞无法回到嵌合蛞蝓的前部位置,这表明分选机制存在缺陷。当用cadA表达载体转染cadA(-)细胞时,野生型表型得以恢复。这些结果表明,除了细胞间粘附外,DdCAD-1在细胞类型比例和模式形成中也发挥作用。

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