8. gene expression Flashcards

1
Q

crispr

A

genome editing
faster than previous methods

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2
Q

pharming

A

genetically modifying animals and plants to make useful products

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3
Q

gene therapy

A

fixing faulty genes
leukaemia

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4
Q

substitution in mutation

A

change in base sequence

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5
Q

nonsense substitution

A

early stop codon
short chain

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6
Q

mis-sense substitution

A

wrong amino acid being made
can effect tertiary structure

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7
Q

silent substitution

A

different base - same amino acid
degenerate nature

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8
Q

deletion/addition/duplication mutation

A

loss or gain of one more bases
changing whole future sequence
frame shift

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9
Q

apoptosis

A

when an organism kills a cell

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10
Q

stem cell define

A

cell which can divide an unlimited no. of times (highly potent)

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11
Q

totipotent stem cell

A

any type of body cell
‘embryonic’
only for limited amount of time in mammalian embryos

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12
Q

pluripotent stem cell

A

can differentiate into any embryonic cell
not extra-cellular (part of placenta)
unlimited no. of times
treat diseases

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13
Q

multipotent stem cell

A

adult stem cell
tissue growth and cell repair

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14
Q

unipotent stem cell

A

only into specific type of cell e.g. heart tissue/cardiomyoctes

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15
Q

oestrogen mechanism epigenetics

A

steroid hormone
moves into blood stream
binds to cell with specific complementary receptor
diffuses through PhosLip Bilayer (lipid soluble)
binds with transcription factors
activates it by releasing inhibitor
moves into nucleus and binds to promotor region of DNA
stimulates RNA polymerase

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16
Q

transcription factor

A

regulating protein
binds to promoter region
stimulates RNA polymerase
signals specific gene production

17
Q

promotor region

A

DNA sequence that controls the transcription of a gene
upstream of the gene’s transcription start site

18
Q

epigenetic

A

inheritable changes to gene function
no change to base sequence
environment stimulates methylation or prevents acetylation

19
Q

DNA methylation

A

methylation of cytosine (next to guanine, CpG regions)
has to be in promoter region
transcription factor cannot bind
RNA polymerase doesn’t transcribe the gene

20
Q

how can DNA methylation treat tumours/cancer

A

removal of methyl groups from tumour suppressor genes
allows gene to be expressed
regulate cell cycle

21
Q

how can acetylation treat tumours/cancer

A

removal of acetyle groups from oncogenes
DNA raps more tightly
genes suppressed

22
Q

oncogenes

A

stimulate cell division too quickly

23
Q

conventional drug use as comparison

A

effective comparison
unethical not to treat

24
Q

negative use of pluripotent cells

A

might differentiate to wrong type of cells
might be out of control
cancer/tumours

25
control group describe
describe relevant comparison
26
5 stages of invivo cloning
isolation insertion into vector (plasmid) transfer of vector to DNA
27
how are successful cloning colonies identified
fluorescent plasmid identified with UV light insertion of protein into plasmid, bind with complementary to make colour change
28
advantages of using mRNA in cloning
no introns already been spliced
29
how to cut gene to make it able to bind to DNA sequence
cut with sticky ends complementary to DNA sequence
30
PCR mechanism
amplifying small part of DNA denaturation (95 degrees C) breaks hydrogen bonds between two strands annealing (55 degrees C) primers bind to complementary sequence in single stranded extension (72 degrees C) DNA polymerase makes another strand (double helix) repeat pH buffer, thermostable DNA polymerase, run out of primers or nucleotides
31
risk of high oestrogen concentrations
breast cancer
32
how is DNA broken into smaller fragments
restriction enzyme break phosphodiester bonds
33
define DNA probe
short single stranded DNA complementary bases