7 1 Chromosomes and Phenotype KEY CONCEPT The

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7. 1 Chromosomes and Phenotype KEY CONCEPT The chromosomes on which genes are located

7. 1 Chromosomes and Phenotype KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.

7. 1 Chromosomes and Phenotype Two copies of each autosomal gene affect phenotype. •

7. 1 Chromosomes and Phenotype Two copies of each autosomal gene affect phenotype. • Mendel studied autosomal gene traits, like hair texture.

7. 1 Chromosomes and Phenotype • Mendel’s rules of inheritance apply to autosomal genetic

7. 1 Chromosomes and Phenotype • Mendel’s rules of inheritance apply to autosomal genetic disorders. – A heterozygote for a recessive disorder is a carrier. – Disorders caused by dominant alleles are uncommon. (dominant)

7. 1 Chromosomes and Phenotype Males and females can differ in sex-linked traits. •

7. 1 Chromosomes and Phenotype Males and females can differ in sex-linked traits. • Genes on sex chromosomes are called sex-linked genes. – Y chromosome genes in mammals are responsible for male characteristics. – X chromosome genes in mammals affect many traits.

7. 1 Chromosomes and Phenotype • Male mammals have an XY genotype. – All

7. 1 Chromosomes and Phenotype • Male mammals have an XY genotype. – All of a male’s sexlinked genes are expressed. – Males have no second copies of sex-linked genes.

7. 1 Chromosomes and Phenotype • Female mammals have an XX genotype. – Expression

7. 1 Chromosomes and Phenotype • Female mammals have an XX genotype. – Expression of sex-linked genes is similar to autosomal genes in females. – X chromosome inactivation randomly “turns off” one X chromosome.

7. 1 Chromosomes and Phenotype • Why are sex-linked genes expressed differently in different

7. 1 Chromosomes and Phenotype • Why are sex-linked genes expressed differently in different cells of a female? • How is the allele for Huntington's disease passed on in the population if it is fatal? • What is the probability of two cystic fibrosis carriers having a child with cystic fibrosis? • How are the X and Y chromosomes different? • What is true about sex-linked traits?

7. 2 Complex Patterns of Inheritance KEY CONCEPT Phenotype is affected by many different

7. 2 Complex Patterns of Inheritance KEY CONCEPT Phenotype is affected by many different factors.

7. 2 Complex Patterns of Inheritance Phenotype can depend on interactions of alleles. •

7. 2 Complex Patterns of Inheritance Phenotype can depend on interactions of alleles. • In incomplete dominance, neither allele is completely dominant nor completely recessive. – Heterozygous phenotype is intermediate between the two homozygous phenotypes – Homozygous parental phenotypes not seen in F 1 offspring

7. 2 Complex Patterns of Inheritance • Codominant alleles will both be completely expressed.

7. 2 Complex Patterns of Inheritance • Codominant alleles will both be completely expressed. – Codominant alleles are neither dominant nor recessive. – The ABO blood types result from codominant alleles. • Many genes have more than two alleles.

7. 2 Complex Patterns of Inheritance Many genes may interact to produce one trait.

7. 2 Complex Patterns of Inheritance Many genes may interact to produce one trait. • Polygenic traits are produced by two or more genes. Order of dominance: brown > green > blue.

7. 2 Complex Patterns of Inheritance • An epistatic gene can interfere with other

7. 2 Complex Patterns of Inheritance • An epistatic gene can interfere with other genes.

7. 2 Complex Patterns of Inheritance The environment interacts with genotype. • Phenotype is

7. 2 Complex Patterns of Inheritance The environment interacts with genotype. • Phenotype is a combination of genotype and environment. • The sex of sea turtles depends on both genes and the environment • Height is an example of a phenotype strongly affected by the environment.

7. 2 Complex Patterns of Inheritance • How can you recognize the heterozygote in

7. 2 Complex Patterns of Inheritance • How can you recognize the heterozygote in an incomplete dominance pattern of heredity? • How are incomplete dominance and codominance similar? • Why are there so many phenotypes in polygenic inheritance? • What term describes the interference of gene expression by another gene? • How is it that identical twins can vary in appearance when they are born?

