cellular control Flashcards

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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
Q

what is a transcriptional factor

A

protein

26
Q

how does a transcriptional factor work at the transcriptional level

A

cell signal –> activates TF –> links to promoter sequence (non-coding) –> recruits RNA polymerase –> increasing the rate of transcription

27
Q

how does oestrogen affect the rate of transcription

A

binds to site on TF

changing shape of the TF molecule

inhibits the protein from binding to a promoter sequence

28
Q

define lac operon

A

group of genes under the control of same regulatory mechanisms expressed at the same time

29
Q

what are two features of lac operon

A

common to prokaryotes

efficient because if a certain protein isn’t needed, all the genes involved in production can be turned off

30
Q

what does the lac operon consist of

A

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
Q

what is the function of LacI

A

codes for a repressor protein

which is constantly produced and binds to operator region

32
Q

what is the function of repressor protein

A

binds to the operator region

prevents the RNA polymerase from binding to DNA (down regulation)

33
Q

what happens when lactose is present

A

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
Q

how do we have more cAMP

A

high lactose

more glucose will be produced

so more undergo respiration synthesising more ATP

so more cAMP is made

35
Q

what is the function of cAMP in lac operon

A

binds to CRP (cAMP receptor protein)

CRP binds to DNA and acts as a TF