Novel plant SUN-KASH bridges are involved in RanGAP anchoring and nuclear shape determination

被引:125
作者
Zhou, Xiao [1 ]
Graumann, Katja [2 ]
Evans, David E. [2 ]
Meier, Iris [1 ]
机构
[1] Ohio State Univ, Dept Mol Genet, Columbus, OH 43210 USA
[2] Oxford Brookes Univ, Fac Hlth & Life Sci, Dept Biol & Med Sci, Oxford OX3 OBP, England
基金
美国国家科学基金会;
关键词
NEMATODE CAENORHABDITIS-ELEGANS; ARABIDOPSIS-THALIANA; FUSION PROTEINS; LAMIN-A; ENVELOPE; COMPLEX; MEMBRANE; MECHANOTRANSDUCTION; TRANSFORMATION; AGROBACTERIUM;
D O I
10.1083/jcb.201108098
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inner nuclear membrane Sad1/UNC-84 (SUN) proteins interact with outer nuclear membrane (ONM) Klarsicht/ANC-1/Syne homology (KASH) proteins, forming linkers of nucleoskeleton to cytoskeleton conserved from yeast to human and involved in positioning of nuclei and chromosomes. Defects in SUN-KASH bridges are linked to muscular dystrophy, progeria, and cancer. SUN proteins were recently identified in plants, but their ONM KASH partners are unknown. Arabidopsis WPP domain interacting proteins (AtWIPs) are plant-specific ONM proteins that redundantly anchor Arabidopsis RanGTPase-activating protein 1 (AtRanGAP1) to the nuclear envelope (NE). In this paper, we report that AtWIPs are plant-specific KASH proteins interacting with Arabidopsis SUN proteins (AtSUNs). The interaction is required for both AtWIP1 and AtRanGAP1 NE localization. AtWIPs and AtSUNs are necessary for maintaining the elongated nuclear shape of Arabidopsis epidermal cells. Together, our data identify the first KASH members in the plant kingdom and provide a novel function of SUN-KASH complexes, suggesting that a functionally diverged SUN-KASH bridge is conserved beyond the opisthokonts.
引用
收藏
页码:203 / 211
页数:9
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