首页> 外文OA文献 >The Nuclear Dbf2-Related Kinase COT1 and the Mitogen-Activated Protein Kinases MAK1 and MAK2 Genetically Interact to Regulate Filamentous Growth, Hyphal Fusion and Sexual Development in Neurospora crassa
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The Nuclear Dbf2-Related Kinase COT1 and the Mitogen-Activated Protein Kinases MAK1 and MAK2 Genetically Interact to Regulate Filamentous Growth, Hyphal Fusion and Sexual Development in Neurospora crassa

机译:核Dbf2相关的激酶COT1和丝裂素激活的蛋白激酶MAK1和MAK2遗传相互作用,以调节神经孢子的丝状生长,菌丝融合和性发育。

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摘要

Ndr kinases, such as Neurospora crassa COT1, are important for cell differentiation and polar morphogenesis, yet their input signals as well as their integration into a cellular signaling context are still elusive. Here, we identify the cot-1 suppressor gul-4 as mak-2 and show that mutants of the gul-4/mak-2 mitogen-activated protein (MAP) kinase pathway suppress cot-1 phenotypes along with a concomitant reduction in protein kinase A (PKA) activity. Furthermore, mak-2 pathway defects are partially overcome in a cot-1 background and are associated with increased MAK1 MAPK signaling. A comparative characterization of N. crassa MAPKs revealed that they act as three distinct modules during vegetative growth and asexual development. In addition, common functions of MAK1 and MAK2 signaling during maintenance of cell-wall integrity distinguished the two ERK-type pathways from the p38-type OS2 osmosensing pathway. In contrast to separate functions during vegetative growth, the concerted activity of the three MAPK pathways is essential for cell fusion and for the subsequent formation of multicellular structures that are required for sexual development. Taken together, our data indicate a functional link between COT1 and MAPK signaling in regulating filamentous growth, hyphal fusion, and sexual development.
机译:Ndr激酶(例如Neurospora crassa COT1)对于细胞分化和极性形态发生很重要,但是它们的输入信号以及它们整合到细胞信号传导环境中仍然难以捉摸。在这里,我们将cot-1抑制剂gul-4鉴定为mak-2,并表明gul-4 / mak-2丝裂原活化蛋白(MAP)激酶途径的突变体抑制了cot-1表型并伴随蛋白质减少激酶A(PKA)活性。此外,mak-2途径缺陷在cot-1背景下得到部分克服,并与增加的MAK1 MAPK信号传导有关。猪笼草MAPKs的比较特征表明,它们在营养生长和无性发育过程中起三个不同的模块的作用。此外,在维持细胞壁完整性期间,MAK1和MAK2信号传导的共同功能将两个ERK型途径与p38型OS2渗透性途径区分开来。与营养生长过程中的单独功能相反,三个MAPK途径的协同活性对于细胞融合以及随后形成性发育所需的多细胞结构至关重要。两者合计,我们的数据表明在调节丝状生长,菌丝融合和性发育中,COT1和MAPK信号传导之间存在功能联系。

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