-recognize specific sequences at the end of introns
Cuts out introns and joins the exons back together
5' UTR EI I1 E2 I2 E3 I3 E4 UTR 3'
Which components of the previous molecule will also be found in mRNA in the cytosol?
C) 5' UTR E1 E2 E3 E4 UTR 3'
Alternative RNA splicing...
C) can allow the production of proteins of different sizes and functions from a single mRNA
Why do we have introns?
Some introns contain sequences which play a role in regulating gene expression
Allows a single gene to code for more than one polypeptide
They let you take out or keep exons
Alternative RNA splicing
Some exons can be left out of final transcript
This allows humans to make 75,000-100,000 proteins with only ~20,000 genes
Translation
mRNA -> protein
Occurs in the cytoplasm
mRNA is "read" 3 bases at a time (codon) to build a polypeptide
Key players of translation
tRNAs
Ribosomes
The codon for serine is UCG. The coding (non-template) strand of the DNA that encoded is ___ and the anticodon of the tRNA that recognizes it is ___.
D) TCG, AGC
Transfer RNA (tRNA)
Translates messages from nucleic acids to amino acids
Transcribed from DNA template and folds to form 3D structure
Contains an anticodon
Carries a specific amino acid
Anticodon
Triplet which is complementary to codon on mRNA
During eukaryotic translation, which of the following is NOT used?
A) RNA polymerase
Aminoacyl-tRNA synthetases
Enzymes which attach the amino acid to the tRNA
Active site can only fit specific combinations of tRNA and amino acids (ensures anticodon brings in correct amino acid)
tRNA with amino acid attached is "charged"
Only ~40 tRNAs (not the 61 you would expect... 1 for each possible codon)
--Flexible base pairing in 3rd position = wobble
How many different aminoacyl-tRNA synthetases are there?
20 different synthetases (1 for each amino acid)
A mutant bacterial cell has a defective aminacyl-tRNA synthetase that attaches a lysine to tRNAs with the anticodon AAA instead of the normal phenylalane. The consequence for the cell will be that...
E) Proteins in the cell will include lysine instead of phenylalanine at amino acid positions specified by the codon UUU
Ribosome
onsist of a small and large subunit composed of protein and ribosomal RNA (rRNA)
Why are prokaryotic and eukaryotic ribosomes differences important in medicine?
Some antibiotic inactivate bacterial ribosomes without harming our own
Otherwise, the two ribosomes are very similar
What catalyzes the formation of peptide bonds?
rRNA not the protein
3 steps of translation
Initiation
Elongation
Termination
Initiation in translation
Small unit of the ribosome, which the initiator tRNA (methione) already attached, binds to leader sequence of mRNA and scans for AUG
Large subunit binds and completes translation initiation complex
Elongation in translation
Ribosome moves along mRNA adding amino acids to the growing polypeptide chain
Termination in translation
Ribosome hits a stop codon and the subunits separate the polypeptide is released
Initiation process in translation
rRNA in small subunit binds to complementary sequence on mRNA (ribosomal binding site)
--helped by initiation factors
Initiator tRNA binds to start codon
Large subunit attaches to form translation initiation complex
Elongation process in translation
Amino acids are added one by one to growing polypeptide chain
-Requires proteins= elongation factors
-Requires energy
3 ribosome sites in elongation
E- empty tRNA exits
P- tRNA with growing polypeptide
A- incoming (active) tRNA
Termination process in translation
Elongation continues until a stop codon is reached
A release factor (protein shaped like a tRNA) binds to the stop codon in the A site
-causes the polypeptide to be released
The translation assembly breaks apart
Polyribosomes
Typically a single mRNA is simultaneously translated by multiple ribosomes (polyribosomes)
1 ribosome can make an average polypeptide in less than a minute
Post-translational modification
Polypeptide must undergo correct secondary and tertiary folding
-may require assistance of molecular chaperons
Chemical post-translational modifications
Attachment of sugars, lipids, phosphate groups
Cleavage of polypeptide chain (i.e insulin)
Interaction of multiple subunits (quaternary structure)