9.8 The Genetic Code and Translation Flashcards

1
Q

________ is the process through which genetic information is converted to protein products

A

translation

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2
Q

how many bases are there per codon?

A

3

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3
Q

the code is _________ (redundant), some amino acids are coded by more than one _______

A

degenerate

codon

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4
Q

_____ are proteins that read the codons and attach the right amino acid. They have non-standard __________ that are essential for enzymes to recognize which protein they are dealing with and attach the right aa.

A

t-RNAs

nucleotides

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5
Q

what enzyme attaches the correct amino acid to the correct tRNA?

A

amino acyl-tRNA synthetase

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6
Q

how many amino acyl-tRNA synthetases are there?

A

20, one for each amino acid

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7
Q

amino acyl-tRNA synthetases are completely specific for both the _____ and _______

A

tRNA and amino acid

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8
Q

The _____________ recognizes specific modified nucleotides within individual tRNAs, allowing correct addition of amino acids.

A

amino acyl tRNA synthetase

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9
Q

are there the same amount of tRNAs as codons? (there are 61 codons not including stop codons). If not, how many tRNAs are there?

A

no. there are 48 tRNAs.

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10
Q

some tRNAs need to recognize more than 1 codon. The non-standard base pairing between the third base of the codon and the corresponding anticodon in the tRNA is called:

A

wobble

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11
Q

the most important modified nucleotide is _____ (closely related to guanine). Is is a purine or pyrimidine? What can it pair with?

A

inosine
purine
C, A, U

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12
Q

a mutation in the mitochondrial gene encoding leucine tRNA causes _______, a human genetic disease that has mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like symptoms.

A

MELAS

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13
Q

in MELAS, a mutation prevents the efficient recognition of the _____ by the appropriate ____________ and therefore interferes with synthesis of mitochondrial proteins.

A

tRNA

leucyl-tRNA synthetase

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14
Q

___________________ disease is a common genetics disease that results in peripheral neuropathy. Associated with mutations in the gene encoding for glycyl-tRNA synthetase.

A

Charcot-Marie-Tooth disease

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15
Q

Charcot-Marie-Tooth disease is caused by a mutation in the ____________, the _______ that attaches _____ to its appropriate _____.

A

glycyl-tRNA sythetase
amino acyl tRNA synthetase
glycine to its appropriate tRNA

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16
Q

the ______ is the fundamental machinery for translation

A

ribosome

17
Q

translation always starts at the start codon ____, which codes for _____

A

AUG

methionine

18
Q

in order to begin translation, an initiation complex is formed from the following factors:

A
  1. tRNAmet
  2. GTP
  3. small subunit of ribosome
  4. initiation factors (ex. eIF-2)
19
Q

the initiation complex for translation recognizes the ____ structure at the 5’ end of an mRNA

A

cap

20
Q

after binding the cap structure at the 5’ end of an mRNA, the initiation complex moves along the mRNA until it comes in contact with the first ____ sequence. ____ provides unwinding for secondary structures in the mRNA

A

AUG

eIF-2

21
Q

In the process of translation: When the first AUG is located, ____ is hydrolyzed and ____ leaves the initiation complex. The large ribosomal subunit joins the complex and translation occurs.

A

GTP

eIF-2

22
Q

What is the enzyme that catalyzes peptide bond formation on the ribosome? (between P and A sites on the large ribosome)

A

peptidyl transferase

23
Q

a single mRNA translated by multiple ribosomes at the same time.

A

polysome

24
Q

what are the three stop codons?

A

UAA

UGA

UAG

25
Q

stop codons are not recognized by ____, thus when a stop codon is in vacant A site, a protein called a ___________ binds to the site. What does it do?

A

tRNA
release factor
attaches a water molecule to the end of the polypeptide chain - severing it.