DNA replication

Last updated: November 01, 2022

DNA replication

Semester 1

Semester 1

Introduction to the skeletal system
Introduction to the muscular system
Anatomical terminology
Anatomy of the breast
Muscles of the thoracic wall
Anatomy clinical correlates: Breast
Introduction to the cranial nerves
Cranial nerve pathways
Anatomy of the thyroid and parathyroid glands
Anatomy of the pelvic girdle
Bones of the vertebral column
Joints of the vertebral column
Muscles of the back
Vessels and nerves of the vertebral column
Anatomy clinical correlates: Bones, joints and muscles of the back
Anatomy clinical correlates: Vertebral canal
Bones of the lower limb
Fascia, vessels and nerves of the lower limb
Anatomy of the anterior and medial thigh
Muscles of the gluteal region and posterior thigh
Vessels and nerves of the gluteal region and posterior thigh
Anatomy of the popliteal fossa
Anatomy of the leg
Anatomy of the foot
Anatomy of the hip joint
Anatomy of the knee joint
Anatomy of the tibiofibular joints
Joints of the ankle and foot
Bones of the upper limb
Fascia, vessels and nerves of the upper limb
Anatomy of the brachial plexus
Anatomy of the pectoral and scapular regions
Anatomy of the arm
Muscles of the forearm
Vessels and nerves of the forearm
Muscles of the hand
Anatomy of the sternoclavicular and acromioclavicular joints
Anatomy of the glenohumeral joint
Anatomy of the elbow joint
Anatomy of the radioulnar joints
Joints of the wrist and hand
Anatomy clinical correlates: Clavicle and shoulder
Anatomy clinical correlates: Axilla
Anatomy clinical correlates: Arm, elbow and forearm
Anatomy clinical correlates: Wrist and hand
Anatomy clinical correlates: Median, ulnar and radial nerves
Suicide
Alcohol use disorder
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
Pyruvate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Carbohydrates and sugars
Glycogen storage disease type I
Glycogen storage disease type III
Phenylketonuria (NORD)
Familial hypercholesterolemia
Hypertriglyceridemia
Glycogen storage disorders: Pathology review
Introduction to biostatistics
Probability
Types of data
Hypothesis testing: One-tailed and two-tailed tests
Type I and type II errors
Sensitivity and specificity
Test precision and accuracy
Positive and negative predictive value
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
Zellweger spectrum disorders (NORD)
Adrenoleukodystrophy (NORD)
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Marfan syndrome
Nuclear structure
Transcription of DNA
Gene regulation
Amino acids and protein folding
DNA structure
Translation of mRNA
Epigenetics
Protein structure and synthesis
DNA replication
Nucleotide metabolism
Lac operon
DNA damage and repair
Mitosis and meiosis
Cell cycle
DNA mutations
Adenosine deaminase deficiency
Xeroderma pigmentosum
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
ELISA (Enzyme-linked immunosorbent assay)
DNA cloning
Gel electrophoresis and genetic testing
Karyotyping
Fluorescence in situ hybridization
Human development days 1-4
Human development days 4-7
Human development week 2
Human development week 3
Ectoderm
Mesoderm
Endoderm
Development of the placenta
Development of the fetal membranes
Hedgehog signaling pathway
Development of the umbilical cord
Development of the axial skeleton
Development of the limbs
Development of the muscular system
Hardy-Weinberg equilibrium
Mendelian genetics and punnett squares
Inheritance patterns
Independent assortment of genes and linkage
Evolution and natural selection
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Huntington disease
Turner syndrome
Klinefelter syndrome
Cri du chat syndrome
Achondroplasia
Hereditary spherocytosis
Albinism
Cystic fibrosis
Hemochromatosis
Primary ciliary dyskinesia
Alpha-thalassemia
Beta-thalassemia
Sickle cell disease (NORD)
Hemophilia
Muscular dystrophy
Mitochondrial myopathy
Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review
Light microscopy and staining methods
Pituitary gland histology
Thyroid and parathyroid gland histology
Adrenal gland histology
Liver histology
Blood histology
Thymus histology
Spleen histology
Lymph node histology
Skin histology
Bone histology
Skeletal muscle histology
Cartilage histology
Central nervous system histology
Peripheral nervous system histology
Mammary gland histology
Bacterial structure and functions
Viral structure and functions
Pediculus humanus and Phthirus pubis (Lice)
Sarcoptes scabiei (Scabies)
Free radicals and cellular injury
Ischemia
Necrosis and apoptosis
Hypoxia
Amyloidosis
Inflammation
Wound healing
Atrophy, aplasia, and hypoplasia
Hyperplasia and hypertrophy
Metaplasia and dysplasia
Oncogenes and tumor suppressor genes
Conn syndrome
Cushing syndrome
Congenital adrenal hyperplasia
Primary adrenal insufficiency
Hyperaldosteronism
Adrenal cortical carcinoma
Hyperthyroidism
Graves disease
Thyroid storm
Hypothyroidism
Thyroid cancer
Hyperparathyroidism
Hypercalcemia
Hypoparathyroidism
Hypocalcemia
Diabetes mellitus
Hyperpituitarism
Pituitary adenoma
Hyperprolactinemia
Prolactinoma
Gigantism
Acromegaly
Hypopituitarism
Hypoprolactinemia
Diabetes insipidus
Syndrome of inappropriate antidiuretic hormone secretion (SIADH)
Androgen insensitivity syndrome
5-alpha-reductase deficiency
Thyroid nodules and thyroid cancer: Pathology review
Parathyroid disorders and calcium imbalance: Pathology review
Jaundice
Non-alcoholic fatty liver disease
Viral hepatitis
Iron deficiency anemia
Sideroblastic anemia
Anemia of chronic disease
Hemolytic disease of the newborn
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Aplastic anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Vitamin K deficiency
Von Willebrand disease
Antithrombin III deficiency
Factor V Leiden
Chronic leukemia
Acute leukemia
Leukemoid reaction
Langerhans cell histiocytosis
Sepsis

