Cell cycle

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Cell cycle

HMBP

HMBP

Glycolysis
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Pentose phosphate pathway
Physiological changes during exercise
Amino acid metabolism
Nitrogen and urea cycle
Fatty acid synthesis
Fatty acid oxidation
Ketone body metabolism
Cholesterol metabolism
Essential fructosuria
Hereditary fructose intolerance
Galactosemia
Pyruvate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Leukodystrophy
Metachromatic leukodystrophy (NORD)
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Cystinosis
Hartnup disease
Alkaptonuria
Ornithine transcarbamylase deficiency
Phenylketonuria (NORD)
Cystinuria (NORD)
Homocystinuria
Maple syrup urine disease
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Disorders of carbohydrate metabolism: Pathology review
Disorders of fatty acid metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Lysosomal storage disorders: Pathology review
Disorders of amino acid metabolism: Pathology review
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Nernst equation
Cytoskeleton and intracellular motility
Cell signaling pathways
Adrenoleukodystrophy (NORD)
Zellweger spectrum disorders (NORD)
Primary ciliary dyskinesia
Alport syndrome
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Marfan syndrome
Vitamin C deficiency
Peroxisomal disorders: Pathology review
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Gene regulation
Epigenetics
Amino acids and protein folding
Protein structure and synthesis
Nucleotide metabolism
DNA replication
Lac operon
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Lesch-Nyhan syndrome
Orotic aciduria
Adenosine deaminase deficiency
Xeroderma pigmentosum
Li-Fraumeni syndrome
Bloom syndrome
Fanconi anemia
McCune-Albright syndrome
Acute radiation syndrome
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
ELISA (Enzyme-linked immunosorbent assay)
Karyotyping
DNA cloning
Fluorescence in situ hybridization
Mendelian genetics and punnett squares
Hardy-Weinberg equilibrium
Inheritance patterns
Independent assortment of genes and linkage
Evolution and natural selection
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Fragile X syndrome
Huntington disease
Myotonic dystrophy
Friedreich ataxia
Turner syndrome
Klinefelter syndrome
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
Cri du chat syndrome
Williams syndrome
Alagille syndrome (NORD)
Achondroplasia
Polycystic kidney disease
Familial adenomatous polyposis
Hereditary spherocytosis
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Hemochromatosis
Sickle cell disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Wilson disease
X-linked agammaglobulinemia
Hemophilia
Muscular dystrophy
Wiskott-Aldrich syndrome
Mitochondrial myopathy
Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review

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.