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GAP Activity, but Not Subcellular Targeting, Is Required for Arabidopsis RanGAP Cellular and Developmental Functions

机译:拟南芥RanGAP细胞和发育功能需要GAP活性,而不是亚细胞靶向

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摘要

The Ran GTPase activating protein (RanGAP) is important to Ran signaling involved in nucleocytoplasmic transport, spindle organization, and postmitotic nuclear assembly. Unlike vertebrate and yeast RanGAP, plant RanGAP has an N-terminal WPP domain, required for nuclear envelope association and several mitotic locations of Arabidopsis thaliana RanGAP1. A double null mutant of the two Arabidopsis RanGAP homologs is gametophyte lethal. Here, we created a series of mutants with various reductions in RanGAP levels by combining a RanGAP1 null allele with different RanGAP2 alleles. As RanGAP level decreases, the severity of developmental phenotypes increases, but nuclear import is unaffected. To dissect whether the GAP activity and/or the subcellular localization of RanGAP are responsible for the observed phenotypes, this series of rangap mutants were transformed with RanGAP1 variants carrying point mutations abolishing the GAP activity and/or the WPP-dependent subcellular localization. The data show that plant development is differentially affected by RanGAP mutant allele combinations of increasing severity and requires the GAP activity of RanGAP, while the subcellular positioning of RanGAP is dispensable. In addition, our results indicate that nucleocytoplasmic trafficking can tolerate both partial depletion of RanGAP and delocalization of RanGAP from the nuclear envelope.
机译:Ran GTPase激活蛋白(RanGAP)对于参与核质运输,纺锤体组织和有丝分裂后核大会的Ran信号很重要。与脊椎动物和酵母RanGAP不同,植物RanGAP具有N末端WPP结构域,是拟南芥RanGAP1的核被膜缔合和几个有丝分裂位置所必需的。两个拟南芥RanGAP同源物的双无效突变体是配子体致死的。在这里,我们通过将RanGAP1无效等位基因与不同的RanGAP2等位基因结合,创建了一系列RanGAP水平降低的突变体。随着RanGAP水平的降低,发育表型的严重性增加,但核输入不受影响。为了剖析RanGAP的GAP活性和/或亚细胞定位是否与观察到的表型有关,用RanGAP1变异体转化了一系列的rangap突变体,这些变异体带有消除GAP活性和/或WPP依赖的亚细胞定位的点突变。数据表明,植物生长受到强度增加的RanGAP突变体等位基因组合的影响,并且需要RanGAP的GAP活性,而RanGAP的亚细胞定位则是必不可少的。此外,我们的结果表明核质运输可以容忍RanGAP的部分耗竭和RanGAP从核被膜上的脱位。

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