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Mount Royal College
CHAPTER
3
Cells: The
Living Units:
Part A
Copyright © 2010 Pearson Education, Inc.
Generalized Cell
• All cells have some common structures and
functions
• Human cells have three basic parts:
• Plasma membrane—flexible outer boundary
• Cytoplasm—intracellular fluid containing
organelles
• Nucleus—control center
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Chromatin
Nucleolus
Nuclear envelope
Nucleus
Smooth endoplasmic
reticulum
Mitochondrion
Cytosol
Lysosome
Centrioles
Centrosome
matrix
Cytoskeletal
elements
• Microtubule
• Intermediate
filaments
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Plasma
membrane
Rough
endoplasmic
reticulum
Ribosomes
Golgi apparatus
Secretion being
released from cell
by exocytosis
Peroxisome
Figure 3.2
Plasma Membrane
• The plasma membrane separates the
intracellular fluid (ICF) from extracellular fluid
(ECF)
• The plasma membrane is semi-permeable
which means that some things can cross the
membrane and some things cannot
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Extracellular fluid
Intracellular fluid
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Figure 3.3
Types of Membrane Transport
• Passive Transport
• No cellular energy (ATP) required
• Substance moves down its concentration
gradient
• Active Transport
• Energy (ATP) required
• Substances are moved or“pumped” against
their gradient
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Passive Transport
•
What determines whether or not a
substance can passively permeate (cross)
a membrane?
1. Lipid solubility of substance
2. Size of the molecule that is passing
PLAY
http://www.youtube.com/watch?v=JShwXBWGMyY
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Passive Transport
• Simple diffusion
• Facilitated diffusion
• Osmosis
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Passive Transport: Simple Diffusion
• Small, nonpolar, hydrophobic substances
diffuse directly through phospholipid bilayer
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Extracellular fluid
Lipidsoluble
solutes
Cytoplasm
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Figure 3.7a
Passive Transport: Facilitated Diffusion
• Larger, hydrophilic molecules (glucose,
amino acids, ions) use carrier proteins or
channel proteins to pass through the plasma
membrane
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Hydrophilic
molecules
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Figure 3.7b
Passive Transport: Osmosis
• Movement of solvent (water) across a
selectively permeable membrane from where
it is most concentrated to where it is less
concentrated
• Water diffuses through plasma membranes:
• Through lipid bilayer
• Through channels (aquaporins)
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Water
molecules
Lipid
billayer
Aquaporin
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Figure 3.7d
Passive Transport: Osmosis
• Osmolarity: The measure of total
concentration of solute particles
• When solutions of different osmolarity are
separated by a membrane, osmosis occurs
until equilibrium is reached
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(a)
Membrane permeable to both solutes and water
Solute and water molecules move down their concentration gradients
in opposite directions.
Both solutions have the
same osmolarity: volume
unchanged
H2O
Solute
Membrane
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Solute
(sugar)
Figure 3.8a
(b)
Membrane permeable to water, impermeable to solutes
Solute molecules are prevented from moving but water moves by osmosis.
Volume increases in the compartment with the higher osmolarity.
Left
compartment
Right
compartment
Both solutions have identical
osmolarity, increases on the right
because only water is
free to move
H2O
Membrane
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Solute
(sugar)
Figure 3.8b
Importance of Osmosis
• When osmosis occurs, water enters or leaves
a cell
• A change in cell volume disrupts cell function
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Tonicity
• Defined as: The ability of a solution to cause a
cell to shrink or swell
• Isotonic: A solution that does not cause a
change in cell volume
• Hypertonic: A solution that causes a cell to
shrink
• Hypotonic: A solution that causes a cell to
swell.