7. 3 Gene Linkage and Mapping KEY CONCEPT Genes can be mapped to specific

7. 3 Gene Linkage and Mapping KEY CONCEPT Genes can be mapped to specific locations on chromosomes.

7. 3 Gene Linkage and Mapping Gene linkage was explained through fruit flies. •

7. 3 Gene Linkage and Mapping Gene linkage was explained through fruit flies. • Morgan found that linked traits are on the same chromosome. • Chromosomes, not genes, assort independently during meiosis. Wild type Mutant

7. 3 Gene Linkage and Mapping • Linked genes are not inherited together every

7. 3 Gene Linkage and Mapping • Linked genes are not inherited together every time. • Chromosomes exchange homologous genes during meiosis.

7. 3 Gene Linkage and Mapping Linkage maps estimate distances between genes. • The

7. 3 Gene Linkage and Mapping Linkage maps estimate distances between genes. • The closer together two genes are, the more likely they will be inherited together. • Cross-over frequencies are related to distances between genes. • Linkage maps show the relative locations of genes.

7. 3 Gene Linkage and Mapping • Cross-over frequencies can be converted into map

7. 3 Gene Linkage and Mapping • Cross-over frequencies can be converted into map units. – gene A and gene B cross over 6. 0 percent of the time – gene B and gene C cross over 12. 5 percent of the time – gene A and gene C cross over 18. 5 percent of the time

7. 3 Gene Linkage and Mapping • • • What term describes the most

7. 3 Gene Linkage and Mapping • • • What term describes the most common phenotype in a species? What conclusion about gene linkage did Thomas Hunt Morgan reach? How is the distance between two genes related to the frequency of crossing over? What does a linkage map show? Genes A, B, and C have these map distances between them: A and B-15 map units; B and C-5 map units; A and C-10 map units. What is the relative order of the three genes on the chromosome?

7. 4 Human Genetics and Pedigrees KEY CONCEPT A combination of methods is used

7. 4 Human Genetics and Pedigrees KEY CONCEPT A combination of methods is used to study human genetics.

7. 4 Human Genetics and Pedigrees Human genetics follows the patterns seen in other

7. 4 Human Genetics and Pedigrees Human genetics follows the patterns seen in other organisms. • The basic principles of genetics are the same in all sexually reproducing organisms. – Inheritance of many human traits is complex. – Single-gene traits are important in understanding human genetics.

7. 4 Human Genetics and Pedigrees Females can carry sex-linked genetic disorders. • Males

7. 4 Human Genetics and Pedigrees Females can carry sex-linked genetic disorders. • Males (XY) express all of their sex linked genes. • Expression of the disorder depends on which parent carries the allele and the sex of the child. Y X

7. 4 Human Genetics and Pedigrees A pedigree is a chart for tracing genes

7. 4 Human Genetics and Pedigrees A pedigree is a chart for tracing genes in a family. • Phenotypes are used to infer genotypes on a pedigree. • Autosomal genes show different patterns on a pedigree than sex-linked genes.

7. 4 Human Genetics and Pedigrees • If the phenotype is more common in

7. 4 Human Genetics and Pedigrees • If the phenotype is more common in males, the gene is likely sex-linked.

7. 4 Human Genetics and Pedigrees Several methods help map human chromosomes. • A

7. 4 Human Genetics and Pedigrees Several methods help map human chromosomes. • A karyotype is a picture of all chromosomes in a cell. XY

7. 4 Human Genetics and Pedigrees • Karyotypes can show changes in chromosomes. –

7. 4 Human Genetics and Pedigrees • Karyotypes can show changes in chromosomes. – deletion of part of a chromosome or loss of a chromosome – large changes in chromosomes – extra chromosomes or duplication of part of a chromosome

7. 4 Human Genetics and Pedigrees • What term describes a chart showing all

7. 4 Human Genetics and Pedigrees • What term describes a chart showing all the chromosomes in a cell? • Can a male be a carrier for hemophilia? • Which genetic disorder is sex-linked? • What does an open square represent in a pedigree? • What must be the genotype of a colorblind female?