Chapter 11: Cell Cycle

11.2. Regulation of Cell Cycle

Learning Objectives

By the end of this section, you will be able to:

  • Explain how the three internal control checkpoints occur at the end of G1, at the G2–M transition, and during metaphase.
  • Describe how cancer is caused by uncontrolled cell growth.

Regulation at Internal Checkpoints

It is essential that daughter cells be exact duplicates of the parent cell. Mistakes in the duplication or distribution of the chromosomes lead to mutations that may be passed forward to every new cell produced from the abnormal cell. To prevent a compromised cell from continuing to divide, there are internal control mechanisms that operate at three main cell cycle checkpoints at which the cell cycle can be stopped until conditions are favorable. These checkpoints occur near the end of G1, at the G2–M transition, and during metaphase (Figure 11.2.1.).

This illustration shows the three major check points of the cell cycle, which occur in G1, G2, and mitosis.
Figure 11.2.1: The cell cycle is controlled at three checkpoints. Integrity of the DNA is assessed at the G1 checkpoint. Proper chromosome duplication is assessed at the G2 checkpoint. Attachment of each kinetochore to a spindle fiber is assessed at the M checkpoint.

The G1 Checkpoint

The G1 checkpoint determines whether all conditions are favorable for cell division to proceed. The G1 checkpoint, also called the restriction point, is the point at which the cell irreversibly commits to the cell-division process. In addition to adequate reserves and cell size, there is a check for damage to the genomic DNA at the G1 checkpoint. A cell that does not meet all the requirements will not be released into the S phase.

The G2 Checkpoint

The G2 checkpoint bars the entry to the mitotic phase if certain conditions are not met. As in the G1 checkpoint, cell size and protein reserves are assessed. However, the most important role of the G2 checkpoint is to ensure that all of the chromosomes have been replicated and that the replicated DNA is not damaged.

The M Checkpoint

The M checkpoint occurs near the end of the metaphase stage of mitosis. The M checkpoint is also known as the spindle checkpoint because it determines if all the sister chromatids are correctly attached to the spindle microtubules. Because the separation of the sister chromatids during anaphase is an irreversible step, the cycle will not proceed until the kinetochores of each pair of sister chromatids are firmly anchored to spindle fibers arising from opposite poles of the cell.

The Cell Cycle Out of Control: Implications

Most people understand that cancer or tumors are caused by abnormal cells that multiply continuously. If the abnormal cells continue to divide unstopped, they can damage the tissues around them, spread to other parts of the body, and eventually result in death. In healthy cells, the tight regulation mechanisms of the cell cycle prevent this from happening, while failures of cell cycle control can cause unwanted and excessive cell division. Failures of control may be caused by inherited genetic abnormalities that compromise the function of certain “stop” and “go” signals. Environmental insult that damages DNA can also cause dysfunction in those signals. Often, a combination of both genetic predisposition and environmental factors lead to cancer.

 

Three situations are shown. In the first, normal cell division and normal apoptosis creates a balanced mixture of cells and results in homeostasis. In the second, increased cell division and normal apoptosis results in a tumor. In the third, normal cell division and decreased apoptosis results in a tumor.
Figure 11.2.2: Cell Division and Apoptosis. In an adult organism, normal cell division is balanced by apoptosis (programmed cell death) to maintain a constant cell number in homeostasis. Either an increase in cell division or a decrease in apo ptosis leads an increase in the number of cells and tumor formation. Credit: Rao, A. and Ryan, K. Department of Biology, Texas A&M University.

The process of a cell escaping its normal control system and becoming cancerous may actually happen throughout the body quite frequently. Fortunately, certain cells of the immune system are capable of recognizing cells that have become cancerous and destroying them. However, in certain cases the cancerous cells remain undetected and continue to proliferate.

If the resulting tumor does not pose a threat to surrounding tissues, it is said to be benign and can usually be easily removed. If capable of damage, the tumor is considered malignant and the patient is diagnosed with cancer.

License and attributions:

  • Concepts of Biology, 2013, Fowler, S. et al. License: CC BY 4.0. Located at https://openstax.org/books/concepts-biology/pages/6-2-the-cell-cycle
  • Anatomy and Physiology, Second edition, 2022, Betts, J.G. et al. License: CC BY 4.0. Located at https://openstax.org/books/anatomy-and-physiology-2e/pages/3-5-cell-growth-and-division
  • Biology, Second edition, 2018, Clark, M.A. et al. License: CC BY 4.0. Located at https://openstax.org/books/biology-2e/pages/10-4-cancer-and-the-cell-cycle

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BIO130: Introduction to Physiology Copyright © 2024 by Dinor Dhanabala; Sandra Fraley; and Gordon Lake is licensed under a Creative Commons Attribution 4.0 International License, except where otherwise noted.

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