Lec 2.2 Control of gene expression 2 Flashcards

1
Q

What keeps mRNAs around and confers stability?

A

poly A tail

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2
Q

What acts a timer to degrade the mRNA?

A

shortening of the poly A tail

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3
Q

What does the 5’Cap do?

A

Protects the mRNA from degradation.

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4
Q

What are the two pathways when the poly-a tail is greatly shortened?

A
  1. 5’ cap is destroyed and thus degradation of the mRNA from 5’ end. 2. degradation from the 3’ end through the poly A tail
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5
Q

What does Ferritin mRNA do?

A

Makes protein to store iron

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6
Q

What does tfR (Transferrin-Receptor) mRNA do?

A

Brings iron into cell

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7
Q

Where is excess iron mainly stored?

A

liver lungs pancreas

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8
Q

What does the cell do during iron starvation?

A

Dont need iron. Decrease Ferritin mRNA, Increase TfR (transferrin receptor) mRNA

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9
Q

what does the cell do during iron excess?

A

Store excess iron. Increase Ferritin mRNA. Decrease TfR (transferrin receptor) mRNA

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10
Q

What are IREs and IRP used for?

A

Used in a system to control TfR mRNA and Ferritin mRNA

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11
Q

What are IREs?

A

Iron Responsive Elements. Recognition sizte on mRNA for binding

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12
Q

What is IRP?

A

Iron responsive regulatory protein. Proteins that bind to mRNA.

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13
Q

What happens if IRP binds to IRE at 5’ ferritin mRNA?

A

No Ferritin.

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14
Q

What happens if IRP binds to IRE at 3’ TfR mRNA?

A

TfR made

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15
Q

What happens if IRP DOESNT bind to IRE at 5’ ferritin mRNA?

A

Ferritin made.

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16
Q

What happens if IRP DOESNT bind to IRE at 3’ TfR mRNA?

A

No transferrin

17
Q

What happens during cell iron starvation?

A

Need more iron, IRP binds to Ferritin (no Ferritin made). IRP binds to TfR (TfR made).

18
Q

What happens during Iron excess in the cell?

A

Need to store. IRP binds to Iron (Ferritin made). No TfR made.

19
Q

What do miRNAs do?

A

Silence expression of specific mRNA targets.

20
Q

Elevated levels of miRNAs suggest what?

A

Cardio disease, stroke, can identify cancers

21
Q

Are changes in miRNA expression causative of disease or responsive?

A

Both

22
Q

What are the 8 ways proteins are regulated by post translational processing and modifications?

A
  1. Post translational modifications. 2. Must fold to 3-d conformations. 3. Molecular chaperones. 4. Bind co-factors.5. Modified by protein Kinases. 6. Glycosylated. 7. Bind to other protein subunits or protein partners. 8. Modifying enzymes act on protein
23
Q

What are molecular chaperones? What do they do?

A

Are heat shock proteins (Hsp). These proteins get activated to fold proteins back to what they were before they were heat shocked

24
Q

What is a proteasome?

A

Degrades misfolded proteins

25
Q

What is the structure of a proteasome?

A

Hollow chamber where proteins are degraded

26
Q

What tells the proteasome what to destroy?

A

Ubiquitin

27
Q

Genomic imprinting is based on what?

A

DNA methylation

28
Q

What is genomic imprinting?

A

Differential expression of genetic material depending on the parent of origin.

29
Q

What is an example of GI?

A

Epigentics

30
Q

What is epigenetics?

A

Regulation of expression of gene activity without altering gene structure.

31
Q

What is an example of a GI disease?

A

PWS. Paternal deletion is lack of gene expression due to GI

32
Q

What is PWS?

A

Inherits gene deletion from father. No gene expression from mother side.

33
Q

What are some symptoms of PWS?

A

Hyperphagia (uncontrollable eating). short stature.

34
Q

What is x chromosome inactivation?

A

How humans deal with extra X’s. So equal number of Xs in both females and males. It is random.

35
Q

Describe the RNA control of Ferritin mRNA and TfR mRNA under iron excess.

A

Need to store. IRP binds to Iron (Ferritin made). No TfR made.

36
Q

Describe genomic imprinting and how it can lead to a disease state.

A

Differential expression of genetic material depending on the parent of origin. Could cause lack of gene expression.