Model organisms/worms/mice Flashcards

1
Q

C. elegans Flashcards
Invariant Cell Lineage

A

Definition: Every individual develops with exactly 959 somatic cells (hermaphrodite) or 1031 (male), following a fixed division pattern.

Significance: Enables precise study of development and apoptosis; mutations can be mapped to specific cell fates.

Example: 131 programmed cell deaths during development; ced-3 and ced-4 genes regulate apoptosis (Horvitz, 2002 Nobel).

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2
Q

C. elegans Genetic Tools

A

RNAi: Gene silencing via double-stranded RNA (Fire & Mello, 2006 Nobel). Used in VIT::GFP assay to study yolk receptor trafficking.

GFP Tagging: First used in animals by Martin Chalfie (2008 Nobel) to visualize neuronal circuits.

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3
Q

C.elegens nervous system

A

Nervous System

Connectome: Fully mapped (302 neurons in hermaphrodites, 381 in males; 5000 synapses). Used to model neurodegenerative diseases (e.g., Alzheimer’s).

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4
Q

Mouse inbred stains

A

C57Bl/6: Th1-skewed immunity (IFN-γ, macrophages); models infections (e.g., tuberculosis).

Balb/c: Th2-skewed immunity (IL-4, eosinophils); models allergic asthma.

Ethics: UK’s ASPA (1986) requires personal/project licenses to minimize distress

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5
Q

Mouse asthma models

A

OVA Model: Intraperitoneal sensitization with alum adjuvant → transient inflammation (poor airway remodeling).

HDM Model: Inhalation of house dust mite → sustained Th2 inflammation, mucus hypersecretion, and fibrosis (Johnson et al., 2004).

IL-4 Role: KO mice lack Th2 responses; adenovirus-mediated IL-4 reintroduction restores airway remodeling (Johnson et al., 2007).

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6
Q

Mouse genetic engineering

A

Cre-LoxP: Cell-specific gene editing (e.g., Gli1:Cre ERT2 mice label pericytes in liver fibrosis).

Conditional Knockouts: Tetracycline/doxycycline systems allow temporal control (e.g., deleting genes in adulthood).

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7
Q

Drosophila Flashcards
Circadian Rhythms

A

Key Genes: period (per), timeless (tim), and Clock (Clk) regulate daily cycles.

Nobel Work: Hall, Rosbash, Young (2017) linked these genes to molecular feedback loops.

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8
Q

Drosophila disease modeling

A

Neurodegeneration: Expressing human tau or α-synuclein in flies induces neuron loss (Parkinson’s/ALS models).

Diabetes: Insulin signaling pathways (e.g., dFOXO) conserved; used to screen anti-diabetic drugs.

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9
Q

Drosophila Genetic Tools

A

GAL4/UAS System: Drives tissue-specific gene expression (e.g., eye-specific GMR-GAL4).

P-Element Transposons: Insert exogenous DNA into the genome for mutagenesis.

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10
Q

Mouse as a Model Organism
Genetic Homology & Differences

A

Similarities: 80% sequence homology; conserved transcription factor networks.

Differences:

Size (human ≈2500x larger), metabolic rate (mouse ≈7x faster).

Organ structure (e.g., lung architecture).

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11
Q

Mouse inbred stains

A

C57Bl/6: Th1-skewed (cell-mediated immunity; infectious disease models).

Balb/c: Th2-skewed (humoral immunity; allergy/asthma models).

Ethics: UK’s ASPA (1986) mandates licenses (personal/project) for vertebrate experiments.

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12
Q

Mouse genetic tools

A

Adoptive Transfer: Bone marrow transplants to track immune cells (e.g., GFP-labeled cells in tumors).

Knockout Mice:

Conventional: Gene deleted in all cells (e.g., IL-4 KO → no Th2 response).

Conditional: Gene deleted in specific cells/times (e.g., tetracycline-inducible systems).

