genetic code Flashcards

(20 cards)

1
Q

what did george gamow suggest

A

suggested the number of nucleotides necessary to code for one amino acid (3-base code)

  • multiple triplets would code for the same amino acid = a redundancy in the code
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2
Q

what is the reading frame of a protein?

A

three codons are read, deduced, and transformed into the amino acids of the protein

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3
Q

what is the open reading frame

A

the entire continuous sequence of a gene that begins at a triplet start codon code and ends with a triplet stop codon code; The coding region of a gene

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4
Q

what are the three ways to read a nucleotide sequence

A

1) first reading frame: codons read from first nucleotide
2) second reading frame: codons read from second nucleotide
3) third reading frame: codons read from third nucleotides

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5
Q

what happens if a single nucleotide was added within the nucleotide sequence?

A
  • the code is misread
  • the series of codons after the added nucleotide are different from the original series; they code for different amino acids in polypeptides
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6
Q

what are frameshift mutations?

A

when one or two nucleotides are added or removed, changing the reading series and coding for new amino acids

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7
Q

what happens if three nucleotides are removed?

A
  • nothing; there is no frameshift (stays the same, no change in reading frame)
  • a triplet codon is removed, meaning a single amino acid in the polypeptide is removed and all the other amino acids are conserved
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8
Q

what happens if a codon is added in the nucleotide sequence?

A
  • one amino acid will get added to the protein
  • the reading frame of the mRNA and remainder of polypeptide sequence is conserved
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9
Q

what direction are codons written in?

A

5’ to 3’ direction

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10
Q

what is the start codon?

A

AUG –> methionine

  • signals the region where protein synthesis should begin
  • first triplet in every protein coding sequence
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11
Q

what are the 3 features of the genetic code

A

1) the genetic code has redundancy

  • this occurs because there are more unique triplets than unique amino acids

2) the genetic code is unambiguous

  • a unique codon triplet will ALWAYS code for a specific amino acid and will never code for more than one amino acid

3) the genetic code is mostly universal

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12
Q

what are the stop codons?

A
  • UAA, UAG, UGA
  • codons found at the end of the protein coding sequence and signal that the translation of mRNA into a polypeptide sequence is complete
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13
Q

what makes the non-template strand the coding strand?

A
  • RNA transcript has the same sequence as the non-template strand of DNA
  • this strand contains the same codons as the mRNA, while the non-coding/template strand contains complementary anticodons
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14
Q

what did Marshall Nirenberg & Johann Matthaei discover

A
  • used a cell-free system to decipher the first level of the code in 1961
  • they were able to determine what specific amino acids a particular RNA nucleotide template could give rise to
  • started by making a simple nucleic acid from a string of uracil; noticed that the nucleic acid produced a repeated polypeptide sequence that contained identical amino acids (phenylalanine)
  • follow up research used a string with alternating uracil and cytosines; produced a polypeptide string of altering serine and leucine
  • these results confirmed that three nucleotides make up a codon that codes for an amino acid
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15
Q

what are some examples that show that the genetic code is not 100% universal

A
  • in some ciliate, ex. paramecium, UAA and UAG are not stop codons; they code for glutamine
  • in mitochondria yeast, CUA codes for threonine but in mammalian mitochondria, CUA codes for leucine
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16
Q

what is retinoblastoma

A

disruption of the Rb protein, which then fails to serve as a cell cycle break and leads to the development of cancer on the retinas

  • treated by the delivery of chemotherapy drugs via liposomes to target areas
17
Q

what are some health conditions leaded to transcription errors

A

diabetes, alzheimer’s disease, parkinson’s disease, aging and cancer, down syndrome (some may be genetic)

18
Q

how do chemotherapy drugs work

A

they inhibit the proper functioning of enzymes (topoisomerases) needed to unwind DNA for replication and transcription

  • this stops cancer cells from dividing and growing
19
Q

what did Dr. Juliet Daniel discover

A
  • discovered and named Kaiso, which regulates the expression of genes which control cell proliferation and cell-cell adhesion (is a transcription factor)
  • Kaiso’s malfunction in tumors (breast, colon, prostrate) contributes to tumor progression and spread of cancer in humans
20
Q

what is triple negative breast cancer

A
  • most aggressive (spreads quickly)
  • no treatment/cure
  • lacks the expression of all 3 biomarkers (estrogen receptor, progesterone receptor, HER 2 receptor)
  • only possible treatment is chemo and radiation
  • African Black women are more targeted