Definition: Process by which the DNA sequence of a gene is transcribed to produce a complementary RNA strand (mRNA).
Steps of Transcription:
Strand Separation: DNA strands are split open to expose the coding sequence.
RNA Polymerase Enzyme:
Role: Binds to the promoter sequence on the DNA strand.
Function: Assembles complementary RNA nucleotides to form mRNA.
Completion: Continues until it reaches a terminator sequence, upon which it detaches from the DNA.
Processing of mRNA:
Addition of Cap and Tail: A 5’ cap and a poly-A tail are added to the mRNA for protection and recognition.
Splicing:
Introns (non-coding regions) are removed.
Exons (coding regions) are joined together to produce the final, mature mRNA.
Codons:
Definition: Sequences of three RNA bases.
Function: Each codon specifies a particular amino acid to be incorporated into a protein.
Definition: The process of converting the sequence of the mRNA into a sequence of amino acids to form a protein.
Steps of Translation:
mRNA Attachment: mRNA attaches to a ribosome, which serves as the site for translation.
tRNA Function:
Reading mRNA: tRNA reads the mRNA code from 5’ to 3' and aligns the appropriate amino acids.
Anticodons: Each tRNA molecule has an anticodon that pairs with the corresponding mRNA codon.
Each tRNA carries a specific amino acid determined by its anticodon.
Amino Acid Binding Sequence:
The tRNA with the matching anticodon binds to the mRNA codon.
The tRNA for the second codon binds as well, and the amino acids on the two tRNAs link together.
The first tRNA leaves, leaving its amino acid behind.
This process is repeated until all codons are translated.
Termination: mRNA contains specific codons that signal the start and stop of translation.
Start Codon: Indicates where translation begins.
Stop Codon: Indicates where translation ends.
Definition: A change in the sequence of bases in DNA, which can lead to changes in the structure and function of proteins.
Types of Mutations:
Base Substitution (Nucleotide Substitution):
Can alter the amino acid sequence of the resulting protein.
Example: Sickle-cell anemia, caused by a single base substitution.
Redundancy in Genetic Code:
The genetic code is said to be redundant, meaning multiple codons can specify the same amino acid, allowing for some variations without effect.
3rd Base Wobble: Refers to the flexibility of the third base in a codon, which can vary without changing the amino acid.
Neutral Mutation:
A mutation that neither benefits nor harms the organism.
Insertion or Deletion:
Involves adding or removing bases from the DNA sequence, potentially leading to frameshift mutations.
Frameshift Mutation: Alters the reading frame of the gene, affecting all subsequent codons.
Mutagens: Agents that increase mutation rates, such as x-rays, radiation, UV light, and certain chemical substances.