Lecture Oct 23, 2024, (end L.7, start L.8) Flashcards

1
Q

What is alternative splicing?

A

Splicing is done at different poitns, depending on the required cell

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2
Q

What are the 100% conserved sequences on an intron

A

Start= 5’ GU
Branch point= A
End= AG 3’

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3
Q

How does splicing occur?

A

U1 binds to start of intron,
U2 binds to end of intron
U4/U6 and U5 bind together at branch point

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4
Q

What is actin?

A

protein for muscle cells

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5
Q

What does the Poly-A tail do?

A

The final maturation step for pre-mRNA

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6
Q

What signal is used to tell the enzyme where to cut?

A
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7
Q

What does the poly-A binding protein do?

A
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8
Q

How does the RNA know when to terminate?

A

It doesn’t?

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9
Q

Where does the export RNA leave to go to the cutoplasm

A

nuclear pore complex

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10
Q

What does acellular mean?

A
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11
Q

Lecture #8

A
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12
Q

Why are 3 nucleiotides used for 1 a.a?

A

Because we need to be able to code 20 a.a (why?), and that allows us to do that

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13
Q

Feautures of genetic code

A
  • no commas
  • no overlap
  • degenrate
  • universal
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14
Q

What does ATG code for?

A

methionine

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15
Q

What is a codon?

A

One unit of the
nucleotide triplet which
specifies an amino acid

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16
Q

What do the stop codons code for?

A

none

17
Q

Names for the 3 kinds of stop codns

A

amber

18
Q

Do all stop codons stop the translation?

A

No, only if they’re within frame

19
Q

What does ORF stand for? What is it?

A

Open reading frame. Includes both START and STOP codon within frame

20
Q

How many different reading frames can a strand have?

A

6

21
Q

What is genetic code degeneracy

A

When one amino acid has multiple nucleiotide codes

22
Q

Stop codons

A

TAG, TGA, TAA (all start with a T, switch the G and A, and double A)

23
Q

What are the color names for the stop codons?

A

TAG (amber), TGA (ochre), TAA (opal)

24
Q

How many reading frames are there? How many open reading frames are there

A

6 different reading frames on a dsDNA, but always only 1 open reading frame

25
Q

What direction is DNA read?

A

5’ to 3’ ALWAYS

26
Q

What mutation causes sickle cell anemia?

A

A point mutation on the β-hemoglobin primary sequence. 6th codon, GAA to GUA

27
Q

What amino acid change causes sickle cell anemia?

A

Glutamic acid (neg charge and polar) to valine(non-polar)

28
Q

Point mutations at ____ codon
position typically makes a larger
change

A

1st