Title: DNA
1DNA GenesChapter 12
- DNA, RNA, Protein Synthesis
2DNA Molecule of HeredityA. Structure
- DNA (polymer) is a long molecule made up of
Nucleotides (monomers) - A Nucleotide consists of
- Deoxyribose (a 5-carbon sugar)
- a phosphate group
- One of 4 Nitrogenous bases (contain nitrogen)
- Adenine (A)
- Guanine (G)
- Cytosine (C)
- Thymine (T)
PURINES
PYRIMIDINES
- The nitrogenous bases of DNA (purines double
ring / pyrimidines single ring)
3DNA
- Deoxyribonucleic acid
- Deoxyribose is sugar
- Nitrogenous bases
- Adenine binds with Thymine
- Cytosine binds with Guanine
One nucleotide of DNA
4Structure of DNA (cont.)
- DNA is like a twisted ladder
- Rungs complementary base pairs (AT, GC)
- Uprights deoxyribose and phosphate groups
- Your Turn Match this DNA base sequence with its
correct complementary DNA bases - T-C-G-A-A-C-T
- A-G-C-T-T-G-A
5DNA.who cares
Is used to catch criminals
Is used to determine the paternity of Children
on shows such as
Is used to make genetically modified food
Is used to compare similarities between species
Is used to make antibiotics and vaccines
6History Griffith and Transformation
- Year 1928
- Examined 2 strains of pneumonia bacteria
- Rough
- Smooth
- Injected mice with bacteria to see if they would
develop pneumonia - Discovered transformation
- Took the heat killed bacteria and combined it
with the harmless bacteria, and mice developed
pneumonia
7History Avery DNA
- 1944
- Used Griffiths experiment. He wanted to know
which molecule in the heat-killed bacteria was
important in transformation - Avery used enzymes to discover that DNA was the
molecule that allowed transformation to happen
8History Hershey-Chase
- 1952
- The Hershey-Chase experiment used viruses known
as bacteriophages. - Question Wanted to know which part of the virus,
protein or DNA, entered the infected core of
bacterium. Preformed the experiment by using
radioactive markers - Concluded, that the genetic material was DNA
9B. History
Source of DNA A T G C
Streptococcus 29.8 31.6 20.5 18.0
Yeast 31.3 32.9 18.7 17.1
Herring 27.8 27.5 22.2 22.6
Human 30.9 29.4 19.9 19.8
- . CHARGAFF (1949) discovered that the of
Cytosine and Guanine were about the same in DNA
the same was true about Adenine and Thymine - This suggests BASE PAIRING.. that C bonds with
G and A bonds with T!
Purines
Pyrimidines
Phosphate group
Deoxyribose
10History (cont.)
- 2. Wilkins and Franklin(1952) took X-Ray
photographs of DNA which suggested a twisted,
helical structure, 2 strands, and bases in the
center - 3. Watson and Crick (1953) using all the
research to date, discovered the structure for
DNA A DOUBLE HELIX (with sugar-phosphate
backbones and bases on the inside held together
by H bonds)
11More DNA info
- DNA contains information that determines an
organisms function and appearance - Some DNA codes for proteins
- DNA is located within genes (sections of a
chromosome) inside of the nucleus of every cell
12Wait a minute
Does that shape remind you of any other shape you
may have seen before?
How about this portion of an apple?
13DNA Flo Rider Featuring T-Pain-less
Shawty got them apple bottom genes with the DNA
(NA)
Nucleotides twisted that way
They start to fold (they start to fold)
Next thing you know
Shawty got chro mo so o o o o omes
The As bond with the Ts and the Cs bond with
the Gs (with the Gs)
Hydrogen bonds in the double helix
They start to fold (they start to fold)
Next thing you know
Shawty got chro mo so o o o o omes
14DNA Replication
- DNA opens up and makes a complete copy of itself
necessary during mitosis and meiosis - New nucleotides float in and pair in a
complementary fashion A to T, C to G and vice
versa
15Figure 16.7 A model for DNA replication the
basic concept (Layer 1)
16Figure 16.7 A model for DNA replication the
basic concept (Layer 2)
17Figure 16.7 A model for DNA replication the
basic concept (Layer 3)
18Figure 16.7 A model for DNA replication the
basic concept (Layer 4)
Semi-conservative process
19C. DNA Replication making more DNA during the
S Phase of the Cell Cycle (in the nucleus)
- 1. The enzyme helicase unwinds DNA double helix
(breaks hydrogen bonds btwn. bases) a
replication fork is created. - (Each old DNA strand will act as a template for
2 new strands to be added on) - 2. Enzyme called DNA Polymerase binds to
replication fork and adds free nucleotides to
each old strand of DNA - 3. DNA Polymerase remains attached until 2 new
DNA strands are created it proofreads the
strands to minimize error in the process.
20Chromosome Structure
Nucleosome
Chromosome
DNA double helix
Coils
Supercoils
Histones
DNA Animation
Go to Section
21DNA Replication (cont.)
- Diagram of DNA Replication
22DNA ? ProteinA. RNA
- RNA Ribonucleic Acid used to make proteins /
Single-stranded - -RNA (polymer) made of nucleotides
(monomer) - -Ribose 5 C sugar Phosphate group N
Base - 4 bases
- Cytosine (C)
- Guanine (G)
- Adenine (A)
- Uracil (U) NO THYMINE in RNA!
