Genetic code: DNA & RNA Flashcards

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1
Q

Nirenberg-Matthaei Poly-U 1961

A
  • determined which RNA coded for which protein
  • found a codon was 3 nucleotides
  • deduction: in order for the 4 nucleotides to account for all 20 amino acids, a minimum of 3 base pairs are required
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2
Q

Degenerate code

A

multiple codons code for the same amino acid

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3
Q

neutral/silent mutation

A

mutation of nucleotide order/ substitution - but does not influence aa encoded

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4
Q

neutral amino acid substitution

A

mutation in different aa produced - but does not affect protein function

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5
Q

how many stop codons are there? codons coding to stops translation

A

3 - no aa is produced - UAG, UAA, and UGA

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6
Q

how many start codons?

A

1 - methionine made

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7
Q

3 types of RNA

A

mRNA - carries transcripts DNA from nucleus to cytoplasm for protein synthesis
tRNA - transfers aas to mRNA to build proteins
rRNA - ribosomal RNA - make up ribosomes w protein

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8
Q

Nucleoside

A

sugar(ribose) + nitrogenous base

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9
Q

Nucleotide

A

nucleoside + phosphate molecule

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10
Q

DNA vs RNA ribose structure

A

Deoxyribose - DNA - H instead of OH on 2nd prime (attached to 2nd carbon in ribose pentagon) = better at long term storage
Ribose RNA - OH = less stable - better for short time/ dynamic use

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11
Q

DNA polymerisation (chain making) phosphate structure?

A

New joining nucleotides with 3 phosphates lose 2 when joining to make phosphodiester bonds - much like ATP (adenosine triphosphate) gives out energy, NTP (nucleoside triphosphates) provides energy for DNA synthesis.

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12
Q

Properties of B-DNA (typical double helix)

A
  • 10 base pairs per turn
  • right handed helix (rotates in clockwise direction)
  • minor and major grooves
  • very -ve charge due to phosphate groups
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13
Q

2 flavours of nitrogenous bases

A

Purines: Adenine, Guanine (double carbon rings)
Pyrimidine: Thymine, Cytosine, Uracil (single carbon rings)

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14
Q

why is Thymine used in DNA over Uracil?

A
  • U makes more stable U-U bonds in mutation under UV radiation - t-t bonds break easier- less likely to be transcribed
  • U paired with A causes kink in double helix backbone
  • Cytosine easily mutates (through deamination- hydrolysis) to U - if U bases also existed in DNA, wouldn’t be able to tell the correct base
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15
Q

dNTPs

A

deoxynucleotide triphosphates = single nucleotides with 3 phosphates (free nucleotides)

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16
Q

chromatin

A

material of chromosomes - consists of: DNA, RNA, Proteins

17
Q

nucleus dna types in microscope images

A

euchromatin - light coloured, sparsely packed dna, 90% of genome, expressed genes

heterochromatin - dark coloured, tight packed - supercoiled, silent genes

each nucleus contains 2m of DNA = supercoiling to fit

18
Q

nucleosome

A

one “bead” of wrapped DNA along strand around histones (linker DNA with histone 1 H1 spans between nucleosomes - space for restriction enzymes to bind)
per nucleosome:
8 histones = “octamers”
147 base pairs
DNA wound 1.6 wraps around histone protein core

supercoil to form cremation fibres 30um

19
Q

chromatin remodelling factors

A

protein complexes that travel along DNA to alter histones:
exchange, remove histones
alter nuclear or histone structure

20
Q

histone tails

A

stick out of nucleosomes to alter gene expression, can be modified with:
methyl groups, acetyl groups, lysine

21
Q

histone methylation

A

decreased DNA expression - inhibits binding of transcription factors by making histone tails wrap around DNA - often methylation can be reversed

22
Q

DNA methylation

A

alters gene expression through modification of DNA - linked to disease - irreversible

23
Q

chromatin fibre

A

Nucleosomes fold up to form a 30-nanometer chromatin fiber, condense into loops to form protein scaffold,

24
Q

facultative heterochromatin

A
  • heterochromatin = tightly packed
  • but still able to be expressed - switches between hetero. and euchromatin states e.g, through histone tail modification
25
Q

constitutive heterochromatin

A
  • always condensed
  • consists fo repetitive sequences, e.g, telomeres, centromeres (connecting sister chromatid)
  • play role in structuring chromosomes
26
Q

telomeres

A
  • repetitive sequences at end of chromosomes
  • shorten with age (oxidisation?) 11 - 4 killobaes thru life
  • to protect genes
27
Q

cause of telomere shortening

A

in DNA replication, RNA primer on lagging strand (is 3-5 so 3’ end of new strand was a primer and has nothing before it so is not replaced by ligase = gap

telomeres will keep shortening every cell division until none left = hayflick limit - cell division stops

solution = telomerase enzyme! - only some cells: germ cells (eggs, sperm), some cancer cells, embryonic stem cells - high volume of telomerase present

28
Q

telomerase

A

enzyme uses reverse transcription from mrna template to dna
on lagging strand, telomere sequence is recognised and dna is added to the parent strand. an RNA primer binds to added length and synthesises 5-3’ to meet original end of RNA = no lost length of telomere, telomerase synthesised extra and primer is then removed.

29
Q

chromosome replication origins

A
  • multiple origins on each chromosome

- each origin only used once per cell cycle - no duplicated dna

30
Q

timing of replication origins

A

euchromatin origins copied earlier than heterochromatin origins