Harispe Laura, Portela Cecilia, Scazzocchio Claudio, Peñalva Miguel A, Gorfinkiel Lisette
Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, Madrid 28040, Spain.
Eukaryot Cell. 2008 Jan;7(1):141-53. doi: 10.1128/EC.00346-07. Epub 2007 Nov 26.
Aspergillus nidulans gapA1, a mutation leading to compact, fluffy colonies and delayed polarity establishment, maps to a gene encoding a Ras GTPase-activating protein. Domain organization and phylogenetic analyses strongly indicate that GapA regulates one or more "true" Ras proteins. A gapADelta strain is viable. gapA colonies are more compact than gapA1 colonies and show reduced conidiation. gapADelta strains have abnormal conidiophores, characterized by the absence of one of the two layers of sterigmata seen in the wild type. gapA transcript levels are very low in conidia but increase during germination and reach their maximum at a time coincident with germ tube emergence. Elevated levels persist in hyphae. In germinating conidiospores, gapADelta disrupts the normal coupling of isotropic growth, polarity establishment, and mitosis, resulting in a highly heterogeneous cell population, including malformed germlings and a class of giant cells with no germ tubes and a multitude of nuclei. Unlike wild-type conidia, gapADelta conidia germinate without a carbon source. Giant multinucleated spores and carbon source-independent germination have been reported in strains carrying a rasA dominant active allele, indicating that GapA downregulates RasA. gapADelta cells show a polarity maintenance defect characterized by apical swelling and subapical branching. The strongly polarized wild-type F-actin distribution is lost in gapADelta cells. As GapA-green fluorescent protein shows cortical localization with strong predominance at the hyphal tips, we propose that GapA-mediated downregulation of Ras signaling at the plasma membrane of these tips is involved in the polarization of the actin cytoskeleton that is required for hyphal growth and, possibly, for asexual morphogenesis.
构巢曲霉gapA1突变导致菌落紧密、蓬松,极性建立延迟,该突变定位到一个编码Ras GTP酶激活蛋白的基因。结构域组织和系统发育分析强烈表明,GapA调节一种或多种“真正的”Ras蛋白。gapA缺失菌株是有活力的。gapA菌落比gapA1菌落更紧密,分生孢子形成减少。gapA缺失菌株的分生孢子梗异常,其特征是在野生型中看不到的两层小梗之一缺失。gapA转录水平在分生孢子中非常低,但在萌发过程中增加,并在与芽管出现同时达到最大值。在菌丝中水平持续升高。在萌发的分生孢子中,gapA缺失破坏了各向同性生长、极性建立和有丝分裂的正常耦合,导致高度异质的细胞群体,包括畸形的幼体和一类没有芽管和多个细胞核的巨型细胞。与野生型分生孢子不同,gapA缺失分生孢子在没有碳源的情况下萌发。在携带rasA显性活性等位基因的菌株中已报道了巨型多核孢子和不依赖碳源的萌发,表明GapA下调RasA。gapA缺失细胞表现出极性维持缺陷,其特征是顶端肿胀和亚顶端分支。在gapA缺失细胞中,强极化的野生型F-肌动蛋白分布消失。由于GapA-绿色荧光蛋白显示皮质定位,在菌丝尖端强烈占优势,我们提出,在这些尖端的质膜上,GapA介导的Ras信号下调参与了菌丝生长以及可能的无性形态发生所需的肌动蛋白细胞骨架的极化。