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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Schizosaccharomyces pombe Adenylate Cyclase Suppressor Mutations Suggest a Role for cAMP Phosphodiesterase Regulation in Feedback Control of Glucose/cAMP Signaling
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Schizosaccharomyces pombe Adenylate Cyclase Suppressor Mutations Suggest a Role for cAMP Phosphodiesterase Regulation in Feedback Control of Glucose/cAMP Signaling

机译:粟酒裂殖酵母腺苷酸环化酶抑制剂突变提示cAMP磷酸二酯酶调节在葡萄糖/ cAMP信号反馈控制中的作用。

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摘要

Mutations affecting the Schizosaccharomyces pombe cAMP phosphodiesterase (PDE) gene cgs2 + were identified in a screen for suppressors of mutant alleles of the adenylate cyclase gene ( git2 +/ cyr1 +), which encode catalytically active forms of the enzyme that cannot be stimulated by extracellular glucose signaling. These mutations suppress both the git2 ? mutant alleles used in the suppressor selection and mutations in git1 +, git3 +, git5 +, git7 +, git10 +, and git11 +, which are all required for adenylate cyclase activation. Notably, these cgs2 mutant alleles fail to suppress mutations in gpa2 +, which encodes the Gα subunit of a heterotrimeric G protein required for adenylate cyclase activation, although the previously identified cgs2-2 allele does suppress loss of gpa2 +. Further analysis of the cgs2-s1 allele reveals a synthetic interaction with the gpa2 R176H-activated allele, with respect to derepression of fbp1-lacZ transcription in glucose-starved cells. In addition, direct measurements of cAMP levels show that cgs2-s1 cells maintain normal basal cAMP levels, but are severely defective in feedback regulation upon glucose detection. These results suggest that PDE activity in S. pombe may be coordinately regulated with adenylate cyclase activity as part of the feedback regulation mechanism to limit the cAMP response to glucose detection.
机译:在筛选腺苷酸环化酶基因(git2 + / cyr1 +)的突变等位基因的抑制剂中筛选出了影响粟酒裂殖酵母cAMP磷酸二酯酶(PDE)基因cgs2 +的突变,该突变体编码的催化活性形式的酶不能被细胞外刺激葡萄糖信号。这些突变抑制了git2?用于抑制子选择的突变等位基因以及git1 +,git3 +,git5 +,git7 +,git10 +和git11 +中的突变,这些都是腺苷酸环化酶激活所必需的。值得注意的是,尽管先前鉴定的cgs2-2等位基因确实抑制了gpa2 +的损失,但这些cgs2突变等位基因未能抑制gpa2 +的突变,后者编码了腺苷酸环化酶激活所需的异三聚G蛋白的Gα亚基。对cgs2-s1等位基因的进一步分析揭示了与gpa2 R176H激​​活的等位基因的合成相互作用,这与葡萄糖饥饿细胞中fbp1-lacZ转录的抑制有关。另外,对cAMP水平的直接测量表明cgs2-s1细胞保持正常的基础cAMP水平,但是在检测到葡萄糖时在反馈调节方面存在严重缺陷。这些结果表明,作为反馈调节机制的一部分,粟酒裂殖酵母中的PDE活性可能与腺苷酸环化酶活性协同调节,以限制cAMP对葡萄糖检测的反应。

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