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Vocabulary-style practice flashcards covering levels of nucleic acid structure, chemistry, and base pairing from Biochemistry 221 (BIOC202) Lecture 1.
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Primary Structure of Nucleic Acids
The linear sequence of nucleotide bases in a nucleic acid chain.
Secondary Structure of Nucleic Acids
The three-dimensional shape or conformation of the polynucleotide backbone.
Tertiary Structure of Nucleic Acids
The complex 3D shape of the molecule resulting from the higher-order folding and interactions of its secondary structure elements.
Quaternary Structure of Nucleic Acids
The higher-order structural arrangements formed when nucleic acid molecules interact with other macromolecules (primarily proteins).
Genetic Code
The order of bases (A, T(U), G, C) along the DNA or RNA polymer which specifies the amino acid sequence of proteins.
Mutation
A small change in sequence that can alter the encoded genetic information.
DNA Secondary Structure
The double helix where two strands are coiled around each other in an antiparallel fashion.
Antiparallel Orientation
The structural arrangement where one DNA strand runs 5′ to 3′ and the complementary strand runs 3′ to 5′.
RNA Secondary Structure
Typically single-stranded but can fold back on itself to form local double-helical regions.
Stem-loop structures
Local double-helical regions in RNA formed when it folds back on itself; also called hairpin loops.
DNA Tertiary Structure
A more compact and organized structure formed through supercoiling where the double helix twists further.
Supercoiling
The process where the DNA double helix twists and coils further to create tertiary structure.
RNA Tertiary Structure
Formed when helices and unpaired regions in secondary structure interact to create an intricate, functional form.
Transfer RNA (tRNA) Secondary Structure
A structure that resembles a cloverleaf.
Transfer RNA ($tRNA$$) Tertiary Structure
An inverted L-shaped structure resulting from interactions between unpaired nucleotides in the loops.
Nucleic Acid–Protein Complexes
The most prevalent form of quaternary organization in nucleic acids, exemplified by ribosomes.
Ribosomes
Functional units essential for protein synthesis consisting of ribosomal RNA (rRNA) complexed with numerous proteins.
Nucleic Acid–Nucleic Acid Complexes
Structured complexes formed by interactions between different nucleic acids, such as tRNA pairing with mRNA during translation.
Transient Nucleic Acid Hybrids
Short-lived DNA−RNA or RNA−RNA structures formed during replication and transcription.
Monomer
The smallest single unit of a polymer; in nucleic acids, these are nucleotides.
Nucleotide
A monomer consisting of a nitrogenous base, a sugar, and a phosphoric acid residue covalently bonded together.
Nitrogenous Bases
Nitrogen-containing biological molecules (nucleobases) that form the building blocks of DNA and RNA.
Purines
Larger, two-ring nitrogenous base structures consisting of Adenine (A) and Guanine (G).
Pyrimidines
Smaller, one-ring nitrogenous base structures consisting of Cytosine (C), Thymine (T), and Uracil (U).
Adenine (A)
A purine base found in both DNA and RNA.
Guanine (G)
A purine base found in both DNA and RNA.
Cytosine (C)
A pyrimidine base found in both DNA and RNA.
Thymine (T)
A pyrimidine base found specifically in DNA.
Uracil (U)
A pyrimidine base found specifically in RNA.
Nucleoside
A molecule consisting of a nitrogenous base and a pentose sugar.
Pentose Sugar
A 5-carbon sugar, either ribose (in RNA) or deoxyribose (in DNA).
Glycosidic Linkage
The covalent bond between the C−1′ carbon of a sugar and the nitrogen of a base (N−1 for pyrimidines or N−9 for purines).
C−1′ carbon
The specific carbon on the pentose sugar that forms a linkage with the nitrogenous base.
N−1 nitrogen
The position on pyrimidine bases that bonds to the pentose sugar.
N−9 nitrogen
The position on purine bases that bonds to the pentose sugar.
Adenosine
A nucleoside formed from the base adenine and the sugar ribose.
Deoxyribose
A sugar found in DNA that lacks an oxygen at the 2′ position.
Ribose
A sugar found in RNA that retains an oxygen at the 2′ position.
Phosphoric acid (H3PO4)
The chemical residue that esterifies to the sugar of a nucleoside to form a nucleotide.
Esterification
The chemical process by which phosphoric acid is attached to the hydroxyl group of a sugar portion of a nucleoside.
5′ carbon
The carbon on the pentose sugar where phosphate groups are typically attached.
-monophosphate
The suffix added to the parent nucleoside name to identify a nucleotide with one phosphate group.
AMP
Adenosine monophosphate, consisting of adenosine plus one phosphate group.
5′−AMP
Adenosine 5′-monophosphate, indicating the phosphate ester is at the 5′ carbon hydroxyl group.
3′−AMP
Adenosine 3′-monophosphate, indicating the phosphate ester is at the 3′ carbon hydroxyl group.
Phosphodiester Bonds
The linkages that connect the 3′ hydroxyl (–OH) group of one sugar to the 5′ phosphate group of the next sugar.
