The Role and Structure of Centrosomes in Cell Division
Examining how centrosomes and their components contribute to cell division.
― 6 min read
Table of Contents
- Structure of Centrioles
- Centrosome Composition and Function
- The Role of Protein Structures in PCM
- Studying Centrosomes in C. Elegans
- Techniques for Observing Centrosomes
- Key Findings on Centrosome Architecture
- Changes During Centriole Development
- Understanding Microtubule Organization
- Exploring the Structure of PCM
- Conclusion and Future Directions
- Original Source
- Reference Links
Centrosomes are important parts of a cell that help organize structures called Microtubules. These microtubules are key for forming the mitotic spindle during cell division. A centrosome is made up of two cylindrical shapes known as Centrioles. These centrioles are surrounded by a zone that contains various proteins. The way these centrioles and proteins work together is crucial for the proper division of cells.
Structure of Centrioles
Centrioles are formed from smaller protein building blocks arranged in a very specific way. Each centriole has an inner structure composed of a core set of proteins, which are the same in many living things. The centrioles can be found in different forms depending on the organism. For example, in some animals, centrioles are arranged in triplets, while in others, they can be found in doublets or singlets. During the cell cycle, centrioles duplicate to provide each new cell with the structures it needs for dividing properly.
Centrosome Composition and Function
The area surrounding the centrioles, known as the Pericentrial Material (PCM), is rich in proteins and plays a key role in organizing microtubules. During the rest phase of the cell cycle, this area is thin, but it grows larger during cell division. This growth is essential for forming the spindle that separates genetic material into new cells.
One important feature of the PCM is the presence of a structure called the gamma-tubulin ring complex. This structure is critical for starting the growth of microtubules. Alongside this complex are various proteins that help maintain microtubules, ensuring they function correctly during cell division.
The Role of Protein Structures in PCM
The PCM is covered with long coiled proteins. These proteins can assemble into larger structures. Some proteins work together to help organize the PCM's structure and function. There are also kinases, which are proteins that add phosphate groups to other proteins, helping in organizing and assembling the PCM during the cell cycle.
While we know many proteins that make up the PCM, how they are organized during cell division remains unclear. Studies using older techniques often show the PCM as a messy area surrounding the centrioles. A special study of a type of clam revealed a network of fibers that could represent a scaffold for the PCM, but it is still uncertain if this is a common feature in other organisms.
Studying Centrosomes in C. Elegans
The roundworm C. elegans is a useful model for studying centrosomes because it has a simpler structure compared to more complex organisms like flies or humans. Much of what we know about how centrioles and the PCM work comes from studies of these worms.
The process of making centrioles in C. elegans involves several proteins working in a specific order. Different proteins come together to form structures that help in the growth of centrioles. Studies on the worms have shown that certain proteins are located next to the centrioles and contribute to the assembly of the PCM.
Techniques for Observing Centrosomes
To better understand how centrosomes change during cell division, researchers used advanced imaging methods. These techniques allow scientists to look closely at the structures within cells while keeping them in their natural state. This is important because traditional methods can damage the very structures researchers want to study.
By using a special cooling technique, researchers preserve cells in a near-natural state, enabling them to visualize different centrosome structures at various stages of cell division. This method led to the discovery of new features in centrioles and provided important details on how centrosomes organize microtubules.
Key Findings on Centrosome Architecture
The research revealed that centrosomes are organized in layers with specific structures. Each centrosome has a central area containing centrioles, surrounded by zones where microtubules and ribosomes are located. The areas where ribosomes are absent indicate the limits of the PCM, while the regions without membranes show where the PCM interfaces with other cellular structures.
Observations during different cell cycle stages showed that the sizes of these zones could change as cells progress through division. For instance, during the mitotic phase, the PCM expands in size compared to interphase, allowing for the organization of microtubules needed for the spindle apparatus.
Changes During Centriole Development
During the maturation of centrioles, important structural changes take place. The new research provided insights into the differences between mother and daughter centrioles. The mother centriole had features not present in the daughter, suggesting that the structure and function of centrioles evolve as they mature.
Some structures observed include an incomplete tube and a star-shaped area surrounding the centriole. These features may help stabilize the centriole, ensuring it can function properly during cell division.
Understanding Microtubule Organization
Microtubules play a significant role in maintaining cell shape and facilitating cell division. The organization of microtubules within the PCM is critical for creating the mitotic spindle. Researchers noted that microtubules nucleated by the PCM consistently had a specific structure, showing that the PCM may influence the shape and function of these microtubules.
The findings showed that centrioles create different microtubule structures compared to those formed by the PCM. This indicates that distinct mechanisms may regulate how microtubules are formed in these areas, demonstrating the complex relationship between the centriole and PCM.
Exploring the Structure of PCM
The study found that the PCM forms a disordered network of proteins creating a flexible but interconnected meshwork. This structure allows the PCM to accommodate smaller proteins while potentially restricting access to larger protein complexes.
The pores formed within this matrix were large enough to permit the passage of important proteins but may also limit the entry of larger structures. Overall, the PCM's architecture is critical for its various functions during cell division, allowing it to adapt as needed throughout the cell cycle.
Conclusion and Future Directions
In summary, the research provides a detailed look at the structure of centrosomes and how they function during cell division. The findings shed light on the arrangement of centrioles and the PCM, illustrating how they work together. These insights could help further our understanding of cell biology and possibly offer new perspectives on how changes in these structures might impact health and disease.
Future research will continue to use advanced imaging techniques to explore other cellular structures and deepen our understanding of the dynamic processes involved in cell division. By studying different organisms, we can begin to uncover the evolutionary significance of these cellular components, leading to broader insights in biology.
Title: Native molecular architectures of centrosomes in C. elegans embryos
Abstract: Centrosomes organize microtubules that are essential for mitotic divisions in animal cells. They consist of centrioles surrounded by Pericentriolar Material (PCM). Questions related to mechanisms of centriole assembly, PCM organization, and microtubule formation remain unanswered, in part due to limited availability of molecular-resolution structural analyses in situ. Here, we use cryo-electron tomography to visualize centrosomes across the cell cycle in cells isolated from C. elegans embryos. We describe a pseudo-timeline of centriole assembly and identify distinct structural features including a cartwheel in daughter centrioles, and incomplete microtubule doublets surrounded by a star-shaped density in mother centrioles. We find that centriole and PCM microtubules differ in protofilament number (13 versus 11) indicating distinct nucleation mechanisms. This difference could be explained by atypical {gamma}-tubulin ring complexes with 11-fold symmetry identified at the minus ends of short PCM microtubules. We further characterize a porous and disordered network that forms the interconnected PCM. Thus, our work builds a three-dimensional structural atlas that helps explain how centrosomes assemble, grow, and achieve function.
Authors: Julia Mahamid, F. Tollervey, M. U. Rios, E. Zagoriy, J. B. Woodruff
Last Update: 2024-04-03 00:00:00
Language: English
Source URL: https://www.biorxiv.org/content/10.1101/2024.04.03.587742
Source PDF: https://www.biorxiv.org/content/10.1101/2024.04.03.587742.full.pdf
Licence: https://creativecommons.org/licenses/by-nc/4.0/
Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.
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