Grade 12 Life Sciences: DNA, RNA, Protein Synthesis, and Genetic Technology

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Comprehensive vocabulary flashcards covering the discovery of DNA, nucleic acid structure, replication, protein synthesis, gene mutations, extraction methods, and DNA technology based on Grade 12 Life Sciences.

Last updated 9:30 AM on 10/13/26
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64 Terms

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Chargaff's Rules

The biochemical principle formulated in 1950 stating that in any double-stranded DNA molecule, the amount of adenine (A\text{A}) always equals thymine (T\text{T}) and the amount of cytosine (C\text{C}) always equals guanine (G\text{G}).

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<p>Photo 51</p>

Photo 51

The famous X-ray diffraction photograph of DNA captured by Rosalind Franklin in 1952, which provided key structural data demonstrating the helical shape, diameter (20 A˚20\,\text{Å}), pitch (34 A˚34\,\text{Å}), and base pair spacing (3.4 A˚3.4\,\text{Å}) of DNA.

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Rosalind Franklin

A physical chemist who utilized X-ray crystallography to produce Photo 51 in 1952, determining DNA's helical dimensions; her critical research data was shown to Watson and Crick without her knowledge or consent.

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Maurice Wilkins

A researcher at King's College London who worked on X-ray crystallography, shared Rosalind Franklin's data with James Watson and Francis Crick, and shared the 1962 Nobel Prize in Physiology or Medicine.

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James Watson and Francis Crick

Scientists at Cambridge University who pieced together physical model representations in 1953 to publish the correct double-helix structure of DNA in Nature.

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Nuclear DNA

The double-stranded, helical chromosomal DNA located within the cell nucleus that binds to histone proteins to form chromatin and encodes genetic traits on chromosomes.

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Mitochondrial DNA (mtDNA)

A small, circular DNA molecule found inside mitochondria that codes for mitochondrial proteins and is inherited strictly through the maternal lineage.

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Chloroplast DNA

The distinct type of circular DNA found inside chloroplasts in plant cells.

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<p>Endosymbiotic Theory</p>

Endosymbiotic Theory

The evolutionary theory proposing that mitochondria originated from primitive, free-living aerobic prokaryotes that were engulfed by ancestral eukaryotic cells billions of years ago and retained their own circular DNA.

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Maternal Inheritance

The inheritance pattern of mitochondrial DNA (mtDNA\text{mtDNA}), wherein offspring receive mitochondria solely from the female egg cell while sperm contribute none, leaving the genetic sequence unaltered across generations.

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<p>Nucleotide</p>

Nucleotide

The basic monomeric building block of nucleic acids, consisting of a phosphate group, a pentose sugar, and a nitrogenous base.

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Phosphate Group

A chemical component of a nucleotide that imparts a negative charge to the nucleic acid molecule and links alternating sugar molecules to build the continuous backbone.

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Deoxyribose

A five-carbon pentose sugar found in DNA nucleotides that lacks one oxygen atom in comparison to ribose.

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Ribose

A five-carbon pentose sugar found in RNA nucleotides that contains an additional oxygen atom missing in deoxyribose.

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<p>Purine</p>

Purine

A class of nitrogenous bases composed of a double-ring structure; examples found in DNA and RNA include adenine and guanine.

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<p>Pyrimidine</p>

Pyrimidine

A class of nitrogenous bases composed of a single-ring structure; examples include cytosine, thymine, and uracil.

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Adenine (A)

A double-ring purine base that pairs with thymine in DNA (or uracil in RNA) via two weak hydrogen bonds.

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Thymine (T)

A single-ring pyrimidine base found exclusively in DNA that pairs with adenine via two weak hydrogen bonds.

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Cytosine (C)

A single-ring pyrimidine base that pairs specifically with guanine via three weak hydrogen bonds in both DNA and RNA.

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Guanine (G)

A double-ring purine base that pairs specifically with cytosine via three weak hydrogen bonds in both DNA and RNA.

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Uracil (U)

A single-ring pyrimidine nitrogenous base found in RNA that substitutes for thymine and pairs with adenine.

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Antiparallel Strands

The structural arrangement of the two complementary strands in a DNA double helix, where one strand runs in the 5′→3′5' \rightarrow 3' direction and the other runs in the 3′→5′3' \rightarrow 5' direction.

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Histones

Basic proteins around which chromosomal DNA wraps in eukaryotic nuclei to form nucleosomes and condense into chromatin.

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Nucleosome

The fundamental subunit of chromatin, consisting of a segment of DNA wrapped around a core of histone proteins.

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Chromatin

The DNA-containing diffuse network found in the eukaryotic nucleus during interphase (the non-dividing stage of the cell cycle).

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Chromatid

One of the two identical individual strands of a replicated chromosome that are joined together at the centromere.

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Centromere

The constricted region of a chromosome that holds two sister chromatids together and serves as the attachment point for spindle fibres during cell division.

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Chromosome

A condensed, thread-like structure of DNA and protein that carries genetic information organized into genes.

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Chromatin Network

Visible thread-like structures composed of DNA and proteins situated in the nucleus of an inactive, non-dividing cell.

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Nucleolus

A distinct dense structure within the cell nucleus responsible for transcribing and assembling ribosomal RNA (rRNA\text{rRNA}).

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Nucleoplasm

The fluid protoplasmic substance enclosed within the nuclear membrane surrounding the chromatin and nucleolus.

