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LO: SWBAT explain how protein shape is determined and differentiate between the different types of mutations. DN: h/0 protein synthesis HW: Read pp 307-308# 1-5 HW: page 306 #1-5 1. Types of RNA: mRNA, tRNA 2. Transcription: mRNA makes a copy of DNA in the nucleus 3. Translation: tRNA reads mRNA codons (3 bases) and brings the correct amino acid to the ribosome 4. Sugar: DNA= deoxribose, RNA= ribose Bases: DNA has T and RNA has U DNA: double stranded, RNA: single stranded 5. UGG CAG UGC Try Glu Cys What do enzymes, antibodies, hormones, hemoglobin and membrane proteins have in common? Enzymes Hemoglobin All are proteins with a specific shape that determines their function. Hormone Antibodies What determines a protein’s Shape? A protein’s shape is determined by its sequence of amino acids. What happens after translation of the genetic code? Proteins do not remain as single strands of amino acids, rather the amino acids chain gets folded into a specific shape. This shape is determined by the ORDER of the amino acids in the chain. Protein Shape: 1) The DNA base sequence (order) determines the sequence of amino acids. 2) The sequence (order) of amino acids in a protein determine its shape. 3) The shape of a protein determines its activity. Transcription & Translation: The processes of transcription and translation, lead to the final shape of a protein. Therefore it is the genetic code: DNA base sequence that ultimately determine a protein’s sequence of amino acids. A–T U C–G G C–G G Tryptophan Mutations Mutations (changes in the genetic code) that can lead to changes in the amino acid sequence and ultimately to the overall shape of the protein. Why? What causes mutations errors in DNA replication? • Chemicals • UV Radiation • X-Ray radiation Mutated Proteins It changes the amino acids sequence which determines protein shape How does a mutated protein affect a cell? •The mutated protein may have a different shape and disrupt its normal activity. Types of Mutation • Substitution Original DNA Strand • Deletion • Insertion • Inversion Copy the Normal DNA Strand: DNA CCT CAA GAT GCG RNA GGA GUU CUA CGC AA Sequence Gly – Val – Leu - Arg Substitution • Substitution – One nitrogenous base is substituted for another. DNA DNA RNA Amino acid CCT CAA GAT GCG CCC CAA GAT GCG GGG GUU CUA CGC Gly - Val - Leu - Arg Deletion • One nitrogenous base is deleted (removed). DNA CCT CAA GAT GCG DNA CTC AAG ATG CG mRNA GAG UUC UAC GC Amino Glu - Ala - Tyracid Insertion (Addition) • Insertion – Extra nitrogenous bases are added to the genetic code. DNA DNA CCT CAA GAT GCG CCT CTA AGA TGC G mRNA GGA GAU UCU ACG C Amino acid Gly - Asp - Ser - Thr - Inversion • Inversion – The genetic code is inverted or reversed. DNA DNA mRNA Amino acid CCT CAA GAT GCG CCT CAA TAG GCG GGA GUU AUC CGC Gly - Val – Iso - Arg Sickle Cell Anemia Point mutation A change in ONE nitrogenous base, the overall number of bases stays the same (Substitution or Inversion) Frame shift mutation A change in the number of overall nitrogenous bases in the genetic code (Addition or Deletion) What type of mutation is it?