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首页> 外文期刊>Eukaryotic cell >Constitutively Active Protein Kinase A Disrupts Motility and Chemotaxis in Dictyostelium discoideum
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Constitutively Active Protein Kinase A Disrupts Motility and Chemotaxis in Dictyostelium discoideum

机译:组成性活性蛋白激酶A破坏盘基网柄菌的运动性和趋化性。

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The deletion of the gene for the regulatory subunit of protein kinase A (PKA) results in constitutively active PKA in the pkaR mutant. To investigate the role of PKA in the basic motile behavior and chemotaxis of Dictyostelium discoideum, pkaR mutant cells were subjected to computer-assisted two- and three-dimensional motion analysis. pkaR mutant cells crawled at only half the speed of wild-type cells in buffer, chemotaxed in spatial gradients of cyclic AMP (cAMP) but with reduced efficiency, were incapable of suppressing lateral pseudopods in the front of temporal waves of cAMP, a requirement for natural chemotaxis, did not exhibit the normal velocity surge in response to the front of a wave, and were incapable of chemotaxing toward an aggregation center in natural waves generated by wild-type cells that made up the majority of cells in mixed cultures. Many of the behavioral defects appeared to be the result of the constitutively ovoid shape of the pkaR mutant cells, which forced the dominant pseudopod off the substratum and to the top of the cell body. The behavioral abnormalities that pkaR mutant cells shared with regA mutant cells are discussed by considering the pathway ERK2 —| RegA —| [cAMP] → PKA, which emanates from the front of a wave. The results demonstrate that cells must suppress PKA activity in order to elongate along a substratum, suppress lateral-pseudopod formation, and crawl and chemotax efficiently. The results also implicate PKA activation in dismantling cell polarity at the peak and in the back of a natural cAMP wave.
机译:蛋白激酶A(PKA)调节亚基基因的缺失导致 pkaR 突变体中的组成型活性PKA。为了研究PKA在盘基网柄菌的基本运动行为和趋化性中的作用,对pkaR 突变细胞进行了计算机辅助的二维和三维运动分析。 pkaR 突变细胞仅以野生型细胞在缓冲液中的速度爬行,在循环AMP(cAMP)的空间梯度中进行了化学趋化,但效率降低,无法抑制颞叶前部的侧假足cAMP的波是自然趋化性的要求,没有表现出响应波前的正常速度激增,并且不能在构成大多数细胞的野生型细胞产生的自然波中向聚集中心趋化。混合培养物中的细胞。许多行为缺陷似乎是 pkaR 突变细胞的本构为卵形的结果,这种突变细胞迫使显性假足离开基底并到达细胞体顶部。通过考虑途径ERK2-|讨论 regA 突变细胞与 pkaR 突变细胞共享的行为异常。 RegA — | [cAMP]→PKA,从波的前面发出。结果表明,细胞必须抑制PKA活性才能沿基质延伸,抑制侧假足形成以及有效地爬行和趋化。结果还暗示了PKA激活会破坏自然cAMP波的峰值和背后的细胞极性。

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