dna & protein synthesis honors biology. history before the 1940’s scientists didn’t know...
TRANSCRIPT
History
• Before the 1940’s scientists didn’t know what material caused inheritance.
• They suspected it was either DNA or proteins.
History
• A series of experiments proved that DNA was the genetic material responsible for inheritance.
Frederick Griffith
• Injected mice with different types of pneumonia bacteria
• Results showed some type of factor was transferred from killed cells to live cells
• Griffith called this transformation
Oswald Avery
• Repeated Griffith’s idea to find how transformation happens
• Result _ DNA was the factor responsible for transformation
History
• In 1952, Alfred Hershey and Martha Chase did an experiment using a virus that infects E. coli bacteria.
• The experiment proved that DNA and not protein is the factor that influences inheritance.
History
• Erwin Chargaff discovered the base pairing rules and ratios for different species.
• Adenine pairs with Thymine
• Cytosine pairs with Guanine.
History• Rosalind Franklin & Maurice Wilkins had
taken the 1st pictures of DNA using X-ray crystallization
History• The Nobel Prize in Medicine 1962
Francis Harry Compton Crick
James Dewey Watson
Maurice Hugh Frederick Wilkins
Rosalind Franklin(Died of cancer 1958)
Wilkins has become a historical footnote and
Watson & Crick are remembered as the
Fathers of DNA
Watson Crick
DNADNA
OO=P-O O
PhosphatePhosphate GroupGroup
N
Nitrogenous baseNitrogenous base (A, T(A, T,, G, C)G, C)CH2
O
C1C4
C3 C2
5
SugarSugar(deoxyribose)(deoxyribose)
Nitrogen Bases
• 2 types of Nitrogen Bases– Purines
• Double ring–G & A
– Pyrimidines• Single ring
–C & U & T
PGA
CUT PY
DNA - double helixDNA - double helix
P
P
P
O
O
O
1
23
4
5
5
3
3
5
P
P
PO
O
O
1
2 3
4
5
5
3
5
3
G C
T A
T A
DNA• DNA is a double-
stranded molecule.
• The strands are connected by complementary nucleotide pairs (A-T & C-G) like rungs on a ladder.
• The ladder twists to form a double helix.
DNA
• During S stage in interphase, DNA replicates itself.
• DNA replication is a semi-conservative process.
DNA• Semi-conservative
means that you conserve part of the original structure in the new one.
• You end up with 2 identical strands of DNA.
DNA Replication
Step 1: Helicase unzips a molecule of DNA @ the hydrogen bonds between base pairs (breaking the H bonds).
Step 2: DNA polymerase joins individual nucleotides to produce a DNA molecule which is a polymer and it also “proofreads” each new DNA strand
Step 3: Ligase links the two sections together.
DNA
• Gene - a segment of DNA that codes for a protein, which in turn codes for a trait (skin tone, eye color, etc.)
• A gene is a stretch of DNA.
DNA
• A mistake in DNA replication is called a mutation.
• Many enzymes are involved in finding and repairing mistakes.
RNARNA
OO=P-O O
PhosphatePhosphate GroupGroup
N
Nitrogenous baseNitrogenous base (A, (A, UU ,, G, C )G, C )CH2
O
C1C4
C3 C2
5
SugarSugar (ribose)(ribose)
3 differences from DNA
1. Single strand instead of double strand
2. Ribose instead of deoxyribose
3. Uracil instead of thymine
3 types of RNA
1. Messenger RNA (mRNA)- copies information from DNA for protein synthesis
Codon- 3 base pairs that
code for a single amino
acid. codon
3 types of RNA
2. Transfer RNA (tRNA)- collects amino acids for protein synthesis
Anticodon-a sequence of 3 bases that are complementary base pairs to a codon in the mRNA
Amino Acids
• Amino acids- the building blocks of protein
• At least one kind of tRNA is present for each of the 20 amino acids used in protein synthesis.
Transcription - mRNA is made from DNA & goes to the ribosomeTranslation - Proteins are made from the message on the mRNA
Transcription
• In order for cells to make proteins, the DNA code must be transcribed (copied) to mRNA.
• The mRNA carries the code from the nucleus to the ribosomes.
Transcription
• RNA polymerase binds to DNA (only to promoters- sections that indicate it to bind on DNA molecule) & separates the DNA strands.
• Uses 1 strand as a template from which nucleotides are assembled into a strand of RNA.
• Signals (like promoters) tell it to stop when RNA is complete.
Translation
• At the ribosome, amino acids (AA) are linked together to form specific proteins.
• The amino acid sequence is directed by the mRNA molecule.
ribosome
Amino acids
Translation
• Begins when mRNA molecule in cytoplasm attaches to ribosome.
• It begins at AUG (the start codon) which always binds methionine (amino acid).
• The tRNA contains the anticodon whose bases are complementary to a codon on the mRNA strand.
• Then another tRNA comes into ribosome and binds the next codon to anticodon.
