4 - Gene organisation and transcription II Flashcards

1
Q

What are the names for the initial RNA produced from a gene?

A

primary transcript
Pre-mRNA
heterogenous nuclear RNA (hnRNA)

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2
Q

Where does RNA processing occur and where does the DNA travel to after this?

A

occurs in the nucleus, and the fully processed RNA is exported to the cell cytoplasm to be translated

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3
Q

Describe the anatomy of a gene

A
  • the gene promoter lies at the 5’ end
  • exons contain the sequences that form part of the final mRNA
  • introns are transcribed but edited out of the final mRNA
  • sequence information is coded discontinuously in DNA
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4
Q

What is the splice donor site?

A

the junction between an exon and an intron

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5
Q

What is the splice acceptor site?

A

the junction between an intron and an exon

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6
Q

What do exons usually end with?

A

AG

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7
Q

What do introns start and end with?

A

start with GU

end with AG

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8
Q

RNA processing uses which type of proteins?

A

small Ribonuclear Proteins (snRNPs)

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9
Q

What end of the mRNA is the cap added to?

A

5’ end

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10
Q

How is the cap formed?

A
  • the hydrolysis of terminal phosphates of mRNA to a diphosphate
  • this reacts with α phosphate of GTP
  • methylation at the N7 position in the purine ring to form 7-methylguanylate cap
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11
Q

What is the role of the cap?

A

to protect the mRNA at the 5’ end and enhance the translation of the mRNA

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12
Q

What virus interferes with the recognition of the cap?

A

Polio Myelitis

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13
Q

How and where is the Poly A tail formed?

A

it is added one base at a time

added 11-30 bases downstream of the sequence AAUAAA

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14
Q

What is thalassemia?

What is β-thalassemia?

A

an inherited disorder where there is an imbalance in the relative amounts of α and β chains making up haemoglobin

β-thalassemia is when there is a relative deficiency of β-chains

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15
Q

What causes β-thalassemia?

A

several types of β-thalassemia feature SPLICE SITE MUTATIONS IN β-GLOBIN GENE

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