Ch 16: How Genes Work Flashcards
Messenger RNA hypothesis
DNA (info storage)–(transcription)–> mRNA (info carrier)–(translation)–> proteins
Central dogma of biology
Particular stretch of DNA (gene) contains info to specify amino sequence of protein
Info in base of DNA = no directly translated into amino sequence
Human genome
20,000 genes humans
Potatoe has 39,000
3 bil base pairs
76% of total genome is transcribed into RNA
Codon
3 nucleotides code for a single amino acid
How do we know it’s 3 nucleotides?
- if each base coded for 1 amino acid= only 4 amino acids
- if pairs of bases codes for amino= max 16
- if triplets= 64 potential amino acids = more than enough
Redundancy
Triplets can code for the same amino acid
Delete/add 3
Sensible message, reading frame restored, slightly altered but functional protein
Francis crick
Making deletions and insertion mutations established code is based on 3 nucleotides for each amino
- triplet code
- reading frame could be resorted if deletions or additions were multiples of 3
Marshall Nirenberg
System for synthesizing specific RNA and codons of known sequence and were able to determine which of 64 codes for each 20 amino acids.
Korana experiments
Alternating synthetic mRNA
Stretch of alternating amino acids
Three stop codons
UAA (U Are Awesome)
UAG (U Are Great)
UGA (U Get As)
Start codon
Methionine
AUG (AUGust start school)
Valine
GU (U,C,A,G) switched in sickle cell
Glutamic acid (Glu)
GAA
GAG
Genetic code is redundant
All amino acids Exocet methionine and tryptophan are coded by more than 1 codon
Genetic code is unambiguous
A single codon never codes for more than 1 amino acids
Genetic code is universal
Few minor exceptions. All codons specify the same amino acids in all organisms
Genetic code is conservative
When several codons specify the same amino acid, first two bases are almost always identical
Silent mutation
Change in NT that does not change amino acid specidified by codon
Change in genotype but not phenotype
Missense mutation
Change in NT changes amino acid specified by codon
Change in primary structure
Nonsense mutation
Change in NT that results in early stop codon
Premature termination: polypeptide truncated
Frameshift
Addition or deletion of a NT
Reading frame is shifted, massive missense (everything beyond that inserted or deleted mutation is changed)