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Genetics and Heredity Part II. Is the study of genetics and heredity really as simple as 2 alleles and a Punnett square?. Unfortunately, NO. Darn . . . The following concepts make genetics more interesting and also more complicated:
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Genetics and Heredity Part II
Is the study of genetics and heredity really as simple as 2 alleles and a Punnett square?
Unfortunately, NO. Darn . . .
The following concepts make genetics more interesting and also more complicated: - incomplete dominance - multiple alleles - polygenic inheritance - environmental factors - chromosome disorders - sex-linked disorders
Incomplete Dominance Incomplete dominance occurs when the offspring of 2 homozygous parents show an intermediate phenotype. (#6)
+ RED WHITE PINK (RR) (WW) (RW)
Red and white are equally dominant colors first generation Second generation: red and white reappear
curly + straight Type of Hair wavy
Multiple Alleles Many traits are controlled by multiple alleles. They produce 3 or more phenotypes.
Ex: blood types 3 alleles for blood A, B, O produce 4 blood types: A, AB, B, O
Polygenic Inheritance Polygenic inheritance occurs when a group of genes work together to produce one trait. #9
As a result, many phenotypes are produced. These 3 gene pairs work together to determine one trait.
Environmental Factors Your environment may help determine which traits are expressed.
Ex: Your diet, exposure to chemicals or sunlight, and temperature can affect genetics.
Chromosome Disorders Every species has a specific # of chromosomes. Humans have 46 chromosomes or 23pairs.
Human Chromosomes Pair #23 determines gender: XX = girl XY = boy.
Sometimes an error occurs during meiosis and a gamete (egg or sperm) has too many or too few chromosomes. # of chromosomes ≠ 23
A zygote formed with one of these defective gametes usually dies. If the zygote survives, the baby will be born with a disorder or disability.
Examples of Chromosome Disorders Down’s Syndrome: 3 copies of chromosome #21; short stature, oversized heart, learning disabilities (#10)
Turner syndrome: only affects girls; are missing part or all of one X chromosome; neck webbing, short, infertile, severe heart and kidney problems (#13)
Autism:brain disorder; repetitive movements, delays in speech, learning, and socialization Marfan’s Syndrome: affects connective tissue; thin body, narrow face, long limbs (#13)
This girl is missing part of her 18th chromosome. This boy is missing part of the 11thchromosome. (Jacobsen’s Syndrome) (#13)
Sex-Linked Disorders Some conditions are passed only on the 23rd or the X or Y chromosome. Since these are our sexcells, the disorders are sex-linked.
All eggs carry the X chromosome. The sperm determines the gender of a child. Females: XX Males: XY X X Y It’s a BOY!! It’s a GIRL!!
If a disorder is carried on the X chromosome, both boys and girls can inherit it. (#12) Males:XY Females:XX If a disorder is carried on the Y chromosome, only boys can inherit it.
Punnett square for a sex-linked disorder that’s carried on the X chromosome. Mother does not have the disorder, but carries and passes on the gene for it. Mother (carrier)
Examples of Sex-Linked Disorders (#14) Baldness Colorblindness
Duchenne Muscular Dystrophy (#14) Calico (cats’ fur)
Hemophilia This hemophilia patient received only one injection (shot). The body reacted with severe bleeding under the skin. (bruising) (#14)
Pedigrees A pedigree is a chart used to trace genetic traits throughout a family’s history.
A pedigree is very useful when trying to find the pattern of inheritance of a genetic disorder. (colorblindness, baldness, hemophilia)