Gene Organisation and Transcription II Flashcards

1
Q

What are the three terms for the RNA directly produced from transcription?

A

Primary transcript or Pre-mRNA or heterogenous nuclear RNA (hn RNA)

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2
Q

Where does RNA processing take place?

A

In the nucleus

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3
Q

What is the splice donor site?

A

Junction between exon and intron

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4
Q

What is the splice acceptor site?

A

Junction between intron and exon

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5
Q

What do exons end with?

A

AF

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6
Q

What do introns start and end with?

A

GU and AG

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7
Q

What are snRNP and what process involves them?

A

Small ribonuclear proteins and RNA splicing

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8
Q

Describe the process of splicing

A

snRNP U1 binds to splice donor sequence. 2. snRNP U2, U4, U5 and U6 bind then, forming the spliceosome. This formation cleaves the splice donor sequence. 3. The end G of the intron bends round and an ‘A residue’ in the intron acts as a branchpoint/2’ -OH and bonds in an intermediate step in splicing. 4. 2’ OH bonds/branchpoint forms between G and A residue. The phosphodiester bond beween end G of intron and the exon breaks so intron is removed as LARIAT structure. Adjacent exons are ligated together.

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9
Q

What two additional modifications do mRNA undergo, not including splicing?

A

PolyA tail addition and cap addition.

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10
Q

How is the mRNA cap formed?

A

By hydrolysis of terminal triphosphate of mRNA to a diphosphate. This then reacts with alpha phosphate of GTP to form 5’-5’phosphate linkage. Cap is further modified by Methylation at the N7 position in the purine ring to form 7-Methylguanylate cap.

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11
Q

What is the purpose of the mRNA cap?

A

To protect mRNA at the 5’ end and also greatly enhance translation

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12
Q

Where is the polyA tail added?

A

11-30 bases downstream of AAUAAA (polyadenylation site)

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13
Q

What is the purpose of the poly A tail?

A

Add stability

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14
Q

What can cause beta-thalassemia?

A

Splice site mutations in the beta globe gene

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