Imaging-based screen identifies novel natural compounds that perturb cell and chloroplast division in <i>Chlamydomonas reinhardtii</i>.
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2025-02
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Abstract
Successful cell division requires faithful division and segregation of organelles into daughter cells. The unicellular alga Chlamydomonas reinhardtii has a single, large chloroplast whose division is spatiotemporally coordinated with furrowing. Cytoskeletal structures form in the same plane at the midzone of the dividing chloroplast (FtsZ) and the cell (microtubules), but how these structures are coordinated is not understood. Previous work showed that loss of F-actin blocks chloroplast division but not furrow ingression, suggesting that pharmacological perturbations can disorganize these events. In this study, we developed an imaging platform to screen natural compounds that perturb cell division while monitoring FtsZ and microtubules and identified 70 unique compounds. One compound, curcumin, has been proposed to bind to both FtsZ and tubulin proteins in bacteria and eukaryotes, respectively. In C. reinhardtii, where both targets coexist and are involved in cell division, curcumin at a specific dose range caused a severe disruption of the FtsZ ring in chloroplast while leaving the furrow-associated microtubule structures largely intact. Time-lapse imaging showed that loss of FtsZ and chloroplast division failure delayed the completion of furrowing but not the initiation, suggesting that the chloroplast-division checkpoint proposed in other algae requires FtsZ or is absent altogether in C. reinhardtii. [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text] [Media: see text].
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Clark-Cotton, Manuella R, Sheng-An Chen, Aracely Gomez, Aditya J Mulabagal, Adriana Perry, Varenyam Malhotra and Masayuki Onishi (2025). Imaging-based screen identifies novel natural compounds that perturb cell and chloroplast division in Chlamydomonas reinhardtii. Molecular biology of the cell, 36(4). p. mbcE24090425. 10.1091/mbc.e24-09-0425 Retrieved from https://hdl.handle.net/10161/32157.
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Masayuki Onishi
The overall goal of the Onishi lab is to understand the fundamental core mechanisms of eukaryotic cell division that have been conserved throughout the evolution from the last eukaryotic common ancestor. To this end, the lab currently uses the unicellular model green alga Chlamydomonas reinhardtii, which is evolutionarily close to plants yet divide like animals by forming a cleavage furrow. Strikingly, unlike animals, this organism does not have a non-muscle type-II myosin that has been believed to be essential for furrowing. In fact, animals, fungi, slime molds, and related species are the exceptions in that they have this myosin motor protein, and the vast majority of the eukaryotes divide by some mechanism that we don't fully understand. Our work aims to understand how the cells without type-II myosin manage to form a cleavage furrow, which should shed light on the questions such as:
(1) How did the ancestral cells divide?
(2) What was the evolutionary advantage of type-II myosin when it emerged in the select lineage?
(3) How did the unique evolution into modern land plants happen?
In the lab, we use the power of genetics, genomics, and molecular and cellular biology. Specific questions include, but not limited to:
How do the three cytoskeletal systems (actin, microtubules, and septin) contribute to cell division?
What is the involvement of extracellular matrix and the ESCRT system?
How do the known and yet-to-be known genes interact with one another to control cell division?
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