MTOControl · Spatiotemporal coordination of microtubule-organizing centers in two evolutionary distant eukaryotes
„Хоризонт Европа“ — Действия „Мария Склодовска-Кюри“
- Период
- 2023-05-15 → 2025-05-14
- Финансиране от ЕС
- 173 847 €
- Участници
- 1
- Схема
- HORIZON-TMA-MSCA-PF-EF
Линиите свързват координатора с партньорите.
Накратко на български
Зелените водорасли се изучават, за да се разбере как центролите и други структури организират деленето на клетките им. Познаването на тези процеси помага за разбирането на размножаването на водораслите, които абсорбират въглероден диоксид от атмосферата.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Spatiotemporal coordination of microtubule-organizing centers in two evolutionary distant eukaryotes
Green algae play a significant role in the global CO2 absorption, removing this greenhouse gas from the atmosphere and using it for photosynthesis. To keep the atmosphere balanced, especially with the growing challenges of climate change, it is important to understand the basic cell biology of green algae proliferation: their cell cycle and especially their mitosis and cell division. During mitosis, a massive reorganization of the microtubule cytoskeleton is critical to ensure mitotic spindle formation, proper segregation of chromosomes and, finally, cell division. In animals, the main microtubule organizing center (MTOC) coordinating microtubules is the centrosome, which contains a central pair of so-called centrioles, cylindrical, complex structures made of microtubules. During mitosis in animals, centrosomes are positioned at the two poles of the mitotic spindle, organizing spindle microtubules. In the evolution of land plants, centrioles were lost and spindle microtubules were organized by a centriole-free, dispersed MTOC. In the eukaryotic tree of life, green algae are in an interesting position “in between” animals and land plants to understand evolution of MTOCs in the green lineage and the impact on mitosis. The unicellular green algae model organism, Chlamydomons reinhardtii, has retained animal-like centrioles which were often assumed to act as MTOCs for mitotic spindle microtubules in the alga. However, there is a clear gap between mitotic spindle poles and the position of the centrioles in the alga cell, questioning whether centrioles are the MTOCs of spindle microtubules in Chlamydomonas. Instead, a second, separated MTOC might coordinate microtubules of the mitotic spindle. In this project, I investigated the dynamics and ultrastructural organization of mitosis, centrioles and associated structures in the green alga Chlamydomonas reinhardtii to understand how the green alga proliferates and which role different MTOCs play during mitosis of the alga in comparison to animals and land plants. The results of my project will help to understand evolution and diversity of MTOC and mitosis biology in green algae and might ultimately give a new view on how the dispersed MTOC of land plants evolved.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Microtubule-organizing centers (MTOCs) are key eukaryotic structures for microtubule nucleation and organization. Many MTOCs contain centrioles, organelles with two critical functions. i) In mitosis, they localize to the pole of the mitotic spindle aiding its organization. ii) After cell division, centrioles are repurposed as basal bodies at the plasma membrane where they are essential for cilia/flagella formation. Defects in centriole/basal body (CBB) repurposing can have devastating consequences and lead e.g. to infertility in human sperm. CBB functions correlate with subcellular localization, but is the spatiotemporal control required for this organelle to fulfill two distinct functions? How did the ancestral CBB evolve these functions? And why are different MTOCs not present simultaneously in a cell? To tackle these questions, I will first analyze and compare CBB repurposing strategies during the cell cycle of the green alga Chlamydomonas rheinhardtii with those in the complex life cycle of the acellular slime mold Physarum polycephalum, two evolutionary distant eukaryotes. To do so, I will develop and apply a correlative microscopy workflow in which time-lapse imaging of cells is followed by cryo-fixation and expansion microscopy (Cryo-ExM) combined with Stimulated Emission Depletion (STED). Using transient overexpression and laser ablation, I will interfere with spatial and temporal control of CBB repurposing to elucidate the role of subcellular location of this bifunctional organelle. Further, I will study how cells cope with several different MTOCs at a time, likely competing for tubulin. This project will provide a novel, high-end correlative live-cell and super-resolution imaging pipeline, which can be easily adapted for various species and cellular structures. Understanding the different strategies of CBB repurposing that evolved will have broad implications as a basis to understand CBB defects in the human cell cycle and during spermatogenesis.
Оригинален текст от CORDIS (на английски).
Участници
- EUROPEAN MOLECULAR BIOLOGY LABORATORY · HeidelbergКоординаторГермания
Връзки
- Виж в CORDIS
- DOI: 10.3030/101109569
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e51c6a82df&appId=PPGMS
- https://ec.europa.eu/research/participants/documents/downloadPublic?documentIds=080166e51c6ab329&appId=PPGMS
Данни: CORDIS, © Европейски съюз
