Overview: The Hershey and Chase experiment was fundamental in demonstrating that DNA is the genetic material.
Conducted by Martha Chase and Alfred Hershey in 1952.
Focused on bacteriophages (viruses that infect bacteria).
Virus Mechanism: A virus attaches to bacteria, injecting its genetic material.
The bacteria then replicate the viral DNA.
This process results in the production of new viruses, which cause the bacterial cell to burst (lyse).
Isotopes for Labeling: The experiment utilized radioactive isotopes to track DNA and proteins.
Phosphorus-32 (32P) was used to label DNA (phosphate groups in DNA).
Sulfur-35 (35S) was used to label proteins (specifically in amino acids).
Two groups of bacteriophages were produced:
Phages with radioactive DNA (32P).
Phages with radioactive protein coat (35S).
Bacteria were infected with these phages.
Centrifuging: After infection, the mixture was blended to separate the viral coats from the bacteria, then centrifuged.
Results showed that the bacteria contained phosphorus (32P), indicating that DNA entered the bacteria during infection.
Conversely, the protein coat, labeled with sulfur, remained outside the bacteria.
Conclusion: This experiment provided solid evidence that DNA, and not protein, serves as the genetic material in viruses.
DNA: Double-stranded helix structure, contains deoxyribose sugar, bases include adenine (A), thymine (T), cytosine (C), and guanine (G).
RNA: Single-stranded molecule, contains ribose sugar, bases are adenine (A), uracil (U), cytosine (C), and guanine (G).
Watson and Crick Findings: Each nucleotide base pairs specifically:
Adenine (A) pairs with Thymine (T) (DNA) or Uracil (U) (RNA).
Cytosine (C) pairs with Guanine (G).
A-T pairs form two hydrogen bonds.
C-G pairs form three hydrogen bonds, contributing to the stability of DNA.
Mechanism of Replication:
Double Helix Unwinding: The DNA strands separate under the action of enzymes (like helicase).
Template Strands: Each original strand serves as a template for a new complementary strand, enhancing accuracy.
Helicase: Unwinds DNA strands at the replication fork.
DNA Polymerase: Synthesizes new strands by adding nucleotides complementary to the templates in a 5' to 3' direction.
Ligase: Joins Okazaki fragments on the lagging strand.
Definition: Genetic information flows from DNA to RNA to Protein.
Transcription: DNA is transcribed into messenger RNA (mRNA) in the nucleus.
Translation: mRNA is translated into proteins in the cytoplasm at ribosomes.
Occurs in the nucleus of eukaryotic cells.
Reactants: DNA is the template; product is mRNA.
Processing: Involves splicing, adding a 5' cap, and a poly-A tail.
Occurs in the cytoplasm at ribosomes.
Reactants: mRNA, tRNA, and ribosomes.
Products: Polypeptide chains (proteins) are formed from amino acids brought by tRNA.
Point Mutation: A single nucleotide change that can lead to silent, missense, or nonsense mutations.
Silent Mutation: No change in protein function.
Missense Mutation: Alters one amino acid in a protein, potentially affecting functionality.
Nonsense Mutation: Creates a premature stop codon, leading to truncated proteins.
Frame Mutation: Involves shifts in the reading frame, altering downstream amino acid sequence.
Definition: Modifications of DNA and histones that can affect gene expression without altering the DNA sequence.
Key Modifications:
Methylation: Addition of methyl groups, typically represses gene expression.
Acetylation: Addition of acetyl groups, usually enhances gene expression by loosening DNA around histones, making it more accessible for transcription.
The combination of knowledge from the Hershey-Chase experiment and understanding the molecular mechanisms of DNA, RNA, and mutations provides essential insights into genetics and cellular biology.