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Ribosome

A cytoplasmic organelle composed of RNA and proteins that reads mRNA codons and serves as the site of protein synthesis (translation).

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DNA Replication

The biological process occurring in the nucleus during interphase whereby an original DNA molecule produces two identical double-stranded DNA molecules.

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<p>Semi-conservative Replication</p>

Semi-conservative Replication

The mechanism of DNA copying wherein each newly synthesized double helix is composed of one conserved parental strand and one newly assembled daughter strand.

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Template Strand

An original single strand of DNA that provides the complementary nucleotide framework upon which a new DNA or RNA strand is assembled.

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Complementary Strand

A newly synthesized polynucleotide strand generated by matching complementary bases against an existing template strand.

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DNA Helicase

An enzyme responsible for unwinding the DNA double helix and breaking the weak hydrogen bonds between complementary base pairs to separate the strands.

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DNA Polymerase

The enzyme that synthesizes new DNA strands by attaching free nucleoplasmic nucleotides to the exposed complementary bases of a template strand during replication.

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DNA Ligase

An enzyme known as the molecular glue that seals breaks in the sugar-phosphate backbone by forming phosphodiester bonds to link DNA fragments.

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Central Dogma of Molecular Biology

The fundamental framework stating that genetic information flows directionally within biological systems from DNA to RNA to Protein.

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Transcription

The first stage of protein synthesis occurring in the nucleus, in which an RNA polymerase enzyme synthesizes a single strand of mRNA from a DNA template.

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RNA Polymerase

The primary enzyme of transcription that separates DNA strands and joins complementary RNA nucleotides to synthesize an mRNA transcript.

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Messenger RNA (mRNA)

A single-stranded RNA molecule transcribed in the nucleus that carries the genetic sequence code from DNA out through the nuclear pore to ribosomes in the cytoplasm.

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<p>Transfer RNA (tRNA)</p>

Transfer RNA (tRNA)

A folded, cloverleaf-like RNA molecule in the cytoplasm possessing a specific anticodon at one end and carrying its designated amino acid to the ribosome.

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Ribosomal RNA (rRNA)

The structural and functional RNA component synthesized in the nucleolus that associates with proteins to form ribosomes.

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Triplet

A sequence of three consecutive nitrogenous bases on a DNA molecule that codes for one specific amino acid in a polypeptide chain.

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Codon

A sequence of three adjacent nitrogenous bases situated on an mRNA molecule that directs the placement of a specific amino acid.

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Anticodon

A sequence of three adjacent nitrogenous bases situated on a tRNA molecule that pairs complementarily with an mRNA codon to deliver the correct amino acid.

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Translation

The second stage of protein synthesis occurring at the ribosome, where the genetic code in mRNA is translated into an amino acid sequence joined by peptide bonds to create a protein.

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Gene Expression

The process by which coded information stored within a gene is used to direct the synthesis of a functional protein molecule.

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Gene Mutation

A permanent alteration in the nucleotide sequence or arrangement of bases in DNA, which can modify mRNA transcription and alter the resulting polypeptide structure.

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Point Mutation

A mutation that affects a single nucleotide within a DNA sequence, typically exemplified by a base substitution.

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Substitution Mutation

A type of point mutation where a single nitrogenous base in DNA is swapped for a different base, categorised as silent, missense, or nonsense.

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Silent Mutation

A base substitution that produces an altered codon that still encodes the identical amino acid due to the degeneracy of the genetic code, leaving the protein unchanged.

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Missense Mutation

A base substitution that changes an mRNA codon such that a different amino acid is incorporated into the growing polypeptide, potentially altering protein structure and function.

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Nonsense Mutation

A base substitution that prematurely converts an amino acid-coding codon into a stop codon, terminating translation early and producing a truncated, non-functional protein.

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Frameshift Mutation

A mutation caused by the insertion or deletion of one or more nucleotides (not in multiples of three) that shifts the entire triplet reading frame for all subsequent codons.

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Insertion Mutation

The addition of one or more nucleotide bases into a DNA sequence, which causes a frameshift and results in abnormal amino acid coding downstream.

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Deletion Mutation

The loss of one or more nucleotide bases from a DNA sequence, causing a frameshift that completely alters downstream codon reading and protein formation.

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Chemical DNA Extraction

A salt-based isolation procedure that uses detergent to dissolve lipid cell and nuclear membranes, salt to neutralize the DNA backbone charge, and ice-cold ethanol to precipitate intact DNA strands.

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Mechanical DNA Extraction

A cell lysis method that utilizes small beads (such as metal, glass, or zirconia) shaken at high velocity to physically shear and shatter tough cell walls and membranes.

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Polymerase Chain Reaction (PCR)

A laboratory technique used to amplify trace quantities of DNA millions of times through sequential thermal cycles of denaturation (∼95∘C\sim 95^\circ\text{C}), primer annealing (∼55∘C\sim 55^\circ\text{C}), and polymerase extension (∼72∘C\sim 72^\circ\text{C}).

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DNA Fingerprinting

A forensic and diagnostic profiling technique that analyzes highly variable, non-coding repetitive DNA regions to generate a unique banding pattern for an individual.

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Non-coding DNA

The approximately 98%98\% of the human genome that does not code for proteins, containing highly variable repetitive sequences known as Short Tandem Repeats (STRs) used in genetic profiling.