Nucleic Acid Discovery And Structure Flashcards

1
Q

Name some functions of dna allowed because of the double helical structure of it

A

Storage within cells

Accessible for transcription(by proteins looking for sequences)

Replication possible

Meiosis - crossing over possible

Genome stability / repair

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2
Q

Explain the griffiths experiment to how they found dna could be the thing ‘transforming’ in strains of strep

A

They took dead pathogenic strain and a non pathogenic strain and this formed progenies that were pathogenic- suggesting something was transformed within the cell to make it pathogenic

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3
Q

What properties did the transforming agent have that showed it was dna in griffiths experiment

A

Contained phosphorus

Was destroyed by deoxyribonuclease enzymes

Wasn’t killed by proteases

= suggests it was dna not protein

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4
Q

Explain the Harvey and chase experiment that lead to discovery of dna being genetic material- not proteins

A

They took a bacteriophage and it had proteins labelled in S and dna was labelled with P

The ecoli was injected by bacteriophage

The bacteriophage was only able to replicate when the P radioactive was present, didn’t replicate when only S

This suggests dna was the thing that encoded for proteins to be assembled into bacteriophages

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5
Q

What is the proper name for bases nucleic acids?

A

Heterocyclic bases

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6
Q

What makes up heterocyclic bases that are purines (A,G)

A

1 pyrimidine N ring (1-6 N)

1 imidazole N ring (7,8,9 N)

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7
Q

What makes up pyrimidines (C,T,U)

A

1 pyrimidine ring (6N)

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8
Q

What is important about the N at 9’ on purines ?

A

That it what attaches to C1 of sugar ribose and deoxyribose

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9
Q

What makes adenine recognisable apart from its ring structure

A

It has an NH2 region attached to its pyrimidine ring

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10
Q

What makes guanine and cytosine recognisable apart from its ring structure

A

Guanine and cytosine both have double O bond

Also an NH2 attached

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11
Q

What makes thymine recognisable from the rest

A

On its pyrimidine ring it has a CH3 group

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12
Q

In nucleic acids there are 2 sugar types - deoxyribose and ribose. What carbohydrate structure do they have?

A

A furanose structure (5 carbon ring and HOC2 at 5’

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13
Q

What makes ribose and deoxyribose different

A

Ribose has an OH on the C2

Deoxyribose only has a H on the C2

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14
Q

At what carbon does phosphate and a base attach on the sugars (via the OH group)

A

Phosphate - at 5’ (and 3’ if in polynucleotide strand)

Base at C1

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15
Q

What are nucleosides

A

A base and sugar joined at N9/N1 and C1

Present in both dna and rna

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16
Q

What are the nucleosides called in dna and rna and what’s the difference

A

RNA- adenosine,guanosine,cytidine, uridine

Dna - deoxyadenosine, deoxyguanosine,deoxycytidine, thymidine

Only difference is the OH on the C2 carbon not present in deoxynucleoside

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17
Q

What are the nucleotides called in RNa and dna (base,phosphate,sugar)

A

Rna - adenylate, guanylate, cytidylate, uridylate

Dna - deoxyadenylate, deoxyguanylate,deoxycytidylate, thymidylate

18
Q

Why is deoxyadenylate special ?

A

The phosphate can be at both 5’c or at 3’C

19
Q

Why is a phosphate attached by a ‘phosphodiester’ bond when in a polynucleotide strand

A

Because it is attached to 1 sugar at C3’ and another sugar at C5’

= 2 ester bonds

20
Q

Why is dna more stable than RNA so used as a long term store?

A

The OH at C2 of the ribose sugar is able to be hydrolysed causing a free phosphate by bases in rna

The OH isn’t present at C2 of dna

21
Q

What is it called when bases are able to hydrolyse the C2 OH on ribose sugars

A

Base catalyses hydrolysis

This causes the breakage of phosphate back bond when base attacks the Oh

22
Q

What are ‘chargaffs rules’ about the base ratio

A

1- A and T are equal and C and G are equal

2- AT pairing can vary aswell as CG pairing in different individuals

23
Q

X-ray fibre diffraction was used to suggest the helical structure of dna. Explain the process of how this works

A

Dna is strawed out into thin fibres and then an X-ray beam is shone

The angle/diffraction site is then detected

24
Q

How did the St. Andrew’s Cross diffraction pattern determine the helixes

A

The diffraction pattern had a 60• angle to it (cross)

These angles are made by the turn of a helix - didn’t know it was double at this point

25
Q

There were dominant diffraction spots on the X-ray fibre diffraction experiment. The spaces between these were found at 34 A and 3.4 A (anxrams)

What did these represent (found by Watson and crick) in the double alpha helix?

A

34A between repeating units (turn of the helixes)

3.4 A between base pairs

26
Q

Explain the basic structure of the alpha helix found by Watson and crick

A

2 anti parallel polynucleotide strands

Base pairs found

5’ to 3’ strand had a free phosphate

3’ to 5’ strand had a free OH on C3

RIGHT HANDED HELIX

27
Q

Base pairs are held by H bonds. Who is the donor and acceptor of the H bond?

A

N-H is the donor

O is the acceptor

28
Q

Why does guanine and cytosine have 3 bonds instead of 2

A

Because they both have a double bonded O on their rings

And also the NH2 groups

29
Q

The backbone enforced the A-T and C-G base pairing. Why do these have to be

A

Because other pairs would be too small, or too large, or misalign the donor from the acceptors

This would change the backbone structure

30
Q

What 3 things give the double helix it’s structural stability

A

Hydrophobic effect- hydrophobic bases are inside and phosphate backbone outside

Base pairs H bonds

Stacked base pairs (van der waal stacking force)

31
Q

What is the importance of the phosphate backbone being negative /acidic (PO43-)

A

Allows binding of proteins such as transcription factors or histones

Which are usually positively charged = attract

32
Q

What is the major and minor grooves of the dna structure

A

The distance between phosphate backbones from one side of helix and the other (in 3D shape)

33
Q

The major groove is called ‘information rich’ why is this

A

The long distance between backbones allows accessibility or molecules such as proteins to bind

Able to read the base sequence easily because backbone isn’t in the way

34
Q

Why is minor groove information poor?

A

Backbones are close together on this side of the helix

The base sequence is not easily read by proteins etc

35
Q

What happens if the proteins such as transcription factors try to bind to minor groove

A

They will alter the dna structure

They have to pull backbone apart to read sequence

36
Q

What 3 dna structures are there (B dna being the Watson and crick model) and what are the slight differences

A

A dna units are shorter

But wider in diameter than B dna

Z dna is left handed helix and is longer repeating units

37
Q

What 4 ways do RNA single strands try to get a double helix (better for them)

A

1- can match base pairs
2- mismatched base pairs
3- unmatched regions
4- tertiary interactions

38
Q

What are tertiary interactions in single stranded rna

A

When base pairs form bonds with other base pairs

39
Q

What is the structure of single stranded things usually called

A

Stem loop structures

40
Q

Why does DNA double stranded absorb more?

A

More UV is absorbed by dna