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Discover the fascinating world of genetics and how traits are passed down from parents to children. Explore the work of Gregor Mendel, learn about monohybrid and dihybrid crosses, and understand concepts such as dominance, codominance, multiple alleles, and sex-linked traits. Dive into the world of genetic disorders and understand how they are inherited.
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Think about this…. • “My parents have brown eyes, why are mine blue?” • “My brother is tall. Why am I short?” • “Why does my sister have blonde hair while mine is brown?”
Are these inherited traits? Your eye color Your hair color and texture Your height
Are these inherited traits? Your personality Your musical, athletic, and artistic abilities
Gregor Mendel • Born in 1822 in Austria • Studied the garden pea plant to determine genetics Father of Genetics
Gregor Mendel • Heredity – the passing on of characteristics from parents to offspring • Characteristics that are inherited are called traits
Gregor Mendel • Mendel studied only 1 trait at a time to control the variable • The tall plants that he worked with had been tall for many generation and had always produced tall offspring • This is calledtrue breeding
Mendel’s Monohybrid Crosses • Mono = one • Ahybrid is the offspring of parents that have different forms of a trait • Such as tall and short
P generation - parents The F1 generation (hybrids) were all purple – self pollinated F2 generation had a ratio of 3:1 3 purple 1 white F stands for filial – son or daughter Mendel’s Monohybrid Crosses
The dominant trait is the trait that is observed The recessive trait is the trait that ‘disappears’ What trait is dominant? The rule of dominance
The rule of dominance • Which is dominant and which is recessive? • TT Tt tt • BB bb Bb • ww WW Ww • HH hh Hh
Phenotypes and Genotypes • The way an organism looks or behaves is called its phenotype
The allele combination an organism contains is its genotype represented as TT for tallness Any plant that is tall has a genotype either TT of Tt Phenotypes and Genotypes
Homo: same Two alleles for the trait are the same (TT or tt) Which ones are homozygous? Homozygous
Hetero = different Two alleles differ from one another (Tt) Heterozygous
A a AA A Aa a Aa aa Monohybrid crosses • a cross that shows the possible offspring for one trait Punnett Square Aa x Aa A: White fur a: Brown fur Genotypic Ratio: 1:2:1 Phenotype: 3 white:1 brown
A A A a Practice! Cross a HOMOZYGOUS dominant female rabbit with a HETEROZYGOUS male rabbit using the same trait. A: White fur a: Brown Fur What is the genotypic ratio? What is the phenotypic ratio?
A A A a Practice! Cross a HOMOZYGOUS dominant female rabbit with a HETEROZYGOUS male rabbit using the same trait. What is the genotypic ratio? AA AA 2 = AA 2 = Aa 2:2 or 50% What is the phenotypic ratio? Aa Aa 4 white fur
Practice!! • Cross a female (Tt) with a male (Tt) using the traits: T: tall t: short T t T t
Practice!! • Cross a female (Tt) with a male (Tt) using the traits: T: tall t: short T t T t
Dihybrid crosses • two traits calculated :RrYy x RrYy
BR Br bR br BR BBRR BBRr BbRR BbRr Br BBRr BBrr BbRr Bbrr bR BbRR BbRr bbRR bbRr br BbRr Bbrr bbRr bbrr Dihybrid Crosses:a cross that shows the possible offspring for two traits BbRr x BbRr Fur Color: B: Black b: White Coat Texture: R: Rough r: Smooth BbRr x BbRr Phenotypic Ratio: 9:3:3:1
More Complex Patterns of Heredity • Codominance/ Incomplete dominance • Multiple Alleles • Sex-Linked Traits
Codominance:two dominant alleles are expressed at the same time CRCR CWCW CRCW
Codominance • Sickle-Cell Anemia is another codominant trait. NA NA NSNA NSNA NS NA=Normal RBC NANA NANA NS=Sickle Cell RBC NA
Multiple Alleles:traits with more than 2 alleles • Blood type has 3 alleles: A, B, O • A and B are codominant over O • O is recessive
What are Sex-Linked Traits? Traits that are located on one of the sex chromosomes (XY) Hemophilia: Failure of blood to clot Alix and Nicholas II Muscular Dystrophy: wasting away of muscles
Can I inherit a sex-linked disease? Mothers (XX) can pass disorders to both sons (XY) and daughters (XX) Fathers (XY) can only pass disorders to daughters (XX) Most disorders are carried on the X chromosome, so males are more likely to inherit them.
How can I tell if I have a genetic disorder? • Karyotypes are a “map” of all 46 (23 pair) of chromosomes.
What’s wrong with this Karyotype? Is this a male or a female?
What’s wrong with this Karyotype? Is this a male or a female?
Down Syndrome Down syndrome occurs because of the presence of an extra 21st chromosome. Down syndrome is also called trisomy 21 Physical Traits • Short stature. A child often grows slowly and, as an adult, is shorter than average. • A short, wide neck with excess fat and skin • Small, low-set ears.
chromosome abnormality that affects only men born with at least one extra X chromosome. The male with Klinefelter Syndrome will be born with 47 chromosomes in each cell, rather than the normal number of 46. Klinefelter Syndrome is also called 47 X-X-Y syndrome. An infant with Kleinnfelter's Syndrome appears normal at birth, but the defect usually becomes apparent in puberty when secondary sexual characteristics fail to develop, and testicular changes occur that eventually result in infertility in the majority of those affected. Klinefelter Syndrome
Trisomy 13 Most cases of Patau syndrome are not inherited, but occur as random events during the formation of reproductive cells (eggs and sperm). Symptoms: Mental & motor challenged polydactyly (extra digits) Heart defects Cleft palate Spinal defects Patau syndrome