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77 Cards in this Set

  • Front
  • Back
Part of chromatin transcribed
Euchromatin
Number of bonds in G and C
3 bonds between these nucleic acids
Purines
Adenosine and Guanine
Number of bonds between A and T
2 bonds between these nucleic acids
Amino acids necessary for purine synthesis
Glycine Asparate and Glutamine
Transition vs Transversion
purine to purine vs purine to pyrimadine (or vice versa)
Number of rings in pyrimadines (C, T and U)
1 ring nucleotides
Number of rings in purines (A and G)
2 rings nucleotides
Direction DNA is opened up and read from
3' to 5'
Direction DNA and RNA are made and RNA read
5' to 3', its all down hill
most, largest, smallest RNAs
rRNA, mRNA, tRNA
DNA Gyrase
A prokaryotic topoisomerase that relieves supercoils for replication (blocked by fluroquinolones)
Problem with mismatch repair
HNPColorectal Cancer has this DNA repair problem
Problem with thymidine dimer repair (base eXcision repair)
Xeroderma pigmentosum (dry skin w/ melanoma ect) have this problem w/ DNA repair
Start and Stop Codons
AUG and UGA,UAA,UAG
Promoter vs Enhancer
Promoter binds both TF and RNA polymerase
RNA polymerases that make tRNA, rRNA, and mRNA
RNA polymerase III, I, and II
Death cap mushrooms (alpha-amanitin) do what?
This toxin inhibits RNA polymerase II
RNA processing (steps inside nucleus before it gets out, INtrons stay IN the nucleus) turning hnRNA (heterogenous) into mRNA, by snRNPs/spliceosome
5' capping w/ 7-methylguanosine, Polyadenylation on 3' (AAUAAA), splicing of introns with
size of Eukaroyotic and Prokaryotic rRNA
even (80) and odd (70)
50S blocking
Chlorophemicol, Clindamycin, Linezolid, Erythromycin (Macrolides- Clarithromycin and Azithromycin)
CLEAN
30S blocking
Tetracyclin (and Doxycyclin), Aminoglycosides (amikacin, gentamicin, neomycin, streptomycin, tobramycin) TAG- AmiNoGlycoSides
Energy to aminoacyclate, load tRNA onto ribosome or Translocate, total energy
ATP-> AMP. GTP-> GDP, total energy is 4 high energy bonds
Cell Cycle
G1 (growth), S phase (synthesis), G2 (growth), Mitosis (prophase, metaphase, anaphase, telophase), G1
Rb and p53 inhibit this
these tumor suppressor genes inhibit the passage from G1 to S phase
These are permanent, not replicating cells, these are stable (quiescent), these are labile
Neurons, skeletal and cardiac muscle, RBCs

