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双态真菌马尔尼菲青霉的CDC42同源物在生长过程中对正确的细胞极化是必需的,但对发育不是必需的。

The CDC42 homolog of the dimorphic fungus Penicillium marneffei is required for correct cell polarization during growth but not development.

作者信息

Boyce K J, Hynes M J, Andrianopoulos A

机构信息

Department of Genetics, University of Melbourne, Parkville, Victoria 3010, Australia.

出版信息

J Bacteriol. 2001 Jun;183(11):3447-57. doi: 10.1128/JB.183.11.3447-3457.2001.

Abstract

The opportunistic human pathogenic fungus Penicillium marneffei is dimorphic and is thereby capable of growth either as filamentous multinucleate hyphae or as uninucleate yeast cells which divide by fission. The dimorphic switch is temperature dependent and requires regulated changes in morphology and cell shape. Cdc42p is a Rho family GTPase which in Saccharomyces cerevisiae is required for changes in polarized growth during mating and pseudohyphal development. Cdc42p homologs in higher organisms are also associated with changes in cell shape and polarity. We have cloned a highly conserved CDC42 homolog from P. marneffei named cflA. By the generation of dominant-negative and dominant-activated cflA transformants, we have shown that CflA initiates polarized growth and extension of the germ tube and subsequently maintains polarized growth in the vegetative mycelium. CflA is also required for polarization and determination of correct cell shape during yeast-like growth, and active CflA is required for the separation of yeast cells. However, correct cflA function is not required for dimorphic switching and does not appear to play a role during the generation of specialized structures during asexual development. In contrast, heterologous expression of cflA alleles in Aspergillus nidulans prevented conidiation.

摘要

机会性人类致病真菌马尔尼菲青霉是双态的,因此能够以丝状多核菌丝或通过裂变进行分裂的单核酵母细胞的形式生长。双态转换取决于温度,需要形态和细胞形状的调节变化。Cdc42p是一种Rho家族GTP酶,在酿酒酵母中,它是交配和假菌丝发育过程中极性生长变化所必需的。高等生物中的Cdc42p同源物也与细胞形状和极性的变化有关。我们从马尔尼菲青霉中克隆了一个高度保守的CDC42同源物,命名为cflA。通过产生显性负性和显性激活的cflA转化体,我们表明CflA启动芽管的极性生长和延伸,并随后维持营养菌丝体中的极性生长。在酵母样生长过程中,CflA也是细胞极化和正确细胞形状确定所必需的,并且活性CflA是酵母细胞分离所必需的。然而,双态转换不需要cflA的正确功能,并且在无性发育过程中产生特殊结构时似乎也不发挥作用。相反,cflA等位基因在构巢曲霉中的异源表达阻止了分生孢子形成。

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