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拟南芥AAA型ATP酶SKD1参与多泡内体功能,并与其正向调节因子LYST相互作用蛋白5相互作用。

The Arabidopsis AAA ATPase SKD1 is involved in multivesicular endosome function and interacts with its positive regulator LYST-INTERACTING PROTEIN5.

作者信息

Haas Thomas J, Sliwinski Marek K, Martínez Dana E, Preuss Mary, Ebine Kazuo, Ueda Takashi, Nielsen Erik, Odorizzi Greg, Otegui Marisa S

机构信息

Department of Botany, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Plant Cell. 2007 Apr;19(4):1295-312. doi: 10.1105/tpc.106.049346. Epub 2007 Apr 27.

Abstract

In yeast and mammals, the AAA ATPase Vps4p/SKD1 (for Vacuolar protein sorting 4/SUPPRESSOR OF K(+) TRANSPORT GROWTH DEFECT1) is required for the endosomal sorting of secretory and endocytic cargo. We identified a VPS4/SKD1 homolog in Arabidopsis thaliana, which localizes to the cytoplasm and to multivesicular endosomes. In addition, green fluorescent protein-SKD1 colocalizes on multivesicular bodies with fluorescent fusion protein endosomal Rab GTPases, such as ARA6/RabF1, RHA1/RabF2a, and ARA7/RabF2b, and with the endocytic marker FM4-64. The expression of SKD1(E232Q), an ATPase-deficient version of SKD1, induces alterations in the endosomal system of tobacco (Nicotiana tabacum) Bright Yellow 2 cells and ultimately leads to cell death. The inducible expression of SKD1(E232Q) in Arabidopsis resulted in enlarged endosomes with a reduced number of internal vesicles. In a yeast two-hybrid screen using Arabidopsis SKD1 as bait, we isolated a putative homolog of mammalian LYST-INTERACTING PROTEIN5 (LIP5)/SKD1 BINDING PROTEIN1 and yeast Vta1p (for Vps twenty associated 1 protein). Arabidopsis LIP5 acts as a positive regulator of SKD1 by increasing fourfold to fivefold its in vitro ATPase activity. We isolated a knockout homozygous Arabidopsis mutant line with a T-DNA insertion in LIP5. lip5 plants are viable and show no phenotypic alterations under normal growth conditions, suggesting that basal SKD1 ATPase activity is sufficient for plant development and growth.

摘要

在酵母和哺乳动物中,AAA型ATP酶Vps4p/SKD1(液泡蛋白分选4/钾离子运输生长缺陷抑制因子1)是分泌性和内吞性货物进行内体分选所必需的。我们在拟南芥中鉴定出了一个VPS4/SKD1同源物,它定位于细胞质和多泡内体。此外,绿色荧光蛋白-SKD1与荧光融合蛋白内体Rab GTP酶(如ARA6/RabF1、RHA1/RabF2a和ARA7/RabF2b)以及内吞标记物FM4-64在多泡体上共定位。SKD1的ATP酶缺陷型版本SKD1(E232Q)的表达会诱导烟草(烟草)BY-2细胞内体系统发生改变,并最终导致细胞死亡。在拟南芥中诱导表达SKD1(E232Q)会导致内体增大,内部囊泡数量减少。在以拟南芥SKD1为诱饵的酵母双杂交筛选中,我们分离出了一个哺乳动物LYST相互作用蛋白5(LIP5)/SKD1结合蛋白1和酵母Vta1p(Vps20相关蛋白1)的假定同源物。拟南芥LIP5通过将其体外ATP酶活性提高4至5倍,作为SKD1的正调控因子。我们分离出了一个LIP5中存在T-DNA插入的敲除纯合拟南芥突变株系。lip5植株能够存活,在正常生长条件下没有表现出表型改变,这表明基础SKD1 ATP酶活性足以支持植物的发育和生长。

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