William S. Klug Michael R. Cummings Charlotte A. Spencer...

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Chapter 8 Lecture Concepts of Genetics Tenth Edition Chromosome Mutations: Variation in Chromosome Number and Arrangement

Transcript of William S. Klug Michael R. Cummings Charlotte A. Spencer...

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    Chapter 8 Lecture

    Concepts of Genetics Tenth Edition

    Chromosome Mutations: Variation in Chromosome Number and Arrangement

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    8.1 Variations in Chromosome Number

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    Nondisjunction during the first and second meiotic divisions

    Variation in the Number of Chromosomes Results from Nondisjunction

  • Copyright © 2009 Pearson Education, Inc. Science (2007) 317:1315-1317

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    8.2 Monosomy and Trisomy Result in a Variety of Phenotypic Effects

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    Partial Monosomy in Humans Cri-du-Chat Syndrome, 46,5p-

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    Trisomy Involves the Addition of a Chromosome to a Diploid Genome

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    During meiosis I three copies of a single chromosome form a trivalent configuration

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    Down Syndrome 47, 21+

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    Father’s Age Is Linked to Risk of Autism and Schizophrenia

    August 22, 2012

    Number of mutations from Dad increases by 2 per year from age 25 on. Number of mutations from Mom is about 15 regardless of Mom’s age.

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    1:19,000

    Patau Syndrome 47,13+

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    1:8,000

    Edwards Syndrome 47,18+

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    Viability in Human Aneuploidy

    Up to 30 percent of all fertilized eggs in humans may contain an error in chromosome number. 45,X has one of the highest incidence rates among abortuses. Also, about 80% of 45,X have the maternal X.

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    8.3 Polyploidy, in Which More Than Two Haploid Sets of Chromosomes Are Present, Is Prevalent in Plants

    But very rare in animals or humans.

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    8.4 Variation Occurs in the Internal Composition and Arrangement of Chromosomes

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    8.5 A Deletion Is a Missing Region of a Chromosome

    Cri du chat Syndrome in Humans: segmental

    deletion

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    Drosophila Heterozygous for Deficiencies May Exhibit Pseudodominance

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    8.6 A Duplication Is a Repeated Segment of the Genetic Material

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    The Bar-Eye Mutation in Drosophila

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    8.7 Inversions Rearrange the Linear Gene Sequence

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    Consequences of Inversions during Gamete Formation

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    8.8 Translocations Alter the Location of Chromosomal Segments in the Genome

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    Robertsonian translocation

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    Translocations in Humans: Familial Down Syndrome

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    8.9 Fragile Sites in Humans Are Susceptible to Chromosome Breakage

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    Fragile X Syndrome (Martin–Bell Syndrome)

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