molecular biology 1 Flashcards

1
Q

what is the difference between deoxyribose and ribose

A

deoxyribose is missing an oxygen hydroxy group on carbon 2

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2
Q

how are the sugars joined together

A

sugars are joined together via a 5’-3’ phosphodiesterase bond which are strong covalent bonds

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2
Q

how are the sugars joined together

A

sugars are joined together via a 5’-3’ phosphodiesterase bond which are strong covalent bonds

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3
Q

nucleoside

A

base and 5 carbon sugar

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4
Q

nucleotide

A

nucleoside and phosphate group

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5
Q

purines

A

adenine and guanine

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6
Q

pyrimidines

A

cytosine, thymine, uracil

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7
Q

describe the DNA structure

A
  • antiparallel double helix
  • phosphate sugar backbone
  • base pairs on the inside are held together with hydrogen bonds.
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8
Q

primary structure of DNA?

A

sequence of nucleotides

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9
Q

secondary structure of DNA?

A

spatial arrangement of the nucleotide chains

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10
Q

how are base pairs held together

A

hydrogen bonds

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11
Q

A-T

A

2 hydrogen bonds

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12
Q

G-C

A

3 hydrogen bonds

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13
Q

chromatin =

A

histone + DNA

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14
Q

genetics

A

the tern used t describe inheritance of changes in base sequences

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15
Q

why does the double helix normally exist in the B-helix form

A

because there are major and minor grooves formed by the structure

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16
Q

what is the polarity of DNA?

A

this is the direction that DNA will run, the way which they are lined together, give DNA polarity.

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17
Q

how can chromosomes be distinguished between each other

A

size and G banding

18
Q

what is a karyotype and what technique is used to find it

A
  • a karyotype is a full set of chromosomes
  • G banding
19
Q

what reaction is chromosomes pulled apart

A

condensation

20
Q

what forms the phosphate sugar backbone?

A

the joining of the sugars via a phosphate

21
Q

what is the charge of the phosphate sugar backbone

A

negative

22
Q

biggest and smaller chromosome?

A

1- biggest
21- shortest

23
Q

how does fluorescent marking work for identifying chromosomes?

A
  • complementary probes of DNA can be made that will match the DNA being analysed
  • these probes have fluorescent markers on them
  • When the DNA strands are separated, they naturally want to be in a double helix so they bind to the fluorescent probe which allows for the image of chromosomes to be made.
24
Q

what are the 2 parts of the chromosome

A

telomere and centromere

25
Q

what does the centromere allow

A

it allows for separation of DNA to opposite ends during mitosis

26
Q

what is a nucleosome consist of

A

147 base pairs of DNA double helix wrapped around a histone core (DNA wrapped around histones)

27
Q

what allows histone and DNA to bind

A

the fact that the histone is positively charged and the DNA is negatively charged

28
Q

what does histone H1 do?

A

it provides a unique role in anchoring the DNA to the histone and telling it to keep folding in the right direction, this helps the nucleosome to become more condensed.

29
Q

how is the chromosome made

A

the nucleosome continues condensing.

30
Q

how are proteins condensed in the cell cycle?

A

enzymes called condensins allow the proteins to adopt a very tight structure

31
Q

why do chromosomes need to be remodelled and how is it done

A
  • chromosomes need to be remodelled to allow protein access in order to use the genetic info.
  • done using a remodelling complex and requires energy
32
Q

what is epigenetic modification and what are examples

A

changes in gene expression that do not cause changes in the DNA sequence.
methylation, acetylation, phosphorylation

33
Q

acetylation

A

this removes the positive charge from the histone which decreases the binding of the positively charged DNA, causing relaxation of the structure.

34
Q

what % of our genome codes for proteins?

A

approx 1.5% with the rest being junk proteins

35
Q

why are repetitions in DNA important in forensics?

A

as consecutive repeats at different locations will be different for different people
this sample can be used in gel electrophoresis to identify the matching repeats.

36
Q

what is myotonia

A

this is the inability to relax muscles at will

37
Q

what causes myotonic dystrophy

A

this is caused by a trinucletide repeat that occurs many times in a row at a particular location.
for most people a trinucleotide repeat is not going to cause any problems, but id the repeat is very large this can lead to muscular dystrophy.

38
Q

structure of mitochondrial DNA

A

17000 base pairs long
circular
2-10 copies in mitochondrion with several mitochondria per cell.

39
Q

why can mitochondria be good for forensics

A

because there are more copies and their smaller culcular structure makes them more stable allowing it to be purified while DNA can’t.

40
Q

where are mitochondria dna inherited and what is this implication on disease?

A
  • inherited from mother
  • this means if there is a defect in the mitochondria it will only come from the mother.
    (it is also useful to see lineage)
41
Q

what are the 2 types of repeat in DNA

A
  • interspersed repeats
  • tandem repeats
42
Q

what is an example of interspersed repeats?

A

SINE and LINE which are often derived from retroviruses

43
Q

what is an example of TANDEM repeats

A

satellites, mini satellites and micro satellites