Sugar-phosphate Backbone
The stable structural framework of nucleic acids formed by repeating phosphodiester linkages.
Direction of sequence reading
The sequence of bases attached to the backbone is read in the 5′ to 3′ direction.
Complementary Base Pairing
The specific hydrogen bonding between bases (A with T, G with C) that stabilizes the DNA double helix.
A−T pair
A base pairing held together by 2 hydrogen bonds.
G−C debt
A base pairing held together by 3 hydrogen bonds, making these regions more thermally stable.
Purine–Pyrimidine pairing
The only base geometry that fits the uniform width of the DNA double helix.
DNA polymerase
An enzyme that can only add nucleotides in the 5′→3′ direction during replication.
Non-covalent forces
Forces like hydrogen bonding, ionic interactions, hydrophobic effects, and van der Waals forces that mediate quaternary structure.
Hydrogen bonding
Non-covalent force that stabilization base pairing and quaternary interactions.
Ionic interactions
Electrostatic forces that help mediate quaternary structural arrangements in nucleic acids.
Hydrophobic effects
Non-covalent forces contributing to the higher-order structural arrangements of nucleic acids.
Van der Waals forces
Weak, short-range electrostatic attractions that help stabilize quaternary structures.
Hierarchical structure
The organization of nucleic acids into levels (primary, secondary, tertiary, quaternary) similar to protein structure.
2′ position
The specific carbon on the sugar molecule that determines if the nucleic acid is DNA (no oxygen) or RNA(oxygen present).
Uniform width of helix
Maintained in DNA by pairing a large purine base with a small pyrimidine base.
Accuracy in decoding
Ensured during translation by the pairing of tRNA with mRNA, forming an RNA−RNA duplex.
Ribosomal RNA (rRNA)
The nucleic acid component of ribosomes that complexes with proteins.
Parent nucleoside
The base plus sugar unit used as the root name when naming a nucleotide (e.g., adenosine in AMP).
Genetic information storage
A function of DNA and RNA sequence determined by the order of bases.
DNA vs RNA sugar difference
DNA contains deoxyribose; RNA contains ribose.
DNA vs RNA base difference
DNA contains Thymine (T); RNA contains Uracil (U).
Cloverleaf interaction
Interaction of unpaired nucleotides in the loops of tRNA results in folding from cloverleaf to inverted L-shape.
Thermal stability
Increases in DNA molecules with higher GC content due to the extra hydrogen bond in G−C pairs.
Backbone protection
The sugar-phosphate backbone is stable and protects the genetic code held in the base sequence.
Complex 3D shape
The definition of the tertiary structure of DNA or RNA.
Glycosidic linkage (Purine)
A bond between the C−1′ carbon of the sugar and the N−9 nitrogen of the purine base.
Glycosidic linkage (Pyrimidine)
A bond between the C−1′ carbon of the sugar and the N−1 nitrogen of the pyrimidine base.
Polynucleotide backbone
The chain of sugars and phosphates that defines the secondary structural conformation.
Hairpin loops
Another name for the stem-loop structures found in RNA secondary structure.
Hierarchical levels of DNA
Organized into four levels: primary, secondary, tertiary, and quaternary.
Linear sequence purpose
Encodes genetic information (the genetic code).
Translation accuracy
Mediated by a short-lived RNA–RNA duplex between tRNA and mRNA.
Nucleic Acid Monomers
Nucleotides, consisting of three covalently bonded parts: base, sugar, and phosphoric acid residue.
Higher-order folding
The process resulting in tertiary structure elements in DNA or RNA.
Base sequence reading convention
Always read from the 5′ end to the 3′ end.
Hydrogen bond count (A-T)
2 hydrogen bonds.
Hydrogen bond count (G-C)
3 hydrogen bonds.
Complexity difference
The distinction between structural levels ranging from linear sequences to intricate protein-complexed units.
Inverted L-shape
The specific tertiary structure adopted by transfer RNA (tRNA).
Covalent polymer parts
Nitrogenous base, sugar, and phosphoric acid residue.
Purine structure
A double-ring nitrogenous structure.
Pyrimidine structure
A single-ring nitrogenous structure.
Nucleoside components
Nitrogenous base and a pentose sugar (ribose or deoxyribose).
Transcription hybrids
Transient DNA–RNA complexes formed during the transcription process.
Replication orientation
Crucially requires the antiparallel orientation of DNA strands for enzyme recognition.
Function of Quaternary Structure
Essential for the execution of specific biological functions in living systems.
DNA-RNA hybrids
Transient complexes formed during DNA replication and transcription.
RNA-RNA duplex
A complex formed between tRNA and mRNA during translation.
Local double-helical regions
Regions in single-stranded RNA where the molecule folds back on itself.
Hierarchical description
The description of nucleic acid structure in levels, similar to protein structural hierarchy.
Biochemistry 202 outcome
Understanding how genetic information is stored, accessed, and used based on structural levels.
Nucleic acids purpose
To carry genetic information in the form of DNA and RNA.
Stable backbone function
Protects the genetic code held in the base sequence.
Uniform width requirement
In a DNA double helix, a large base (purine) must always pair with a small base (pyrimidine).