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DNA, RNA, and Protein Synthesis
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10.1 Discovery of DNA
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10.2 DNA Structure LEARNING TARGETS I will be able to:
Evaluate the contributions of Franklin and Wilkins in helping Watson and Crick discover DNA’s double helix structure Describe the 3 parts of a nucleotide Relate the role of base-pairing rules to the structure of DNA
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Rosalind Franklin
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Rosalind Franklin Took the first ever picture of DNA using x-ray diffraction This information was then used by Watson and Crick
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James Watson and Francis Crick (1953)
Watson (American) & Crick (British) 2. Watson and Crick developed the structure of DNA as a double helix Looks like a twisting staircase
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James Watson and Francis Crick (1953)
Looks like a twisting staircase a. The shape of DNA is a double helix
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DNA Nucleotides Nucleotides are the building blocks (monomers) of ………?
A. proteins B. lipids C. carbohydrates D. nucleic acids
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DNA Nucleotides Nucleotides are the building blocks (monomers) of ………?
NUCLEIC ACIDS!!!!!!!!!!! If answered correctly… =3GwjfUFyY6M
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DNA Nucleotides (3 parts)
Made up of 3 parts: Phosphate group
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DNA Nucleotides (3 parts)
Made up of 3 parts: Phosphate group Deoxyribose sugar
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DNA Nucleotides (3 parts)
Made up of 3 parts: Phosphate group Deoxyribose sugar Nitrogen base
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DNA Nucleotides (3 parts)
Sugar and phosphate groups are identical in all nucleotides Bases are different
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DNA Nucleotides (3 parts)
Deoxyribose sugar and phosphate make up the “backbone” of DNA Sides of the ladder (yellow)
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DNA Nucleotides (3 parts)
Nitrogen bases make up the middle of DNA Rungs of the ladder (multicolor)
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Nitrogenous Bases (4 types)
T - Thymine C - Cytosine
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Nitrogenous Bases (4 types)
G - Guanine A - Adenine
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Erwin Chargaff (1949) American biochemist Noticed that amount of A = amount of T Amount of C = amount of G
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Base-Pairing Rules C always pairs with G A always pairs with T These are complementary bases connected by hydrogen bonds
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Base-Pairing Rules
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Base-Pairing Rules
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10.3 DNA Replication
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10.3 DNA Replication LEARNING TARGETS I will be able to:
Summarize the process of DNA replication Identify the role of enzymes if the replication of DNA Describe how complementary base pairing guides DNA replication Describe mutations that occur during DNA replication
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10.3 DNA Replication
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DNA Replication Amount of DNA is doubled in preparation for cell division
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DNA Replication – 3 Steps
One DNA strand is separated into two strands a. Helicase – enzyme that separate DNA strands
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DNA Replication – 3 Steps
Almost like using a zipper on a jacket b. replication fork - Y shaped region where strands are being separated
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DNA Replication – 3 Steps
Complementary bases are added to new strands What gets added to A? What gets added to C?
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DNA Replication – 3 Steps
DNA polymerase – enzyme that adds nucleotides to new strands
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DNA Replication – 3 Steps
d. DNA has 5’ end and 3’ end e. DNA polymerase always works from 5’ to 3’
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DNA Replication – 3 Steps
f. Leading strand – where DNA polymerase works toward split in DNA g. Lagging strand – where DNA polymerase works away from split in DNA
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DNA Replication – 3 Steps
DNA polymerase falls off Forms two new strands
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Mutations Mutation – change in nucleotide sequence of DNA
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Mutations Addition – nucleotide is added to the sequence
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Mutations Deletion – one nucleotide is removed from sequence
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Mutations Substitution – one nucleotide is exchanged for another
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What is the enzyme responsible for splitting DNA apart?
Front door left: DNA polymerase Front door right: RNA polymerase Back right corner: helicase Back left corner: peptase
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What is the mutation called when you add a nucleotide (letter?
Front door left: addition Front door right: deletion Back right corner: substitution Back left corner: transfiguration
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10.4 Protein Synthesis
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10.4 Protein Synthesis LEARNING TARGETS: I will be able to:
Outline the flow of genetic information from DNA to protein Compare the structures of DNA and RNA Summarize the process of transcription Compare the role of mRNA, tRNA, and rRNA Identify the importance of learning about the human genome
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10.4 Protein Synthesis
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Protein Synthesis Overview
Consists of transcription and translation Transcription – DNA mRNA (happens in nucleus)
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Protein Synthesis Overview
Consists of transcription and translation Translation – mRNA amino acids (happens on ribosome)
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RNA Structure single helix Ribose sugar, not deoxyribose sugar
Has uracil (U) instead of thymine (T) U-A and C-G base pairing
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2 Types of RNA mRNA – messenger RNA
Takes info from DNA in nucleus to ribosome in cytoplasm
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2 Types of RNA tRNA – transfer RNA
Transfers amino acids during translation Aka “anticodon”
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Transcription Steps RNA polymerase attaches to START
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Transcription Steps DNA unwinds
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Transcription Steps RNA polymerase adds complementary bases
Complementary mRNA is formed!
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Transcription Steps #1 on back of notes DNA: TAC CGT ATC mRNA: ?????
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Transcription Steps #1 on back of notes DNA: TAC CGT ATC mRNA: AUG GCA UAG
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Genetic Code Explains how a sequence of bases creates a specific amino acid
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Genetic Code 3 nucleotides code for a specific amino acid
Codon – a 3 nucleotide sequence in mRNA that codes for an amino acid
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Codon Table
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Codon Table
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Translation Steps mRNA attaches to rRNA of ribosome
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Translation Steps 2. tRNA brings amino acids to ribosome
Don’t forget that amino acids are the building blocks of proteins! Anticodon on tRNA starts the translation process
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Translation Steps Codon = CGA Anticodon = GCU
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Translation Steps Amino acids form bond together tRNA leaves
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Translation Steps STOP codon reached and translation stops
Ribosome leaves and protein forms
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Translation Steps #3 on back of notes mRNA = AUG GCA UAG Amino acids = ??????
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Translation Steps #3 on back of notes mRNA = AUG GCA UAG Amino acids = start alanine stop
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Translation Steps #5 on back of notes mRNA = AUG GCA UAG Anticodons = ?????????
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Translation Steps #5 on back of notes mRNA = AUG GCA UAG Anticodons = UAC CGU AUC
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Translation Steps
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Translation Steps If DNA strand = TAC CGA GAT ATT What would be the complementary mRNA strand? What would be the amino acids formed? What would be the anti-codons?
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Human Genome We’ve figured out the order of 3.2 billion base pairs in the 23 human chromosomes!!!!!!!!!!!!!! About 30,000 genes in human genome Can help find genes responsible for specific diseases
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