Mission
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D1.2 Protein synthesis

태그
transcription
translation
RNA polymerase
promoter
alternative splicing
ribosome
codon
anticodon
intron
exon
sickle cell anemia
Date

Understanding points

D1.2.1 Transcription as the synthesis of RNA using a DNA template D1.2.2 Role of hydrogen bonding and complementary base pairing in transcription D1.2.3 Stability of DNA templates D1.2.4 Transcription as a process required for the expression of genes D1.2.5 Translation as the synthesis of polypeptides from mRNA D1.2.6 Roles of mRNA, ribosomes and tRNA in translation D1.2.7 Complementary base pairing between tRNA and mRNA D1.2.8 Features of the genetic code D1.2.9 Using the genetic code expressed as a table of mRNA codons D1.2.10 Stepwise movement of the ribosome along mRNA and linkage of amino acids by peptide bonding to the growing polypeptide chain D1.2.11 Mutations that change protein structure D1.2.12 Directionality of transcription and translation (HL only) D1.2.13 Initiation of transcription at the promoter (HL only) D1.2.14 Non-coding sequences in DNA do not code for polypeptides (HL only) D1.2.15 Post-transcriptional modification in eukaryotic cells (HL only) D1.2.16 Alternative splicing of exons to produce variants of a protein from a single gene (HL only) D1.2.17 Initiation of translation (HL only) D1.2.18 Modification of polypeptides into their functional state (HL only) D1.2.19 Recycling of amino acids by proteasomes (HL only)

Transcription

Production of mRNA from DNA by RNA polymerase
RNA polymerase unwinds DNA and binds to the promoter with the help of transcription factors*(AHL) RNA is synthesized in 5’ → 3’ direction by complementary base pairing of A-U and G-C ↓ RNA and RNA polymerase detach from template + DNA rewinds into double helix

Translation

Production of a polypeptide from mRNA by ribosomes
Ribosomes are made of rRNA and protein
Large subunit: 3 binding sites (A,P E) for tRNA
Small subunit: mRNA binding site
Codon: 3 bases on mRNA that code for an amino acid
Complementary base pairing with anticodon on tRNA
*(AHL) Translation initiates at start codon (AUG) ↓ mRNA binds to ribosome small subunit ↓ tRNA binds with αα then attaches to ribosome (1st tRNA at P site) ↓ Anticodon on tRNA pairs with codon on mRNA ↓ Peptide bond forms between the amino acids of consecutive tRNAs ↓ The 1st tRNA leaves via the E site and the 2nd tRNA enters the A site ↓ As ribosome moves along the mRNA, polypeptide elongation occurs ↓ Translation stops when it reaches a stop codon (UAA, UAG, UGA)

Sickle cell anemia

Cause
Base substitution mutation in hemoglobin gene Single base change from CTC to CAC 𝛼𝛼 change from glutamic acid to valine
Result
Hemoglobin forms fibrous, insoluble strands RBC becomes sickle shaped and cannot carry sufficient oxygen
Genetics
Sickle-cell allele is codominant Heterozygous = malaria resistant carrier Homozygous = anemia

*(AHL)

Post-transcriptional modification

In the nucleus
Removal of introns
Introns are removed and exons are spliced together Alternative splicing: different exons joined to produce different polypeptides
Addition of 5’ cap
Methylguanine is added to 5’ end of mRNA
Addition of 3’ tail
100~200 adenine nucleotides are added to 3’ end of mRNA

Post-translational modification

Noncoding sequences

Gene regulators
Promoters and repressors 
Introns 
Removed from mRNA before translation 
Telomeres 
Repetitive sequences at the ends of chromosomes that protects DNA
tRNA and rRNA genes
Transcripted, but not translated 

Proteasomes

Degrade damaged proteins marked with ubiquitin