UNIT 1 TEST Flashcards

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1
Q

What is differentiation?

A

process that cells become specialised for a particular function and can’t change into different cell types

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2
Q

What are embryonic stem cells involved in

A

growth repair and renewal of cells found in the tissue

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3
Q

Germline cells

A

If mutation occurs then mutation is PASSED onto the offspring

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4
Q

Somatic cells

A

If mutation occurs its NOT PASSED onto the offspring

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5
Q

Therapeutic use of stem cells

A

bone marrow transplant

skin grafts

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6
Q

what is cancer

A

uncontrolled growth of cells

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7
Q

why do cancer cells divide uncontrollably

A
  • dont respond to the usual regulatory signals and chemical messengers inside and outside the cell to produce a mass of abnormal cells
  • if cancer cells fail to attach to each other, they can spread throughout the body to form secondary tumours.
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8
Q

what is a tumour

A

abnormal cells produced by uncontrollable cell division

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9
Q

what forms DNA nucleotides

A
  • phosphate
  • deoxyribose sugar
  • base
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10
Q

whats the backbone called

A

sugar phosphate backbone

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11
Q

prevent tangling in dna

A

molecules of the DNA are tightly coiled around proteins

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12
Q

what does DNA polymerase do

A

adds complementary DNA nucleotides to the 3’ end

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13
Q

what does ligase do

A

enzyme that joins DNA fragments together

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14
Q

what is the structure of RNA

A
  • phosphate
  • ribose sugar
  • base
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15
Q

differences between DNA and RNA

A
  • rna is single stranded and DNA is double stranded
  • RNA contains uracil and DNA contains Thymine
  • RNA contains ribose sugar and DNA contains deoxyribose sugar
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16
Q

Transcription

A

mRNA carries a copy of the DNA code out the nucleus to the ribosome

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17
Q

tRNA

A

bring specific amino acids to the ribosome where the mRNA and the genetic information is translated into a protein

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18
Q

what enzyme is responsible for transcription

A

RNA polymerase

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19
Q

what is a mutation

A

change to the genetic structure of an organism

20
Q

missense mutation

A

altered codon for amino acid still makes sense but not the original sense.

21
Q

Nonsense mutation

A

a codon used to code for an amino acid is exchanged for one that acts as a premature stop codon. it causes protein synthesis to be halted prematurely and results in a polypeptide chain shorter than normal and unable to function

22
Q

splice site mutation

A

if one or more introns have been retained by modified mRNA, they may in turn be translated into an altered protein that doesn’t function properly

23
Q

frameshift

A

every codon after the site of mutation to be altered. altered protein will not be able to function

24
Q

PCR

A

1- dna strands separate
2-primers bind to the DNA strands
3- DNA polymerase builds nucleotides into the DNA strands

25
Q

what does amplification of DNA mean

A

process of taking a tiny sample of DNA and producing vast numbers of copies of it

26
Q

enzyme involved in PCR

A

Taq polymerase

27
Q

what is a DNA probe

A

detect the presence of a specific sequence of nucleotide and they have a fluorescent label so they can be detected easily

28
Q

what is anabolic pathway

A

building up complex molecules and REQUIRE energy

29
Q

what is catabolic pathway

A

breakdown of molecules. they RELEASE energy

30
Q

what factors can affect enzyme activity

A
  • ph
  • temperature
  • inhibitors
31
Q

how does competitive inhibitor work

A

bind with the active site and block it from the substrate . it can be reversed by adding more substrate

32
Q

how does non competitive inhibitor work

A

bind to the enzyme NOT the active site. they change the shape of the active site so the substrate no longer fits, it can’t bind

33
Q

what is phosphorylation

A

phosphate groups added to a molecule

34
Q

where does glycolysis take place

A

cytoplasm

35
Q

state what glycolysis is

A

glucose is broken down to pyruvate

doesnt require energy

36
Q

energy investment stage

A

2 ATP are used up

37
Q

energy pay off stage

A

4 ATP are produced

38
Q

what enzyme controls the release of hydrogen ions from substrate

A

dehydrogenase

39
Q

where does the citric acid cycle take place

A

central matrix of the mitochondria

40
Q

how is citrate formed

A

acetyl coenzyme A combines with oxalocetate to form citrate

41
Q

what is formed during citric acid cycle

A

ATP and Carbon dioxide

42
Q

where does the electron transport chain found

A

inner membrane of the mitochondria

43
Q

what is the final hydrogen acceptor and what substrate does it form when combined with hydrogen

A

oxygen which combines with hydrogen ions and electrons to form water

44
Q

what inhibits phosphofruitokinase?

A

high levels of ATP and citric acid

45
Q

what is type of activity is slow twice muscle fibre good for

A

long distance running

46
Q

what type of activity is fast twitch muscle fibre good for

A

weighlifting

sprinting