Gorovits Rena, Yarden Oded
Department of Plant Pathology and Microbiology. The Otto Warburg Center for Agricultural Biotechnology, Faculty of Agricultural, Food and Environmental Quality Sciences, The Hebrew University of Jerusalem, Rehovot 76100, Israel.
Eukaryot Cell. 2003 Aug;2(4):699-707. doi: 10.1128/EC.2.4.699-707.2003.
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, H(2)O(2), 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.
cot-1突变体属于粗糙脉孢菌菌落温度敏感(cot)突变体类别,当在限制温度下生长时,它们会表现出异常的极性延伸和分支模式。cot-1编码一种丝氨酸/苏氨酸蛋白激酶,其结构与人强直性肌营养不良激酶相关,后者受损时会引发一种涉及细胞结构和离子稳态变化的疾病。在限制条件下生长时,cot-1培养物表现出增强的培养基酸化速率、钠相对丰度增加以及细胞内甘油含量增加,表明超分支突变体中存在离子稳态缺陷。离子转运阻滞剂的应用仅导致cot-1表型的轻度抑制。培养基中NaCl或山梨醇、H₂O₂或乙醇水平的增加显著抑制了cot-1表型,恢复了离子稳态,并伴随着环磷酸腺苷依赖性蛋白激酶(PKA)活性水平的降低。用KT-5720直接抑制PKA也可部分抑制cot-1表型。可发酵碳源可用性的降低对cot-1表型也有抑制作用。与cot-1的基因外粘性抑制子的作用相反,与环境应激相关的cot-1抑制并未改变突变体中COT1多肽的表达模式。我们认为COT1功能与环境应激反应信号传导相关,并且改变PKA活性绕过了对完全功能性COT1的需求。