Chapter 7: RNA and the Genetic Code Flashcards
What are interferons?
What do they do?
Interferons interfere with viral replication.
They do so by curtailing the process of transcription and translation.
Briefly walk through the process of expressing genetic information.
The first step in expressing genetic information is transcription of the information in the base sequence of double straight DNA molecule to form a single strand molecule of RNA.
The second step is translating that nucleotide sequence into a protein.
What is the central dogma of molecular biology?
We have DNA. DNA contains genes. DNA is transcripted to RNA. RNA can be reverse transcribed to DNA. RNA is translated to proteins.
Which way is mRNA synthesized, which directionality does it have relating to DNA.
Which way do ribosomes translate the mRNA? Why?
mRNA is synthesized in the 5’-3’ direction and is complimentary and antiparallel to the DNA template strand (RNA transcriptase READS in the 3’-5’ direction)
The ribosome translates the mRNA in the 5’-3’ direction, as it synthesize as the protein from the amino terminus (N) to the carboxy terminus (C).
There are three types of RNA. What are they?
mRNA: messenger RNA carries information, specifying the amino acid sequence of the protein to the ribosome.
tRNA: transfer RNA is responsible for converting the language of nucleic acids to the language of amino acids and peptides.
rRNA: ribosomal RNA is synthesized in the nucleus and functions as an integral part of the ribosomal machine machinery used during protein assembly in the cytoplasm.
What is mRNA?
What enzyme transcribes mRNA?
What is a codon?
What is monocistronic, polycistronic?
mRNA is the messenger of genetic information. mRNA takes the information from the DNA to the ribosomes, where creation of the primary protein structure occurs. mRNA is the only type of RNA that contains information that is translated into protein.
RNA polymerase transcribes mRNA from DNA.
A codon is a three nucleotide segment that codes for an amino acid.
Monocistronic (eukaryotic mRNA): each mRNA molecule translates into only one protein product.
Polycistronic: (prokaryotic mRNA): mRNA can result in different proteins by starting the process of translation at different locations in the mRNA.
What is tRNA?
What is aminoacyl-tRNA synthase?
Where does the AA attach to the tRNA molecule?
What is rRNA?
What are ribozymes?
Ribosomes are enzymes made of RNA molecules rather than peptides.
What is a codon?
How many codons are there?
Which way are codons written? Why?
Consists of three bases that code for a specific AA.
There are 64 codons, 61 for one of the 20 AA, 3 for encoding for the termination of translation.
Codons are written in the 5’-3’ direction because that’s the way the DNA is structured.
Speak to the antiparallel nature of tRNA anticodon and codon on mRNA.
Every preprocessed eukaryotic protein starts with the exact same AA. That AA is what?
What is the start codon for that AA?
What are the stop codons?
Every eukaryotic protein starts with methionine Met M, codon for methionine is AUG and is considered the start codon.
The three stop codon are UGA, UAA, and UAG.
Mnemonic for remembering the stop codons.
What two AA only have one codon?
Methionine Met M
Tryptophan Trp W
What is the wobble position of a codon?
What is wobble?
Bring it all together.
The genetic code is degenerate because more than one codon can specify a single amino acid.
For the 18 amino acids that have multiple codons, the first two bases are the same. The third base is variable and is referred to as the wobble position.
Wobble is an evolutionary development designed to protect against mutations in the coding regions of our DNA.
Mutations in the wobble position tend to be called silent or degenerate, which means there is no effect on the expression of the amino acid, and therefore no adverse effects on the polypeptide sequence.
What is a point mutation?
If a mutation occurs, and it affects one of the nucleotides in a codon, it is known as a point mutation.
Point mutations can affect the primary amino acid sequence of the protein and are called expressed mutations. There are two categories of expressed mutations. What are they?
Missense mutation: mutation where one amino acid substitute for another.
Nonsense mutation: mutation were the codon now encodes for a premature stop codon (aka truncation mutation).
What is a missense mutation? Nonsense?
Missense: incorrect AA
Nonsense: premature stop codon
What is a frameshift mutation?
The three nucleotides of a codon referred to as the reading frame.
Frameshift mutation occurs when some number of nucleotides are added to or deleted from the mRNA sequence.
Caused by insertion or deletion of nucleotides.
What is cystic fibrosis?
Cystic fibrosis is caused by a frameshift mutation: a deletion at codon 508 in the polypeptide chain of the CFTR (Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene) chloride channel gate.
The loss of phenylalanine residue at this position results in defective chloride ion channels, leading to blocked passage of salt and water into and out of cells.
This causes abnormally thick sticky mucus in cells that line the passageway of the lungs and pancreas and other organs.
The sticky mucus traps bacteria in increasing the likelihood of infection in patients.
MCAT concept check the genetic code 7.1 page 256 question 1
What are the roles of the three main types of RNA?
mRNA carries information from DNA by traveling from the nucleus (where it is transcribed) to the cytoplasm (where it is translated).
tRNA translates nucleic acids to amino acids by pairing its anticodon with mRNA codons, it is charged with an amino acid which can be added to the growing peptide chain.
rRNA forms much of the structural and catalytic components of the ribosome, and act as a ribozyme to create peptide bonds between amino acids.
MCAT concept check the genetic code 7.1 page 256 question 2
Write out the sequence from 5’-3’. Then write the mRNA sequence antiparallel (3’-5’). The reverse of this will be the sequence of the mRNA, or the codon, that translates to an AA.
MCAT concept check the genetic code 7.1 page 256 question 3
MCAT concept check the genetic code 7.1 page 256 question 4
What is wobble? What role does it serve?
Wobble refers to the fact that the third base in a codon often plays no role in determining which amino acid is translated from that codon.
For example, any codon starting with CC codes for proline, regardless of which base is in the third position (the wobble position)
This is protective because of mutations in the wobble position will not have any effect on the protein translated from that gene.