Lecture 11-12 Flashcards

1
Q

What are the types of mutations

A

i. point mutations
transition purine -> purine - purine or pyrimidine -. pyrimidine
transversion -> purine to pyrimidine vice versa
ii. silent - no change in aa
iii. neautral - properties of aa are simular
iv. missense - aa change that affects protein function
v. nonsence - mutation to a termintion codon
vi. framshift- changes reading frame on mRNA

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2
Q

What are tautomeric shifts and how do that cause mutation

A

Tuatomeric shifts occure from movment of hydrogren atoms bbetween keto and amino forms and rare (enol and imino) position on a base, leak to replicaiton erroe due to incorrect base pariing

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3
Q

Describe muations induced by cheimicals

A

alkylatin agents: alter base pairing specifiity, donate methy or ethly groups that modifiy bases

base analogs: subsitutes for usual bases, ex. 5 bromouracil 5BU is a thyminine analog, incrases probability of tautomeric shift

oxidative deamination: nitrous acids converts amino to keto group

intercalting agnets: same dimenations as base pari, wedge between base paris and disorts DNA, causes gaps during replication, inseration or deletion of a SINLGE nucleotide creates frame shifts mutatison

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4
Q

Mutations induced by radiation

A

ultra violet (UV) light: bases absorb UV at 254 nm, can form thyamine dimers, distrupt base paring during replication

x-rays can break N-glycosidic bond between sugar and base creating apurnic or apyrimidinic sites

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5
Q

What is the ames test

A

screen for mutagenic compouds measuring ability to convert histide minus (unable to synthesize histidine) mutatnst of salmonella to histidine plus (able to synthesize histidine

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6
Q

Describe the photo reactivation repair mechanisms

A

only occurs in prokayrotes and uses light eneryg to activate DNA phtolase enzyme to repair thymine dimers

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7
Q

Describe base excisiton repair

A

a cut and past machansism that removes modified nucleotides and requires a specific glycoasylase (removes base), AP endonuclease and phosphdiesterase (removes sugar-phosphate) followed be inseration of correct nuecltotide by DNA pol and phsphodiester bod formation by DNA ligase

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8
Q

Describe nucelotide excision repair

A

cut and paste mechanism that can reparin thymine dimers bt removing 12 base stran and requires the acitivies of uvr A, B, C and D proteins in E. coli

in euks, remoes larger stechend of DNA and requires XPA rpetones (mutatined in xerderma pismentosum)

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9
Q

Describe mis match repair

A

corrects replication errors by a mechanims tha tin E.coli require the mutS, H,L and U proteins, which recognize te newly synthesizes strand by the absence of a mthelyates A in the sequence GATC

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10
Q

Desctibe the SOS response in E.coli

A

eorro prone repair response that in induced by the Lex A and RecA proteins

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11
Q

Describe post replication rapir in E.coli

A

usues homolgous recbintion (mediated by RecA) to repair gaps created when the replication fork skps over an unrepaired thymine dimer

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12
Q

How does the doubl strand break repair work

A

joins nonhomologous end-joining (in which end trimming and blut end ligation reults in some loss of DNA) or by homologous recombination (in which reuqires the Rad proteins

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