Binary division of plastids involves endoplasmic reticulum mediation.

IF 5.7 2区 生物学 Q1 PLANT SCIENCES Journal of Experimental Botany Pub Date : 2025-12-16 DOI:10.1093/jxb/eraf064
Puja Puspa Ghosh, Thomas Kadanthottu Kunjumon, Jaideep Mathur
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Abstract

Plastids divide through binary division, involving the cytosolic protein Accumulation and Replication of Chloroplast 5 (ARC5), suggested to constrict and sever the plastid envelope membrane. However, the mechanisms involved in ARC5 recruitment to the mid-plastid division site and the final separation of daughter plastids are not fully understood. Using time-lapse imaging of Arabidopsis thaliana stable transgenics expressing fluorescently tagged endoplasmic reticulum (ER) and ARC5 proteins, we investigated the role played by the ER in the late stages of plastid division. Our observations establish that prior to its mid-plastid localization at the division plane, ARC5 associates with ER membranes. ARC5-ER association generates an ER band around the plastid mid-plane that persists throughout division. Progressive tightening of the ER band narrows the middle of the plastid to form an isthmus. Concomitantly, tandem plastid-ER dynamics facilitated by membrane contact sites (MCSs) move and rotate the dividing plastid and ultimately lead to the separation of daughter plastids. Our findings strongly indicate a pivotal role for the ER in facilitating plastid division.

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质体的二元分裂涉及er介导。
质体通过二元分裂进行分裂,涉及胞质蛋白积累和叶绿体5 (ARC5)的复制,提示质体包膜的收缩和断裂。然而,ARC5在中质体分裂位点募集和子质体最终分离的机制尚不完全清楚。通过对表达荧光标记内质网和ARC5蛋白的拟南芥稳定转基因基因的延时成像,研究了内质网在质体分裂后期的作用。我们的观察证实,在分裂平面的中质体定位之前,ARC5与内质网膜相关。在整个分裂过程中,ARC5-ER结合在质体中间面周围产生一个持续存在的ER带。逐渐收紧的er带使中间的质体变窄,形成峡部。同时,在膜接触位点(MCSs)的促进下,串联质体-内质网动力学移动和旋转分裂的质体,最终导致子质体的分离。我们的研究结果强烈表明,内质网在促进质体分裂中起着关键作用。
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来源期刊
Journal of Experimental Botany
Journal of Experimental Botany 生物-植物科学
CiteScore
12.30
自引率
4.30%
发文量
450
审稿时长
1.9 months
期刊介绍: The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology. Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.
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