Human Genetics Module 9.

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Presentation transcript:

Human Genetics Module 9

Studying Human Genetics A PEDIGREE is used to study the inheritance of a single trait in a family Symbols used in pedigrees:

Pedigrees Inheritance of an autosomal dominant trait Individuals need ONE dominant allele to express the trait Trait is present in every generation Trait is expressed in both males AND females

Pedigrees Inheritance of an autosomal recessive trait Individuals need TWO recessive alleles to express the trait Trait skips a generation Trait is expressed in both males AND females

Pedigrees Inheritance of an sex-linked recessive trait Males need ONE recessive allele to express the trait Females need TWO recessive alleles to express the trait Females can “carry” the trait Trait skips a generation Trait is expressed more often in males and is inherited from mother to son

What is a trait? TRAITS include “normal” characteristics as well as genetic DISORDERS

Karyotypes A karyotype is a picture of chromosomes A karyotype may show chromosomal disorders / aneuploidy (an abnormal #) Autosomes: the first 22 pairs Sex chromosomes: the 23rd pair

Karyotypes How do we obtain chromosomes for a karyotype? All cells contain a complete copy of the chromosomes We can obtain cells from a fetus using 2 methods: Amniocentesis Chorionic Villi Sampling

Gene disorders Can NOT be “seen” on a karyotype! Involve the inheritance of a faulty GENE GENE: a section of DNA that codes for a particular protein; PROTEINS DETERMINE TRAITS

Gene Disorders Huntington’s Disease HH – has trait Inherited as: autosomal dominant HH – has trait Hh – has trait hh – no trait Appears after age 40; leads to gradual deterioration of the brain and eventual death

Gene Disorders Sickle-Cell Anemia SS – has disease Inherited as: autosomal co-dominant SS – has disease SN – has trait NN – no trait (normal blood cells) Sickle-shaped red blood cells lead to poor circulation and pain; predominant in African/ African-American populations Tiki Barber

Gene Disorders Cystic Fibrosis CC – normal Inherited as: autosomal recessive CC – normal Cc – normal, but “carries” the trait cc – has disease Leads to mucous build-up in lungs and digestive tract, usually fatal; predominant in Caucasian populations

Gene Disorders Tay-Sachs TT – normal Inherited as: autosomal recessive Tt – normal, but “carries” the trait tt– has disease Breaks down the central nervous system leading to death by age 4; predominant in Jewish populations

Gene Disorders Phenylkentonuria (PKU) PP – normal Inherited as: autosomal recessive PP – normal Pp – normal, but “carries” the trait pp– has disease Inability to break down the amino acid phenylalanine, so it builds up in the brain; leads to decreased mental function, but can be controlled by diet

Gene Disorders Hemophilia XHXH or XHY – normal Inherited as: sex-linked recessive XHXH or XHY – normal XHXh – normal, but “carries” the trait XhXh or XhY – has disease Low production of blood clotting factors leads to excessive bruising or bleeding

Gene Disorders Red-Green Colorblindness XBXB or XBY – normal Inherited as: sex-linked recessive XBXB or XBY – normal XBXb – normal, but “carries” the trait XbXb or XbY – has disease Inability to distinguish between colors (especially reds and greens)

Chromosomal disorders CAN be diagnosed using a karyotype! Involve problems with an entire chromosome, which may contain 1000’s of genes! ANEUPLOIDY: an abnormal number of chromosomes resulting from mistakes in meiois 23 24 23 23 VS. 46 47

Chromosomal Disorders Down’s Syndrome Inherited as: autosomal aneuploidy; Trisomy 21 Leads to mental impairment, heart defects, flat facial features, enlarged tongue

Chromosomal Disorders Turner’s Syndrome Inherited as: sex chromosome aneuploidy; XO Leads to mental impairment and infertility

Chromosomal Disorders Klinefelter’s Syndrome Inherited as: sex chromosome aneuploidy; XXY Leads to mental impairment and infertility

Replacing a defective gene with a normal gene Gene Therapy Genetic disorders can often be treated but can NOT be cured The Human Genome Project has given us information that allows the development of gene therapies GENE THERAPY: Replacing a defective gene with a normal gene