Transcription
Process Overview: Transcription occurs in the nucleus and involves the synthesis of mRNA from a DNA template.
Steps Involved:
- Strands Separation: The DNA strands are split open to expose the genetic code.
- RNA Polymerase Function:
- Attachment: The enzyme RNA polymerase attaches to a specific region known as the promoter sequence on the DNA strand.
- Nucleotide Addition: It subsequently adds appropriate RNA nucleotides to form a complementary strand of mRNA.
- Termination: The process continues until the RNA polymerase reaches a terminator sequence, at which point it detaches from the DNA.
- Processing of mRNA:
- A 5' cap and a poly-A tail are added to the mRNA for stability and protection.
- Splicing: Introns (non-coding regions) are removed from the pre-mRNA, while exons (coding regions) are retained and spliced back together to form mature mRNA.
Codon Structure: The information in mRNA is encoded in codons, which are sequences of three bases; each codon specifies a particular amino acid.
Translation
Process Overview: Translation occurs at the ribosome, where the mRNA is decoded to build proteins.
Steps Involved:
- Attachment of mRNA: The mRNA strand attaches to a ribosome.
- tRNA Function:
- Transfer RNA (tRNA) molecules “read” the mRNA code, working from the 5' to 3' direction, and align the corresponding amino acids to form the protein.
- Each tRNA has:
- An anticodon that pairs with the mRNA codon.
- An attached amino acid, which depends on the anticodon.
- Binding Process:
- The tRNA with the anticodon that matches the first codon binds to the mRNA.
- The tRNA that matches the second codon attaches to the mRNA.
- The amino acids on both tRNAs bind together.
- The first tRNA leaves, releasing its amino acid, while the process repeats for subsequent codons.
- Start and Stop Codons: mRNA contains specific codons that signal the beginning (start codon) and the end (stop codon) of the translation process.
Mutation
Definition: A mutation is a change in the sequence of bases in DNA, which can affect protein synthesis.
Types of Mutations:
- Base Substitution (Nucleotide Substitution): This may change the amino acid sequence of a protein.
- Example: Sickle-cell anemia is a result of a base substitution mutation.
- Genetic Code Redundancy: The genetic code is described as redundant because the third base of a codon can often wobble (change) without affecting the amino acid.
- Neutral Mutation: This mutation does not impact the organism positively or negatively.
- Insertion or Deletion: This involves adding or removing bases from the DNA sequence, potentially leading to significant changes.
- Frameshift Mutation: Such mutations change all subsequent codons in the gene, which can radically alter protein function.
Mutagens: External factors that increase the rate of mutations, such as x-rays, radiation, UV light, and certain chemicals.