DNA, RNA and Protein Synthesis

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DNA, RNA and Protein Synthesis TAKS Review Spring 2012

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DNA, RNA and Protein Synthesis. TAKS Review Spring 2012. Structure of DNA. DNA is deoxyribonucleic acid DNA is a large molecule that has subunits called nucleotides . The nucleotides come together to make the DNA molecule in the shape of a double helix (looks like a twisted ladder). - PowerPoint PPT Presentation

Transcript of DNA, RNA and Protein Synthesis

Page 1: DNA, RNA and Protein Synthesis

DNA, RNA and Protein Synthesis

TAKS Review

Spring 2012

Page 2: DNA, RNA and Protein Synthesis

Structure of DNA

• DNA is deoxyribonucleic acid

• DNA is a large molecule that has subunits called nucleotides.

• The nucleotides come together to make the DNA molecule in the shape of a double helix (looks like a twisted ladder).

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Nucleotides

• Nucleotides are the subunits that make up DNA and they have 3 major parts:

1. A sugar molecule (deoxyribose sugar)

2. A phosphate group 3. A nitrogen base

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Nitrogen bases

There are 4 kinds of nitrogen bases:

Adenine (A)

Guanine (G)

Thymine (T)

Cytosine (C)

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DNA Structure

• DNA is a double helix (twisted ladder)

• The handrails of the ladder are made of phosphate and sugar

• The rungs of the ladder are made of nitrogen bases.

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Bonding

• Sugar and phosphate bond using covalent bonds (strong) and nitrogen bases bond using hydrogen bonds (weak)

• Nitrogen bases are specific: Adenine (A) always attaches to Thymine (T); and Cytosine (C) always attaches to Guanine (G)

• (Think apples in trees, cars in garages)

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DNA Replication

A review:

A cell will make an exact copy of itself during a process called mitosis

Before the cell can copy itself it must copy all of it’s DNA so that both daughter cells have the same number of chromosomes.

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DNA replication takes place in 3 steps

• 1. DNA unwinds at the hydrogen bonds

• 2. nucleotides are added to the exposed nitrogen bases. It follows base pairing rules. (A –T and C-G)

• 3. The DNA winds back up producing 2 new strands.

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What’s the complementary strand?

• If one side is CAG, what is the complementary strand?

• Answer: GTC

• If one side is AAC, what is the complementary strand?

• Answer: TTG

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RNA vs DNA

Characteristic RNA DNA

Strands 1 2

Sugar molecule Ribose Deoxyribose

Bases A, U, C, G A, T, C, G

Found Nucleus and cytoplasm

Nucleus only

Building block Nucleotide Nucleotide

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Kinds of RNA

• There is only one kind of DNA, but there are 3 kinds of RNA.

– Messenger RNA (mRNA)

– Transfer RNA (tRNA)

– Ribosomal RNA (rRNA)

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http://onlinetc.its.brooklyn.cuny.edu/Core81/chap5.html#jump2

Gene Expression

DNA (double-stranded)

RNA (single-stranded)

Protein (amino acid chain)

Transcription Translation

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Central Dogma of Molecular Biology

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http://www.wappingersschools.org/RCK/staff/teacherhp/johnson/visualvocab/mRNA.gif

Transcription= taking DNA and making an RNA copy of it. Uses complementary

nucleotides. C=G, G=C, T=A, A=U

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The Genetic Code

• Remember that messenger RNA – mRNA- is a copy of the DNA. It carries instructions for making a protein.

• The instructions (nucleotides) have to be translated into proteins (amino acids).

• A sequence of three nucleotides is called a codon, and it corresponds to an amino acid.

• We use a codon chart for translation

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Genetic Mutations

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Mutation• A mutation is any change in a genetic code (DNA).• It may not change the resulting amino acid chain and

is called a silent mutation• EXAMPLE: Notice how the resulting a.a. sequence is

the same in spite of the change:– Original DNA: CAA CCC AAA– Resulting mRNA: GUU GGG UUU– Resulting amino acid: Val – Gly - Phe– Mutated DNA: CAA CCC AAG– Resulting mRNA GUU GGG UUC– Resulting amino acid: Val – Gly – Phe

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Point Mutation or Substitution Mutation• A point mutation is a change in one nucleotide. It

can be silent or it can cause a change in one amino acid

• Can be devestating if the resulting amino acid has a STOP codon inserted as a result– Original DNA: ATG CCC AAA– Resulting mRNA: UAC GGG UUU– Resulting amino acid: Tyr – Gly - Phe– Mutated DNA: ATG ACC AAA– Resulting mRNA UAC UGG UUU– Resulting amino acid: Tyr – Trp – Phe– Mutated DNA: ATT CCC AAA– Resulting mRNA: UAA GGG UUU– Resulting amino acid: Stop

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Insertion and Deletion Mutations• Insertion – addition of one or more nucleotides• Deletion – deletion of one or more nucleotides• Insertion and deletion mutations are almost

always devastating because it will cause a frame-shift to occur.

• Imagine if a sentence of 3-letter words lost a letter?

• Original sentence: The cat and dog are fat.• A mutation occurs that deletes the c in cat.• Mutated sentence: Thc ata ndd oga ref at.• The same things happen to DNA when it mutates

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Frame Shift Mutation

• Original DNA: CAT AGC TAG GAT• Resulting mRNA: GUA UCG AUC CUA • Resulting amino acid: Val–Ser-Ile-Leu • Mutated DNA: CAA GCT AGG AT• Resulting mRNA: GUU CGA UCC UA

• Resulting amino acid: Val-Arg-Ser-?

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Mendel’s Theory and Studying Heredity

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The Flower

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Mendelian Theory of Heredity

• 2 sets of chromosomes = 2 copies of each gene

• Alleles—alternative forms of a gene– Purple vs. white flowers

• Dominant allele—trait that is expressed or seen.

• Recessive allele—trait that is not seen. To be seen, must be present in 2 copies.

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Terms and Notations

• Dominant alleles = capital letters

• Recessive alleles = lower case letters

• Dominant allele is always written first

• Homozygous individual—alleles are the same (EX: PP or pp)

• Heterozygous individual—alleles are different (EX: Pp)

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Terms and Notations Continued

• Genotype—set of alleles, or genes.

• Phenotype—physical appearance of a trait.

Genotype PhenotypePP purple flowers, homozygous

dominant

Pp purple flowers, heterozygous

pp white flowers, homozygous recessive

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Punnett Squares

• Diagram that predicts the outcome of a genetic cross

• Top represents one parent, side the other

• Letters in the box indicate the possible genotypes of the offspring.

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Example Punnett Square

Y y

Y

y

Yy—heterozygote

Yy—heterozygote

YY Yy

Yy yy

¼=YY homozygous dominant

2/4=Yy heterozygous

¼=yy homozygous recessive

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Inheritance of Traits

• Pedigree—family history that shows how a trait is inherited over several generations.

• Helps identify carriers of genetic disorders

• Carriers—individuals who are heterozygous for a genetic disorder but do not show symptoms—can pass the mutant allele to their offspring

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Example Pedigree

Male

Female

Male with disorder

Female with disorder