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DNA Mutations. What Are Mutations? Changes in the nucleotide sequence of DNA.

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Presentation on theme: "DNA Mutations. What Are Mutations? Changes in the nucleotide sequence of DNA."— Presentation transcript:

1 DNA Mutations

2 What Are Mutations? Changes in the nucleotide sequence of DNA

3  May occur in somatic cells & aren’t passed to offspring  May occur in gametes (eggs & sperm) and be passed to offspring

4  Mutations happen regularly (its very common)  Almost all mutations are neutral (doesn’t harm organism)

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6  Chemicals & UV radiation cause mutations – skin cancer

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8  Many mutations are repaired by enzymes

9  Some type of skin cancers and leukemia result from somatic mutations  Can you “catch” cancer from someone? NO!

10  Some mutations may improve an organism’s survival (beneficial)

11 Types of Mutations 1. Chromosomal 2. Gene

12 Chromosomal Mutations  May Involve:  Changing the structure of a chromosome  The loss or gain of part of a chromosome

13 Chromosomal Mutations  Five types exist:  Deletion  Inversion  Duplication  Translocation  Nondisjunction

14 Deletion  Due to breakage  A piece of a chromosome is lost

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16 Inversion  Chromosome segment breaks off  Segment flips around backwards and reattaches

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18 Duplication  Occurs when a gene sequence is repeated

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20 Translocation  Involves two chromosomes that aren’t homologous (similar)  Part of one chromosome is transferred to another chromosomes

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22 Nondisjunction  Failure of chromosomes to separate during meiosis (making of sperm or egg)  Causes gamete to have too many or too few chromosomes

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24 Chromosome Mutation Animation http://highered.mcgraw- hill.com/sites/0072556781/student_vie w0/chapter11/animation_quiz_4.html

25 Disorders caused by nondisjunction: Down Syndrome Turner Syndrome Klinefelter’s Syndrome

26 Normal Female Karyotype 2n = 46

27 Normal Male Karyotype 2n = 46

28 Female Down’s Syndrome 2n = 47

29 Male, Trisomy 21 (Down’s) 2n = 47

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32 Turner’s Syndrome 2n = 45

33 Klinefelter’s Syndrome 2n = 47

34 http://www.dailymail.co.uk/health/articl e-1082293/The-XYY-Factor-How-rare- chromosome-disorder-brought-son- world-pain.html

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36 Gene Mutations  Change in the nucleotide sequence of a gene  May only involve a single nucleotide  May be due to copying errors, chemicals, viruses, etc.

37 Types of Gene Mutations  Include:  Point Mutations  Substitutions  Insertions  Deletions  Frameshift Mutations

38 Point Mutation Change of a single nucleotide Includes the deletion, insertion, or substitution of ONE nucleotide in a gene

39 Point Mutation  Sickle Cell disease is the result of one nucleotide substitution  Occurs in the hemoglobin gene

40 Deletion

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42 Substitution  a single nucleotide is substituted with (or exchanged for) a different nucleotide that may result in an altered sequence of amino acidnucleotide amino acid

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44 Insertion  Nucleotides are inserted into sequence altering codon pattern

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47 Frameshift Mutation Inserting or deleting one or more nucleotides Changes the “reading frame” like changing a sentence Proteins built incorrectly

48 Frameshift Mutation  Original:  The fat cat ate the wee rat.  Frame Shift (“a” added):  The fat caa tet hew eer at.

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50 Gene Mutation Animation

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52 Mutations Lab Gene Therapy http://www.news- medical.net/health/What-is-Gene- Therapy.aspx http://www.youtube.com/watch?v=bLI1G fb0ynw


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