Protein Translation and Mutations Flashcards

1
Q

The process of translating the sequence of a messenger RNA (mRNA) molecule to a sequence of amino acids during protein synthesis.

A

TRANSLATION

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2
Q

It is the unit used for sedimentation coefficients and is indirect
measure of particle size

A

Svedberg unit

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3
Q

Svedberg unit of Large subunit and small subunit

A

60s Large
40s Small

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4
Q

What are the steps in translation

A

Initiation
Elongation
Termination

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5
Q

Each tRNA has a triplet called an _________ that complements a codon on mRNA.

A

anticodon

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6
Q

it is cloverleaf shaped

A

tRNA

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7
Q

An error in base sequence reproduced during DNA replication.

A

MUTATIONS

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8
Q

Errors in genetic information is passed on
during ______________

A

transcription.

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9
Q

Type of mutation that arises naturally
and not as a result of exposure to mutagens

A

SPONTANEOUS MUTATION

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10
Q

It occurs due to error in DNA replication,
depurination, deamination and transposable
genetic elements

A

SPONTANEOUS MUTATION

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11
Q

Type of mutation that is produced by treatment with a physical or chemical agent (mutagens) that affects the DNA

A

INDUCED MUTATION

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12
Q

It occurs due to the incorporation of base
analogs, base mispairing and base damage

A

INDUCED MUTATION

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13
Q

What is the cause of mutations?

A

mutagens

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14
Q

These are substances or agents that causes a change in the structure of a gene, i.e., radiation or chemical

A

mutagens

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15
Q

Mutation: Purine replaces another purine
Pyrimidine replaces another Pyrimidine

A

Transitional Mutation

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16
Q

Mutation: Purine replaces pyrimidine or vice
versa

A

Transversional Mutation

17
Q

Mutation: Codon containing the changed base results to the same amino acid

A

SILENCE

18
Q

Mutation: Codon containing the changed base results to a different amino acid

A

MISSENSE

19
Q

Mutation: Codon containing the changed base results to a STOP CODON

A

NONSENSE

20
Q

Where one or more bases is added or removed and can be caused by an aromatic compound inserting between bases in stacked DNA.

A

FRAMESHIFT MUTATION

21
Q

Condition where Inability to repair tissue damage No exonuclease

A

Xeroderma Pigmentosa

22
Q

Condition where MISSENSE Mutation
Valine replaces Glutamic acid

A

Sickle Cell Anemia

23
Q

Condition where NONSENSE Mutation
Insufficient production of Hgb

A

Thalassemia

24
Q

Condition where Short stature, aplastic anemia
Induced by Mitomycin C

A

Fanconi’s Anemia

25
Q

Condition where Proximal Tubule is Impaired

A

Fanconi’s Syndrome

26
Q

Condition where deficiency in HGPRT (Hypoxanthine- guanine phosphoribosyl transferase)

A

Lesch Nyhan Syndrome