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ToggleThe heart is the first functional organ to develop in a fetus. Around the third week of pregnancy, cells begin to differentiate and form the heart tube, which starts beating spontaneously by the end of the third week or early in the fourth week. This early heartbeat helps to pump blood through the developing circulatory system, which is crucial for the growth and development of other organs.
Simultaneously, the brain begins its development process. It starts as a simple neural tube, which closes by the end of the fourth week of pregnancy. From this tube, the complex structure of the brain will eventually develop. The brain’s early development is critical as it controls the growth of other vital systems and organs in the body.
The Cell Cycle: Essential for Growth and Division
It all starts with just a single fertilized egg.
That tiny cell begins to divide and multiply through mitosis, creating more and more cells that are genetically identical to each other.
As weeks pass, the embryo transforms into a fetus.
The rapid mitotic divisions enable the fetus to develop the necessary tissues and structures for survival outside the womb.
This is simply the power of the cell cycle!
In the realm of life’s building blocks, there exists a remarkable process that orchestrates growth, repair, and reproduction. It is the Cell Cycle.
The Cell cycle is a series of events that take place in a cell as it grows and divides. The cell cycle is divided into two major phases: Interphase and the Mitotic phase.
Interphase: Setting the Stage for Division
To start with the interphase, this phase prepares the cell for division by duplicating the DNA.
Interphase itself is three phases: G one phase, S phase and G two phase.
G One phase:
In humans, at the beginning of interphase which means in G one phase, each cell has 46 chromosomes. Each of these chromosomes is made up of one chromatid.
S Phase:
During S phase, DNA duplicates.
G Two Phase:
At the end of interphase which means in G two phase, the number of chromosomes remains the same which is 46.
But now each chromosome is made up of two identical sister chromatids connected by a centromere.
After Interphase, the cell is now ready for division through the mitotic phase.
Mitotic Phase:
The Mitotic phase includes mitosis followed by cytokinesis.
During Mitosis, the nucleus divides through four phases: Prophase, Metaphase, Anaphase and Telophase.
Prophase:
At the beginning of prophase, the nuclear envelope and the nucleolus of the cell disappears.
The thin, thread like chromatin condenses to form visible chromosomes.
The pair of centrioles in the cell moves apart and forms the spindle fibers.
Later, during prophase, the centrioles reach the opposite poles of the cell and spindle fibers extend from each centriole towards the edge of the cell, forming a structure called the aster.
After that, chromosomes attach to spindle fibers through the kinetochore.
The kinetochore is a patch of protein found on the centromere of each sister chromatid. The two kinetochores of each chromosome should be attached to spindle fibers from opposite poles.
It is important to note that each chromosome attaches to a separate spindle fiber.
After Prophase, the cell starts with Metaphase.
Metaphase:
During Metaphase, the chromosomes line up the equator of the cell forming the equatorial plate.
Metaphase is proceeded with Anaphase.
Anaphase:
Throughout Anaphase, the glue holding the sister chromatids together is broken down. And the spindle fibers shorten toward the poles. This pulls sister chromatids of the same chromosomes apart.
Then we can say during Anaphase sister chromatids separate.
The last phase of Mitosis is the Telophase.
Telophase:
In telophase, the cell’s nucleus is nearly done dividing.
We notice that the nuclear envelope re-forms around each lot of chromatids at the poles, nucleolus re-appears as well, the spindle fibers are broken and the chromosomes de-condense back to the chromatin state.
Besides the division of nucleus, constrictions of the cytoplasmic membrane starts.
By the end of Telophase, the same cytoplasm shares two identical nuclei.
Mitosis ends with Telophase but cell division is not done yet. The cytoplasm still has to split into two cells.
Following Mitosis, the cell undergoes cytokinesis.
Cytokinesis:
Cytokinesis involves the division of the cytoplasm.
This process differs between animal and plant cells.
In animal cell, cytokinesis is contractile as the cell pinches into two. This process is known as the cleavage furrow.
However, in plant cells, due to the presence of a rigid cell wall, the cell can’t constrict. Instead, a structure called
Watch Complete Video of Cell Cycle with Step by Step Examination:
Assuming the intended query was about the “cell cycle,” it refers to the series of events that take place in a cell leading to its division and duplication (replication). It consists of the four stages outlined above, through which the cell grows, replicates its DNA, and divides.
In GCSE biology, the cell cycle is explained as the process through which a cell replicates itself, crucial for growth, repair, and reproduction in organisms. It encompasses:
While traditionally described in four or five stages, a detailed breakdown could include:
The G1 phase primarily serves for cell growth and preparation for DNA replication. During this phase, the cell increases in size, produces RNA, synthesizes proteins, and accumulates the resources necessary for DNA synthesis and mitotic division.
DNA replication occurs during the S phase (Synthesis phase) of the cell cycle. This phase is dedicated to copying the cell’s genetic material so that each new cell will have a complete set of chromosomes.
Mitosis is the division of the nucleus, where the cell’s chromosomes are equally divided between two new nuclei. It includes stages like prophase, metaphase, anaphase, and telophase. Cytokinesis, on the other hand, is the division of the cell’s cytoplasm, resulting in two separate daughter cells. It begins during or after the late stages of mitosis.
Checkpoints in the cell cycle are critical control mechanisms that ensure the proper progression of the cycle. They help verify whether the processes at each phase have been accurately completed before the cell moves into the next phase. This regulation prevents errors that could lead to cell death or disease, such as cancer, ensuring genetic stability and cellular function.
During the S phase, the entire DNA content of the nucleus is replicated. This replication must be precise to maintain genetic fidelity in daughter cells. Enzymes like DNA polymerase play a crucial role in this process, ensuring that each base pair is copied correctly to avoid mutations.
