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Genetic Mutations Standards: • CLE 3210.4.6 Describe the connection between mutations and human genetic disorders. Objectives: • Investigate the affect of mutations on protein production • Differentiate between point mutations and chromosomal mutations. What is a gene mutation? • Mutations are changes in gene code – changes in DNA code – which means changes in a gene(s) • In gene mutations, the DNA code will have one or more bases missing, added, or changed in a codon. How common are mutations? • Mutations occurs at a frequency of about 1 in every 1 billion base pairs • Everybody has about 6 mutations in each cell in their body! Does that mean I have a chance to become a super hero/villian? If I have that many mutations, why don’t I look weird? • Mutations are not always seen. The affected gene may still function. • Mutations may be harmful. • Mutations may be beneficial. • Mutations may have no effect on the organism. How do mutations affect a population? • Mutations are a major source of genetic variation in a population increasing biodiversity. • Some variations may help them to survive better. Beneficial or Harmful? How are mutations inherited? Only mutations that occur in gametes, or were present when the organism was fertilized, are passed onto offspring. Mutations that occur in body cells (somatic cells) (after an organism has developed) only affect the organism in which they occur and are not passed on. Types of Mutations • Point mutation occurs when a codon is changed. – (ex. GCA is changed to GAA) • Chromosome mutations - Changes in the number or structure of chromosomes Types of Point Mutations • Point mutation occurs when the base sequence of a codon is changed. (ex. GCA is changed to GAA) • There are 3 types: •Substitution •Deletion •Insertion Also called frameshift mutations Substitution Mutations Normal DNA: CGA – TGC – ATC Alanine – Threonine - stop Mutated DNA: CGA – TGC – TTC Alanine – Threonine - Lysine What This What Theis has will adenine a substitution happened happen wastoto replaced the the amino mutation with DNA? acids? thymine Substitution Mutations • This is a substitution mutation. • A single nitrogen base is substituted for another in a codon. • It may or may not affect the amino acid or protein. Normal DNA: CGA – TGC – ATC Alanine – Threonine - stop Mutated DNA: CGA – TGC – TTC Alanine – Threonine - Lysine The benefit of 64 codons and only 20 amino acids TRY THIS! • On your note paper write: The cat ate the rat • Change one letter in the sentence to represent a substitution mutation. Think – Pair - Share • Why are we using 3 letter words? • Share with your partner the substitution change that you made • Can you still “read” your sentence fairly easily? • How damaging is a substitution mutation? Analogy The cat ate the rat. SUBSTITUTION #1 Thc cat ate the rat. May have little effect. You can still get the overall idea. Like a typo on a test. SUBSTITUTION #2 The hat ate the rat. Changes the thought of the sentence. The effect of the mutation depends on where the substitution happens Insertion Mutations Normal DNA: CGA – TGC – ATC Alanine – Threonine – stop Mutated DNA: CGA – TAG – CAT – C Alanine – Isoleucine – Valine An This adenine is an was insertion inserted What What will has happen happened to the mutation, thereby pushing also a type all the of amino to the acids? DNA? other frameshift bases over mutation. a frame. Insertion Mutations • This is an insertion mutation. • A nitrogen base is inserted/added to the sequence. • It causes the triplet “frames” to shift. • It always affects the amino acids that follow the mutation – changing the protein. Normal DNA: CGA – TGC – ATC Alanine – Threonine - stop Mutated DNA: CGA – TAG – CAT – C Alanine – Leucine - Valine Think – pair - share • Predict the effect an insertion mutation cause to our sentence: THE CAT ATE THE RAT •Remember: the sentence must remain with 3letter words (codons) TRY THIS! • On your notebook paper write: The cat ate the rat. • Insert a letter into any word above. • Rewrite the sentence . Each word must have only 3 letters to represent the codon. • What were the effects of the insertion? Analogy The cat ate the rat. Insertion The cca tat eth era t. Inserting the c causes a FRAMESHIFT THE SENTENCE NO LONGER MAKES SENSE!! Think – pair - share • Where in the gene sequence would an insertion mutation cause the most damage to the DNA code? • In the beginning, middle or end? Why? At the beginning of the gene sequence – it changes all the following codons, thus changing