Course review

D1.2 Protein synthesis

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Learning objective

D1.2.1—Transcription

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• Transcription makes mRNA as a mobile copy of gene information • RNA polymerase synthesizes RNA complementary to the DNA template strand

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Learning objective

D1.2.2—Hydrogen bonding in transcription

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• Free RNA nucleotides align by complementary base pairing and hydrogen bonding • DNA adenine pairs with RNA uracil, while cytosine pairs with guanine

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D1.2.3—DNA template stability

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• DNA template strands are transcribed without altering the base sequence • Sugar-phosphate backbone and base pairing preserve genetic information

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Learning objective

D1.2.4—Transcription for gene expression

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• Transcription is the first stage of gene expression • Cells regulate which genes are transcribed according to tissue, stage, and signals

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D1.2.5—Translation

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• Translation decodes mRNA at ribosomes to synthesize polypeptides • mRNA codon order determines amino acid sequence

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Learning objective

D1.2.6—Roles in translation

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• mRNA provides codons; tRNA carries activated amino acids with anticodons • Ribosomes hold mRNA and tRNAs so peptide bonds can form

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D1.2.7—Complementary base pairing

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• tRNA anticodons pair with complementary mRNA codons by hydrogen bonding • Specific tRNA-amino acid attachment helps ensure correct amino acid addition

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Learning objective

D1.2.8—Genetic code features

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• The genetic code is triplet, degenerate, and almost universal • Codons specify amino acids, a start signal, or stop signals

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Learning objective

D1.2.9—Using genetic code table

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• Genetic code tables use mRNA codons, not DNA triplets • Convert template DNA to mRNA first, then read codons 5' to 3'

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Learning objective

D1.2.10—Elongation of polypeptide

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• Ribosomes move along mRNA one codon at a time from start to stop • Peptide bonds join amino acids; multiple ribosomes can form a polysome

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Learning objective

D1.2.11—Mutations changing protein structure

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• Mutations can change codons and therefore amino acid sequence • Changed primary structure may alter folding and function, such as sickle-cell haemoglobin

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Learning objective

D1.2.12 (HL)—Directionality

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• RNA polymerase reads template DNA 3' to 5' and synthesizes RNA 5' to 3' • Ribosomes translate mRNA codons in the 5' to 3' direction

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D1.2.13 (HL)—Initiation of transcription at promoter

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• Promoters mark transcription start regions and orientation • Transcription factors help RNA polymerase bind and initiate in eukaryotes

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Learning objective

D1.2.14 (HL)—Non-coding sequences in DNA

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• Non-coding DNA does not code for polypeptide amino acid sequences • Includes introns, regulatory sequences, telomeres, rRNA genes, and tRNA genes

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D1.2.15 (HL)—Post-transcriptional modification

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• Eukaryotic pre-mRNA is modified before export and translation • Processing adds a 5' cap and poly-A tail and removes introns by splicing

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D1.2.16 (HL)—Alternative splicing

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• Alternative splicing joins different exon combinations from one pre-mRNA • One gene can produce multiple protein variants in different cells or stages

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D1.2.17 (HL)—Translation initiation

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• Translation initiation assembles ribosomal subunits at the start codon AUG • Initiator tRNA enters the P site; A, P, and E sites organize tRNA movement

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D1.2.18 (HL)—Polypeptide modification

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• Newly made polypeptides may be folded, cleaved, or chemically modified • Preproinsulin processing to active insulin is a key example

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D1.2.19 (HL)—Amino acid recycling by proteasomes

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• Proteasomes degrade tagged, damaged, or unneeded proteins • Amino acid recycling supports new protein synthesis and proteome quality control

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