Molecular medicine Flashcards

1
Q

Outline transcription?

A

1) Topoisomerase unwinds DNA supercoils
2) DNA helicase breaks H+ bonds and exposes the nucleotides
3) Single stranded binding proteins stop DNA strands reannealing
4) RNA polymerase binds at TATA promoter region
5) Read 3’ to 5’ direction , form 5’ to 3’
6) Adds one ribonucleotide at a time until stop codon is reached (UAA/UAG/UGA)
7) mRNA strand produced with a poly-A tail and 5’ cap

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2
Q

What is start codon?

A

AUG methionine

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3
Q

State stop codon?

A

UAA
UAG
UGA

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4
Q

Function:
topoisomerase
DNA helicase
SSB
RNA polymerase

A

topoisomerase- unwind DNA supercoil
DNA helicase- break H bond expose nucleotides
SSB- prevent DNA strands reannealing
RNA polymerase- add ribonucleotide

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5
Q

Which direction does RNA polymerase read, form?

A

read- 3’-5’
form- 5’ to 3’

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6
Q

What are introns?

A

Non-coding

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7
Q

Explain splicing?

A

1) Removal of introns (non-coding segments) to form fully coding strand
2) Carried out in nucleus by slicosomes
3) Exons spliced back together
4) Mature mRNA leaves nucleus via nuclear pores

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8
Q

Where does splicing occur? By what?

A

Nucleus- slicosomes

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9
Q

How does mature mRNA leave nucleus?

A

Nuclear pores

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10
Q

Explain translation?

A

1) mRNA binds to ribosome which has small and large subunits
2) tRNA carries anticodons
3) tRNA binds to ribosome
4) mRNA moves in a 3’ to 5’ direction and the anticodon binds to mRNA
5) As each amino acid bound- mRNA shifts along ribosome
6) Termination codon- ribosome detaches and mRNA is broken down in the cytosol

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11
Q

What comes first transcription or translation?

A

Transcription- 1st stage
Translation- 2nd stage

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12
Q

What are 3 main types RNA?

A

messenger RNA (mRNA)
transfer RNA (tRNA)
ribosomal RNA (rRNA)

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13
Q

What are 3 stop codons?

A

1) UAA
2) UAG
3) UGA

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14
Q

Define single nucleotide polymorphism? (SNP)
Example?

A

Single nucleotide differs

Sickle cell
CF

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15
Q

What subunits in haemoglobin?

A

2 alpha and 2 beta

Normal adult- HbA
Sickle cell- HbS

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16
Q

What is SNP in sickle cell?

A

GAG to GTG- 17th nucleotide

17
Q

Is sickle cell autosomal recessive or dominant?
Both parents- chance?
SNP?

A

Autosomal recessive
1 in 4, 50% carrier
GAG to GTG in 17th nucleotide

18
Q

What functional change in sickle cell?

A

1) Cells don’t live as long
2) Lower affinity for oxygen
3) Stuck in blood vessels
Reduced delivery of O2 to muscles

19
Q

State diff protein structure?

A

1o - linear chain of amino acids- covalent bonds
2o = alpha helix, beta pleated sheets- H+ bonds
3o = 3D structure of a single chain of amino acids
VdW, H+ bonds, Electrostatic, Ionic, Disulphide bridges
4o = overall 3D structure of a polypeptide- interaction chains