Unit 3: DNA & Genetic Technologies Notes
Unit 3: DNA & Genetic Technologies
Organelles in Cells
Animal Cell
Plant Cell
Organelles to identify:
Smooth ER
Golgi Body
Cell membrane
Rough ER
Nucleus
Ribosome
Lysosome
Vacuole
Mitochondrion
Cytoplasm
Chloroplast
Cell Wall
Introduction to DNA
DNA is the blueprint for a living thing, containing the genetic information in cells.
Nearly every cell in an organism has the same genetic information.
In animal and plant cells, DNA is stored in the nucleus.
DNA (deoxyribonucleic acid) determines organ and part development, assembly order, and how they work together.
Key Terms
Cell: Smallest unit of living things.
Nucleus: Control center of the cell.
DNA: Deoxyribonucleic acid, encoding genetic information, composed of nucleotides linked in a chain.
Chromosome: Thread-like structures where DNA is tightly packaged.
Gene: Segment of DNA molecule with coded instructions, determining an organism's characteristics.
Allele: Alternative forms of a gene arising by mutation, found at the same place on a chromosome.
DNA Structure
DNA stands for deoxyribonucleic acid, a chemical substance in the nucleus of all living cells.
DNA controls all chemical changes in a cell.
DNA determines the type of cell produced (muscle, blood, bone, etc.).
DNA determines the type of organism produced (buttercup, giraffe, penguin, human, etc.).
Genome
Genetic information is carried by DNA, a polymer of nucleotides in a double helix.
DNA is found within chromosomes.
A gene is a DNA section that carries coding for a protein, containing instructions for an organism's characteristic.
Structure of DNA
DNA is a long-chain molecule made of repeating sub-units (monomers) called nucleotides.
DNA usually has two strands twisted into a double helix.
Each nucleotide includes:
A phosphate group
A deoxyribose sugar
An organic base
Deoxyribose vs Ribose Sugars
Ribose is a five-carbon sugar.
Deoxyribose is similar but has one less oxygen atom.
Nitrogenous Bases
Four different nitrogenous bases in DNA:
Adenine (A)
Cytosine (C)
Guanine (G)
Thymine (T)
DNA: A Polynucleotide
DNA is a polymer of mononucleotides.
Mononucleotides join between the sugar of one nucleotide and the phosphate group of the next.
The sugar and phosphate units make up the “backbone” of the nucleic acid.
A base is attached to each sugar molecule.
DNA Base Pairing
DNA usually has a double strand of nucleotides pairing up to form a “ladder”, then twisted into a double helix.
Sugar-phosphate “backbones” are on the outside, held by hydrogen bonds between bases.
Hydrogen bonds are weak individually but strong collectively.
Bases always pair up:
Adenine (A) with Thymine (T)
Cytosine (C) with Guanine (G)
The Genetic Code
DNA bases make up the genetic code.
The Human Genome Project found approximately 3.3 billion base pairs in our genome.
Human genes vary in size from a few hundred bases to more than 2 million.
Chemical cross-links between DNA strands are formed by base pairs (A-T & C-G), known as complementary base pairing.
The sequence of base pairs in a gene provides the code for the cell to build a protein.
DNA Adaptation to Function
DNA is heredity material for passing genetic information from cell to cell.
The structure of DNA has advantages:
It is stable.
Two strands can separate for self-replication.
It is a large molecule that carries lots of information.
Base pairing prevents corruption from outside chemicals or physical forces.
Summary of Key Points
A person’s genome consists of a complete set of genes.
DNA contains the genetic code that controls protein production in living things.
DNA is a polymer consisting of millions of nucleotides.
A nucleotide consists of sugar, phosphate, and a nitrogenous base.
The four bases pair complimentary (A-T and C-G).
The order of nitrogenous bases (AGCT) creates variation.
Watson and Crick DNA Model
Sugar-phosphate backbone.
Base pairs (Cytosine, Guanine, Adenine, Thymine).
Hydrogen bonds.
DNA Structure Activity
Cut & Paste activity to learn about DNA Structure.
Key includes Adenine, Cytosine, Thymine, Guanine, Phosphate, Deoxyribose.
The Double Helix
Sugar-phosphate chain.
A and T are complimentary base pairs.
C and G are complimentary base pairs.
History of DNA Structure
Rosalind Franklin
British chemist.
