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AQA A LEVEL BIOLOGY 4: GENETIC INFORMATION, VARIATION AND RELATIONSHIPS BETWEEN ORGANISMS NOTES

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MASTER AQA A-LEVEL BIOLOGY – TOPIC 4: GENETIC INFORMATION, VARIATION AND RELATIONSHIPS BETWEEN ORGANISMS Everything you ACTUALLY need. Nothing more, nothing less. These are razor-sharp, exam-focused notes written exactly for the AQA mark scheme – no waffle, no filler, just pure grade-boosting content. What makes these different: Precise wording examiners reward Clear, step-by-step explanations of every concept Perfect definitions, processes & required practicals Structured exactly like the spec for easy recall Ideal for quick revision OR full topic mastery These are the exact notes that helped me hit A/A* in every class test, every mock, and the real exam. If you want to walk into Topic 1 questions feeling untouchable, this is your shortcut. ⏳ Don’t waste hours drowning in textbooks – learn what actually gets marks and move on. Your future A* starts here. Revise smarter. Score higher. Stress less.

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4.1 DNA, genes, and chromosomes
Eukaryotic Prokaryotic, mitochondria, chloroplast
Same nucleotide structure joined by phosphodiester bonds
Long Short
Linear Circular
Associated with histone proteins Not associated with proteins
Have introns No introns

● Chromosome: long, coiled DNA molecule and its associated proteins
● Gene: base sequence of DNA that codes for: the amino acid sequence of a
polypeptide, a functional RNA
● Locus: fixed position of a gene on a DNA molecule
● Triplet: sequence of 3 DNA bases that codes for a specific amino acid

● Genetic code is universal, non-overlapping, degenerate
○ Universal: each triplet codes for the same amino acid in all organisms
○ Non-overlapping: each base is part of only one triplet
○ Degenerate: an amino acid can be coded for by more than one triplet

● Exon: sequence of DNA that codes for an amino acid sequence
● Intron: non-coding sequence of DNA


4.2 DNA and protein synthesis
● Genome: the complete set of genes in a cell
● Proteome: the full range of proteins a cell is able to produce




● tRNA has a cloverleaf structure made of nucleotides
● 3 bases form an anticodon at one end, allowing it to bind to a complementary
mRNA codon
● Amino acid binding site at the other end carries a specific amino acid that is
complementary to the mRNA codon

, Transcription:
● DNA helicase breaks H bonds between complementary base pairs, separating the
DNA molecule
● Only one strand acts as a template and the bases are now exposed
● Free RNA nucleotides align by complementary base pairing
● RNA polymerase then joins the adjacent nucleotides by forming phosphodiester
bonds
● pre-mRNA is then spliced to remove sections of non-coding introns
● Mature mRNA strand leaves the nucleus

● In prokaryotic cells, mRNA is directly formed and splicing does not occur as there
are no introns

Translation:
● mRNA attaches to a ribosome which moves to the start codon
● tRNA brings an amino acid to the ribosome, its anticodon binds to the
complementary mRNA codon
● The ribosome then moves along the mRNA to read the next codon, allowing the
next tRNA to bind, bringing another amino acid
● The 2 amino acids that have been brought by the tRNA molecules join by a peptide
bond with the use of ATP
● Once the amino acid brought by the tRNA molecule has been added to the growing
polypeptide chain, the tRNA is released
● The process of adding amino acids to the polypeptide chain repeats until the
ribosome reaches a stop codon, releasing the polypeptide chain


4.3 Genetic diversity can arise as a result of mutation or
during meiosis
● Mutation: change in the base sequence of chromosomes
● Occurs spontaneously during DNA replication and includes base deletion and
substitution
○ Base deletion: when one or more bases are removed from a DNA sequence
causing frame shift, resulting in a different amino acid that is coded for
○ Base substitution: when one base is replaced by another. As the genetic
code is degenerate, not all base substitutions will result in a different amino
acid being coded for so may have no effect

○ Mutations cause change in base sequence of DNA, changing primary
structure, changing tertiary structure

● Mutations in number of chromosomes can occur due to non-disjunction during
meiosis
○ Non-disjunction: homologous chromosome pair failed to separate leading to
a gamete with one more or one less chromosomes

● Mutagenic agent: increases rate of mutations

Meiosis:

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