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Translation Packet #11 Chapter #8
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Introduction Translation
The actual process of protein synthesis where the mRNA, made during transcription, is utilized along with ribosomes.
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RNA Utilized During Translation
Review, And Types, of RNA
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Types of RNA Continued…
tRNA Transfer RNA Transports amino acid molecules to the ribosome Class of small RNA molecules that bear/carry specific amino acids to the ribsome during translation What are the building blocks of proteins? Amino Acids The amino acids will be used to create a protein chain rRNA Ribosomal RNA RNA found within the ribosomes used during translation. Two sizes 30S Large ribosome (subunit) 15S Small ribosome (subunit) Types of RNA mRNA snRNA tRNA rRNA
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Types of RNA Continued…
mRNA Messenger RNA An RNA molecule transcribed from the DNA of a gene Proteins are translated from mRNA by the help of RIBOSOMES Carries the GENETIC CODE, from DNA, used to create proteins Types of RNA mRNA snRNA tRNA rRNA
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The Ribosomes
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Ribosomes Ribosome The large subunit has three sites
Acts as the site of protein synthesis in the cell There are two sized ribosomes used during translation Large 30S Small 15S The large subunit has three sites Attachment Site (A site) Polypeptide Site (P site) Exit Site (E site)
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mRNA & The Genetic Code
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Introduction mRNA carries the genetic code in the form of codons.
A codon is a group of three nucleotides that provide information necessary for a single, specific amino acid.
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List of Codons & Amino Acids
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tRNA and the Genetic Code
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The Role of tRNA Recall that the role of tRNA is carry individual amino acids to the location where the polypeptide chain is growing. Hence, it must have something to match the codon found on the mRNA. This is called the anticodon A nucleotide triplet, found on tRNA, that aligns with a particular codon in the mRNA. However, it MUST be noted that the codon is the one that indicates what the amino acid will be.
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Steps of Translation
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Peptide Bond Formation
Introduction There are five basic steps during the process of translation. Initiation Peptide Bond formation Elongation Translocation Termination Initiation Peptide Bond Formation Elongation Translocation Termination
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Initiation Ribosome binds to the mRNA
Small subunit binds to mRNA Initiator tRNA binds at start codon Start codon = AUG tRNA carries anti-codon UAC Initiator tRNA carries amino acid MET Ribosome binds to mRNA Large subunit binds to mRNA Initiator tRNA will be located at the P site of large subunit
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Peptide Bond Formation
Ribosome (rRNA) catalyzes the formation of a peptide bond between the new amino acid and the carboxyl end of the growing polypeptide
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Elongation Elongation occurs when the incoming amino acid binds to the polypeptide chain through the formation of a peptide bond.
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Translocation The ribosomes move allowing the tRNA’s to switch sites
tRNA in the A (addition) site is translocated to the P (polypeptide) site tRNA in the E (exit site) leaves the ribsome mRNA shifts position New tRNA with anticodon enters the A site
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Termination Release factor (a protein) binds at stop codon
There are THREE stop codons UUA UGA UAG Polypeptide chain released from tRNA tRNA released from P site Ribosomes released from mRNA.
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Special Note As the polypeptide chain is being completed, attaches and enters into another organelle known as the endoplasmic reticulum. Hence creating what is known as the rough endoplasmic reticulum.
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The Danger of Mutations
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Introduction Mutations occur when a nucleotide base, or nucleotide bases, has either been changed, inserted or deleted within a gene.
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Gene Mutations When the base sequence of a molecule of DNA is altered, the sequence of nucleotides for the mRNA will also be altered. This results in a change in the amino acid sequence for the polypeptide change and hence changes a protein/enzyme. Mutation in gene Change in mRNA Change in the polypeptide sequence Change in the structure of a protein/enzyme Results in a severe consequence for the human body.
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Types of Mutations
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Types of Mutations Point Mutation
Change a single nucleotide of a gene.
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Types of Mutations Frameshift Mutation
Addition or deletion of one or more nucleotides. Results in a change in the improper grouping of nucleotides in subsequent codons.
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Types of Mutations Missense Mutation Nonsense Mutation
The most common type of mutation where the new codon still codes for AN amino acid (not necessarily the same amino acid) Nonsense Mutation A mutation that changes an amino acid codon to an amino acid codon that is a stop codon--usually resulting in a shorter, and non-functional form, of a protein
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Genetic Disorders Resulting From Mutations
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Genetic Disorders Frameshift Mutations Huntington Disease
Dominant allele disorder that results in death by the age of 40 Cystic Fibrosis Autosomal recessive disorder that results in excess excretion of lung mucous Hemophilia X-linked recessive disorder that results in the inability to clot blood
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Genetic Disorders II Point Mutation Skin Cancer
Proliferation genes have nucleotide bases thymine changed into uracil. UV light rays that enter skin cells. This results in the proliferation genes being constantly turned on
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Review
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Review I Translation Process Mutations Initiation
Peptide Bond Formation Elongation Translocation Termination Mutation in gene Change in mRNA Change in the polypeptide sequence Change in the structure of a protein/enzyme Results in a severe consequence for the human body.
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Review II Types of Mutations Point Frameshift Nonsense Missense
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