Genetic code and Transcription (Week 3) Flashcards

1
Q

What is the Central Dogma and who coined the idea of it?

A
  • DNA to RNA to protein
  • Francis Crick coined the idea
  • viruses can preform reverse transcription
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2
Q

How do viruses use RNA?

A
  • Reverse transcribed into dsDNA
  • Moves to nucleus where it uses the host machinery for transcription
  • Host machinery for translation
  • New proteins assemble
  • New virus particles released
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3
Q

How do retroviruses use reverse transcription?

A
  • viruses have RNA genomes

- enzymes catalyze RNA genome into DNA then integrate the DNA into the host

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4
Q

What is important about coding sequences?

A
  • triplet codons can be read in various combinations
  • each codes for unique polypeptide chain (alternate splicing)
  • can have long strands of non-coding DNA
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5
Q

What is important about genetic codes?

A

-can have some different codes for same codon (degenerate)
-Non-overlapping - each nucleotide is a part of one, and only one, triplet
-Nucleotide triplet in mRNA – Codon
-Unambiguous - each codon specifies a particular amino acid and only that amino acid
Important: AUG is start, UAA, UGA and UAG are stop

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6
Q

What are the different types of mutations?

A

-Missense mutation: one nucleotide changes, changes amino acid in protein
-Nonsense mutation: one nucleotide changes, causes premature stop codon
-Silent mutation: often in last nucleotide; one nucleotide changes but amino acid is still the same
-Frameshift mutation: adding or deleting a nucleotide in the sequence; can cause missense and nonsense mutations
Mutations in long DNA segments: insertion, duplication, inversion (reverse of pairs), translocation (switch spots; “crossing over”)

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7
Q

What is important about the reading frame?

A
  • Open reading frame(ORF) - the part of areading framethat contains nostop codons.
  • read in grouplets of 3 (triplets)
  • code for amino acid or nothing (stop codon)
  • if stops before the stop codon, get incomplete protein
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8
Q

What are the main effects of frameshift mutations?

A
  • single mutant: like addition or deletion causes reading frame to shift
  • if two deletion or two addition, reading shift off; if one addition and one deletion, doesn’t effect very much (one codon wrong)
  • if three addition, cause a few to be wrong but most will be ok; same idea with three deletion
  • frame shift least effected by triplet codon
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9
Q

What experiment proved that genetic code is non-overlapping?

A
  • added codon to a DNA sequence, observed results; saw that codes didn’t overlap
  • Crick and Brenner’s frameshift mutations would not have been observed if code were overlapping
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10
Q

Describe the transcription of mRNA to DNA

A

2 strands:Template strand and Non-template strand (coding strand)
-Utilizes the same base pairing rules as DNA replication, except uracil (U) in place of thymine
-Since mRNA molecules are synthesized in the
5’ 3’ direction (like DNA), 64 codons are also written in 5’ 3’ direction
-involves four stages; Binding, Initiation, Elongation and Termination

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11
Q

What is important factor in bacteria transcription?

A
  • A large protein – a and b subunits and sigma factor

- Sigma factor promotes binding of RNA polymerase to specific DNA sequences called promoters

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12
Q

How does initiation of RNA synthesis begin?

A
  • Initiation of RNA synthesis takes place once the DNA is unwound
  • One of the DNA strands serves as a template for RNA synthesis, using incoming NTPs (nucleotide triphosphates) that are complementary to the template strand
  • RNA polymerase catalyzes the formation of a phosphodiester bond between the NTPs
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13
Q

How does transcription occur in bacteria?

A
-RNA polymerase binds to promoter
sigma (σ) factor
-Initiation of synthesis
-Elongation of RNA
T-ermination of synthesis; termination signal - Use of GC loop or ‘rho factor’
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14
Q

What is the promoter sequence in bacteria?

A
  • Six-nucleotide sequence at -10 (TATAAT) – called ‘-10 sequence’ or ‘pribnow box’
  • Six nucleotide sequence at -35 (TTGACA) – called ‘-35 sequence’
  • must see this before AUG start codon
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15
Q

What can be noted about Termination of Transcription in Bacterial Genes?

A

-the Hairpin loop filled with GC

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16
Q

How does transcription occur in Eukaryotic cells?

A
  • More complicated
  • 3 different RNA polymerases
  • Promoters are more varied
  • Require transcription factors
  • Protein-protein interactions play a prominent role
  • Extensive RNA processing
17
Q

What are the 3 types of RNA polymerases? How sensitive are they to a-aminitin?

A

1 is for pre-rRNA; resistant to a-amanitin; found in nucleolus
2 is for pre-mRNA ; very sensitive to a-amanitin; found in nucleoplasm
3 is for pre-tRNA; moderately sensitive to a-amanitin; found in nucleoplasm
-a-aminitin – a deadly toxin produced by the mushroom, Amanita phalloides an inhibitor of RNA polymerase

18
Q

What are snRNA?

A
  • Also known as U-RNA - a class of small RNA molecules that are found within the nucleus ofeukaryoticcells.
  • Primary function - processing of pre-mRNA in the nucleus
  • Also aid in regulation oftranscription factors and maintaining thetelomeres
  • snRNA help to regulate telomeres
19
Q

What is micro RNA?

A
  • A microRNA (abbreviated miRNA) is a small non-coding RNA molecule (containing about 22 nucleotides) found in plants, animals and some viruses, that functions in RNA silencing and post-transcriptional regulation of gene expression.
  • Functions in transcriptional and post-transcriptionalregulation of gene expression
20
Q

Explain transcription in prokayrotes

A

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21
Q

Explain transcription in eukaryotes; RNA poly 1

A
  • Consists of core promoter and upstream control element
  • RNA polymerase binds to the core promoter
  • Upstream control elements- improve promoter’s efficiency
22
Q

Explain transcription in eukaryotes; RNA poly 2

A

-need TFs; RNA poly 2 doesn’t bind to promoter on its owns; TFs guide to promoter
promoter for RNA 2: 4 sequences involved; Short initiator (Inr) sequence- surrounding startpoint
TATA box, followed by 2 or 3 more ‘A’s, located ca. 25 nt upstream of start point
The TFIB recognition element (BRE) located slightly upstream of the TATA box (
The Downstream Promoter Element (DPE) located ca. 30 nt downstream from the start point

23
Q

Explain transcription in eukaryotes; RNA poly 3

A
  • Entirely downstream of the startpoint - for transcribing tRNA and 5S-rRNA
  • A third type of RNA polymerase III promoter, an upstream promoter is used for transcribing small RNA molecules
24
Q

What are some Upstream Control Elements?

A

-Some upstream control elements – common to many different genes
-CAAT box (GCCCAATCT consensus sequence, most frequent residues, in animals and yeast)
GC box (GGGCGG consensus sequence)
-The location of upstream control elements varies from gene to gene
-Those within 100–200 nucleotides of the startpoint are called proximal control elements
-Those farther away are called enhancer elements