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Chapter 19: Genetics and Inheritance

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1 Chapter 19: Genetics and Inheritance
Alleles Different forms of homologous genes Humans have 23 pairs of chromosomes Homozygous Both alleles identical Heterozygous Alleles are different Genotype Complete set of genes and alleles Phenotype Observed physical and functional traits Pearson - The Biology Place

2 Punnett Squares: predicts patterns of inheritance
Figure 19.1

3 Patterns of Genetic Inheritance
Mendel developed basic rules of inheritance Law of segregation Reproductive cells carry only one copy of each gene Law of independent assortment Genes for different traits are separated from each other independently during meiosis Applies in most cases

4 Allelic Interactions Genotype and environment affect phenotype
Dominant alleles Gene always expressed, even if heterozygous Recessive alleles Two copies of gene needed to be expressed; must be homozygous

5 Allelic Interactions Incomplete dominance Codominance
Heterozygote is an intermediate phenotype Codominance Both phenotypes equally expressed Polygenic inheritance Multiple genes involved Linked alleles May be inherited together if close on a chromosome

6 Pedigree Chart: Inheritance Pattern for an X-Linked Recessive Disease
Figure 19.16

7 Sex-Linked Inheritance: X and Y Chromosomes
Origin of sex chromosomes Chance mutations Y determines sex Sex-linked genes located on sex chromosomes Sex-linked or X-linked inheritance Characteristics Mostly males with disease Passed to sons by mother Father cannot pass the gene Sex-influenced traits Affected by presence of testosterone, estrogen

8 Chromosomes May Be Altered in Number and Structure
Nondisjunction during meiosis Examples Down syndrome: trisomy 21 Alterations of the number of sex chromosomes: XYY: double-Y syndrome XXY: Klinefelter syndrome XXX: trisomy-X syndrome XO: Turner syndrome; no Y

9 Chromosomes May Be Altered in Number and Structure
Altered chromosome structure

10 Inherited Genetic Disorders
Mechanism Most mutations usually involve recessive alleles Phenylketonuria Tay-Sachs disease Dominant lethal allele Huntington disease Always expressed, though at midlife Always lethal

11 Genes and Behavior Mechanism Protein functions
Product of gene-specific proteins Proteins have specific functions leading to phenotypes Protein functions Hormones, enzymes, structural, neurotransmitters


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