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Vocabulary flashcards covering fundamental terms from the lecture on molecular biology and cellular organelles.
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Central Dogma
Flow of genetic information: DNA → RNA → Protein.
DNA
Double-helical molecule storing genetic information; composed of A-T and C-G base pairs.
DNA Replication
Process by which DNA makes an identical copy of itself before cell division.
Reverse Transcription
Synthesis of DNA from an RNA template.
Chromatin
DNA-protein complex that packages eukaryotic DNA inside the nucleus.
Chromosome
Condensed form of chromatin visible during cell division.
mRNA
Messenger RNA; carries coding information from DNA to ribosomes.
tRNA
Transfer RNA; adaptor that delivers specific amino acids during translation.
rRNA
Ribosomal RNA; forms the structural and catalytic core of ribosomes.
miRNA
MicroRNA; small non-coding RNA that down-regulates gene expression, often dysregulated in cancer.
siRNA
Small interfering RNA; short double-stranded RNA that silences gene expression.
snRNA
Small nuclear RNA; functions in RNA splicing within the nucleus.
snoRNA
Small nucleolar RNA; guides chemical modifications of other RNAs.
lncRNA
Long non-coding RNA; regulates gene expression at multiple levels.
Transcription
Synthesis of RNA from a DNA template in the nucleus.
Translation
Protein synthesis from an mRNA template on ribosomes.
Ribosome (80S)
Eukaryotic protein factory composed of 60S and 40S subunits.
Ribosome (70S)
Prokaryotic ribosome targeted by many antibiotics.
Nucleus
Double-membrane organelle housing DNA and site of transcription.
Nucleolus
Nuclear substructure that synthesizes rRNA and assembles ribosomal subunits.
Rough Endoplasmic Reticulum
Membrane network with bound ribosomes; site of synthesis/folding of secretory and membrane proteins.
Smooth Endoplasmic Reticulum
Ribosome-free ER; functions in lipid synthesis, detoxification, glycogen metabolism, and Ca²⁺ storage.
Golgi Apparatus
Organelle that modifies, sorts, and packages proteins and lipids; has cis and trans faces.
I-cell Disease
Congenital disorder caused by failure to phosphorylate mannose on lysosomal enzymes.
Mitochondria
ATP-producing organelles with their own maternal DNA; regulate apoptosis and Ca²⁺.
Oxidative Phosphorylation
Mitochondrial process that couples electron transport to ATP synthesis.
Lysosome
Acidic vesicle containing hydrolytic enzymes for degradation and autophagy.
Tay-Sachs Disease
Lysosomal storage disorder due to hexosaminidase A deficiency; presents with cherry-red macula.
Peroxisome
Organelle that performs β-oxidation of very long-chain fatty acids and detoxifies H₂O₂.
Zellweger Syndrome
PEX gene mutation causing absent peroxisomes and accumulation of VLCFAs.
Cytoskeleton
Network of actin filaments, intermediate filaments, and microtubules providing structure and transport.
Microtubule
Tubulin polymer involved in intracellular transport, cilia, flagella, and mitotic spindle.
Centrosome
Microtubule-organizing center containing two orthogonally arranged centrioles.
Kartagener Syndrome
Dynein arm defect leading to immotile cilia, sinusitis, infertility, and dextrocardia.
Plasma Membrane
Phospholipid bilayer with proteins and cholesterol; controls transport and cell signaling.
CFTR
Chloride channel defective in cystic fibrosis; encoded on chromosome 7.
Cystic Fibrosis
Autosomal recessive disease due to CFTR mutations causing thick secretions and salty sweat.
Cytoplasm
Cellular contents outside the nucleus; includes cytosol and organelles.
Cytosol
Aqueous component of cytoplasm; site of glycolysis, protein translation, and fatty-acid synthesis.
Actin (Microfilament)
Thin filament involved in cell movement, cytokinesis, and muscle contraction.
Intermediate Filament
Cytoskeletal fiber providing mechanical strength; examples include keratin and lamins.
Prokaryotic Cell
Unicellular organism lacking a nucleus and membrane-bound organelles; has circular DNA.
Eukaryotic Cell
Cell with membrane-bound organelles and a true nucleus containing linear chromosomes.
Laminopathies
Diseases caused by mutations in nuclear lamina proteins, e.g., Hutchinson-Gilford progeria.
Colchicine
Drug that inhibits microtubule polymerization, disrupting mitosis and neutrophil migration.
Paclitaxel
Chemotherapy agent that stabilizes microtubules, preventing their depolymerization.
Vincristine
Anticancer drug that inhibits microtubule assembly, blocking mitotic spindle formation.
Maternal Inheritance
Transmission pattern of mitochondrial DNA where traits are passed from mother to all offspring.