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(a)
Isotonic solutions
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(b)
Hypertonic solutions
(c)
Hypotonic solutions
Figure 3.9
Active Transport
• The Sodium-potassium pump (Na+-K+ ATPase) is a
specific example of active transport
• Located in all plasma membranes
• Maintains electrochemical gradients essential for
functions of muscle and nerve tissues
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Vesicular Transport
• Transports large particles, macromolecules, &
fluids across plasma membranes
• Is active transport = requires energy ATP
• Examples:
• Exocytosis—moves substances out of cell
• Endocytosis—moves substances into cell
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ECF
Cytoplasm
Transport
vesicle
Endosome
Lysosome
(a)
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Other Organelles
• Membranous structures
• Nucleus with chromatin• Mitochondria –
• Endoplasmic Reticulum (ER) (rough and
smooth) –
• Golgi Apparatus• Lysosomes-
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Nucleus
Nuclear envelope
Smooth ER
Rough ER
Vesicle
Plasma
membrane
Lysosome
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Golgi
apparatus
Transport
vesicle
Figure 3.22
Smooth ER
Nuclear
envelope
Rough ER
Ribosomes
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Figure 3.18a
Rough ER
Phagosome
ER
membrane
Plasma
membrane
Vesicle becomes
lysosome
Golgi
apparatus
Secretory
vesicle
Secretion by
exocytosis
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Extracellular fluid
Figure 3.20
Mitochondria
• Organelle with shelflike
folds called cristae
• Provide most of cell’s
ATP (enzymes for this
process are located on
cristae)
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Other Organelles
• Non-Membranous structures
• Centrioles- involved in cell division
• Cytoskeleton- includes
microfilaments, intermediate
filaments and microtubules
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Centrosome matrix
Centrioles
(a)
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Microtubules
Figure 3.25a
Microfilaments
• Function in cell
motility and aid
in cell shape
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(a) Microfilaments
Intermediate Filaments
(b) Intermediate filaments
• Resist pulling forces
on the cell and
attach to
desmosomes
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Microtubules
• Most radiate from
centrosome
• Determine overall
shape of cell and
distribution of
organelles
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(c) Microtubules
Extensions of the plasma membrane
• Cilia are: short, hairlike structures that move
substances across cell surfaces
• Flagella are: Whiplike, tails that move entire
cell
• Microvilli are: fingerlike extensions found on
absorptive cells
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Power, or
propulsive,
stroke
1
2
3
4
Recovery stroke, when
cilium is returning to its
initial position
5
6
7
(a) Phases of ciliary motion.
Layer of mucus
Cell surface
(b) Traveling wave created by the activity of
many cilia acting together propels mucus
across cell surfaces.
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Figure 3.27
Microvillus
Actin
filaments
Terminal
web
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Figure 3.28
The Cell Cycle
• Includes:
• Interphase
• Period from cell formation to cell division
• Three sub phases of Interphase:
• G1 (gap 1)—growth and metabolism
• S (synthetic)—DNA replication
• G2 (gap 2)—preparation for division
• Cell division (mitotic phase)
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S
Growth and DNA
synthesis
G1
Growth
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M
G2
Growth and final
preparations for
division
Figure 3.31
DNA Replication
• Helicase untwists the double helix and
exposes complementary chains
• Each nucleotide strand serves as a template
for building a new complementary strand
• DNA polymerase forms new DNA strand
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DNA Replication
• End result: two DNA molecules formed from
the original
• This process is called semiconservative
replication
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Chromosome
Free nucleotides
DNA polymerase
Template for synthesis
of new strand
Leading strand
Old DNA
Helicase unwinds
the double helix and
Exposes bases
Replication
fork
Adenine
Thymine
Cytosine
Guanine
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Lleading and lagging strands are
synthesized in opposite directions
Lagging
strand
DNA polymerase Old (template) strand
Figure 3.32
Cell Division
• Mitotic (M) phase of the cell cycle
• Essential for body growth and tissue repair
• Does not occur in most mature cells of
nervous tissue, skeletal and cardiac muscle
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Cell Division
•
Includes two distinct events:
1. Mitosis—four stages of nuclear division:
•
Prophase
•
Metaphase
•
Anaphase
•
Telophase
2. Cytokinesis—division of cytoplasm by
cleavage furrow
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S
Growth and DNA
synthesis
G1
Growth
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G2
Growth
M
Figure 3.31
Prophase
