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Protein Synthesis
How does the information coded in DNA affect a cell?
DNA directs protein synthesis
The sequence of nitrogen bases contains the coded information
in DNA and is translated into the amino acid sequence of a protein according to
a set of rules called the genetic code. The DNA nucleotides are read in
sequence, in groups of three called a triplet. Each triplet specifies 1 amino
acid. The sequence of nucleotides that codes for a specific polypeptide is
called a gene. Each gene also contains regulator sequences such as
promoter and repressor areas or those that indicate "start" and "stop"
ends.
Transcription Process:
In eukaryotes
- DNA is transcribed into mRNA, process occurs in the
nucleus
- Need precursor nucleotides (A, G, C, U) & RNA
polymerase
- A portion of DNA (gene) separates & 1 DNA strand acts as
a template to form mRNA
- RNA polymerase attaches to DNA promoter site and binds free
nucleotides to complementary nitrogen bases and links nucleotides together to
form mRNA. Multiple copies can be made. 3-base mRNA is called a
codon
- Single strand mRNA is released & double-stranded DNA
reforms (conservative process)
- RNA processing occurs in the nucleus. mRNA contains
introns that are noncoding and exons that code for protein. Introns are
cut out and exons are spliced together
There are three types of RNA involved in protein synthesis:
- mRNA
-
- single strand
- produced in nucleus & travels into cytoplasm
- half-life of minutes to hours
- rRNA
-
- combined with protein forms two subunits of the
ribosome
- ribosomes act as nonspecific mechanisms for assembling
amino acids into proper sequence
- ribosomes are found attached to RER or in groups in the
cytoplasm
- tRNA
-
- short molecule with clover shape that transports amino
acids
- stalk attaches to a specific amino acid
- on upper loop is an anticodon complementary to a mRNA
codon & able to bind to it
Translation Process
- Codons of mRNA are translated into amino acid sequences
(polypeptide) in the cytoplasm
- mRNA attaches to the light subunit of ribosome & is read
sequentially from "start" codon (AUG) to "stop" (3') codon, generally
nonoverlapping, occurs in about 20 sec
- A complementary tRNA binds to 1st codon and heavy
ribosomal subunit attaches
- A complementary tRNA binds with 2nd codon,
enzymes of the heavy subunit detach amino acid from 1st tRNA and
attach it to 2nd amino acid
- Ribosome moves along one codon on mRNA, process repeats
until reaching the “stop” codon
- Ribosomal subunits detach from the mRNA, polypeptide is
released into ER or cytoplasm
- mRNA can be read multiple times or by multiple
ribosomes
Effects of mutations on protein synthesis:
- Point mutation
- 1 base change codes for wrong amino acid {ex. sickle cell
anemia}
- Frame-shift mutation
- insert or delete 1 base, whole sequence is read out of phase
Despite thousands of changes per cell per day, only a few
mutations accumulate in a cell each year because DNA repair mechanisms (based
on double-stranded characteristic of DNA) fix most changes |