The Human Genome Chapter 14 The Human Genome

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The Human Genome Chapter 14

The Human Genome Chapter 14

The Human Genome In humans, diploid (2 n) = 46 That 44 means somatic

The Human Genome In humans, diploid (2 n) = 46 That 44 means somatic cells have 46 chromosomes autosomal chromosomes and a pair of sex chromosomes

Pedigrees A pedigree is a diagram that traces a single trait through several generations

Pedigrees A pedigree is a diagram that traces a single trait through several generations

Individuals shaded in have attached earlobes. Is this trait dominant or recessive? RECESSIVE!! Partially

Individuals shaded in have attached earlobes. Is this trait dominant or recessive? RECESSIVE!! Partially shade carriers and label genotypes

Solution:

Solution:

A Pedigree for a sex-linked recessive trait: Shade in known carriers and label genotypes.

A Pedigree for a sex-linked recessive trait: Shade in known carriers and label genotypes.

Solution:

Solution:

The Human Genome Chapter 14 Blood Typing and Chromosomal Genetic Disorders

The Human Genome Chapter 14 Blood Typing and Chromosomal Genetic Disorders

Use only to type blood in lab (serum reacts to antigens present) Blood Typing

Use only to type blood in lab (serum reacts to antigens present) Blood Typing Chart Blood Type A B AB O Rh+ Rh Genotypes Antigens Antibodies Donate to Receive from Reaction to Anti-A Reaction to Anti-B Reaction to Anti-Rh

Use only to type blood in lab (serum reacts to antigens present) Blood Typing

Use only to type blood in lab (serum reacts to antigens present) Blood Typing Chart Blood Type Genotypes A IAIA, IAi B IBIB, IBi AB IAIB O ii ++, +Rh+ dominant -Rhrecessive Antigens Antibodies Donate to Receive from Reaction to Anti-A Reaction to Anti-B Reaction to Anti-Rh

Use only to type blood in lab (serum reacts to antigens present) Blood Typing

Use only to type blood in lab (serum reacts to antigens present) Blood Typing Chart Blood Type Genotypes A IAIA, IAi B IBIB, IBi AB IAIB O ii ++, +Rh+ dominant -Rhrecessive Antigens Antibodies A Anti-B B Anti-A AB none Anti-A Anti-B Rh none *only if exposed to antigen Donate to Receive from Reaction to Anti-A Reaction to Anti-B Reaction to Anti-Rh *Rh- mothers can be exposed to the Rh antigen if the fetus is Rh+

Use only to type blood in lab (serum reacts to antigens present) Blood Typing

Use only to type blood in lab (serum reacts to antigens present) Blood Typing Chart Blood Type Genotypes A IAIA, IAi B IBIB, IBi AB IAIB O ii ++, +Rh+ dominant -Rhrecessive Antigens Antibodies Donate to Receive from A Anti-B A, AB A, O B Anti-A B, AB B, O AB none AB, A, B, O none Anti-A Anti-B A, B, AB, O O Rh none pos or neg none *only if exposed to antigen pos or neg only Reaction to Anti-A Reaction to Anti-B Reaction to Anti-Rh *Rh- mothers can be exposed to the Rh antigen if the fetus is Rh+

Use only to type blood in lab (serum reacts to antigens present) Blood Typing

Use only to type blood in lab (serum reacts to antigens present) Blood Typing Chart Blood Type Genotypes A IAIA, IAi B IBIB, IBi AB IAIB O ii ++, +Rh+ dominant -Rhrecessive Antigens Antibodies Donate to Receive from Reaction to Anti-A Reaction to Anti-B Reaction to Anti-Rh A Anti-B A, AB A, O clumps - B Anti-A B, AB B, O - clumps AB none AB, A, B, O clumps none Anti-A Anti-B A, B, AB, O O - - Rh none pos or neg clumps none *only if exposed to antigen pos or neg only - *Rh- mothers can be exposed to the Rh antigen if the fetus is Rh+

Nondisjunction Occurs when a chromosome or chromosomes fail to separate in meiosis Individuals end

Nondisjunction Occurs when a chromosome or chromosomes fail to separate in meiosis Individuals end up with the wrong number of chromosomes ( < or > 46 total) Risk factor increases with age

Nondisjunction of Autosome Down Syndrome caused by trisomy 21 (3 copies of chromosome #21)

Nondisjunction of Autosome Down Syndrome caused by trisomy 21 (3 copies of chromosome #21)

Nondisjunction of Sex Chromosomes Turner Syndrome (karyotype 45, XO): Female; sterile; sex organs do

Nondisjunction of Sex Chromosomes Turner Syndrome (karyotype 45, XO): Female; sterile; sex organs do not develop at puberty Klinefelter’s Syndrome (Karyotype 47, XXY): Male; infertility; fewer secondary sex characteristics; variations are 48, XXXY and 49, XXXXY