Showed phosphates must lie on the outside of the molecule in the early 1950s.
Obtained images of DNA using x-ray crystallography, including photo 51.
Independently concluded that DNA must have a double helical structure.
Her manuscript was published in the same edition of Nature as Watson & Crick’s.
Died in 1958 from cancer; her contribution was acknowledged much later.
Maurice Wilkins
New Zealand-born physicist.
Introduced the idea to study DNA with x-ray crystallography.
Franklin’s colleague; relationship was poor.
Wilkins shared photo 51 with Watson & Crick, without Franklin’s knowledge or consent.
Awarded Nobel Prize, along with Watson & Crick, for his work on DNA in 1962.
James Watson & Francis Crick
American zoologist (Watson) and British physicist (Crick).
Put together several models of DNA, attempting to incorporate all available evidence.
Used Franklin’s data (without her knowledge/consent) to arrive at the correct structure.
Awarded Nobel Prize, along with Wilkins, for their work on DNA in 1962.
The Genetic Code – Brief History
In the mid-1800s, Gregor Mendel proved that traits were passed on from parent to child.
Our understanding of cell biology and genetics increased through the early 1900s, leading to the discovery of DNA structure in 1952.
Scientists were unsure how genes encoded in DNA become the proteins that give us our phenotype (observable trait).
Protein Synthesis: Transcription & Translation
The processes where the genes encoded in DNA become the proteins.
Proteins
Proteins are large, complex molecules made up of one or more polypeptides.
Polypeptides are long chain molecules made up of amino acids.
Each protein has a specific function, such as enzymes, structural components of cells, hormones, etc.
Messenger RNA (mRNA)
DNA contains genes that work as instructions for protein synthesis.
DNA cannot leave the nucleus; ribosomes responsible for protein synthesis are outside the nucleus.
Messenger RNA (mRNA) is created as a copy of the genetic code that can leave the nucleus; it is a single-strand nucleic acid.
mRNA is made from the DNA template during transcription.
The role of mRNA is to carry information from the DNA to the ribosomes, which will translate the genetic code to synthesize appropriate proteins.
DNA vs RNA
DNA is double-stranded, while RNA is usually single-stranded.
The “backbone” of DNA is made of deoxyribose sugars and phosphate groups, RNA is made of ribose sugars and phosphate groups.
Both contain four possible nucleobases; thymine (T) is only in DNA, uracil (U) is only in RNA.
Adenine (A) can pair with both thymine (T) & uracil (U). Uracil (U) replaces thymine (T) in RNA.
Key Terms
Amino Acid: A small molecule that joins with others to form proteins. Amino acids are the building blocks of proteins, which are the building blocks of cells.
Polypeptide: A continuous, unbranched chain of amino acids joined by peptide bonds. Proteins are made up of one or more polypeptides.
Protein: A large molecule made up of amino acids. Proteins form structures and perform functions in an organism. DNA contains instructions for building proteins.
RNA: Ribonucleic acid. A nucleic acid with similar structure to DNA, however, unlike DNA RNA is single stranded. An RNA molecule has a backbone made of alternating phosphate groups and the sugar ribose, rather than the deoxyribose found in DNA.
mRNA: Messenger RNA. A type of RNA molecule created from the DNA template during transcription. mRNA acts as a copy of the genetic code that can leave the nucleus and provides instructions to the ribosomes during translation.
Protein Synthesis – Overall Process
Since the DNA instructions must remain in the nucleus, an intermediate molecule, messenger RNA (mRNA), is created, carrying a transcribed copy of relevant instructions from the nucleus to ribosomes in the cytoplasm.
Ribosomes translate the message carried by mRNA into a cell product such as protein.
Transcription
Transcription is the first step in synthesising a protein from the information contained in a gene. It involves copying the gene’s DNA sequence to make an RNA molecule known as messenger RNA (mRNA).
This process occurs in the nucleus of the cell.
Transcription is performed by enzymes called RNA polymerases, which link nucleotides to form an RNA strand (using a DNA strand as a template).
Phase 1: Initiation
RNA polymerase binds to a sequence of DNA called the promoter, found near the beginning of a gene.
Each gene has its own promoter.
Once bound, RNA polymerase separates the DNA strands, providing the single-stranded template needed for transcription.
Phase 2: Elongation
One strand of DNA acts as a template for RNA polymerase.
As it