Hepatocytes, lymphocytes

Bone marrow, gut epithelium, skin/hair
Site of packaging and secretion of proteins through glycosylation, rich in goblet cells (mucous), and Ab secreting plasma cells
Rough ER role in protein transport
Site of steroid synthesis and detoxification
Smooth ER (Hepatocytes and adrenal cortex)
Golgi apparatus function
Distribute proteins from ER to plasma membrane, lysosomes and secretory vessicles, adds oligosaccharides, targets proteins to lysosomes, makes proteoglycans and sulfation of these sugars and other tyrosines
How does the Golgi target proteins to lysosomes
mannose-6-phosphate to protein
Clathrin does what?
This protein does plasma-membrane receptor mediated endocytosis, and moving things from trans-Golgi network to lysosomes
Microtubules structure and function
alpha and beta tubulin make flagella, cilia, axoplasmic transport, and mitotic spindles
Motor proteins that go forward on microtubules)
Kinesin (vs Dynein)
Drugs that act on microtubules
Vincristine/vinblastin (anti-cancer), Colchicine (gout, also raises pH to stop uric acid crystalization and NSAID by blocking PMNs), Griseofulvin (antifungal), and Mebendazole/thiabendazole (anti-helminthic), Paclitaxel (anti-breast cancer)
Chediak-Higashi syndrome ((ashy white skin, checked phagocytosis leads to pyogenic infection)
Microtubule polymerization defect -> low phagocytosis: PYOGENIC INFECTIONS, PARTIAL ALBANISM, PERIPHERAL NEUROPATHY
ashy white skin, checked phagocytosis leads to pyogenic infection)
Kartagener's Syndrome
Immotile cilia from dynein arm defect on cilia. Infertility, bronchiectasis, sinusitis, related to sinus inversus
Cilia
cilia are 9+2 arrangement of microtubule doublets
Intermediate filaments
desmin (Dsg) of skin, GFAP, neurofilaments, cytokeratin
What is I-Cell Dz
No mannose-6-P to lysosomal bound proteins -> accumulation -> course facial features, clouded cornea, restricted ROM, high plasma lysosymal enxymes (often childhood fatal)
Vimentin stains
Connective tissue is stained by
Desmin stains
Muscle is stained by
Cytokeratin stains
Epithelial cells are stained by
GFAP stains (glial fibrillary acid proteins)
Neuroglia stain
Neurofilaments stain
Neurons are stained by
Digoxin/Digitoxin mechanism of action
This drug inhibits Na/K ATPase, indirectly inhibiting Na/Ca exchange which gets rid of Ca by letting in Na, increasing [Ca+], increasing CTY
Collagen Type I
Collagen in Bone, Skin, Tendon, dentin, fascia, cornea, late wound repair
Collagen Type II
Collagen in cartilage, nucleus pulposus, vitreous body
Type III Collagen
Collagen in skin, blood vessels, uterus, fetal tissue, granulation tissue (aka Reticulin)
Type IV col
Collagen in basement membrane (FLOOR), kidneys, eyes, ears
Type VII collagen
Collagen in dermis (epidermolysis bullosa)
Collagen synthesis inside fibroblasts
Vit C, glycine, proline, anydroxyproline, or hydroxylysine, glycosylation, formation of triple-helix and exocytosis
Outside fibroblasts collagen gets
Proteolytic processing of procollagen (terminal regions get cleaved) to make tropocollagen, and cross-linking to make collagen fibrils (by lysyl oxidase)
Osteogensis imperfect (brittle bone dz)
Collagen type I stops formation of triple helix to make procollagen

blue sclera, hearing loss, dental problems, AUTOSOMAL DOMINANT
Ehlers-Danlos syndrome
Hyper extensible skin, bleeding, hyperflexibilty from Type III collagen mutation (berry aneurysms, organ rupture, joint dyslocation)
Alports Syndrome
Type IV col disorder, X-linked recessive

progressive nephritis and deafness, vision changes
Marfans
fibrillin-1 defect (AD) (makes elastin which makes making lungs, arteries, ligmants, vertebrae flexible),
Regulation of Elastin
This molecule is broken down by elastase, which is inhibited by alpha1-antitrypsin (emphysem can be caused by anti-trypsin deficiency)
cDNA
library of all a organisms translated genetic material that w/ introns
Imprinting Diseases
Prader-Willi (retardation, developmental delay followed by hyperphagia, parental is deleted in dz) and AngelMan's Syndrome (maternal is deleted in dz,intellectual and developmental delay, hand flapping, happy super smiley), both on 15
Locus Heterogeneity
When one phenotype can be produced by mutations in different places
Heteroplasmy
A result of inheriting lots of mtDNA, it describes how the expression is very variable in mitochondrial inherited diseases
Hardy Weinberg

carrier frequency
affected frequency
allele frequency
prevalence in men if x-linked
1 = p2 + 2pq + q2

carrier = 2pq
affected = q^2
allele frequency= p and q, p+q = 1
if x-linked, male prev = q
Vit D resistant rickets inheritance pattern
X-linked dominate, (phosphate wasting in proximal tubules)
Leber's hereditary optic neuropathy, other myopathies
Mitochondrial inheritance
Location of FA oxidation (beta-oxidation)
Mitochondria
Location of acetyl-CoA production
Mitochondria
Location of TCA cycle
Mitochondria
Location of oxydative phosphorylation
Mitochondria
Location of glycolysis
cytoplasm
Location of FA synthesis
cytoplasm
Location of HMP shunt
Cytoplasm
Location of Protein synthesis
cytoplasm (RER)
Location of steroid synth
cytoplasm (SER)
Location of Heme synth
Both Mito and Cyto
Location of Urea Cycle
Both Mito and Cyto
Location of Gluconeogensis
Both Mito and Cyto
what goes up the most in ketoacidosis
Beta-hydroxybuterate