DNA REPAIR Flashcards

1
Q

WHAT IS THE FUNCTION OF EXONUCLEASES

A

‘PROOF READ’ DNA TO CORRECT ERRORS MADE IN REPLICATION

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2
Q

WHAT TYPES OF DAMAGE CAN DNA BE EXPOSED TO

A
  1. THERMAL DEGRADATION
  2. METABOLIC BYPRODUCTS
  3. ENVIRONMENTAL SUBSTANCES
  4. RADIATION
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3
Q

WHY IS IT IMPORTANT THAT DNA CAN BE REPAIRED COMPARED TO OTHER MOLECULES

A

DNA HAS TWO MOLECULES ONLY AND HARBOURS MOST INFORMATION

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4
Q

WHICH BASES ARE CONSIDERED PURINES

A

ADENINE AND GUANINE

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5
Q

WHAT STRUCTURALLY MAKES PURINES DIFFERENT TO PYRAMIDINES

A

TWO CARBON NITROGEN RING BASES

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6
Q

WHICH BASES ARE CONSIDERED PYRIMADINES

A

CYTOSINE, THYMINE AND URACIL

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7
Q

WHY IS THE CYTOSINE GUANINE PAIR A MORE STABLE MOLECULE

A

BECAUSE IT CAN FORM 3 H BONDS

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8
Q

WHAT STRUCTURALLY STOPS THYMINE FORMING 3 H BONDS

A

CH3 GROUP

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9
Q

DEAMINATION (ADDITION OF H2O AND REMOVAL OF NH3) OF CYTOSINE RESULTS IN WHAT

A

CONVERSION TO URACIL

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10
Q

THERE ARE SITES ON ALL BASES THAT ARE VULNERABLE TO WHAT

A
  1. HYDROLYTIC ATTACK

2. OXIDATIVE DAMAGE

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11
Q

URACIL IS ALMOST CHEMICALLY IDENTICAL TO WHICH BASE

A

THYMINE

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12
Q

WHAT IS THE DIFFERENCE BETWEEN URACIL AND THYMINE

A

ONE METHYL GROUP

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13
Q

FAILURE TO UNDERTAKE DNA REPAIR RESULTS IN

A

MUTATION

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14
Q

IF REPAIR IS NOT UNDERTAKEN BEFORE REPLICATION WHAT OCCURS

A

ONE OF THE NEW DAUGHTER STRANDS WOULD CARRY THE MUTATION

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15
Q

WHAT ARE THE TWO CATEGORIES OF MUTATION

A

TRANSVERSION

TRANSITION

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16
Q

WHAT IS TRANSVERSION

A

MUTATION OF A PURINE FOR A PYRIMIDINE OR VICE VERSA

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17
Q

WHAT IS A TRANSITION

A

MUTATION OF A PURINE FOR A DIFFERENT PURINE OR PYRIMIDINE FOR ANOTHER PYRMIDINE

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18
Q

HOW MANY TYPES OF TRANSVERSION IS THERE

A

4 TYPES

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19
Q

HOW MANY TYPES OF TRANSITION IS THERE

20
Q

IS TRANSVERSION OR TRANSITION MORE COMMON

A

TRANSITION MUTATIONS ARE MORE COMMON

21
Q

TRANSITION MUTATIONS ARE ……….. LIKELY TO RESULT IN AMINO ACID SUBSTITUTIONS

22
Q

MULTIPLE POTENTIAL …………… ALLOW FOR THE ………… AMINO ACID

A

CODONS

SAME

