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 Mutations are a result in a change in DNA sequence › A protein with a different AA sequence could be produced. › Germ Cell - If mutations occur in sex.

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Presentation on theme: " Mutations are a result in a change in DNA sequence › A protein with a different AA sequence could be produced. › Germ Cell - If mutations occur in sex."— Presentation transcript:

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2  Mutations are a result in a change in DNA sequence › A protein with a different AA sequence could be produced. › Germ Cell - If mutations occur in sex cells they may be passed on to the next generation. › Somatic- A mutation occurring only in body cells may be a problem for the individual but will not be passed on to the offspring.  Mutations may be classified as chromosomal alterations or gene mutations › Chromosomal alterations are generally more severe because many genes are usually involved.

3 Significance of Mutations Most are neutral Eye color Birth marks Some are harmful Cystic Fibrosis Down Syndrome Some are beneficial Sickle Cell Anemia to Malaria Immunity to HIV

4 What Causes Mutations? There are two ways in which DNA can become mutated: – Mutations can be inherited. Parent to child – Mutations can be acquired. Environmental damage Mistakes when DNA is copied

5  Silent mutation › any mutation that is not expressed because it does not cause a change in amino acid chain.  Point mutation › base-pair substitution › 1 base is replaced by a different base

6 Point mutation Only one nucleotide changes, but it makes a different protein

7 Gene Mutations Point Mutations – changes in one or a few nucleotides – Substitution THE FAT CAT ATE THE RAT THE FAT HAT ATE THE RAT – Insertion THE FAT CAT ATE THE RAT THE FAT CAT XLW ATE THE RAT – Deletion THE FAT CAT ATE THE RAT THE FAT ATE THE RAT

8 Frameshift Causes every codon in the DNA sequence to be changed after the mutation: Insertion- one or more bases are added Deletion- one or more bases are removed A

9  Deletion - part of chromosome is left out.  Duplication - part of chromatid breaks off add attaches to the sister chromatid creating a duplication of genes on the same chromosome. › Deletion and duplication mutations are errors that occur during crossing over in Meiosis I.  Translocation - when part of one chromosome breaks off and is added to a different chromosome.  Inversion - when part of a chromosome breaks off and is reinserted backwards.

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11 Chromosome Mutations Changes in number and structure of entire chromosomes Original Chromosome ABC * DEF DeletionAC * DEF DuplicationABBC * DEF TranspositionACB * DEF InversionAED * CBF TranslocationABC * JKL GHI * DEF

12 A dinky Y chromosome and the hairy ear gene on the Y chromosome Chromosomal Deletion


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