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Transcription and
Translation
From DNA to RNA to protein
Overview
• Genes in DNA contain
information to make
proteins.
• The cell makes mRNA
copies of genes that are
needed.
• The mRNA is read at the
ribosomes in the rough
ER.
• Protein is produced.
Key Players
• mRNA carries the
information from a gene
in DNA.
• Ribosomes, made of
rRNA, consist of
subunits and carry out
an enzyme-like role.
• tRNA carries specific
amino acids to the
ribosome.
Transcription
1. DNA unzipped by helicase.
2. RNA polymerase transcribe DNA into mRNA by
complementary base pairing
Transcription
RNA polymerase matches bases in the sense strand with
RNA bases, building a strand of mRNA that carries the
information encoded in the DNA.
Transcription
Encoded in DNA is a signal telling RNA polymerase where
to stop. Transcription ends at that point.
Transcription
The completed mRNA molecule then moves from the
nucleus to the rough ER for translation.
Translation
• On the ribosome,
specific tRNA will bring
in specific amino acid
towards the mRNA by
complementary base
pairing
Translation
• The ribosomal unit binds
to mRNA where the
code for met is located
(AUG). The anticodon
(UAC) of the tRNA
matches the “start”
codon on mRNA (AUG).
Translation
• Another tRNA carrying
different amino acid will
come in, as the
ribosome reads through
the mRNA sequence
Translation
• Ribosome will catalyze
the formation of peptide
bonds between the
adjacent amino acids
Translation
• A catalytic site on the
larger subunit binds the
two amino acids
together using
dehydration synthesis,
forming a peptide bond
between them.
Translation
• The first tRNA now
detaches and goes of to
find another met in the
cytoplasm. The mRNA
chain shifts over one
codon, placing the
second codon (CAU)
over the second active
site.
Translation
• A tRNA with an
anticodon (GUA)
matching the exposed
codon (CAU) moves
onto the ribosome. This
tRNA carries histidine
(his).
Translation
• A new peptide bond
forms between val and
his on the catalytic site.
The tRNA that carried
val will detach and find
another val in the
cytoplasm. The mRNA
strand will then shift over
one more codon.
Translation
• The process continues
until the ribosome finds
a “stop” codon. The
subunits detach from
one another, the mRNA
is released, and the
polypeptide chain moves
down the ER for further
processing. The initial
met is removed and the
chain is folded into its
final shape.
Summary
Transcription Animation
• http://learn.genetics.utah.edu/units/basics/tra
nscribe/
Mutations
• Any mistakes in the DNA code can result
in a “broken” (non-functional) protein.
• A mutation affecting only a few somatic
cells (body cells) might not have any
effect, unless the mutation turns the cell
cancerous.
• A mutation affecting a sex cell can be
passed on to the offspring.
Types of Mutations
• Point mutation: base substitution that may
or may not code for a different amino acid.
• Insertion mutation: one or more bases is
inserted into the DNA strand.
• Deletion: one or more bases is deleted
from the DNA strand.
Effects of mutations
• Original: THE FAT CAT SAT
• Point mutation: THA FAT CAT SAT
• Insertion: THE FTT ATC ATS AT
• Deletion: THE FTC ATS AT
Hemoglobin mutations
DNA mRNA Amino Acid
Properties of
AA
Effect on protein Disease
Original
codon 6
CTC GAG Glutamic Acid Hydrophilic Normal None
Mutation 1 CTT GAA Glutamic Acid Hydrophilic Neutral None
Mutation 2 GTC CAG Glutamine Hydrophilic Neutral None
Mutation 3 CAC GUG Valine Hydrophobic
Loses water
solubility
Sickle Cell
Anemia

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transcription-translation.ppt

  • 2. Overview • Genes in DNA contain information to make proteins. • The cell makes mRNA copies of genes that are needed. • The mRNA is read at the ribosomes in the rough ER. • Protein is produced.
  • 3. Key Players • mRNA carries the information from a gene in DNA. • Ribosomes, made of rRNA, consist of subunits and carry out an enzyme-like role. • tRNA carries specific amino acids to the ribosome.
  • 4. Transcription 1. DNA unzipped by helicase. 2. RNA polymerase transcribe DNA into mRNA by complementary base pairing
  • 5. Transcription RNA polymerase matches bases in the sense strand with RNA bases, building a strand of mRNA that carries the information encoded in the DNA.
  • 6. Transcription Encoded in DNA is a signal telling RNA polymerase where to stop. Transcription ends at that point.
  • 7. Transcription The completed mRNA molecule then moves from the nucleus to the rough ER for translation.
  • 8. Translation • On the ribosome, specific tRNA will bring in specific amino acid towards the mRNA by complementary base pairing
  • 9. Translation • The ribosomal unit binds to mRNA where the code for met is located (AUG). The anticodon (UAC) of the tRNA matches the “start” codon on mRNA (AUG).
  • 10. Translation • Another tRNA carrying different amino acid will come in, as the ribosome reads through the mRNA sequence
  • 11. Translation • Ribosome will catalyze the formation of peptide bonds between the adjacent amino acids
  • 12. Translation • A catalytic site on the larger subunit binds the two amino acids together using dehydration synthesis, forming a peptide bond between them.
  • 13. Translation • The first tRNA now detaches and goes of to find another met in the cytoplasm. The mRNA chain shifts over one codon, placing the second codon (CAU) over the second active site.
  • 14. Translation • A tRNA with an anticodon (GUA) matching the exposed codon (CAU) moves onto the ribosome. This tRNA carries histidine (his).
  • 15. Translation • A new peptide bond forms between val and his on the catalytic site. The tRNA that carried val will detach and find another val in the cytoplasm. The mRNA strand will then shift over one more codon.
  • 16. Translation • The process continues until the ribosome finds a “stop” codon. The subunits detach from one another, the mRNA is released, and the polypeptide chain moves down the ER for further processing. The initial met is removed and the chain is folded into its final shape.
  • 19. Mutations • Any mistakes in the DNA code can result in a “broken” (non-functional) protein. • A mutation affecting only a few somatic cells (body cells) might not have any effect, unless the mutation turns the cell cancerous. • A mutation affecting a sex cell can be passed on to the offspring.
  • 20. Types of Mutations • Point mutation: base substitution that may or may not code for a different amino acid. • Insertion mutation: one or more bases is inserted into the DNA strand. • Deletion: one or more bases is deleted from the DNA strand.
  • 21. Effects of mutations • Original: THE FAT CAT SAT • Point mutation: THA FAT CAT SAT • Insertion: THE FTT ATC ATS AT • Deletion: THE FTC ATS AT
  • 22. Hemoglobin mutations DNA mRNA Amino Acid Properties of AA Effect on protein Disease Original codon 6 CTC GAG Glutamic Acid Hydrophilic Normal None Mutation 1 CTT GAA Glutamic Acid Hydrophilic Neutral None Mutation 2 GTC CAG Glutamine Hydrophilic Neutral None Mutation 3 CAC GUG Valine Hydrophobic Loses water solubility Sickle Cell Anemia