• Chromosomes condense and become visible
• Mitotic spindle form
• Nuclear envelope fragments
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Early Prophase
Early mitotic
spindle
Aster
Early Prophase
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Chromosome
consisting of two
sister chromatids
Centromere
Figure 3.33
Microtubule
Late Prophase
Late Prophase
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Fragments
of nuclear
envelope
Microtubule
Figure 3.33
Metaphase
• Chromosomes are aligned at the equator
• Metaphase plate = The plane midway
between the poles of the cell
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Metaphase
Spindle
Metaphase
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Metaphase
plate
Figure 3.33
Anaphase
• Shortest phase
• Chromosomes are pulled to opposite poles by
microtubules
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Anaphase
Anaphase
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Daughter
chromosomes
Figure 3.33
Telophase
• Begins when chromosome movement stops
• Nuclear membrane forms around each
chromatin mass
• Spindle disappears
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Cytokinesis
• Begins during late anaphase
• Ring of actin microfilaments contracts to form
a cleavage furrow
• Two daughter cells are pinched apart, each
containing a nucleus identical to the original
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Nuclear
envelope
forming
Nucleolus
forming
Contractile
ring at
cleavage
furrow
Telophase and Cytokinesis
Telophase
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Figure 3.33
PROTEIN SYNTHESIS
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Protein Synthesis
• DNA is the master blueprint for protein
synthesis
• Gene: Segment of DNA with blueprint for one
polypeptide
• Each triplet (3 base sequence) in DNA
specifies an amino acid
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Nuclear
envelope
Transcription
RNA Processing
DNA
Pre-mRNA
mRNA
Translation
Nuclear
pores
Ribosome
Polypeptide
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Figure 3.34
Roles of the Three Main Types of RNA
• Messenger RNA (mRNA)
• Carries instructions for building a polypeptide,
from a gene in DNA to ribosomes in cytoplasm
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Roles of the Three Main Types of RNA
• Ribosomal RNA (rRNA)
• Helps form ribosome
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Roles of the Three Main Types of RNA
• Transfer RNAs (tRNAs)
• Transfer amino acids from cytoplasm to
mRNA attached to ribosome to begin process
of protein synthesis
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Transcription
• Transfers triplet code into a complementary
base sequence in mRNA
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Transcription
• RNA polymerase
• Enzyme that oversees synthesis of mRNA
• Unwinds DNA
• Adds complementary RNA nucleotides using a
DNA template and joins them together
• Stops when it reaches termination signal
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RNA polymerase
Coding strand
DNA
Promoter
region
1
Template strand
Termination
signal
Initiation: Once transcription factors are bound to promoter, RNA
pol binds promoter, unwinds DNA strands,
and initiates mRNA synthesis .
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Figure 3.35 step 1
mRNA
Template strand
2 Elongation: RNA pol moves along the template
strand, elongating the mRNA transcript one base at a time.
mRNA transcript
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Figure 3.35 step 2
3 Termination: mRNA synthesis ends when the termination signal
is reached. RNA poly and mRNA transcript are released.
Completed mRNA transcript
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RNA
polymerase
Figure 3.35 step 3
Steps of Translation
• Converts base sequence of nucleic acids into
the amino acid sequence of proteins
• Involves mRNAs, tRNAs, and rRNAs
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Genetic Code
• Each three-base sequence on DNA (triplet) is
represented by a codon
• Codon—complementary three-base sequence
on mRNA
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SECOND BASE
C
A
U
UUU
U
UUC
UUA
UUG
Phe
Leu
CUU
C
CUC
CUA
A
Leu
UCC
UAC
UCA
Ser
UAA
UCG
UAG
CCU
CAU
CCC
CCA
Pro
CAC
CAA
CCG
CAG
AUU
ACU
AAU
ACC
AAC
AUC
Ile
ACA
Thr
AAA
Met or
AUG Start ACG
AAG
GUU
GCU
GAU
GUC
GCC
GAC
GUA
GUG
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UAU
CUG
AUA
G
UCU
Val
GCA
GCG
Ala
GAA
GAG
G
Tyr
UGU
UGC
U
Cys
C
Stop UGA Stop A
Stop UGG
Trp G
His
Gln
Asn
Lys
Asp
Glu
U
CGU
CGC
CGA
C
Arg
A
CGG
G
AGU
U
AGC
AGA
AGG
Ser
C
A
Arg
G
GGU
U
GGC
C
GGA
GGG
Gly
A
G
Figure 3.36
Translation
• mRNA attaches to a small ribosomal subunit that
moves along the mRNA to the start codon (AUG)
• Large ribosomal unit attaches, forming a functional
ribosome
• Anticodon of tRNA binds to complementary codon
and adds its amino acid to the forming protein chain
• New amino acids are added by other tRNAs as
ribosome moves along mRNA, until stop codon is
reached
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Nucleus
RNA polymerase
mRNA
Leu
Template
strand of
DNA
1 After mRNA synthesis in the
nucleus, mRNA leaves the nucleus
and attaches to a ribosome.
