Chapter 10 Notes
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Transcript Chapter 10 Notes
Chapter 10: DNA, RNA,
and Protein Synthesis
Objectives:
Analyze and investigate emerging
scientific issues (e.g., genetically
modified food, stem cell research,
genetic research and cloning).
Describe advances in life sciences
that have important long-lasting
effects on science and society
(e.g., biological evolution, germ
theory, biotechnology and
discovering germs).
Analyze and investigate emerging scientific issues
(e.g., genetically modified food, stem cell
research, genetic research and cloning).
I. DNA Structure
A.
Double helix
A.
B.
Double twisted Ladder
Watson and Crick
A.
1953
II. DNA Nucleotides
Make up the long chains of the DNA Helix
Parts of the ladder
Consists of 3 parts:
Five carbon sugar (deoxyribose)
Phosphate group
Nitrogen base
III. Nitrogen bases
4 Nitrogen bases make up DNA
T (thymine)
A (Adenine)
C (Cytosine)
G (Guanine)
Base pairing rules
Cytosine always pairs with Guanine
Guanine always pairs with Cytosine
Thymine always pairs with Adenine
Adenine always pairs with Thymine
IV. Example
If you have the
sequence
A
T
C
G
It will be paired with
T
A
G
C
V. DNA Replication
Process by which DNA is copied before a cell
divides
Steps:
Enzymes, called helicases, separate the DNA
strand
Enzymes, called polymerase, add complimentary
bases pairs (T’s to A’s etc.)
DNA polymerase fall off and there are 2 identical
strands
helicase
polmerase
-T
-A
-G
-C
-T
-A
-G
-G
ATCGATCC-
-T
-A
-G
-C
-T
-A
-G
-G
A–
T–
C–
G–
A–
T–
C–
C–
VI. DNA errors in
replication
Mutation
A change in the nucleotide
sequence
Have serious effects on the
function of cells
Mutations that are not repaired are
called cancer
VII. Flow of Genetic Material
How does information from DNA get to
cell?
DNA – RNA - protein
Transcription
DNA
acts as a template for RNA synthesis
Translation
Directs
assembly of proteins
Protein synthesis
Forming
proteins bases on information
VIII. Protein Synthesis
Steps:
DNA double helix unwinds
Messenger RNA comes and copies
A (adenine) pairs with U (uracil)
Other bases pairs combine with usual complimentary
bases
RNA codes for codons, (3 base pair) see chart
Each codon is used to make an amino acids
Each amino acid combination makes proteins
Proteins control ALL functions of the cell!
The nearly universal genetic code identifies
the specific amino acids coded for by each
three-nucleotide mRNA codon.
Translation: Assembling Proteins
IX. The Human Genome
The entire gene sequence of the human
genome, the complete genetic content, is
now known.
To learn where and when human cells use
each of the proteins coded for in the
approximately 30,000 genes in the human
genome will take much more analysis.
10.4 Genetic Changes
Mutation – any change in a gene or
chromosome.
*Leading cause of evolution.
Mutations that occur in gametes can be
inherited while mutations that occur in the
body cells are not passed to offspring. You
may have a genetic predisposition to the
defect.
Example Breast Cancer
A. Types of mutations
Point mutation – change in one base pair.
AAT, AAC.
( the amino acids are leucine,
still leucine) sometimes there is no effect on
the protein
Inversion – where two letters are switched.
Instead of AAT you could get ATA. (leucine
becomes tyrosine)
Frameshift – when an entire sequence is altered.
Deletion shifts the frame left – ATATTC, delete the A
You get TATTC
-Insertion shifts the frame to the right – ATATTC, add a T you get TATATTC
Insertion of a base or deletion of a base will
cause frameshift mutations. Could affect the
entire chromosome
Translocation – piece of chromosome
attaches to an entirely different
chromosome.
B. Causes of Mutations
Spontaneous – just happen, no
explanation
Mutagens – things that can cause
cancer. Such as: drugs, alcohol,
smoke, pollution, radiation (sun &
X-Ray, nuclear), chemicals
(dioxins, asbestos, benzene,
cyanide) and even high
temperatures.
Repairing DNA: Enzymes proof
read and correct nucleotides, but
the more mutations the more likely
a mistake will be missed and not
corrected. You need to limit your
exposure to mutagens to reduce
your risk of causing a mutation.