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Chloroplast Division Protein ARC3 Regulates Chloroplast FtsZ-Ring Assembly and Positioning in Arabidopsis through Interaction with FtsZ2

机译:叶绿体分裂蛋白ARC3通过与FtsZ2的相互作用调节叶绿体FtsZ环装配和拟南芥中的位置。

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摘要

Chloroplast division is initiated by assembly of a mid-chloroplast FtsZ (Z) ring comprising two cytoskeletal proteins, FtsZ1 and FtsZ2. The division-site regulators ACCUMULATION AND REPLICATION OF CHLOROPLASTS3 (ARC3), MinD1, and MinE1 restrict division to the mid-plastid, but their roles are poorly understood. Using genetic analyses in Arabidopsis thaliana, we show that ARC3 mediates division-site placement by inhibiting Z-ring assembly, and MinD1 and MinE1 function through ARC3. ftsZ1 null mutants exhibited some mid-plastid FtsZ2 rings and constrictions, whereas neither constrictions nor FtsZ1 rings were observed in mutants lacking FtsZ2, suggesting FtsZ2 is the primary determinant of Z-ring assembly in vivo. arc3 ftsZ1 double mutants exhibited multiple parallel but no mid-plastid FtsZ2 rings, resembling the Z-ring phenotype in arc3 single mutants and showing that ARC3 affects positioning of FtsZ2 rings as well as Z rings. ARC3 overexpression in the wild type and ftsZ1 inhibited Z-ring and FtsZ2-ring assembly, respectively. Consistent with its effects in vivo, ARC3 interacted with FtsZ2 in two-hybrid assays and inhibited FtsZ2 assembly in a heterologous system. Our studies are consistent with a model wherein ARC3 directly inhibits Z-ring assembly in vivo primarily through interaction with FtsZ2 in heteropolymers and suggest that ARC3 activity is spatially regulated by MinD1 and MinE1 to permit Z-ring assembly at the mid-plastid.
机译:叶绿体分裂是通过组装包含两个细胞骨架蛋白FtsZ1和FtsZ2的中叶叶绿体FtsZ(Z)环而启动的。叶绿体3(ARC3),MinD1和MinE1的分裂部位调节剂的积累和复制将分裂限制在中间质体,但人们对其作用的了解甚少。使用拟南芥中的基因分析,我们显示ARC3通过抑制Z环装配以及通过ARC3的MinD1和MinE1功能来介导分裂位点的位置。 ftsZ1空突变体表现出一些中质体FtsZ2环和收缩,而在缺少FtsZ2的突变体中未观察到收缩和FtsZ1环,表明FtsZ2是体内Z环组装的主要决定因素。 arc3 ftsZ1双突变体表现出多个平行但无中质体FtsZ2环,类似于arc3单突变体的Z环表型,表明ARC3影响FtsZ2环和Z环的定位。 ARC3在野生型和ftsZ1中的过表达分别抑制Z环和FtsZ2环的组装。与其在体内的作用一致,ARC3在两个杂交试验中与FtsZ2相互作用,并抑制异源系统中的FtsZ2装配。我们的研究与其中ARC3主要通过与杂聚物中的FtsZ2相互作用直接直接抑制体内Z环组装的模型相一致,并表明ARC3的活性在空间上受MinD1和MinE1的调节,以允许Z环在质体中间组装。

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