Cell cycle

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Cell cycle

HMBP

HMBP

Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Gene regulation
Epigenetics
Amino acids and protein folding
DNA replication
DNA damage and repair
Cell cycle
DNA mutations
Cellular structure and function
Introduction to pharmacology
Enzyme function
Pharmacodynamics: Agonist, partial agonist and antagonist
Human development days 1-4
Human development week 2
Human development days 4-7
Human development week 3
Ectoderm
Mesoderm
Endoderm
Ionic bonding
Covalent bonding
Physiologic pH and buffers
Buffering and Henderson-Hasselbalch equation
Acid-base disturbances: Pathology review
Electron transport chain and oxidative phosphorylation
Glycogen metabolism
Pentose phosphate pathway
Gluconeogenesis
Cell membrane
Cytoskeleton and intracellular motility
Selective permeability of the cell membrane
Cell signaling pathways
Mitosis and meiosis
Light microscopy and staining methods
Pharmacodynamics: Drug-receptor interactions
Pharmacodynamics: Desensitization and tolerance
Arsenic poisoning
Pharmacokinetics: Drug absorption and distribution
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Independent assortment of genes and linkage
Inheritance patterns
Drug administration and dosing regimens
Cholesterol metabolism
Ketone body metabolism
Fatty acid synthesis
Nitrogen and urea cycle
Amino acid metabolism
Protein structure and synthesis
Nucleotide metabolism
Gout
Gout and pseudogout: Pathology review
Severe combined immunodeficiency
Fatty acid oxidation
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
ELISA (Enzyme-linked immunosorbent assay)
Gel electrophoresis and genetic testing
Karyotyping
Fluorescence in situ hybridization
Citric acid cycle
Glycolysis
Carbohydrates and sugars
Cystinosis
Friedreich ataxia
Achondroplasia
Niemann-Pick disease type C
Gaucher disease (NORD)
Fabry disease (NORD)
Niemann-Pick disease types A and B (NORD)
Krabbe disease
Adrenoleukodystrophy (NORD)
Fragile X syndrome
Cystinuria (NORD)
Hartnup disease
Lesch-Nyhan syndrome
Rett syndrome
Ataxia-telangiectasia
DiGeorge syndrome
Myasthenia gravis
Charcot-Marie-Tooth disease
Autosomal trisomies: Pathology review
Miscellaneous genetic disorders: Pathology review
Tay-Sachs disease (NORD)
Cystic fibrosis
Williams syndrome
Cri du chat syndrome
Angelman syndrome
Prader-Willi syndrome
Turner syndrome
Patau syndrome (Trisomy 13)
Edwards syndrome (Trisomy 18)
Down syndrome (Trisomy 21)
Fanconi anemia
Xeroderma pigmentosum
Osteogenesis imperfecta
Marfan syndrome
Ehlers-Danlos syndrome
Primary ciliary dyskinesia
Disorders of carbohydrate metabolism: Pathology review
Glycogen storage disorders: Pathology review
Glycogen storage disease type II (NORD)
Glycogen storage disease type IV
Glycogen storage disease type V
Glycogen storage disease type III
Glycogen storage disease type I
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Galactosemia
Essential fructosuria
Pyruvate dehydrogenase deficiency
Hereditary fructose intolerance
Proteins

Transcript

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The cell cycle refers to the events that somatic cells - which includes all of the cells in our bodies except the reproductive cells - go through from the moment they’re formed until the moment they divide in two identical daughter cells.

This cycle varies in length depending on the type of cell - for rapidly dividing cells, like skin cells, it takes less than a day, whereas for other cells, like liver cells, the cell cycle can last years.

The cell cycle has two phases: interphase, and mitosis.

Interphase the longest part of the cell cycle, and it’s a state of preparation, during which the cell carries out its cell functions, grows and replicates its DNA to prepare for mitosis - or cellular division.

After a parent cell divides, each of the two daughter cells enter interphase again.

Now, interphase can further be broken down in three subphases: G1, S, and G2. G1 stands for “gap” or “growth” 1, and it’s the longest phase of the cell cycle.

During G1, the cell mostly grows and the organelles take care of regular cellular business - like the synthesizing proteins and producing energy.

Inside the cell nucleus, there’s our DNA, organized as chromosomes - and during G1, each chromosome is made up of a single, thin spaghetti of DNA, called a chromatid.

At the end of G1, there’s a cell cycle control point called the G1 checkpoint - where the cell checks to see if the DNA is not damaged, and it synthesized the right proteins in the correct amount.

If it turns out that there is any reason for the cell not to divide - such as DNA damage, things can go one of two ways: the cell can either enter a non-dividing state, called the G0 phase, where the DNA repair mechanisms try to fix the problem, or the cell can self-destruct in a process called apoptosis.

Now, if the cell does get the go-ahead at the G1 checkpoint, it enters the S phase. S stands for “synthesis”, because during this phase, DNA is replicated, so that each daughter cell receives identical copies of the genetic material.

So for each chromosome from G1, an identical copy is created.

This happens with the help of a number of proteins, both structural proteins and enzymes, as well as energy.

Now, just to be clear - this doesn’t mean that the number of chromosomes increases - human somatic cells have 46 chromosomes throughout the cell cycle.

However, the amount of DNA they have - and, in turn, their aspect - changes throughout the cell cycle.

So each chromosome enters the S phase with a single copy of the genetic information, called a chromatid.

During replication, each chromatid is copied and pasted, so the amount of DNA doubles up.

The two resulting chromatids are identical to each other and to the original genetic template, and they join together in the center in a region called the centromere - - but they still make up a single chromosome.

So while the amount of genetic information has doubled, there are still 46 chromosomes that contain that genetic information.

The cell can now enter the G2 phase. G2 stands for “gap” or “growth” 2.

Even after synthesizing copies of the DNA, the cell still has to duplicate organelles so that there are enough for both daughter cells.

In fact, by the end of G2, the cell looks like a big balloon of cytoplasm and organelles, just waiting to split.

Key Takeaways

The cell cycle is a process that somatic cells go through that involves the duplication of DNA, growth, and division of the cell. The cell cycle can be divided into four phases: G1, S, G2, and M. G1 is the growth phase, where the cell performs all of its functions, and S is the synthesis phase, where DNA replication occurs. G2 is the growth phase, where the cell grows in size and prepares for Mitotic division, and M is the mitotic cell division phase, dividing the cell into two identical daughter cells.