DNA Structure, Replication, and Chromosomes
DNA Structure
DNA has a ladder-like spiral structure called a double helix.
During the cell cycle:
Interphase: DNA is in chromatin form.
Mitosis: DNA is in chromosome form.
A DNA molecule comprises millions of subunits called nucleotides.
Nucleotides
Each nucleotide consists of:
Phosphate group
Pentose sugar
Nitrogenous base
Structure of a Nucleotide
Pentose Sugar
A 5-carbon sugar.
In DNA, the sugar is deoxyribose.
In RNA, the sugar is ribose.
Pentose Sugar Details
Carbons are numbered 1 through 5.
RNA (Ribose) vs. DNA (Deoxyribose):
The difference lies in the hydroxyl group on the #2 carbon.
Nucleotide: Phosphate Group
Phosphate Group
Links two sugars together.
Primary Structure of DNA
The sugar-phosphate backbone of a DNA strand.
Phosphodiester bonds link deoxyribonucleotides.
Nitrogen-containing bases project from the backbone.
Strand has a 5' end and a 3' end.
Phosphodiester Bonds
Join two sugars via the phosphate group.
Formation of Phosphodiester Bond
Chemical bonds form, releasing H2O.
Structure of a Nucleotide: Nitrogenous Base
Nitrogenous Base
In DNA, the four bases are: Thymine, Adenine, Cytosine, Guanine.
In RNA, the four bases are: Uracil, Adenine, Cytosine, Guanine.
DNA Strand
A strand of nucleotides is joined by covalent bonds (very strong).
The sequence of bases makes up the genetic code.
Bases are read in triplets.
These triplets send instructions to switch genes on and off, to make proteins and enzymes.
The 4 Nucleotides
Purines: Adenine (A) and Guanine (G)
Pyrimidines: Cytosine (C), Thymine (T), and Uracil (U; in RNA)
The 4 Nucleotides (Simplified)
Adenine (A)
Thymine (T)
Cytosine (C)
Guanine (G)
Nitrogenous Base Pairing
Each base bonds with one other specific base, called complementary base pairs.
Adenine (A) pairs with Thymine (T) - 2 hydrogen bonds.
Cytosine (C) pairs with Guanine (G) - 3 hydrogen bonds.
In RNA, Uracil (U) binds to Adenine (A).
Nitrogenous Base Pairing (Hydrogen Bonding)
Due to complementary base pairing, the order of bases in one strand determines the order of bases in the other strand.
Mutations
Mutation (genetic mutation) is a change in the nucleotide sequence of DNA.
Example of normal vs. mutated DNA sequence.
Nature of Genetic Material
Property 1: Contains, in a stable form, information encoding the organism’s structure, function, development, and reproduction.
Property 2: Replicates accurately so progeny cells have the same genetic makeup.
Property 3: Capable of some variation (mutation) to permit evolution.
DNA Replication
Two DNA molecules are made from one DNA molecule.
Each new DNA molecule (double helix) has one strand from the original molecule and one new strand.
DNA Replication Outcome
Parent DNA molecule and two daughter molecules are identical.
DNA Replication - Base Pairing
Adenine binds with Thymine.
Cytosine binds with Guanine.
Knowing the order of one strand allows you to know the order of the other.
DNA Replication Process
Step 1: Enzyme (helicase) breaks the hydrogen bonds between nitrogenous bases, causing the DNA helix to unzip or unwind.
Step 2: As DNA unzips, DNA polymerase moves along the single strands and helps each free nucleotide bind to a new corresponding base.
Step 3: A new strand is formed by pairing complementary bases with the old strand (A-T, C-G).
The process continues until the original molecule has been entirely unzipped and replicated, producing two new DNA molecules.
One strand acts as a template to make a new strand.
The process is semiconservative because each daughter strand is paired with a parent (original) strand (one old and one new).
Inheritance
Passing on genetic information from parents to offspring.
Chromosomes
Each chromosome contains many genes.
Gene Definition
A segment of a chromosome that contains the code for a single protein (enzyme).
The enzyme causes a chemical reaction that allows a trait to be expressed (hair/eye color, etc.).
Alleles
Alleles are alternate/different forms of a gene.
Homozygous individuals have two identical alleles for a trait.
Heterozygous individuals have two different alleles for a trait.
Chromosome Count
The number of chromosomes varies from species to species.
The number of chromosomes does not correlate with the complexity of organisms.
Human somatic cells have 46 chromosomes (organized into 23 pairs).
Each pair consists of one chromosome from the father and one from the mother.
Sex Chromosomes & Autosomes
Sex Chromosomes: 1 pair out of 23 (X and Y), determine individual’s sex (Female XX, male XY).
Autosomes/Somatic Chromosomes: 22 pairs out of 23; all chromosomes but sex chromosomes, paired based on similar characteristics.
Sex Chromosomes & Autosomes (Visual)
Illustration of autosomes and sex chromosomes.
Homologous Chromosomes
Pairs of chromosomes that are similar but NOT identical based on:
Length
Centromere location
Banding patterns (when dyed)
Carry genes for the same trait at the same location.
Homologous Chromosomes (cont.)
They are not identical because they carry different forms of the same gene (different DNA pattern/alleles).
Genes are sections of DNA that contain genetic information for specific traits (e.g., hair/eye color).
Karyotype
A photograph of a particular set of chromosomes for an individual.
Prepared by taking a sample cell in metaphase, staining the chromosomes to reveal banding patterns, then sorting and pairing them.