23
Q

MOST OF THE TIME MUTATION IN THE FIRST OR SECOND BASE WILL RESULT IN WHAT

A

AMINO ACID SUBSTITUTION

24
Q

MUTATIONS IN THE THIRD BASE OF A CODON, MOST ARE …………………….. ALTERNATIVES

A

TRANSITIONAL

25
WHAT OCCURS AS A RESULT OF UV LIGHT
PHOTOLYTIC CONVERSION
26
WHAT DOES PHOTOLYTIC CONVERSION CAUSE
PYRMIDINE DIMERS
27
WHAT IS A PYRIMIDINE DIMER
THE DOUBLE BONDS IN PYRIMIDINES ARE HIGHLY REACTIVE AND WHEN UV LIGHT BREAKS THE BONDS, THEY FORM BOND WITH THEMSELVES INSTEAD OF THE COMPLIMENTARY PURINE
28
HOW CAN PHOTOLYTIC CONVERSION BE REPAIRED
NUCLEOTIDE EXCISION REPAIR (NER/LONG PATCH) USES AN EXCISION NUCLEASE TO CLEAVE A 12 NUCLEOTIDE LONG SSDNA AROUND THE DIMER. DNA HELICASE UNWINDS IT FROM THE STRAND SO IT CAN BE EXPOSE TO DNA POLYMERASE AND SEALED BACK WITH DNA LIGASE.
29
HOW IS DEPURINATION REPAIRED
VIA THE BASE EXCISION REPAIR PATHWAY (BER/SHORT PATCH)
30
WHAT IS THE BER PATHWAY
REPAIR ENZYMES(GLYCOSYLASES) FIND AN INAPPROPRIATE BASE, IT IS CLEAVED AN ENDONUCLEASE AND PHOSPHODIESTERASE REMOVE THE BACKBONE DNA POLYMERASE ADDS THE NEW NUCLEOTIDE DNA LIGASE SEALS IT IN
31
WHAT METHOD DO GLYCOSYLASES USE TO FIND ERRORS
BASE FLIPPING
32
WHAT HAPPENS WHEN DNA POLYMERASE REACHES ABNORMAL DNA THAT HAS NOT BEEN REPAIRED
IT RELEASES FROM THE STRAND AND TRANS-LESIONAL DNA POLYMERASE BINDS VIA ASSEMBLY FACTORS
33
WHAT IS THE DISADVANTAGE OF TRANS LESIONAL DNA POLYMERASE
THEY LACK PRECISION AND ARE MORE LIKELY TO MAKE ERRORS WHEN CROSSING THE POINT OF DAMAGE
34
WHAT IS THE MAIN CAUSE OF BASE SUBSTITUTION AND SINGLE NUCLEOTIDE DELETION MUTATIONS
TRANS LESIONAL DNA POLYMERASE
35
WHAT ARE THE ADVANTAGES OF TRANS LESIONAL DNA POLYMERASE
1. ITS MISTAKES ARE A DRIVER OF EVOLUTION | 2. IT IS THE BEST CASE SCENARIO IN TERMS OF REPAIR THAT HAS NOT HAPPENED PRIOR TO REPLICATION
36
WHY ARE DOULE STRANDED BREAKS HAZARDOUS
THERE IS NO TEMPLATE FOR REPAIR
37
WHAT ARE THE CAUSES OF DS BREAKS
IONISING RADIATION REPLICATION ERRORS OXYGEN RADICALS
38
WHAT ARE THE TWO MECHANISMS THAT EXIST TO REPAIR DS BREAKS
1. NON HOMOLOGOUS END JOINING | 2. HOMOLOGOUS RECOMBINATION
39
WHAT HAPPENS IN NON HOMOLOGOUS END JOINING
THE ENDS OF THE BROKEN DNA MOLECULES ARE JOINED TOGETHER AFTER EACH END IS PROCESSES
40
WHAT ARE THE DISADVANTAGES OF NON HOMOLOGOUS END JOINING
THERE IS A CHANCE OF LOSS OF NUCLEOTIDES | THERE IS A CHANCE THAT THERE IS JOINING OF THE WRONG STRANDS
41
WHAT IS HOMOLOGOUS RECOMBINATION
NUCLEASE DIGESTS THE ENDS OF BROKEN STRANDS | THE STRAND INVADES THE HOMOLOGOUS STRAND ALLOWING TEMPLATED REPLICATION IN ORDER TO GET AN ACCURATE COPY
42
WHAT IS THE ADVANTAGE OF HOMOLOGOUS RECOMBINATION
IT IS MORE ACCURATE
43
WHAT IS THE DISADVANTAGE OF HOMOLOGOUS RECOMBINATION
YOU GET LOSS OF HETEROZYGOSITY AS THE LOST ALLELE MAY HAVE BEEN DIFFERENT FROM WHAT IS BEING COPIED
44
GIVE AN EXAMPLE OF A DISEASE THAT ARISES FROM LACK OF DNA REPAIR ENZYMES
XERODERMA PIGMENTOSUM
45
FAILURES IN DNA REPAIR SYSTEMS HAVE STRONG LINKS TO WHAT
CANCERS