RNA Synthesis And The Genetic Code Flashcards

1
Q

What is the purpose of transcription?

A

Retrieval of information for synthesis of the cells proteins in the form of messenger RNA (mRNA)

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2
Q

What are the classes of RNA?

A
Transfer RNA (tRNA)-carrier for Amina acids
Ribosomal RNA (rRNA)-major component of the protein synthesizing machinery
Messenger RNA (mRNA)- carries information encoded in the DNA to the cytoplasm for translation into proteins
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3
Q

What is the sequence in transcription?

A

Transcription has a start site on the DNA
There are a few consensus sequences:
-10 region-Tata box
-35 region
Consensus sequences at -10 and -35 form the promoter
RNA polymerase binds to region near the promoter
Helicase unwinds the DNA

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4
Q

What are the characteristics of termination?

A

Rho independent terminators-hairpin loops

Rho dependent-Rho binds to 5 prime end of messages, ribosomes stall and termination occurs

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5
Q

What is the location and product of RNA polymerase?

A

RNA polymerase I in nucleolus -product ribosomes; RNA
RNA polymerase II in nucleoplasm- hnRNA (precursor of mRNA)
RNA polymerase III in nucleoplasm- small RNA

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6
Q

What is the structure of the promoter?

A

TATA box-directs RNA polymerase to correct start site
CAAT box-controls frequency of transcription initiation
Enhancer/silencer elements-can be located either upstream or downstream

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7
Q

What is the difference in MRNA between prokaryotes and eukaryotes?

A
In prokaryotes:
MRNA is polycistronic message
No introns
Message short lived and immediately translated
In eukaryotes:
mRNA is monocistronic
Possess introns and exons
mRNA must be processed 
Long lived
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8
Q

What are the modifications of mRNAs?

A

Caps-consisting of methylated guanine and methylated ribose at the 5 prime end of the molecule.
Function in protecting 5 prime from attack by Rnase, permit binding of mRNA to the 40S ribosomal subunit
PolyA tails-Prevents early degradation of message.
messenger RNBAs which code for histones don’t contain polyA

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9
Q

What are introns and exons?

A

Exons: coding sequences
Introns: non coding sequences removed when mRNA processed

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10
Q

What is splicing?

A

Removal of introns
GU rich found in 5 prime end where intron meet 5 prime exon
AG site where 3 prime end of intron meets 3 prime of exon
Adenosine is part of the branch site located 40 nucleotides upstream from 3 prime splice site
Intron removed by 2 transesterification reactions: between 5 prime splice site and branch site, between 5 prime exon and 3 prime splice site.

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11
Q

What is a spliceosome?

A

Large protein plus RNA complex which catalyzed slicing out of the intron

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12
Q

What is a snurp?

A

Complex associated with a particular small RNA molecule
Protein portion has at least 7 proteins
Hydrogen bonding between small RNas and sequences near intron splice sites are required for proper splicing

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13
Q

What is the genetic code?

A

Sequence of 3 nucleotide coding for amino acids
64 possible codes: 61 for amino acids, 3 termination scodons (UAA, UGA, UAG)
Initiation codon and methionine similar=AUG

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14
Q

What are the characteristics of the genetic code/

A

Degenerate-more than one code for most AA
Degeneracy is not uniform
Wobble-3rd position AA less specific than first 2
Code almost universal except mitochondria and chloroplasts

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15
Q

What are the mutations of the genetic code?

A

Transitions-purine is replaced by another purine (A->G, T–>C)
Transversions-Purine is replaced by pyrimidine or vice versa (T–>A or G, or G–>T or C)
Transitions and transversions also known as point mutations

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16
Q

What are the consequences of point mutations?

A

Silent mutations-Change in codon but no change in AA no effects is seen
Missense mutations-inactive or partially active protein (sickle cell anemia)
Nonsense mutation- Results in synthesis of nonfunctional protein, introduction of an early stop codon

17
Q

What are the types of frame shift mutations?

A

Insertions-new base pair inserted into the DNA

Deletions-Base pair removed from the DNA