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首页> 外文期刊>Eukaryotic cell >Environmental Suppression of Neurospora crassa cot-1 Hyperbranching: a Link between COT1 Kinase and Stress Sensing
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Environmental Suppression of Neurospora crassa cot-1 Hyperbranching: a Link between COT1 Kinase and Stress Sensing

机译:环境抑制的神经孢霉cot-1超支化:COT1激酶和压力感测之间的联系。

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cot-1 mutants belong to a class of Neurospora crassa colonial temperature-sensitive (cot) mutants that exhibit abnormal polar extension and branching patterns when grown at restrictive temperatures. cot-1 encodes a Ser/Thr protein kinase that is structurally related to the human myotonic dystrophy kinase which, when impaired, confers a disease that involves changes in cytoarchitecture and ion homeostasis. When grown under restrictive conditions, cot-1 cultures exhibited enhanced medium acidification rates, increased relative abundance of sodium, and increased intracellular glycerol content, indicating an ion homeostasis defect in a hyperbranching mutant. The application of ion transport blockers led to only mild suppression of the cot-1 phenotype. The presence of increased medium NaCl or sorbitol, H2O2, or ethanol levels significantly suppressed the cot-1 phenotype, restored ion homeostasis, and was accompanied by reduced levels of cyclic AMP-dependent protein kinase (PKA) activity. The cot-1 phenotype could also be partially suppressed by direct inhibition of PKA with KT-5720. A reduced availability of fermentable carbon sources also had a suppressive effect on the cot-1 phenotype. In contrast to the effect of extragenic ropy suppressors of cot-1, environmental stress-related suppression of cot-1 did not change COT1 polypeptide expression patterns in the mutant. We suggest that COT1 function is linked to environmental stress response signaling and that altering PKA activity bypasses the requirement for fully functional COT1.
机译: cot-1 突变体属于一类 Neurospora crassa 殖民地温度敏感( cot )突变体,生长时表现出异常的极性延伸和分支模式在极限温度下。 cot-1 编码的Ser / Thr蛋白激酶与人的肌强直性营养不良激酶在结构上有关,当受损时,它会导致涉及细胞结构和离子稳态变化的疾病。在限制性条件下生长时, cot-1 培养物显示出中等的酸化速率,钠的相对丰度增加和细胞内甘油含量增加,表明超支化突变体中的离子稳态缺乏。离子转运阻滞剂的应用仅导致 cot-1 表型的轻微抑制。培养基中NaCl或山梨糖醇,H 2 O 2 或乙醇水平的升高显着抑制了 cot-1 表型,恢复了离子稳态,并伴有环AMP依赖性蛋白激酶(PKA)活性水平降低。通过用KT-5720直接抑制PKA,也可以部分抑制 cot-1 表型。可发酵碳源的减少也对 cot-1 表型产生抑制作用。与 cot-1 的外源 ropy 抑制剂的作用相反,与环境胁迫相关的 cot-1 抑制不改变COT1多肽的表达。突变体中的模式。我们建议,COT1功能与环境应激反应信号相关,并且改变PKA活性可以绕开对功能全面的COT1的需求。

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