Unit 5 Study Guide
DNA Structure
Nucleotides: Building blocks of DNA, composed of:
DNA Backbone: Made of alternating 5-carbon sugar (deoxyribose) and phosphate groups.
Nitrogenous Bases: Adenine (A), Thymine (T), Cytosine (C), and Guanine (G).
Complementary Base Pairing:
A pairs with T (2 hydrogen bonds)
C pairs with G (3 hydrogen bonds)
Purines vs. Pyrimidines:
Purines: Adenine (A) and Guanine (G) (double-ringed structures)
Pyrimidines: Cytosine (C) and Thymine (T) (single-ringed structures)
Phosphodiester Bonds: Covalent bonds linking nucleotides in the DNA backbone.
Hydrogen Bonds: Hold complementary bases together.
Gene: A segment of DNA that codes for a protein.
DNA Function
Double Helix: Allows for compact storage and stable transmission of genetic information.
Nitrogenous Bases: Provide the genetic code that determines protein synthesis.
Phosphodiester Bonds: Maintain the integrity of the DNA strand.
Hydrogen Bonds: Allow for easy separation during replication and transcription.
DNA vs. RNA
Feature | DNA | RNA |
---|---|---|
Location | Nucleus | Nucleus & Cytoplasm |
Function | Stores genetic info | Transmits genetic info & aids in protein synthesis |
Sugar | Deoxyribose | Ribose |
Structure | Double-stranded helix | Single-stranded |
Bases | A, T, C, G | A, U (Uracil), C, G |
Transcription
Purpose: To create an mRNA copy of a DNA sequence.
Location: Nucleus
Role of RNA Polymerase: Unzips DNA and synthesizes mRNA by pairing RNA bases with complementary DNA bases.
Transcription Example:
DNA: TAC GGC TAA
mRNA: AUG CCG AUU
Translation
Purpose: To convert mRNA into a protein.
Location: Ribosome (in the cytoplasm or rough ER)
Roles in Translation:
Ribosome: Reads mRNA and facilitates protein synthesis.
tRNA: Brings amino acids to the ribosome.
Anticodons: Found on tRNA, complementary to mRNA codons.
Amino Acids: Linked together to form proteins.
Translation Example:
mRNA: AUG CCG AUU
Amino Acid Sequence: Met - Pro - Ile
Mutations
Mutation: A change in DNA sequence.
Types of Mutations:
Substitution Mutations: One nucleotide is replaced with another.
Silent Mutation: No change in amino acid sequence.
Missense Mutation: One amino acid changes, potentially altering protein function.
Nonsense Mutation: Creates a stop codon, leading to a shortened protein.
Frameshift Mutations: Insertion or deletion of a nucleotide shifts the reading frame.
Insertion: Extra nucleotide added, altering the sequence.
Deletion: A nucleotide is removed, changing the sequence.
Impact of Mutations:
DNA Sequence: Changes base pairs.
mRNA Sequence: Alters codons transcribed from DNA.
Amino Acid Sequence: Could change protein structure and function.
Protein Structure & Folding:
No Change in Function: If mutation does not affect folding or active sites.
Change in Function: If mutation disrupts protein shape or active sites, altering biological activity.