Ch 7 - RNA and Genetic Code Flashcards
1
Q
central dogma
A
- DNA replication
- DNA to RNA via transcription
- opposite via reverse transcription
- mRNA synthesized in 5-3 direction and is complementary to DNA template strand
- RNA to protein via translation
- translate RNA from 5-3 direction
- synthesize protein from N terminus to C terminus
2
Q
mRNA
A
- specify amino acid sequence for proteins
- transcribed via rna polymerase in the nucleus
- read in codons
- monocistronic - each mRNA molecule translates to one protein
- eukaryotes
- polycistronic - different proteins depending on where on mRNA translation begins
- prokaryotes
3
Q
tRNA
A
- transfer RNA
- anticodon to match codon on mRNA and retreive amino acid
- charged (activated) - when connected to amino acid
- aminoacyl-tRNA synthetase - activates amino acid
- uses 2 high energy bonds from ATP
- energy rich process
- CCA sequence where amino acid binds to 3’ end of tRNA
4
Q
rRNA
A
- ribosomal RNA
- synthesized in nucleolus
- ribosomal machinery
- ribozymes - enzyme made of RNA
- important in splicing out introns
5
Q
Codons
A
- anticodons - antiparallel to codons
- AUG - start codon (methionine)
- stop codons - UGA, UAA, UAG
6
Q
Mutations
A
- silent/degenerate - due to wobble base
- no change to amino acid
- point - affect one nucleotide
- missense - affect one amino acid
- nonsense - introduce a stop codon
- frameshift - nucleotides added or deleted
- insertion or deletion
7
Q
transcription
A
- helicase and topoisomersae unwind and prevent supercoiling
- synthesized from template strand
- synthesized by RNA polymerase
- RNA polymerase II - mRNA and snRNA in eukaryotes
- RNA polymerase I - rRNA in nucleolus
- RNA polymerase III - tRNA and rRNA
- starts at promoter region
- binds to TATA box
- trasncription factors help polymerase bind
- travel in 3-5 direction in order to synthesize in 5-3
- +1 base is first to be transcribed
- upstream from here are negative numbers
- downstream are positive numbers
- TATA box near -25
- continue until termination sequence
- DNA double helix reforms
- hnRNA - heterogeneous nuclear RNA is unmodified transcript
8
Q
Posttranscriptional processing
A
- splicing: introns and exons
- 5’ cap
- 3’ poly A tail
9
Q
Splicing
A
- remove introns (noncoding sequences)
- ligate exons (coding sequences) together
- Spliceosome - snRNA and small nuclear ribonucleoproteins (snRNPs)(snurps)
- recognize introns and remove
- lariat - lasso shaped structure of intron
- intron degraded
- Alternatice splicing - make many different proteins from a limited number of genes
- splice together in different ways
10
Q
5’ Cap
A
- 7-methylguanylate triphosphate cap
- protect from degradation in cytoplasm
- recognized by ribosome as the binding site
11
Q
3’ Poly A tail
A
- 3’ end of transcript
- protect from degradation
- longer tail will mean longer life outside of nucleus
12
Q
Ribosome
A
- A site - aminoacyl
- P site - peptidyl
- E site - exit
- Eukaryotes - 4 rRNA strands
- RNA polymerase I and III transcribe rRNA
- polymerase I in the nucleolus
- 40S and 60S subunits join to make 80S (whole ribosome)
- RNA polymerase I and III transcribe rRNA
- Prokaryotes - 70S made from 50S and 30S subunits
13
Q
Translation Initiation
A
- eukaryotes - small subunit binds to 5’ cap
- initiator tRNA binds anticodon to AUG in P site of ribosome
- large subunit binds to small subunit
- assisted by initiation factors
- prokaryote - small subunit binds to Shane Dalgarno Sequence (5’ untranslated region)
14
Q
Translation Elongation
A
- ribosome moves 5-3
- synthesize N to C terminus
- A site - hold aminoacyl-tRNA complex, next amino acid, determined by codon
- P site - hold growing peptide chain
- form peptide bond - polypeptide transferred from P to A site tRNA via peptidyl transferase
- GTP used
- form peptide bond - polypeptide transferred from P to A site tRNA via peptidyl transferase
- E site - uncharged tRNA pauses and then leaves
- EF factors - elongation factors - locate and recruit amnioacyl tRNA and GTP, remove GTP
15
Q
Translation Termination
A
- release factor binds to terminal codon (stop codon)
- UAA, UAG, UGA
- add water to peptide chain - peptidyl transferase and termination factors hydrolyze peptide from last tRNA
- released from P site
- ribosome subunits dissociate
16
Q
Posttrasnlational processing
A
- chaperones - fold protein
- cleavage - inactive peptide must be cleaved before active
- phosphorylation - add PO4 2- via kinase
- carboxylation - add carboxylic acid
- glycosylation - add oligosaccharides in ER and golgi
- prenylation - add lipids to membran bound enzymes
17
Q
signal sequences
A
- designate destination for a protein
- some direct to endoplasmic reticulum
- ribosomes on ER to complete translation
- then to Golgi apparatus and secrete via vesicle and exocytosis
18
Q
Prokaryote Gene expression
A
- Operon - cluster of genes transcribed as a single mRNA
- described by Jacob-Monod Model
- strucutreal gene - protein of interest
- operator site - binds repressor protein
- promoter site - RNA polymerase binds
- regulator gene - codes for repressor protein
- Inducible and Repressible Systems
19
Q
Inducible System (operator system)
A
- repressor binds to operator system and stops transcription
- negative control - reduce transcription due to binding of molecule
- Inducer binds to repressor to allow RNA polymerase to transcribe the gene
- similar to competitive inhibition
- ex. Lac operon (negative inducible)
- only used when lactose is high and glucose is low
- induced by presence of lactose
- catabolite activator protein (CAP) - transcriptional activator when glucose is low
- low glucose - high cAMP - binds to CAP - CAP conformational change - CAP bind to promoter - increase transcription of lactase gene
- positive control - increase transcription of gene due to binding of molecule
- only used when lactose is high and glucose is low
20
Q
Repressible Systems
A
- constant production of protein
- repressor must bind to corepressor to be active
- complex binds operator site
- negative feeback
- final structure may be the corepressor
- trp operon - negative repressible
- trp operon - tryptophan is high - acts as corepressor
- repressor binds to operator when 2 tryptophans bound to it - stop making tryptophan
21
Q
Transciption factors
A
- Eukaryotes
- search DNA for DNA binding motifs
- DNA binding domain - binds specific sequence in promoter region or DNA response element
- Activation domain - binds other transcription factors and regulatory proteins
22
Q
Gene Amplification
A
- increase transcription due to hormones, growth factors, intracellular conditions
- Enhancers - several response elements (DNA sequences) grouped together to cause increase in transcription
- form hairpin turn in DNA to mean up with promoter region
- enhancer binds transcription factors that cooperate with the promoter region transcription factors
- Gene duplication - can duplicate to have many duplicates on one chromosome
23
Q
Chromatin Structure
A
- Heterochromatin - tightly coiled DNA, dark under microscope
- Euchromatin - looser, light under microscope
- genes are active
- Histone acetylation - histone acetylase, acetylate lysine residue on histone proteins
- decreases positive charge and weaken interaction with DNA
- open chromatin and easier access
- histone deacetylase - closes chromatin to decrease expression
- DNA methylation - DNA methylase - add methyl group to cytosine and adenine
- silences gene expression
- heterochromatin is more methylated