Translation
• The ribosome will then bind the two amino acids together, using peptide bonds, and breaks the bond between methionine and its tRNA.
• The tRNA floats away from the ribosome allowing ribosome to bind another tRNA.
• The ribosome will move along mRNA binding new tRNA molecules and amino acids.
Translation
• Process continues until ribosome reaches one of the three stop codons:– UAA– UAG– UGA
Then it releases the formed polypeptide and the mRNA molecule, completing translation.
Make mRNA
• tRNA sequence
AUG UAC AAC AAG GUA AUU
• mRNA sequence
UAC AUG UUG UUC CAU UAA• Amino Acid sequence
met lys asp lys val stop
Mutations
• What causes mutations?– Can occur spontaneously– Can be caused by a mutagen
• Mutagen: An agent, such as a chemical, ultraviolet light, or a radioactive element, that can induce or increase the frequency of mutation in an organism.
Mutations
• Some mutations can:
• Have little to no effect
• Be beneficial (produce organisms that are
better suited to their environments)
• Be deleterious (harmful)
Mutations• Types of mutations
– Point Mutations : involves changes in one or a few nucleotides that occur at a single point in the DNA sequence.• Substitutions- one base changed to
another• Insertions- one base is inserted in the
DNA sequence• Deletions- one base is removed from
the DNA sequence
Sickle Cell Mutation
• Mutation in the haemoglobin gene – Oxygen carrying protein found on red blood
cells.
Life expectancy is 50- 60 years old!
Mutations• Types of mutations
– Frame Shift Mutations: changes the “reading frame” of the genetic message, so that every codon beyond the point of insertion or deletion is read incorrectly during translation.
• Ex.: Crohn’s disease
Crohn’s Disease
• Bacterial products activate inflammation in digestive system causing– Diarrhea– Constipation– Cramps
• Mutation in a gene that produces kininogen protein.
• Mutation on Chromosome 16 too!
Huntington’s disease
• A progressive brain disorder that causes uncontrolled movements, emotional problems, and loss of thinking ability.
• Mutations in HTT gene causes disease.
• HTT-produces huntingtin protein. – CAG trinucleotide repeat
Mutations• Types of mutations
– Chromosomal Inversions: an entire section of DNA is reversed.
– Ex.: Hemophilia
a bleeding disorder
DNA Repair
• A complex system of enzymes, active in the G2 stage of interphase, serves as a back up to repair damaged DNA before it is dispersed into new cells during mitosis.
Mutations
• Many (most) are neutral and have little or no effect.
• Polyploidy- a complete set of chromosomes fails to separate during meiosis, can produce gametes with:– 3N (Triploid)– 4N (Tetraploid)
Ex. Polyploid plants are larger and stronger than diplid plants.
Gene Regulation
• Only a fraction of the genes in a cell are expressed at a given time.
• Expressed gene- a gene that is transcribed into RNA.
How does cell decided which will be “expressed” and which will be “silent”?
Gene Regulation
• Certain DNA sequences serve as promoters for DNA-binding proteins to attach and they help to regulate gene expression.
• There are “regulatory sites” next to the promoter in which the action of these proteins determines whether a gene is turned on or turned off.
Gene Regulation
• Most Eukaryotic genes are controlled individually and have regulatory sequences
• Why is Gene Regulation Important?
Gene Regulation
• Regulation of gene expression is important in shaping the way a complex organism develops.
• Differentiation- cells don’t just grow and divide during embryonic development they become specialized in structure and function.
Gene Regulation
• Hox genes- a series of genes that control the differentiation of cells and tissues in the embryo. – A mutation in one of these “master control
genes” can completely change the organs that develop in specific parts of the body.
– Ex. Fruit fly mutation can replace fly’s antennae with legs growing on its head!
Human Genome Project
• The Human Genome Project is a
collaborative effort of scientists around the
world to map the entire gene sequence of
humans.
• This information will be useful in detection,
prevention, and treatment of many genetic
diseases.
DNA Technologies
• DNA technologies allow scientists to identify, study, and modify genes.
• Forensic identification is an example of the application of DNA technology.
Gene Therapy• Gene therapy is a technique for correcting
defective genes responsible for disease development.
• Possible cures for:– diabetes– cardiovascular disease– cystic fibrosis– Alzheimer's– Parkinson’s– and many other diseases is possible.
Genetic Engineering
• The human manipulation of the genetic
material of a cell.
• Recombinant DNA- Genetically
engineered DNA prepared by splicing
genes from one species into the cells of
a different species. Such DNA becomes
part of the host's genetic makeup and is
replicated.
Genetic Engineering • Genetic engineering techniques are used in
a variety of industries, in agriculture, in
basic research, and in medicine.
This genetically engineered cow resists infections of the udders and can help to increase dairy production.
Genetic Engineering • There is great potential for the development
of useful products through genetic
engineering• EX., human growth hormone, insulin, and pest-
and disease-resistant fruits and vegetables
Seedless watermelons are genetically engineered