Energized by ATP, the correct amino
acid is attached to each species of
tRNA by aminoacyl-tRNA synthetase
enzyme.
Amino acid
Nuclear pore
tRNA
Nuclear
membrane
G A A
2 Translation begins as incoming
aminoacyl-tRNA recognizes the
complementary codon calling for
it at the A site on the ribosome. It
hydrogen-bonds to the codon via
its anticodon.
Released mRNA
Aminoacyl-tRNA
synthetase
Leu
3 As the ribosome moves along
the mRNA, and each codon is
read in sequence, a new amino
acid is added to the growing
protein chain and the tRNA in
the A site is translocated to the
P site.
Ile
tRNA “head”
bearing
anticodon
Pro
4 Once its amino acid is released
from the P site, tRNA is ratcheted
to the E site and then released to
reenter the cytoplasmic pool,
ready to be recharged with a new
amino acid. The polypeptide is
released when the stop codon is
read.
E
site
P
site
G G C
A
site
A U A C C G
C U U
Codon
15
Codon
17
Codon
16
Large
ribosomal
subunit
Small
ribosomal
subunit
Direction of
Portion of mRNA ribosome advance
already translated
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Figure 3.37
Nucleus
mRNA
RNA polymerase
Template
strand of
DNA
1
mRNA leaves the
nucleus and attaches to a
ribosome.
Leu
Amino acid
Nuclear pore
tRNA
Nuclear
membrane
GAA
Released mRNA
Aminoacyl-tRNA
synthetase
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Figure 3.37 step 1
Leu
2 Translation begins;.
Ile
tRNA “head”
bearing
anticodon
Pro
E
site
P
site
G G C
A
site
Large
ribosomal
subunit
A U A C C G C U U
Codon Codon
15
16
Codon
17
Small
ribosomal
subunit
Direction of
Portion of
ribosome advance
mRNA already
translated
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Figure 3.37 step 2
Leu
3
The ribosome moves
along the mRNA, and each
codon is read in sequence. a
new amino acid is added to
the growing protein chain .
Ile
tRNA “head”
bearing
anticodon
Pro
E
site
P
site
G G C
A
site
Large
ribosomal
subunit
A U A C C G C U U
Codon Codon
15
16
Codon
17
Small
ribosomal
subunit
Direction of
Portion of
ribosome advance
mRNA already
translated
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Figure 3.37 step 3
Leu
3
2
Ile
tRNA “head”
bearing
anticodon
Pro
4 tRNA is released to reenter the
cytoplasmic pool, ready to be
recharged with a new amino
acid. The polypeptide is
released when the stop
codon is read.
E
site
P
site
G G C
A
site
Large
ribosomal
subunit
A U A C C G C U U
Codon Codon
15
16
Codon
17
Small
ribosomal
subunit
Direction of
Portion of
ribosome advance
mRNA already
translated
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Figure 3.37 step 4
Nucleus
RNA polymerase
mRNA
Leu
Template
strand of
DNA
1
Energized by ATP, the correct amino
acid is attached to each species of
tRNA by aminoacyl-tRNA synthetase
enzyme.
Amino acid
Nuclear pore
tRNA
Nuclear
membrane
G A A
2
Released mRNA
Aminoacyl-tRNA
synthetase
Leu
3
Ile
tRNA “head”
bearing
anticodon
Pro
4
E
site
P
site
G G C
A
site
A U A C C G
C U U
Codon
15
Codon
17
Codon
16
Large
ribosomal
subunit
Small
ribosomal
subunit
Direction of
Portion of mRNA ribosome advance
already translated
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Figure 3.37