cellular control Flashcards

1
Q

why is it important that genetic information is conserved accurately when replicating DNA

A

3 bases code for an AA

sequence of triplets determines the sequence of amino acids for proteins

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2
Q

how does an allele form

A

change to base sequence of a gene

produces no change if the mutation is silent or takes place in an intron

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3
Q

why can changed codons still code for the same AA

A

more than more triplet codon can code for the same AA

changed codon can still code for the same AA

because the code is degenerate

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4
Q

define degenerate code

A

more than one triplet can code for the same AA

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5
Q

if there are four bases in DNA and these code for 20 AA, what is the basis for the genetic code

A

if three bases code for one AA

possible AA = 4x4x4 = 64

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6
Q

define mutation

A

change in base sequence in DNA

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7
Q

how does genetic variation occur

A

random, spontaneous mutations

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8
Q

what types of mutations pass onto successive generations

A

only in gametes

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9
Q

why is there is no effect when mutation occurs

A

mutation occurs in non-coding part of DNA (intron)

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10
Q

define mutagens and the different types

A

changes the rate at which mutations occurs

ionisation – break one/both DNA strands
alkylating agent – adds methyl/ethyl groups
de-aminating agent – alters bases
viruses – insert viral DNA into host genome

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11
Q

when does genetic mutation and chromosomal mutation occur

A

genetic – during DNA replication

chromosomal – during cell division

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12
Q

what are the types of point mutations

A

silent – no change to primary sequence
(degenerate code)

nonsense – changes a codon into stop-codon leading to truncated protein

missense – change to primary sequence
changes the properties to their opposite ones

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13
Q

what are the types of chromosomal mutations

A

deletion – section lost

translocation – substition of a section of chromosome

duplication – of a section

inversion – section of DNA from chromosome breaks off and reversed joined back

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14
Q

what is rate of cell division controlled by

A

proto-oncogene – stimulates cell division

tumour suppressor gene – slows/inhibits cell division

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15
Q

what happens when the proto-oncogene undergoes point mutation

A

turns into oncogene

stimulates excessive cell division

forms tumour

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16
Q

what happens when tumour suppressor gene undergoes point mutation

A

inactivated

rate of cell division increases unregulated

17
Q

what is gene expression important for

A

responding to receptors

growth

18
Q

how is chromatin formed

A

DNA is negative
histones are positive

they associate –> coil

19
Q

describe the processes involved in development of an organism

A

fertilisation –> form zygote (pluripotent)

mitosis (responsible for the quantity of cells in an organism = 37.2 trillion)
differentiation (responsible for the organisms having 200+ different specialised cels)

20
Q

describe the cell signalling mechanism in glucose to move from the intestines to the blood

A

glucose binds to receptor

causes gene expression in nucleus

to produce proteins (carriers on the c.s.m)
which transports glucose through cell to blood

21
Q

what happens if a gene turns ‘on’ and ‘off’

A

‘on’ = more of a protein produces

‘off’ = less of a protein produces

22
Q

what is transcription controlled at

A

transcriptional level

post-transcriptional level

translational level

post-translational level

23
Q

how does chromatin remodelling occur at the transcriptional level

A

remodel chromatin into:

heterochromatin – tightly wound (present during c.division) –> down regulates transcription

euchromatin – loosely wound (during DNA replication interphase) –> up regulates transcription

24
Q

how does histone modification occur at the transcriptional level

A

makes histone more or less positive

more => heterochromatin
adding methyl groups to become more hydrophobic or removing acetyl groups

less => euchromatin
adding acetyl groups by phosphorylation

25
what is a transcriptional factor
protein
26
how does a transcriptional factor work at the transcriptional level
cell signal --> activates TF --> links to promoter sequence (non-coding) --> recruits RNA polymerase --> increasing the rate of transcription
27
how does oestrogen affect the rate of transcription
binds to site on TF changing shape of the TF molecule inhibits the protein from binding to a promoter sequence
28
define lac operon
group of genes under the control of same regulatory mechanisms expressed at the same time
29
what are two features of lac operon
common to prokaryotes efficient because if a certain protein isn't needed, all the genes involved in production can be turned off
30
what does the lac operon consist of
3 genes: Lac2 -- codes for beta-galactosidase --> breaks down lactose LacY -- codes for permease --> binds to membrane for lactose to be pumped into cell LacA
31
what is the function of LacI
codes for a repressor protein which is constantly produced and binds to operator region
32
what is the function of repressor protein
binds to the operator region prevents the RNA polymerase from binding to DNA (down regulation)
33
what happens when lactose is present
lactose binds to R-protein causing change in T.structure so the R-protein can no longer bind to DNA RNA polymerase binds to promoter uninhibited
34
how do we have more cAMP
high lactose more glucose will be produced so more undergo respiration synthesising more ATP so more cAMP is made
35
what is the function of cAMP in lac operon
binds to CRP (cAMP receptor protein) CRP binds to DNA and acts as a TF