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Chromosomal Basis of Inheritance. Chapter 7. Objectives. Be familiar with patterns of inheritance for autosomal and sex linked genes Understand the concept of “Linked Genes”
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Chromosomal Basis of Inheritance Chapter 7
Objectives • Be familiar with patterns of inheritance for autosomal and sex linked genes • Understand the concept of “Linked Genes” • Understand how traits affected by incomplete dominance and codominance differ from autosomal dominant and autosomal recessive traits • Understand how nondisjunction of chromosomes can lead to disorders.
Linked Genes • Linked genes are those that reside on the same chromosome and tend to be inherited together • Humans have 23 pairs of chromosomes • Autosomal genes reside on the autosomal chromosomes (pairs 1-22) • Sex-linked genes are found on the sex chromosomes (pair 23, usually on the X)
Autosomal Genes • Autosomal genes are usually represented by a pair of alleles • The phenotype of the gene reflects the dominant/recessive relationship of the alleles
Autosomal Disorders • Most autosomal genetic diseases are autosomal recessive meaning the individual need to be homozygous recessive to exhibit the condition (example: cystic fibrosis) • Huntington’s disease is an autosomal dominant disorder meaning that is a single Huntingtons allele is inherited, the individual will have the disease.
Incomplete and Codominance • Some alleles do not show a dominance hierarchy • Incomplete dominance: the phenotype of a heterozygous genotype is intermediate in appearance • Codominance: each allele in the genotype for a particular gene will be expressed in the phenotype
Incomplete Dominance(heterozygous genotype is intermediate in appearance)
Sex Linked Inheritance • Males and females differ in their sex chromosome combination (females XX; males XY) • Because the X contains genes and the Y “does not”, inheritance patterns of sex-linked genes vary between the sexes • recessive traits more prevalent in males
Is the Disorder an Autosomal Recessive Disorder or Is It Sex Linked?
Errors In Chromosomal Inheritance • Genetic disorders can also occur due to errors in the number of inherited chromosomes • This condition arises through a problem that occurs during meiosis
Nondisjunction • Failure of a pair of chromosomes to separate during gamete formation • Genetic disorders like: • Down’s syndrome (#21, 3n) • Turner syndrome (XO) • Metafemale (XXX) • Kleinfelter Male (XXY) • Jacob’s Male (XYY)