Genetics Heredity passing down of traits or characteristics from _____________________ Genetics study of _________________ Gregor Mendel (1822-1884) Worked with ___________________. 2 major traits for each plant Plants were either _________________________ Plants were either _________________________ Mendel’s Experiment Male and Female sex organs in pea plants are on the _________________ (___________have pollen and ______________ contains the egg) Pure Traits Traits established through _______________________ Stamen Stigma Genetics •Pure white individuals x pure purple individuals •F1 ____________________________ •F1 x F1 ______ ratio of purple to white pea plants •Out of 1000 plants ______________ were purple and _______________ were white •Results of the Parental cross showed that one trait _______________________ the other trait X = Genetics Vocabulary Dominant Trait Trait that _______________ the recessive trait Recessive Trait Trait that is ___________________ up In this cross PURPLE color was dominant Mendel’s Hypothesis Gene sequence of ___________ on a chromosome Each pea plant trait is a combination of _________genes, one from __________ and one from ____________ Each alternative gene is called an ______________ Dominant Gene shown by a capital letter (P) Recessive Gene shown by a lower case letter (p) Pure Purple plants ________ Pure white plants _______ PP x pp all _________ Pp x Pp ____________________________ Mendel’s Terms Homozygous 2 of the same allele (PP or pp) Heterozygous 2 different alleles (Pp) Punnett Square Results of a cross can be predicted Incomplete Dominance Some traits do not have dominant alleles Heterozygotes appear as a mix between 2 parents 1 trait = ___ phenotypes 4 O’clock Flowers Rr x Rr Ratio of Offspring 1 _______ 2 _______ 1 _______ Codominance Neither allele is dominant Presence of heterozygote means both alleles are _________________________ ____________________is an example Sex Determination Thomas Morgan discovered that chromosomes differed in males and females Females- ______ Males- ________ Called _______ Chromosomes All other chromosomes are called __________ Sex-linked Inheritance Morgan crossed _________ male with _______________ female F1Ratio: _________________ F2 Ratio: 3:1 ratio, but ______ any white females Reasoned that there are genes on __________chromosomes Allele for eye color is on ______chromosome No gene for eye color on ______ chromosome Presence of homozygous recessive, or ONLY a _______________, yields recessive trait Morgan’s Crosses Sex Influenced Traits (Not on test!) • Sex-influenced traits are autosomal traits that are influenced by sex. If a male has one recessive allele, he will show that trait, but it will take two recessive for the female to show that same trait. One such gene is baldness. • BB normal male & female • Bb bald male; normal female • bb bald male; bald female Dihybrid Crosses Dihybrid Cross: Cross: Cross of 2 individuals for 2 different traits Example: In Pea Plants Tall(T) is dominant to short Purple(P) is dominant to white Crossing homozygous tall, purple plant with a homozygous short, white plant _______________ Crossing heterozygous tall, purple plant with a heterozygous tall, purple plant TtPp x TtPp Pedigrees & Genetic Diseases Autosomal dominant disease Presence of dominant allele means that _________________________________________ Autosomal recessive disease Disease only present when ______________recessive alleles are present Sex-linked Dominant Disease present when dominant allele is present on ______________________________ Sex-linked Recessive Disease present when recessive allele is ________________________________ Common Genetic Diseases Huntington’s Disease ___________________________; ____________________; degeneration of muscle tissue; onset in early 30’s. Folk Singer Woody Guthrie had the disease Cystic Fibrosis _______________________________; Defective Protein is made that creates excess mucus; clogs lungs. Color Blindness _________________________________ Inablity to distinguish colors (_______________of male population) Some Genetics Diseases Hemophilia Sex-linked recessive __________________________ Nicholas, Czar of Russia (Mid 1800’s) child was _________________________ Muscular Dystrophy _______________________ Tay-Sach’s Disease _______________________ Degeneration of _____________________; infant mortality Changes in Chromosome Number Nondisjunction – occurs when: In meiosis I, homologous pair both go into the same daughter cell or In meiosis II, the sister chromatids both go into the same gamete. The result: ___________ (3 copies of a single chromosome) or ___________ (1 copy of a single chromosome) Nondisjunction in meiosis I Changes in Chromosome Structure • Mutation - a permanent ____________________. • Chromosome mutation - a change in _____________________structure • Radiation, organic chemicals, or even viruses may cause chromosomes to break, leading to mutations. • Types of chromosomal mutations: inversion, translocation, deletion, and duplication. Deletions Deletions occur when a single break causes a ___________, or two breaks result in a loss in the interior. An individual inherits a normal chromosome from one parent and a chromosome with ______________from the other parent No longer has a pair of ______________________ A syndrome can result – type depends on chromosome(s) affected. Williams Syndrome • Chromosome ________________________ • Children have a pixie look (turned-up noses, wide mouth, small chin, large ears) • Poor academic skills, good verbal and musical abilities • Skin ages prematurely from lack of the gene that controls the production of elastin (also affects cardiovascular health). Duplication Duplication results in a chromosome segment being __________________________________ Produces extra alleles for a trait. Ex: An inverted duplication in chromosome 15 causes inv dup 15 syndrome Poor muscle tone, mental retardation, seizures, curved spine, and autistic characteristics Duplication Translocation Translocation is _________________________________ between two, non-homologous chromosomes. Ex: Alagille syndrome results from a deletion of chromosome 20 or a translocation that disrupts an allele on chromosome 20. Distinctive face, abnormalities of eyes & internal organs, and severe itching. Translocation Inversion • Inversion involves a segment of a chromosome being ____________________________ • The reverse sequence of alleles can alter gene activity. • Crossing-over between inverted and normal chromosomes can cause duplications and deletions in resulting chromosomes. Inversion