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Cell Cycle

For medical students2 min readUpdated 2026-10-10

The cell cycle is the entire sequence of events from the formation of a cell by the division of a mother cell until its own division or death. The ability (or inability) to enter the cycle determines a cell's entire lifespan and its function in the body.

Diploid set2n — characteristic of normal somatic cells
DurationApproximately 24 hours for rapidly dividing human cells
Synthetic periodDNA replication occurs from 2n to 4n

DNA Dynamics and Types of Division

Understanding the cycle is based on changes in the amount of DNA, denoted by the Latin letter n (the haploid set, typical of mature gametes). Most somatic cells in our body are diploid (2n).

There are two main types of cell division:

Periods of the Mitotic Cycle

For cells capable of dividing, the life cycle is identical to the mitotic cycle. It consists of the division phase itself (mitosis) and a prolonged preparation phase — interphase.

Interphase includes three phases:

  1. $G_1$ (presynthetic phase). Begins immediately after mitosis. The cell grows and restores cytoplasmic volume. At the end of the phase is the "restriction point": if the cell receives external signals (mitogens) and passes this point, it irreversibly commits to the next division. DNA set — 2n.
  2. $S$ (synthetic phase). The main event is the replication of DNA and chromosomal proteins. The DNA content increases from 2n to 4n. Centrioles duplicate near the nucleus. Centromeric regions of chromosomes are not copied in this phase, holding sister chromatids together until the start of mitosis anaphase.
  3. $G_2$ (postsynthetic phase). A relatively short stage before division. DNA set — 4n. The cell actively synthesizes substances for mitosis, primarily the protein tubulin, which builds the mitotic spindle.

Classification of Cells by Proliferative Capacity

Based on proliferative activity, all cells of the adult body can be divided into three functional groups:

Resting Phase ($G_0$) and Cell Fate

If a cell leaves the mitotic cycle at the $G_1$ stage, it enters the resting phase — $G_0$.

Exit to $G_0$ can occur for various reasons: temporary "dormancy" of stem cells, resource depletion, the need to repair DNA damage, or the initiation of specialization (differentiation).

For some cells (conditionally postmitotic), this exit is reversible: upon receiving specific signals, they can return directly from $G_0$ to the $S$ phase.

For others (postmitotic), specialization means an irreversible exit from the cycle. For example, in the epidermis, cells shift from the basal layer to the spinous, granular, and translucent layers, where they function but no longer divide, and eventually die in the cornified layer. Long-lived postmitotic cells (neurons, cardiomyocytes) function throughout the organism's entire lifespan and die either from aging or damaging factors.

Frequently asked questions

What phases are included in the process of mitosis?

Mitosis is classically divided into four sequential phases:

  • Prophase — chromatin condenses, and distinct condensed chromosomes become visible.
  • Metaphase — the mitotic spindle forms, and chromosomes align at the equatorial metaphase plate.
  • Anaphase — spindle fibers shorten, and sister chromatids separate toward opposite poles of the cell.
  • Telophase — chromosomes reach the poles, followed by the disassembly of the mitotic apparatus.
Which cyclin-dependent kinases and cyclins regulate cell cycle progression?

Cell cycle progression is controlled by complexes of cyclins and cyclin-dependent kinases (CDKs).

  • G1/S-cyclins D and E prepare cells for DNA replication.
  • Cyclins D1, D2, D3 + Cdk4/Cdk6 are necessary to cross the restriction point; cyclin D–Cdk4 and cyclin D–Cdk6 complexes help initiate a new cell cycle.
  • Cyclin E–Cdk2 is associated with cell cycle entry; in G1b phase, this complex phosphorylates the Rb protein, leading to E2F activation.
  • Cyclin A–Cdk2 triggers the S phase and initiates DNA replication.
  • Cyclin B–Cdk1 promotes the transition to mitosis and helps trigger mitotic entry.

After completing their controlled phase, cyclins are degraded via ubiquitination and proteasomal degradation.

What factors trigger apoptosis during cell cycle abnormalities?

During mitotic cycle abnormalities, apoptosis ("intrinsic pathway") is triggered by unresolvable defects detected at checkpoints:

  • DNA damage — e.g., double-strand breaks. If repair is impossible, p53 protein accumulation initiates apoptosis by activating Bax and Bak.
  • Chromosome segregation errors — incorrect distribution of genetic material in the previous division.
  • Mitotic apparatus defects — abnormal microtubule structure or improper mitotic spindle assembly checked during metaphase.

This mechanism protects against mutation accumulation and prevents malignant transformation.

How does mitosis differ from meiosis in terms of DNA?

In mitosis, DNA replicates once and the cell divides once, maintaining a diploid set (2n). In meiosis, following DNA replication, two successive divisions occur (the second without replication), yielding a haploid set (n).

What is the restriction point?

It is a checkpoint at the end of the $G_1$ phase. Once a cell passes this point, it is committed to completing the cell cycle (entering the S phase), even if stimulating signals (mitogens) disappear.

Does all DNA replicate during the S phase?

No, centromeric regions do not replicate during the S phase. They duplicate later, at the beginning of mitosis anaphase, to keep sister chromatids held together until that moment.

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