DNA structure

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DNA structure

HMBP Exam

HMBP Exam

Introduction to pharmacology
Light microscopy and staining methods
Cytoskeleton and intracellular motility
Pharmacodynamics: Agonist, partial agonist and antagonist
Cellular structure and function
Primary ciliary dyskinesia
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Epigenetics
DNA damage and repair
DNA mutations
Rett syndrome
Amino acids and protein folding
Protein structure and synthesis
Osmosis
Myasthenia gravis
Cell membrane
Human development days 1-4
Human development days 4-7
Human development week 2
Selective permeability of the cell membrane
Prions (Spongiform encephalopathy)
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Cystic fibrosis
Ectoderm
Mesoderm
Endoderm
Diabetes mellitus
Beta-thalassemia
Inheritance patterns
Independent assortment of genes and linkage
Mitosis and meiosis
Karyotyping
Glycolysis
Gluconeogenesis
Essential fructosuria
Hereditary fructose intolerance
Amino acid metabolism
Arsenic poisoning
Patau syndrome (Trisomy 13)
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Turner syndrome
Klinefelter syndrome
Angelman syndrome
Prader-Willi syndrome
Marfan syndrome
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Pharmacokinetics: Drug metabolism
Pharmacokinetics: Drug elimination and clearance
Pentose phosphate pathway
Glycogen metabolism
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type V
Glycogen storage disease type IV
Glycogen storage disease type III
Ketone body metabolism
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Cri du chat syndrome
Williams syndrome
Fatty acid synthesis
Fatty acid oxidation
Nucleotide metabolism
Cystinosis
Antimetabolites for cancer treatment
Severe combined immunodeficiency
Lesch-Nyhan syndrome
Megaloblastic anemia
Hartnup disease
Cystinuria (NORD)
Drug administration and dosing regimens
Nitrogen and urea cycle
Cell cycle
Cholesterol metabolism
Fragile X syndrome
Huntington disease
Friedreich ataxia
Polycystic kidney disease
Achondroplasia
Neurofibromatosis
Albinism
Niemann-Pick disease types A and B (NORD)
Tay-Sachs disease (NORD)
Fabry disease (NORD)
Alkaptonuria
Ornithine transcarbamylase deficiency
Homocystinuria
Maple syrup urine disease
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease type C
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Phenylketonuria (NORD)
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Wernicke-Korsakoff syndrome
Zellweger spectrum disorders (NORD)
Vitamin C deficiency
Adenosine deaminase deficiency
Xeroderma pigmentosum
Fanconi anemia
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
Fluorescence in situ hybridization
ELISA (Enzyme-linked immunosorbent assay)
Hardy-Weinberg equilibrium
Hemochromatosis
Alpha-thalassemia
Hemophilia
Muscular dystrophy
Mitochondrial myopathy
Pharmacokinetics: Drug absorption and distribution
Pharmacodynamics: Drug-receptor interactions

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Buried deep within the nucleus, lies our genetic information, called DNA - which stands for deoxyribonucleic acid.

DNA is made up of two strands that are coiled around one another in a double helix.

Each of the two strands that make up DNA is a polynucleotide chain - so it’s a string of nucleotides one after another.

Nucleotides are organic molecules that are made up of a 5-carbon sugar, a phosphate group and a nitrogenous base - also called a nucleobase - or, simply, a “base”.

For DNA, the 5-carbon sugar is deoxyribose. Deoxyribose looks like a pentagon, and the tips of the pentagon are 4 carbons and an oxygen molecule.

The 5th carbon is outside the ring, and it binds to the phosphate group.

The sugar and phosphate elements are the same for the 4 nucleotides that make up DNA - the difference comes from the nucleobase, which is attached to the first carbon of the sugar.

There are four nucleobases that make up and give DNA nucleotides their name - adenine, or A, thymine, or T, cytosine, or C and guanine, or G.

Structurally, these bases can be either purines or pyrimidines - the purines, guanine and adenine, are made up of 2 heterocyclic rings.

The pyrimidines, cytosine and thymine, are made up of a single ring.

You can remember this with “CUT PYe (pie)” - because cytosine and thymine along with uracil, which is a nucleotide found in RNA, are all Pyrimidines.

The nucleotides bind to one another using their sugar and phosphate groups.

The phosphate group on the 5th carbon of the sugar of one nucleotide - also called the 5’ carbon - forms a covalent bond with the 3rd carbon on the sugar of the next nucleotide - also called the 3’ carbon.

This gives each DNA strand a sugar-phosphate backbone, as well as a “direction” - one of the strands runs from the 5’ end towards the 3’ end, while the other one runs from 3’ to 5’.

This makes DNA an “antiparallel” molecule - it’s a bit like two snakes coiled up together but facing different directions.

However, to form the double helix, the nucleotides use their bases - A, T, C, G to form hydrogen bonds with bases on the opposing strand.

Bases form bonds according to the rule of “complementary base pairing” - which states that in DNA, A always pairs with T, by means of two hydrogen bonds, while C always pairs with G, through three hydrogen bonds.

The hydrogen bonds are much weaker than the covalent bonds that hold the strands together - so they can be easily broken and reformed when DNA is being transcribed into RNA or being replicated during cell division.

Now, DNA is actually a very organized molecule, because the two strands coil around each other once every 10 base pairs.

This twisting and turning makes the DNA molecule develop major and minor grooves, which are larger or smaller spaces between the strands where proteins can bind to DNA in order to regulate its functions.

DNA is also a surprisingly long molecule - over 2 meters long when fully stretched.

To make 46 of these DNA molecules - meaning one molecule for each chromosome - fit into a tiny nucleus, our cells rely on a few packaging tricks.

Key Takeaways

The basic structure of DNA is a double helix, which consists of two long strands of DNA wrapped around each other. Each strand consists of many nucleotides, each consisting of a sugar and phosphate group, which form the sugar-phosphate backbone of DNA, and a nitrogenous base, which determines the identity of each nucleotide. The order of the bases (A, T, C, and G) on each strand determines the DNA sequence. DNA strands are held together by hydrogen bonds between the bases.