Epigenetics

Last updated: November 01, 2022

Epigenetics

Modulo 3 BPT

Modulo 3 BPT

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
Familial hypercholesterolemia
Hereditary spherocytosis
Marfan syndrome
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Gaucher disease (NORD)
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
Hemochromatosis
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Krabbe disease
Leukodystrophy
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Primary ciliary dyskinesia
Phenylketonuria (NORD)
Sickle cell disease (NORD)
Tay-Sachs disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Wilson disease
Alport syndrome
X-linked agammaglobulinemia
Fabry disease (NORD)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hemophilia
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Muscular dystrophy
Ornithine transcarbamylase deficiency
Wiskott-Aldrich syndrome
Mitochondrial myopathy
Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review
Blood histology
Blood components
Erythropoietin
Blood groups and transfusions
Platelet plug formation (primary hemostasis)
Coagulation (secondary hemostasis)
Role of Vitamin K in coagulation
Clot retraction and fibrinolysis
Iron deficiency anemia
Sideroblastic anemia
Anemia of chronic disease
Lead poisoning
Hemolytic disease of the newborn
Autoimmune hemolytic anemia
Pyruvate kinase deficiency
Paroxysmal nocturnal hemoglobinuria
Aplastic anemia
Megaloblastic anemia
Folate (Vitamin B9) deficiency
Vitamin B12 deficiency
Diamond-Blackfan anemia
Acute intermittent porphyria
Porphyria cutanea tarda
Vitamin K deficiency
Bernard-Soulier syndrome
Glanzmann's thrombasthenia
Hemolytic-uremic syndrome
Immune thrombocytopenia
Thrombotic thrombocytopenic purpura
Von Willebrand disease
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Antiphospholipid syndrome
Hodgkin lymphoma
Non-Hodgkin lymphoma
Chronic leukemia
Acute leukemia
Myelodysplastic syndromes
Polycythemia vera (NORD)
Myelofibrosis (NORD)
Essential thrombocythemia (NORD)
Langerhans cell histiocytosis
Mastocytosis (NORD)
Microcytic anemia: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Macrocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Coagulation disorders: Pathology review
Platelet disorders: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Lymphomas: Pathology review
Leukemias: Pathology review
Plasma cell disorders: Pathology review
Myeloproliferative disorders: Pathology review
Ribonucleotide reductase inhibitors
Topoisomerase inhibitors
Platinum containing medications
Anti-tumor antibiotics
Microtubule inhibitors
DNA alkylating medications
Monoclonal antibodies
Antimetabolites for cancer treatment
Prostate cancer
Benign prostatic hyperplasia
Testicular cancer
Ovarian surface epithelial tumors
Ovarian germ cell tumors
Ovarian sex-cord stromal tumors
Endometrial cancer
Cervical cancer
Breast cancer
Disorders of sex chromosomes: Pathology review
Testicular tumors: Pathology review
Ovarian cysts and tumors: Pathology review
Cervical cancer: Pathology review
Breast cancer: Pathology review
Colorectal cancer
Carcinoid syndrome
Irritable bowel syndrome
Colorectal polyps and cancer: Pathology review
Seizures and epilepsy
Dementia: Pathology review
Movement disorders: Pathology review
Demyelinating disorders: Pathology review
Neuromuscular junction disorders: Pathology review
Adult brain tumors: Pathology review
Inflammatory bowel disease: Pathology review
Bowel obstruction

Flashcards

Epigenetics

0 of 6 complete

Questions

USMLE® Step 1 style questions USMLE

0 of 1 complete

A researcher conducts an experiment that studies epigenetic modifications in human cells. During this study, cells are cultured in vitro, and an epigenetic modification is made to Gene A. This change results in decreased production of the protein encoded by Gene A. Which of the following epigenetic modifications most likely took place?  

Transcript

Watch video only

Epigenetics is a process of gene regulation - turning genes on and off.

Think about it - you have about 37 trillion cells, and over 200 different types of cells in your body.

For example, there are muscle cells, for looking great at the beach as well as neurons that tell your muscles to flex when it’s time to show off.

And both muscle cells and neurons have the same origin and genetic material - meaning, 46 chromosomes, with each chromosome made up of a single DNA molecule.

Along that chromosome are sequences of DNA that code for genes, with thousands of genes on each one.

It makes sense that there would have to be a process to control all of those genes.

Now, it turns out, that DNA is a very long molecule - over 2 meters when fully stretched.

So to save space, DNA is wrapped around special proteins called histones.

Now - histones actually come in groups of 8 - 4 stacks of 2, like poker chips - and the DNA molecule wraps around each group of 8 histones twice, forming a nucleosome.

Different sections of DNA - meaning, different genes - wrap around different stacks of histones.

Finally, the nucleosomes are packed together even more tightly - resulting in chromatin which looks like threads of cotton-candy within the nucleus.

Now - a cell type boils down to what a cell does - and, in turn, what a cell type does boils down to the kind of proteins it makes to carry out its role.

Proteins are made based on genes - so our collection of genes, or genotype is actually like an incredible wardrobe - it contains something for every occasion.

And different cell types wear different attires.

For example, our muscle cells are usually doing the hard work of contracting and relaxing all day, so they would require the equivalent of athletic gear to do their job.

Posh neurons, on the other hand, might prefer a tuxedo to tend to their synapses in.

So, the muscle cell needs only certain parts of that wardrobe and the neuron needs a very different part of that wardrobe.

This is achieved through selectively activating or silencing certain genes.

The final appearance of how a cell looks depends on which genes are activated - and we call that the phenotype.

All of this happens through epigenetics - which specifically refers to mechanisms that can selectively activate or silence certain genes without modifying the nucleotide sequence of the gene.

Let’s start with histones. Histones can be influenced to either release their DNA or lock down their DNA, through chemical changes, like acetylation or methylation.

For example, when an acetyl group is added to the histone, there’s less attraction between DNA and histones.

Key Takeaways

Epigenetics is the study of how environmental and lifestyle factors can change the way our genes are expressed without actually changing the DNA sequence. These epigenetic changes can be passed down from one generation to the next, which means that they can influence our health even if we don't have any direct descendants.

There are a number of different epigenetic mechanisms, but some of the most common ones include DNA methylation, histone modification, and microRNA expression. Each of these mechanisms can either promote or suppress gene expression, and they can be affected by things like diet, stress, exposure to toxins, and social interactions.