Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand

被引:7
作者
Anderson, Heidi L. [1 ]
Casler, Jason C. [1 ]
Lackner, Laura L. [1 ]
机构
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
基金
美国国家卫生研究院;
关键词
DYNEIN-DEPENDENT INTERACTIONS; ENDOPLASMIC-RETICULUM; CYTOPLASMIC DYNEIN; CELL CORTEX; SACCHAROMYCES-CEREVISIAE; ORGANELLE INHERITANCE; MITOTIC SPINDLE; CORTICAL ANCHOR; QUALITY-CONTROL; YEAST NUM1P;
D O I
10.1091/mbc.E21-12-0610-T
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Positioning organelles at the right place and time is critical for their function and inheritance. In budding yeast, mitochondrial and nuclear positioning require the anchoring of mitochondria and dynein to the cell cortex by clusters of Num1. We have previously shown that mitochondria drive the assembly of cortical Num1 clusters, which then serve as anchoring sites for mitochondria and dynein. When mitochondrial inheritance is inhibited, mitochondrial-driven assembly of Num1 in buds is disrupted and defects in dynein-mediated spindle positioning are observed. Using a structure-function approach to dissect the mechanism of mitochondria-dependent dynein anchoring, we found that the EF hand-like motif (EFLM) of Num1 and its ability to bind calcium are required to bias dynein anchoring on mitochondriaassociated Num1 clusters. Consistently, when the EFLM is disrupted, we no longer observe defects in dynein activity following inhibition of mitochondrial inheritance. Thus, the Num1 EFLM functions to bias dynein anchoring and activity in nuclear inheritance subsequent to mitochondrial inheritance. We hypothesize that this hierarchical integration of organelle positioning pathways by the Num1 EFLM contributes to the regulated order of organelle inheritance during the cell cycle.
引用
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页数:18
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