The cell cycle is regulated by a complex system of proteins and enzymes including cyclins, cyclin-dependent kinases (CDKs), and tumor suppressors like p53. These proteins ensure the cell cycle progresses at the correct rate and that cells only divide when appropriate. They control the activation and deactivation of key points in the cycle through phosphorylation and other chemical modifications.
During the G2 phase, the cell continues to grow and produces proteins and organelles. It also makes necessary repairs to DNA and begins the initial steps required to prepare for mitosis, such as the synthesis of microtubules essential for chromosome separation.
The cell cycle can become dysregulated through mutations in genes that encode for critical regulatory proteins (like CDKs, cyclins, and tumor suppressors). This can result in unchecked cell growth and division, a hallmark of cancer. Environmental factors and viral infections can also lead to disruptions in cell cycle regulation.
Mitosis consists of four stages:
In prokaryotic cells, the cell cycle is simpler and usually consists of a form of cell division known as binary fission. Prokaryotes lack a nucleus, so their DNA replication and segregation occur in the cytoplasm. In contrast, eukaryotic cells undergo a complex cell cycle that includes interphase (G1, S, G2 phases) and mitosis, involving intricate mechanisms of DNA replication, chromosome segregation, and cell division.
A malfunction in the G1/S checkpoint can lead to the progression of cells with DNA damage into the S phase, where they replicate their DNA. This can result in the accumulation of mutations, which may contribute to the development of cancer.
Nutrients and growth factors influence the cell cycle by providing the necessary signals that encourage or inhibit cell growth and division. These factors activate specific signaling pathways that can lead to the activation of cyclins and cyclin-dependent kinases, pushing the cell cycle forward.
Apoptosis plays a critical role in eliminating damaged, diseased, or unwanted cells, thus maintaining cellular health and tissue homeostasis. It helps prevent the development of cancer by removing cells with potentially harmful mutations.
Protein p53 acts as a guardian of the genome, pausing the cell cycle in response to DNA damage. It activates DNA repair genes when damage is detected and can initiate apoptosis if the damage is irreparable, preventing the propagation of faulty cells.
Proto-oncogenes promote cell division and growth, acting as accelerators for the cell cycle. Conversely, tumor suppressor genes act as brakes, halting the cell cycle to allow for DNA repair or to prevent excessive cell growth. Mutations in these genes can lead to unchecked cell proliferation, characteristic of cancers.
The metaphase checkpoint ensures that all chromosomes are properly aligned and attached to the mitotic spindle before cell division proceeds. This checkpoint prevents the unequal distribution of chromosomes, which could lead to genetic disorders or cell death.
During the G1 phase, cells employ several DNA repair mechanisms such as nucleotide excision repair, base excision repair, and mismatch repair to correct errors that occurred during DNA replication or due to environmental insults, thus preserving genome integrity.
During embryonic development, the cell cycle is characterized by rapid divisions to facilitate growth. As development progresses and cells differentiate, the cell cycle slows, and controls become stricter to maintain tissue and organ integrity in the mature organism.
Telomeres are repetitive nucleotide sequences at the ends of chromosomes that protect them from deterioration or fusion with neighboring chromosomes. As cells divide, telomeres shorten, eventually leading to cell senescence or apoptosis, influencing aging and the risk of age-related diseases.
In stem cells, the cell cycle is highly regulated to maintain a balance between self-renewal and differentiation. Stem cells typically have a shorter G1 phase to facilitate rapid division, which is essential for tissue growth and regeneration. In contrast, fully differentiated cells often have a longer cell cycle or exit the cell cycle entirely (entering the G0 phase), focusing on specialized functions rather than proliferation.
Checkpoints in the cell cycle ensure that each stage is completed correctly before the cell proceeds to the next stage. They help prevent cells from duplicating damaged DNA or dividing prematurely, which is crucial for maintaining genetic stability.
If a cell’s DNA is damaged beyond repair, the cell will typically initiate a process called apoptosis, or programmed cell death. This mechanism prevents the damaged DNA from being passed on to daughter cells, which could lead to mutations and cancer.
Growth factors stimulate cell division by binding to specific receptors on the cell surface. This binding triggers a cascade of signaling pathways that ultimately activate proteins necessary for progressing through the cell cycle phases.
Mitosis is the process of nuclear division in eukaryotic cells where one cell divides to produce two genetically identical daughter cells. It is essential for growth, tissue repair, and asexual reproduction in multicellular organisms.
Cancer is related to the cell cycle because it involves the uncontrolled growth and division of cells. Mutations in genes that regulate the cell cycle can lead to unchecked cellular proliferation, which forms tumors and spreads through tissues.
Cyclins and cyclin-dependent kinases (CDKs) are proteins that regulate the cell cycle’s progression. Cyclins bind to CDKs, activating them; the activated CDKs then phosphorylate target proteins to drive the cell cycle forward.
Cytokinesis is the process of cytoplasmic division, which occurs after mitosis. It involves the splitting of the cell’s cytoplasm into two daughter cells, each with its own nucleus following mitosis, resulting in the physical separation of the cells.
The G1 phase is significant because it is the primary period of cell growth before DNA replication occurs. During this phase, cells increase in size, produce RNA, and synthesize proteins necessary for DNA synthesis and the subsequent phases of the cell cycle.
The transition from the G2 phase to mitosis is regulated by the G2/M checkpoint. This checkpoint ensures that the cell is ready to enter mitosis, checking for DNA damage and ensuring all DNA has been replicated correctly.
Binary fission is the method by which prokaryotic cells, such as bacteria, reproduce. It is a simpler and quicker process than mitosis, involving the replication and division of the cell into two parts, each with an identical copy of the original DNA, closely related to the principles of the cell cycle in eukaryotic cells.