Transcript

Watch video only

At a quick glance, the life of a cell - it’s cell cycle - is pretty routine.

It’s either actively dividing, or preparing to divide into two daughter cells.

The cell cycle itself has an interphase, made up of subphases G1, S and G2, during which the cell is preparing for division, and mitosis, during which the cell actively divides.

During the S phase, the cell performs DNA replication - which is when its 46 chromosomes are duplicated so that each daughter cell can get its own copy of the genetic material.

A single chromosome is made up a single DNA molecule that has two strands, which wrap one around one another to form a double helix.

Each single strand of DNA is composed of a sequence of four types of nucleotides - which are the individual letters or building blocks of DNA.

Nucleotides of DNA are made up of a sugar - deoxyribose, a phosphate, and one of the four nucleobases - adenine, cytosine, guanine, and thymine - or, commonly, A, C, G, T for short.

The nucleotides on one strand form hydrogen bonds to complementary nucleotides on the other strand; specifically, A bonds with T via two hydrogen bonds, and C bonds with G, via three hydrogen bonds.

Additionally, the two DNA strands also have a “direction” - meaning, one of them runs from the 3’ end to the 5’ end, while the other one runs from the 5’ end to the 3’ end.

Kinda like two snakes coiled up together, but facing in different directions.

DNA replication can be described as semiconservative.

That means that each strand of the double helix acts as a “template”, based on which a new, complementary strand will form.

Eventually the original chromosome will split into two exact copies, each made of one of original strands, and one of the newly made ones.

Overall, DNA replication has 3 steps: initiation, elongation, and termination.

Initiation kicks off when a group of proteins get together to form the pre-replication complex.

This pre-replication complex looks for specific nucleotide sequences along the DNA strand - called origins of replication.

And yes, we’re talking plural! That’s because our DNA strand is so long that DNA replication actually starts in several origins along the chromosomes simultaneously.

These special nucleotide sequences have a ton of A and T bases.

Because A and T are joined by only two hydrogen bonds, the enzyme DNA helicase has a relatively easy time separating the two strands.

This creates a replication fork, with the two prongs of the fork being the two strands that are separate from one another.

Single strands of DNA can get a bit unstable, so to help keep them from getting back together again, helper molecules called single stranded DNA binding proteins come in and bind to each of the lonely strands.

Also, as DNA helicase breaks down bonds, the segments of DNA ahead of it start to overwind - meaning, the double helix becomes more tightly wound.

You can try this with a close friend who has braided hair - if you pull the braid apart in the middle then the ends get tighter.

Again - make sure it’s a friend and not a stranger.

Overwinding of the DNA can slow down replication, so the enzyme DNA topoisomerase works ahead of DNA helicase to loosen up the tight DNA coils.

It achieves this by gently snapping one strand, loosening the overwinding tension, and then patching it back up, tension free.

The second step is elongation, and for that we need a new enzyme - RNA primase. Yes, you heard that correct, RNA this time.

It’s kinda like DNA, it uses ribose instead of deoxyribose in its nucleotides, and instead of thymine, it uses uracil.

Key Takeaways

DNA replication is the process by which a DNA molecule is copied into two identical DNA molecules. This process is essential to ensure the accurate transmission of genetic information from one generation to the next.

DNA replication occurs in three main steps: initiation, elongation, and termination. Initiation involves the unwinding of the DNA molecule, and it happens thanks to DNA helicase and topoisomerase enzymes. Next, elongation consists of making RNA primers by RNA primase and synthesizing the DNA leading strand by DNA polymerase. In termination, converging replication forks meet, and the whole process is complete.