all the amino acids. Let’s examine the effect of location THE CAT ATE THE RAT INSERTION #1 – THE CAT ATE THA ERA T – Would any of the codons code correctly? INSERTION #2 – TAH ECA TAT ETH ERA T – Would any of these codons code correctly? Deletion Mutations Normal DNA: CGA – TGC – ATC Alanine – Threonine – stop Mutated DNA: CGA – TCA- TC Alanine – Serine This What A What guanine iswill called has happen was happened a deleted, deletion to the mutation, thereby amino to the pushing also acids? DNA? a type all the of bases frameshift downmutation. a frame. Deletion Mutations • This is a deletion mutation. • A nitrogen base is deleted/removed from the sequence. • It causes the triplet “frames” to shift. • It always affects the amino acids and, consequently, the protein. Normal DNA: CGA – TGC – ATC Alanine – Threonine – stop Mutated DNA: CGA – TCA- TC Alanine – Serine TRY THIS! • Write the sentence on your paper: The cat ate the rat. • Delete one letter from any word. • Rewrite the sentence. Remember: each word can only have 3 letters. Analogy DELETION The cat ate the rat. Thc ata tet her at FRAMESHIFT The sentence no longer makes sense!! Deletions can have huge effects. DNA Mutations DNA CA AG C T A A C T Normal gene CA AG C G AA C T Single base change CA A G G C G C T A A C T Additions C T CA A G A A C T Deletions Gene Mutations Activity • Complete the worksheet Standards: • CLE 3210.4.6 Describe the connection between mutations and human genetic disorders. Objectives: • Investigate the affect of mutations on protein production • Differentiate between point mutations and chromosomal mutations. Think – pair - share • Which type of mutation would have the least damaging affect on an organism? Normal DNA: CGA – TGC – ATC Alanine – Threonine - stop Mutated DNA: CGA – TGC – ATT Alanine – Threonine - stop Mutated DNA: CGA – TGC – ATG Alanine – Threonine - Tyrosine • Substitution has the least affect because it changes only one amino acid or it may change no amino acid. An example of a substitution mutation is sickle cell anemia • Only one codon in the gene sequence is affected by the mutation • So, only one amino acid changes in the hemoglobin protein. • The hemoglobin still functions but it folds differently changing the shape of the rbc. Think – pair - share • Which type(s) of mutation would have the most affect on an organism? • Insertion and deletion mutations have the most effect on an organism because they affect many amino acids and consequently the whole protein. CGA – TGC – ATC Alanine – Threonine – stop Mutated DNA: CGA – TCA- TC Alanine – Serine Mutated DNA: CGA – TAG – CAT – C Alanine – Leucine - Valine Normal DNA: An example of a frameshift mutation disorder is Tay Sachs disease. • Children born with this disorder cannot make an enzyme that is critical in breaking down fat and toxic substances in the brain. • The disease is terminal. Most will die before age 4. Think – pair - share • In which cells would a gene mutation have the greatest affect on an organism? Egg being fertilized • When it is inherited from the gametes or develops early in embryonic development (in stem cells or first few days). Four cell Zygote Embryo Mutagens • What causes mutations? – natural errors during replication – an environmental mutagen/carcinogen • What is a mutagen (carcinogen)? something that causes the DNA code to change (mutate) – x-ray, chemicals, UV light, radiation, etc • What happens to a person who has a mutation? Chromosomal Mutations think – pair - share • How do you think we could mutate (change/damage) a chromosome? • List at least 3 ways Chromosomal Mutations • Changes in the number or structure of chromosomes • Deletions • Duplication • Inversion • Translocation • Nondisjunction Deletions • removal of a gene and/or entire chromosome Duplication • repeat of a gene or chromosome Inversion • gene sequences are switched on the chromosome Translocation • part of one chromosome breaks off and reattaches to a non-homologous chromosome Think - pair - share • Compare and contrast translocation with crossing – over –How are they similar? –How are they different? Non-disjunction • A chromosome fails to separate from its homologue during meiosis Down’s Syndrome • Result of nondisjunction of the chromosomes at pair #21 Standards: • CLE 3210.4.6 Describe the connection between mutations and human genetic disorders. Objectives: (DID WE…) • Investigate the affect of mutations on protein production • Differentiate between point mutations and chromosomal mutations. Exit Ticket • How do mutations affect the production of a protein?