- 3 types of RNA
- 1. messenger RNA (mRNA) single stranded
- transmits info from DNA to protein syn.
- 2. transfer RNA (tRNA) - single stranded/
- 20 or more varieties ea. w/ ability to bond to
only - 1 specific AA
- 3. ribosomal RNA (rRNA) globular / major
- component of ribosome
23B. Protein Synthesis (overview)
- 2 Stages in making proteins
- Transcription using DNA template to make mRNA
strand - Translation using mRNA strand to create
polypeptides
DNA
RNA
Protein
Transcription
Translation
241. Transcription
- The Goal of Transcription is to produce a
single-stranded mRNA helix that contains
information from DNA to make proteins - How its done (This happens in the Nucleus!)
- 1. DNA strand unwinds/unzips complementary DNA
strands - 2. Enzyme called RNA Polymerase binds to DNA
promoter regions and plugs in complementary
RNA nucleotides to the DNA template. - Example DNA Template ATTGGCAGT
- new RNA Strand UAACCGUCA
25Transcription (cont.)
26Transcription (cont.)
- 3. Once produced, this pre-mRNA strand breaks
away when RNA polymerase reaches a sequence of
bases on DNA that act as a stop sign. - The finished product (mRNA) moves out of the
Nucleus through a nuclear pore into the
cytoplasm. - 4. 2 DNA complementary strands rejoin
272. The Genetic Code
- How do we get proteins from mRNA strands?
- The mRNA strand must be read in groups of 3
nucleotides, called a CODON. - Different Codons translate for different Amino
acids.
28Codons in mRNA
29Codons in mRNA
- Start codon AUG (Methionine)
- Stop codons UAA, UAG, and UGA
- Example
- mRNA Strand
- U-C-A-U-G-G-G-C-A-C-A-U-G-C-U-U-U-U-G-A-G
-
- methionine glycine threonine cysteine
phenylalanine STOP
303. Translation
- The Goal of Translation is to translate these
mRNA codons into their amino acids to form a
polypeptide. - How its done
- 1. mRNA strand attaches to a ribosome (rRNA)
- 2. Each mRNA codon passes through ribosome
- 3. Free-floating Amino Acids from cytosol are
brought to ribosome by tRNA - 4. Each tRNA has an anticodon to match up to mRNA
codons - 5. Amino Acids are joined as tRNA keeps bringing
them - 6. Polypeptide chain grows until stop codon is
reached
31Translation (cont.)
1st. mRNA strand attaches to a ribosome (rRNA)
32Translation (cont.)
2nd, Each mRNA codon passes through ribosome
33Translation (cont.)
3rd, Free-floating Amino Acids from cytosol are
brought to ribosome by tRNA
34Translation (cont.)
4th, Each tRNA has an anticodon to match up to
mRNA codons
35Translation (cont.)
5th, Amino Acids are joined as tRNA keeps
bringing them
36Translation (cont.)
. Polypeptide chain grows until stop codon is
reached
37Genetic Changes MutationsA. Types of
Mutations
- 1. Gene Mutations changes in nucleotides
- Point Mutations
- Frameshift mutations
- 2. Chromosome Mutations changes in or
structure of chromosome - Deletion
- Insertion/Duplication
- Inversion
- Translocation
381. Gene Mutations
- a. Point Mutation the substitution, addition or
removal of a single nucleotide - b. Frameshift Mutations types of point
mutations that shift the reading frame of the
genetic message
39Example of Point Mutation
Induced Point mutation in growth hormone gene
causes semi-dominant dwarfism obesity
image borrowed from www.science.ngfn.de/6_164.htm
40B. Chromosome Mutations
- 1. Deletion
- 2. Insertion/Duplication
- 3. Inversion
- 4. Translocation.
41- A chromosomal mutation involves changes in the
number or structure of chromosomes. Chromosomal
mutations may change the locations of genes on
chromosomes and even the number of copies of some
genes. - Deletion involves the loss of all or part of a
chromosome. - The opposite of a deletion is a
- Duplication, in which a segment of a chromosome
is repeated. - When part of a chromosome becomes oriented in the
reverse of its usual direction, the result is an
Inversion. - A Translocation occurs when part of one
chromosome breaks off and attaches to another,
non-homologous, chromosome. In most cases,
nonhomologous chromosomes exchange segments so
that two translocations occur at the same time.
42- A chromosomal mutation involves changes in the
number or structure of chromosomes. Chromosomal
mutations may change the locations of genes on
chromosomes and even the number of copies of some
genes. - Deletion involves the loss of all or part of a
chromosome. - The opposite of a deletion is a
- Duplication, in which a segment of a chromosome
is repeated. - When part of a chromosome becomes oriented in the
reverse of its usual direction, the result is an
Inversion. - A Translocation occurs when part of one
chromosome breaks off and attaches to another,
non-homologous, chromosome. In most cases,
nonhomologous chromosomes exchange segments so
that two translocations occur at the same time.
43Gene Regulation in Prokaryotes
The lac operon enables the production of
lactose-processing enzymes in E. coli, but only
when needed.
- In the absence of lactose, the repressor protein
binds to the operator on DNA and inhibits
transcription of lactose-processing enzymes.
- In the presence of lactose, the repressor is
inhibited from binding with the operator this
all ows transcription to take place to produce
lactose-processing enzymes.