Cre-LoxP: Cell-specific gene expression (e.g., Gli1:Cre ERT2 mice for fibrosis studies).

CRISPR/Cas9: Gene editing (e.g., MCAM KO in mammary epithelial cells).

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13
Q

C. elegans as a Model Organism

A

Anatomy: 1 mm, transparent, 959 somatic cells (hermaphrodite), invariant cell lineage.

Genetics:
Short life cycle (3 days), large brood size, conserved genes (40% human disease homologs).
Males (XO) arise via X chromosome non-disjunction.

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14
Q

c.elegans
genetic technique

A

Forward Genetics: Mutagenesis → phenotype analysis (e.g., lin-14 mutants).

Reverse Genetics: RNAi silencing (e.g., VIT::GFP assay for yolk receptor trafficking).

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15
Q

Drosophila as a Model Organism

A

Life Cycle: Egg → adult in ~10 days.

Genetics: 8 chromosomes (XX = female, XY = male), 75% disease gene homology with humans.

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16
Q

Drosophila as a Model Organism Tools & Applications

A

Genetic Tools: GAL4/UAS system, P-element transposons.

Disease Models:

Neurodegeneration (Alzheimer’s, Parkinson’s).

Diabetes (insulin signaling pathways).

17
Q

Drosophila Limitations in study

A

Simplified physiology (e.g., no adaptive immune system).

Environmental factors absent in lab settings.

18
Q

Microbes as Tools Flashcards

Industrial Applications of Microbes

A

Glucose to Fructose Conversion

Chemical Method: Low yield (5%), requires harsh conditions (KOH, 3.5 months).

Microbial Method: Glucose isomerase (bacterial enzyme); 100% yield, no cofactors, cost-effective.

19
Q

Microbes as Tools Flashcards
Single-Cell Protein (SCP)

A

Examples:

Spirulina (algae).

Fusarium venenatum (Quorn).

Saccharomyces cerevisiae (Marmite).

Advantages: High protein/nutrient content, sustainable.

20
Q

Microbes as Tools Flashcards
Antibiotic Production

A

Penicillin: Penicillium spp.

Streptomycin: Streptomyces griseus.

Vancomycin: Amycolatopsis orientalis.

21
Q

Microbes as Tools
Fermentation Processes

A

Alcohol Fermentation
Microbe:Saccharomyces cerevisiae (anaerobic).
Product: Ethanol (e.g., beer, wine).
Acetic Acid Fermentation

Microbe: Acetobacter aceti (aerobic).Product: Vinegar.
Lactic Acid Bacteria
Examples: Lactobacillus plantarum, Pediococcus spp.
Process: Glycolysis → lactate; regenerates NAD+ (key in yogurt/cheese production).

22
Q

Microbes Bioremediation

A

Hydrocarbon Degradation

Mechanism: Oxygenases break down petroleum into CO₂/H₂O (e.g., Pseudomonas TOL plasmid degrades toluene).

Example: Kenyan farmer using chicken waste for biogas (methane via anaerobic digestion).

23
Q

Microbes bioremediation

A

Wastewater Treatment

Aerobic: Zooglea ramigera reduces BOD (biological oxygen demand).

Anaerobic: Produces methane for energy.

24
Q

Microbial Enzymes

A

Specificity:Regioselective (site-specific) and stereoselective (optical isomer-specific).
Advantages: Mild conditions, energy-efficient, safer than chemical synthesis.

Commercial Sources
Bacteria: Bacillus (amylase, subtilisin).
Fungi: Aspergillus (invertase, lactase).
Yeast: Saccharomyces (pectinase).

25
Microbes Recombinant Protein Production
Host Systems E. coli: Fast, cheap, but forms inclusion bodies (insoluble proteins); lacks glycosylation. Yeast (e.g., Pichia pastoris): High yield (>10g/L), eukaryotic post-translational modifications (e.g., glycosylation). Animal Cells: Expensive, low yield, but proper glycosylation.