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6 BIO
6.1.1 Cellular control
Gene expression
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Cell structures and functions vary
not all
genes
are
expressed
genes are selectively
switched
on or off
proteins
produced determine
cell structure
and processes
During
transcription
transcription factors
operons
During mRNA modification (pre-mRNA -> mature mRNA)
RNA splicing
RNA editing
caps and tails
Protein modification and activation
addition of non-protein groups
modifications of
amino acids
modifications of protein folding
removal of a part of a
polypeptide chain
activation with
cAMP
cofactors
coenzymes
inhibitors
Transcription rate
determines how much of a
protein
is made
transcription rate is determined by
transcription factors
Transcription factors
bind to
DNA
or
operons
with its
specific
shape, this shape can be altered
in DNA they bind to specific DNA sites neat the start of a
target gene
on an operand they bind to the
operator
Activators
transcription factor
turns a
gene
on to increase rate of transcription
Repressor
transcription factor
turns a gene off to decrease rate of transcription
Operons
a group or a cluster of
genes
that are controlled by the same
promoter
Structural genes
code for the
protein
itself
Regulatory genes
Code for
transcription factors
Control elements of operons
promoter - where
RNA polymerase
binds
operator - where
transcription factors
bind
the
lac operon
controls production of
LACTASE
allows the breakdown of
lactose
so it can be used as an energy source
lactase is an
inducible
protein - only made when lactose is present
The
lac operon
P -
promoter region
Lacl - codes for the
lac repressor
P - promoter region
O - operator region
lacZ
- LACTASE
lacY
- permease
lacA
- transacetylase
The
lac repressor
two
binding sites
one binds to the
operator region
other site binds to
lactose
(the
effector molecule
)
when lactose binds to the repressor, shape of other binding site changes so it cannot bind to the operator region of the operon
splicing
removal of
introns
,
exons
remain, ends reconnect
pre-
mRNA
becomes mature mRNA
occurs in the
nucleus
editing
pre-mRNA
can have changes made to the base sequence
caps
added to
5'
end of DNA
to regulate
nuclear export
, increases stability in
cytoplasm
, promotes translation
poly-A tail
lots of
adenine
nucleotides on 3' end
less
mRNA
is
hydrolysed
in the
cytoplasm
, so it lasts longer
allows for more protein to be
synthesised
caps and tails
improves
stability
lengthens
half-life
of
mRNA
allows for higher
quantities
of protein to be produced
Translation
caps
aid binding of
mRNA
to
ribosomes
inhibitory
or
initiation
factors can bind to mRNA, affecting binding of mRNA to ribosomes
Addition of non-protein groups
components that make it functional (e.g.
haem group
)
tags that indicate what is is for (e.g.
carbohydrate tags
)
occurs in the golgi body
Modifications of amino acids
adapting their
chemical properties
changes shape and therefore function of
protein
e.g.
methyl
and
acetyl
groups of
histones
Modification of protein folding
CHAPERONE PROTEINS
control how proteins are folded
there are multiple ways a protein can be folded, influencing its
function
Removal of part of a poly-peptide chain
MASKING SEQUENCE can be removed to activate it
e.g.
pepsinogen
is the inactive form of pepsin
cAMP activation
a molecule binds to
cell membrane
to stimulate the production of cAMP
cAMP alters the 3D shape of proteins to change the activity of them
cAMP acts as a secondary messenger
e.g.
PKA
is 4
units
bound together which must be released by changing the 3D structure
cofactors
loosely binds to
proteins
to hold their shape and perform their function
regulating their
availability
/
concentration
therefore regulates a proteins activity
coenzymes
organic co-factors
deliver
ions
, atoms or chemical groups to an enzyme
e.g.
NAD
,
FAD
,
NADP
delivering H+
Inhibitors
a way to regulate
protein
action post
translation