mRNA processing Flashcards

0
Q

How is mRNA process before exiting out of the nucleus?

A
  • Addition of a cap to the 5’ end.
  • Addition of a poly-A tail to the 3’ end.
  • Cutting out of introns from mRNA.
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1
Q

What’s is 5’ to 5’ linkage?

A

Nose??????????

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2
Q

In what type of cell is mRNA

Process?

A

In eukaryotic cell, because mRNA is in the nucleus and it has to be processed before exiting the cell.
- ( it is not required in prokaryotes because mRNA is in the cytoplasm already .

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3
Q

Function of the 5’ CAP?

A
  • protection
  • binding site for CAP binding proteins
    (Cap binding protein attract ribosomes once it gets out of the nucleus)
    -
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4
Q

Steps in the addition to the CAP to the 5’ end?

A
  • Guanine is added to the absolute 5’end. Via to the 5’ to 5’ linkage.
  • That guanine and the first few nucleotide are then methylated.

Cap binding proteins then attached to it and atract ribosome once mRNA exits the nucleus.

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5
Q

Function of the poly A tail added to the 3’ end?

A
  • Protection against nucleases.
  • provide a lifespan
  • allow mRNA - ribosomal attachment.
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6
Q

What are introns?

A

Junk sequence does not code for any gene.

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7
Q

Steps in adding a pol-A tail to the 3’ end.

A

Most genes are transcribed beyond coding sequence , the extra sequence will be cut off and the poly A tail will added.

  • Poly-A polymerase detects a consensus sequence near the end of mRAN and cuts it 25 nucleotides downstream.
  • poly-A polymerase adds 50-200 adenines to the cut end.
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8
Q

Is it good to have a mRNA STABLE FOREVER.

A

No, because condition might change. You might one a gene on now but maybe not in different condition.

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9
Q

Where introns might come from?

A
  • rreoviruses
  • trtansposomes
  • mutated portions of a former exon.
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10
Q

Common propeerties of all introns ?

A

-Common in eukaryotes rare in prokaryotes
- the more complex the organism the more complex/ abundant the introns
-intron abundance and size vary per gene within species.
( some genes have no introns other have many)

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11
Q

Classification of introns?

A

Introns are classified by how they are removed.

  • group 1 and group 2 introns ( in rRNA)
  • Nuclear pre-mRNA introns
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12
Q

Group 1 and group 2 introns?

A
  • Found in rRNA & few bacteria gene
  • small
  • uses guanosine to excise itself out. ( exon then glue)
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13
Q

Nuclear pre mRNA introns?

A
  • Larger and more complex
  • Require help from splicesomes in order to be removed
  • Usually contain consensus sequence at the end that attract splicesosomes.( c.s in between intron/ exons)
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14
Q

Alternative splicing?

A

mRNA is spliced in different ways

  • 100% of introns are removed.
  • exons are differently Cut/Retained.
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15
Q

The more exons?

A

The more potential different isoforms..

16
Q

Isoforms?

A

Different protein products from the same gene caused by alternate splicing

17
Q

One gene can code for more than one protein. true or false?

A

Yes, one gene can code for more than one protein through alternate splicing.

18
Q

Advantage of isoforms/ isoforms?

A

A way of coping more information in less space.

19
Q

What happen right before mRNA is ready to exit the nucleus?

A

mRNA get scanned by the pos of the nucleus.

And will only exit with a cap, poly A tail and not introns.

20
Q

What is mRNA EXPORTER.?

A

mRNP + (nuclear) Pore Complexes.

21
Q

Function proteins called mRNP?

A

mRNP associate with processed mRNA and diret them to and through the nuclear pore.

22
Q

Example of a disease caused because introns were never cut of and never mRNA never made it out of the cell?

A

Beta hemoglobin and thalassemia .