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biology: whole course
unit 1
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Nucleotides
Made up of a
phosphate
molecule, a
sugar
molecule (
deoxyribose
), and a
base
molecule
DNA structure
Double-stranded
helix
Nucleotides
run in opposite directions (
anti-parallel)
Bases
(A, T, C, G) form
complementary
base pairs held together by
hydrogen
bonds
Sugar-phosphate backbone
Phosphate
and sugar
molecules
are joined together by stronger
sugar-phosphate
bonds
Deoxyribose sugar
Contains
5
carbon molecules
5' end
Has a
phosphate
group
3' end
Where new
nucleotides
are added
Prokaryotes
No
membrane-bound
organelles
Have a
single
circular
chromosome
May have smaller circular
plasmids
Eukaryotes
Have membrane-bound organelles including a
nucleus
Have
linear
chromosomes
Also have
circular
chromosomes in organelles like
mitochondria
and chloroplasts
Yeast is a special example of a
fungal
cell that contains
plasmids,
even though it is a
eukaryote
Linear chromosomes in eukaryotes
DNA is very tightly coiled and packaged into
histone
proteins
DNA replication
The process by which DNA makes an exact
copy
of itself
Steps of DNA replication
1. DNA
Helicase
unwind DNA
double
helix
2. Primer is added to
3’
end.
3. New
complementary
bases are added to each strand following
base
rules.
4. Two new DNA
strands
are formed
Leading strand
DNA is added
continuously
to the
3'
end
Replication proceeds in a
continuous
'zipper-like' fashion
Lagging strand
DNA is added in fragments to the
5'
end
Replication
is
discontinuous
Primers
Short
complementary
sequences of nucleotides blinded to the
3’
end to provide a
starting
point for DNA polymerase to
initiate
replication
DNA polymerase
Enzyme that adds complementary
nucleotides
to form new
DNA strands
Ligase
Enzyme that
joins
DNA fragments
together
on the
lagging
strand
Requirements
for DNA replication
Original
DNA
template
Free DNA
nucleotides
Primers
DNA
polymerase
Ligase
ATP
Polymerase Chain Reaction (PCR)
A technique used to
amplify
or make many copies of a specific
DNA
sequence in a
laboratory
setting
Steps of PCR
1. Heat DNA sample to
94
degrees to break the weak
hydrogen
bonds between bases to
separate
strands.
2. Cool DNA sample to
55
degrees to allow the
primers
to bond to their
specific
target sequences on
DNA.
3. Heat DNA sample again to
72
degrees to allow the
TAQ
Polymerase to add
nucleotides
to the
3’
ends.
Thermal cycler
Machine that cycles through different
temperatures
to
automate
the
PCR
process
Uses of PCR
Forensics
Paternity
testing
Medical diagnosis
Requirements for PCR
Original DNA template
Primers
DNA
nucleotides
pH
buffer
Heat-resistant
DNA
polymerase
Thermal cycler
Gene expression
The
process
of using
information
from a
gene
in order to
synthesize
or make a
protein
Genotype
The sequence of
bases
and
genes
that an organism has
Phenotype
What an organism
physically
looks like, determined by the
proteins
that are
synthesised
when genes are
expressed
Protein synthesis
DNA
-> mRNA ->
Ribosome
-> Amino acids ->
Protein
Transcription
The synthesis of an
mRNA
strand from a section of DNA
Translation
The synthesis of a
protein
using the genetic instructions from mRNA at the
ribosome
RNA
Single-stranded
Uses
ribose
sugar
Adenine
pairs with
uracil
mRNA
A
copy
of the genetic code from the
nucleus
to the
ribosome
tRNA
Carries a
specific
amino acid to the
ribosome
rRNA
Part of the
ribosome,
made up of proteins and
RNA
Transcription
1.
DNA unwinds
2.
RNA
polymerase
synthesizes
mRNA strand
3.
Stop
codon reached
Codon
A
triplet
of bases on
mRNA
that codes for a
specific
amino acid
Splicing
1.
Introns
removed
2.
Exons
joined together to form
mature
mRNA
The same gene can produce multiple mature
mRNA
transcripts and different
proteins
due to
alternative
RNA splicing
Translation
1.
mRNA
attaches to
ribosome
2.
tRNA
brings
amino
acids
to match
codons
3.
Peptide
bonds form between
amino acids
4.
Protein
folding
The
shape
of a protein determines its
function
Alternative RNA Splicing
Creates a range of different
proteins
from the same gene by varying the
combination
of
exons
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