CH7 RNA and the Genetic Code Flashcards

1
Q
  • mRNA (polymerase 2) (what is hnRNA)
  • tRNA (Polymerase 3
  • rRNA (Polymerase 1 and 3 )
A
  • mRNA: Transcribed from template DNA by RNA polymerase enzymes. Takes info to ribosomes to make proteins. hnRNA is mRNA before it is spliced
  • tRNA: Folded RNA strand with a 3 nucleotide anti-codon and with amino acid attacched
  • rRNA: Synthesized in the nucleolus. Some function as ribozymes and help catalyze the formation of peptide bonds
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2
Q

Degeneracy and wobble

Point mutations

  1. Missense mutation:
  2. Nonsense mutation:

Frameshift mutations

1.

A

1 AA can by specified by multple codons, the first 2 bases are usually the same.

3rd one is variale = in wobble postion and if affected it will be a silent/degenerate mutation. bc it will still code for that AA

i.e glycine is coded by GG and third can be A, C, G, or U

Point mutations

  1. Missense mutation: Substitution of a codon which cause substitution of AA
  2. Nonsense mutation: It changes that codon to a stop codon = stops prematurely also called truncation mutation

Frameshift mutaiton: Nucleotides are added or deleted

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3
Q

Splicing: Introns and exons

Alternative Splicing

5’ Cap

3’ Tail

A

Spliceosome splices the hnRNA and removes the introns and ligates the exons together

Alternative Splicing: Allows for the making of many different proteins from the same gene

At the 5’ end a triphosphate cap is added to be recognized for the ribosome as the binding site

At the 3’ a polyadenosyl tail is added to protect from rapid degradation in the cytoplasm

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4
Q

Translation:

Need energy? peptidyl transferase

  1. Initiation
  2. Elongation
  3. Termination
A

All stages require energy

peptidyl transferase: catalyzes peptide bond formation b/w incoming amino acid to A site with the growing amino chain on the P site

  1. Initiation
  2. Elongation
  3. Termination
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5
Q

Posttranslational processing

  1. Phosphorylation
  2. Carboxylation
  3. Glycosylation
  4. Prenylation
A
  1. Phosphorylation: Adding phosphate group (PO4-2) to activate or deactivate proteins
  2. Carboxylation: Adding carboxylic acid, usually to serve as calcium biding sites
  3. Glycosylation: Addition of oligosaccharides in the ER and Golgi apparatus to determine cellular destination
  4. Prenylation
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6
Q

Prokaryotic gene regulation:

what is the promotor and operator

The Lac operon (positive control)

Trp operon (negative control)

A

Promotor = Where RNA polymerase binds

Operator = the door that allows RNA polymerase to move. It can be locked by the repressor

The Lac operon: no lactose = repressor on, lactose binds and allows RNA polymerase to transcribe mRNA

Trp: Trp presents = repressor on

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7
Q
  • Eukaryotic Gene Regulation
  • Enhancers and transcription factors
  • Histone Acetylation and Deacetylases
  • DNA Methylation
  • Heterochromatin vs Euchromatin regions
A
  • Prior to the promotor, there are enhancers in the DNA where transcription factors can bind. They enhance the activity of RNA polymerase at a single promotor site
  • DNA bends and allows RNA polymerase to start transcription
  • Histone Acetylation: Decreases + charge of lysine residues and weakens the interaction of the histone with DNA. Deacetylases remove acetyl groups and close the chromatin to reduce transcription
  • DNA Methylation: Adds methyl groups to cytosine and adenine to silence the gene expression
  • Heterochromatin: Tightly coiled DNA appears dark under microscope usually inactive genes that are highly methylated
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8
Q
A
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