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The Complex Dance of Cell Division

Explore the vital process of cell division and the role of key proteins.

Ryo Fujisawa, Karim P.M. Labib

― 5 min read


Cell Division: The Cell Division: The Essential Process in cell division. Discover the crucial roles of proteins
Table of Contents

Cell division is the process by which a single cell divides to form two identical daughter cells. It is a fundamental process in life, allowing growth, repair, and reproduction. In animals, cell division primarily occurs through a process called mitosis. During mitosis, the genetic material of the cell, found in the DNA, is duplicated and evenly distributed to ensure that each daughter cell receives an identical set of chromosomes.

DNA: The Blueprint of Life

DNA, or deoxyribonucleic acid, is the molecule that contains the genetic instructions for the development, functioning, growth, and reproduction of all known living organisms. Think of it as a recipe book where each recipe is a specific gene that guides how the organism should be built and operated.

The Cell Cycle: Phases of Life

The process of cell division is organized into a series of stages known as the cell cycle. The cell cycle has several phases, but the main ones include:

  1. Interphase: This is when the cell spends most of its time. It is divided into three parts:

    • G1 Phase (Gap 1): The cell grows and prepares for DNA replication.
    • S Phase (Synthesis): DNA is replicated. The cell makes a copy of its DNA.
    • G2 Phase (Gap 2): The cell continues to grow and prepares for mitosis.
  2. M Phase (Mitosis): This is when the cell divides its copied DNA and cytoplasm to form two new cells.

The Importance of DNA Replication

During the S phase of interphase, the cell duplicates its DNA. This is crucial because each daughter cell needs an exact copy of the DNA to function properly. If DNA replication is not completed before mitosis starts, it can lead to errors, which might cause problems for the daughter cells.

What Happens If DNA Isn't Replicated on Time?

In some cases, especially in cells with large genomes or in certain abnormal cell conditions like cancer, DNA replication can continue even as the cell is preparing to divide. This can create a tricky situation, as any remaining unreplicated DNA may disrupt the even distribution of genetic material. This could be likened to trying to serve a meal that isn't fully cooked.

Entering Mitosis: The Transition

When a cell gets ready to divide, it transitions from interphase to mitosis. This transition is tightly regulated to ensure that everything is in order. If there are leftover DNA fragments, the cell has to find a way to deal with them quickly to avoid chaos during division.

The Role of Various Proteins

Several proteins play crucial roles during cell division and DNA replication. Notably, three key players include TRAIP, TTF2, and DNA polymerase epsilon (Polε). Here’s what they do in a nutshell:

  • TRAIP: This protein is like a skilled chef who ensures that the DNA is properly prepared before serving. It helps with repairing any issues and encouraging the proper breakdown of the DNA replication machinery when it's time to divide.

  • TTF2: Think of TTF2 as a helper who makes sure the chef has all the right tools. TTF2 gets involved during the final stages of DNA preparation and helps move other proteins where they need to be during division.

  • DNA Polymerase Epsilon: This protein is like the main cook who actively builds new DNA strands during replication. It works alongside TRAIP and TTF2 to ensure everything is just right before the cell splits.

How These Proteins Work Together

When cells enter mitosis, these proteins form a complex to navigate through the tricky business of DNA replication and division. For example, TRAIP gets activated during mitosis, which leads to the dismantling of leftover DNA assembly lines (replisomes) and error correction. This process is essential for maintaining the integrity of the cell's genome.

Why Do Errors Matter?

Imagine driving a car and suddenly finding the map is incomplete. You might end up in the wrong place, or worse, crash! The same applies to cells. If DNA errors are not corrected before the cell divides, it can lead to malfunctioning cells, which might promote diseases like cancer.

Mitotic DNA Synthesis (MiDAS)

Sometimes cells encounter issues during DNA replication due to stress or damage. Under such circumstances, some cells can perform what’s called Mitotic DNA Synthesis (MiDAS). This is a process where the cell continues to replicate DNA even during mitosis. It’s like trying to fix the car while driving-risky but occasionally necessary!

The Importance of TRAIP and TTF2 in MiDAS

Both TRAIP and TTF2 are essential during MiDAS. They help the cell to handle any errors that arise when replicating the DNA under stressful conditions. Without them, the chance of problems occurring during cell division increases significantly.

Conclusions on the Dance of Cell Division

The process of cell division is intricate, like a carefully choreographed dance. It involves numerous proteins that must work together effectively. If any part of the process goes wrong-like an uncoordinated dancer-the entire performance can suffer. The understanding of how these proteins function and interact is essential in areas such as cancer research, where errors in cell division lead to serious health issues.

As scientists continue to dive deeper into the world of cell biology, they hope to uncover new insights that could help improve health outcomes and develop new treatments for diseases caused by cellular malfunction.

Original Source

Title: TTF2 drives mitotic replisome disassembly and MiDAS by coupling the TRAIP ubiquitin ligase to Pol epsilon

Abstract: Mammalian cells frequently enter mitosis before DNA replication has finished, necessitating the rapid processing of replication forks to facilitate chromosome segregation. The TRAIP ubiquitin ligase induces mitotic replisome disassembly, fork cleavage, and repair via Mitotic DNA Synthesis (MiDAS). Until now, it was unclear how TRAIP is regulated in mitotic cells. Here we show that TRAIP phosphorylation mediates a complex with the TTF2 ATPase and DNA Polymerase {varepsilon} (Pol{varepsilon}). Whereas TTF2 ATPase activity removes RNA polymerase II from mitotic chromosomes, replisome disassembly involves an unanticipated mechanism. The TTF2 amino terminus couples TRAIP to Pol{varepsilon}, via tandem Zinc fingers that recognise phosphorylated TRAIP, and a motif that binds to POLE2. Thereby, TTF2 and Pol{varepsilon} cause TRAIP to ubiquitylate the CDC45-MCM-GINS (CMG) helicase, triggering replisome disassembly and MiDAS. These data identify TTF2 as a multifunctional regulator of chromatin transactions during mitosis.

Authors: Ryo Fujisawa, Karim P.M. Labib

Last Update: 2024-12-02 00:00:00

Language: English

Source URL: https://www.biorxiv.org/content/10.1101/2024.12.01.626218

Source PDF: https://www.biorxiv.org/content/10.1101/2024.12.01.626218.full.pdf

Licence: https://creativecommons.org/licenses/by/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.

Thank you to biorxiv for use of its open access interoperability.

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