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Involvement of Botrytis cinerea Small GTPases BcRAS1 and BcRAC in Differentiation, Virulence, and the Cell Cycle

机译:灰葡萄孢小GTP酶BcRAS1和BcRAC参与分化,毒力和细胞周期

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Small GTPases of the Ras superfamily are highly conserved proteins that are involved in various cellular processes, in particular morphogenesis, differentiation, and polar growth. Here we report on the analysis of RAS1 and RAC homologues from the gray mold fungus Botrytis cinerea. We show that these small GTPases are individually necessary for polar growth, reproduction, and pathogenicity, required for cell cycle progression through mitosis (BcRAC), and may lie upstream of the stress-related mitogen-activated protein kinase (MAPK) signaling pathway. bcras1 and bcrac deletion strains had reduced growth rates, and their hyphae were hyperbranched and deformed. In addition, both strains were vegetatively sterile and nonpathogenic. A strain expressing a constitutively active (CA) allele of the BcRAC protein had partially similar but milder phenotypes. Similar to the deletion strains, the CA-BcRAC strain did not produce any conidia and had swollen hyphae. In contrast to the two deletion strains, however, the growth rate of the CA-BcRAC strain was normal, and it caused delayed but well-developed disease symptoms. Microscopic examination revealed an increased number of nuclei and disturbance of actin localization in the CA-BcRAC strain. Further work with cell cycle- and RAC-specific inhibitory compounds associated the BcRAC protein with progression of the cell cycle through mitosis, possibly via an effect on microtubules. Together, these results show that the multinucleate phenotype of the CA-BcRAC strain could result from at least two defects: disruption of polar growth through disturbed actin localization and uncontrolled nuclear division due to constitutive activity of BcRAC.
机译:Ras超家族的小GTPases是高度保守的蛋白质,参与各种细胞过程,特别是形态发生,分化和极性生长。在这里,我们报告从灰霉菌灰葡萄孢的RAS1和RAC同源物的分析。我们表明,这些小的GTPases是极个别的增长,生殖和致病性所必需的,通过有丝分裂(BcRAC)进行细胞周期进程所需,并且可能位于应激相关的促丝裂原激活的蛋白激酶(MAPK)信号通路的上游。 bcras1 bcrac 缺失菌株的生长速率降低,其菌丝超支化并变形。此外,两种菌株均为营养无菌且无致病性。表达BcRAC蛋白的组成型活性(CA)等位基因的菌株具有部分相似但较温和的表型。与缺失菌株相似,CA-BcRAC菌株不产生任何分生孢子,并具有肿胀的菌丝。但是,与这两个缺失菌株相反,CA-BcRAC菌株的生长速度正常,并引起延迟但发展良好的疾病症状。显微镜检查显示CA-BcRAC菌株中细胞核数目增加和肌动蛋白定位受到干扰。细胞周期特异性和RAC特异性抑制化合物的进一步研究可能将BcRAC蛋白与细胞周期通过有丝分裂的进程联系起来,可能是通过对微管的影响。总之,这些结果表明,CA-BcRAC菌株的多核表型可能是由至少两个缺陷引起的:通过扰动的肌动蛋白定位破坏极性生长,以及由于BcRAC的组成活性而导致的不受控制的核分裂。

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