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Genetics

This chapter explores Gregor Mendel's groundbreaking work on heredity, focusing on his study of garden peas and the transmission of traits from one generation to the next. The chapter discusses Mendel's methods, conclusions, and the concepts of dominant and recessive traits, as well as the use of Punnett squares to predict offspring. It also delves into topics such as incomplete dominance, co-dominance, dihybrid crosses, sex determination, sex linkage, blood types, pedigrees, chromosome mutations, and more.

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Genetics

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  1. Genetics Chapter 9 and 12

  2. Gregor Mendel • 1842 • Studied heredity- the transmission of characteristics from parents to offspring. • Studied garden peas- Pisum sativum

  3. Mendel's Work • Looked at peas’ traits • Height (tall or short) • flower position (axial or terminal) • pod appearance (inflated or constricted) • pod color (green or yellow) • seed texture (smooth or wrinkled) • Flower color (purple or white)

  4. Mendel’s Methods • Pollination - from anther to stigma • Self-pollination • Cross-pollination

  5. Types of Pollination

  6. His experiments • Mated pure plants through self pollination. • Created strains of plants. • Created P1 or parent generations. • Crossed the plants to get F1 or first filial generations. AKA 1st offspring. • Then crossed F1 plants to create F2 Plants. AKA 2nd generation offspring.

  7. Conclusions (pg 167-168) • Axial + terminal = axial • Green + yellow = green • Purple + white = purple • THEREFORE…. • Found factors – pairs for each trait. • 2 Alleles per trait (ex Gg)

  8. Recessive vs Dominant Traits • Dominant = controlling or over powering allele. • Recessive= overpowered not controlling allele. Can be masked • Law of segregation= pair of factors is segregated, or separated, during the formation of gametes. • AKA one from dad, one from mom -> join to make a pair.

  9. Chromosomes and Genes • Molecular genetics= study of structure and function of genes. • Alleles- one half of a pair of genes • ex. Aa, “A” is an allele. “a” is an allele. • Probability- the likelihood that a specific event or trait will occur. • ratios

  10. Genotype and Phenotypes • Genotype= genetic makeup of an organism. (Gg) • Phenotype= Physical appearance of organism as a result of its genotype. (green) • Homozygous= both alleles are the same (GG) • Heterozygous= alleles are different (Gg)

  11. Punnett Squares and Crosses • Monohybrid Crosses- cross for ONE pair on contrasting traits. • Homozygous Dominant (PP) x Homozygous Recessive (pp)

  12. Homozygous (BB) x heterozygous (Bb) Heterozygous (Bb) x heterozygous (Bb) Monohybrid Cont.

  13. Test Crosses • Unknown genotypes of parents • Known phenotypes of offspring BB=black, Bb= black, bb=brown • 2 black:2brown • One parent is brown (bb)

  14. Incomplete Dominance • Two or more alleles influence the phenotype. AKA “mixing” • Neither allele is dominant • EX: RR=red, Rr=pink, rr=white • Geno=1RR:2Rr:1rr • Pheno=1red:2pink: • 1white

  15. Co dominance Page 176 • Both alleles are expressed in heterozygous offspring. • Example- a horse has a gene for both red and white hair. Therefore he has strands of white hair and strands of red hair.

  16. Dihybrid Crosses • Involves two pairs of contracting traits. • EX= seed texture and seed color • Homo Dom x Homo Recessive • R (round) is dominant over r (wrinkled) • Y (yellow) is dominant over y (green) • Cross rryy (homogenous wrinkled green) with RRYY (homogenous round, yellow)

  17. RRYY X rryy (Homozygous dominant X recessive)

  18. Heterozygous X Heterozygous RrYy X RrYy

  19. Hetero X Hetero Results • Genotypic ratio • 1RRYY: 2RRYy: 2RrYY: 4 RrYy: 1RRyy: 2Rryy: 1rrYY: 2rrYy: 1rryy • Phenotypic Ratio • Always 9:3:3:1 (total 16) • 9 dominant for both traits • 1 recessive for both traits

  20. Results Continued • 9/16 round and yellow • 3/16 round and green • 3/16 wrinkled and yellow • 1/16 wrinkled and green • **Remember** • 9:3:3:1

  21. Sex determination of Offspring • Cross XX (mom) with XY (dad) • Geno Always = 2XX:2XY • Pheno Always= 2females:2males

  22. Sex Linkage • Genes that are found only on the “X” chromosome or the “Y” chromosome. • color blindness (inherited from mom) • hemophilia • Ex Fly eye color (Morgan) • F1= all red eyes • F2= 3 red: 1white • White was ALWAYS male • THUS, eye color is carried on the “X” chromosome.

  23. Results • F1- all red eye because they all carry “R” • F2- • 3 red eyed (carry “R” • 1 white (does not carry “R” )

  24. X- Influenced • Traits influenced by sex hormones. • Phenotypes differ even is genotypes are the same. • Pattern baldness • B=bald • B’=non bald • Dominant in males, Recessive in females • **Females only show if both alleles are dominant. **

  25. Blood Type • Controlled by multiple alleles • iA, iB, and i (iO). • A and B are co dominant. • A and B are dominant to O.

  26. Pedigrees (see page 227) • Record of how a trait is inherited over several generation. • Determines carriers- organisms that have the gene but do not show the phenotypic trait. • Used to determine genetic disorders.

  27. Additional Info • Chromosome Map- diagram that shows a linear sequence of genes on a chromosome. • Mutation- some sort of change in the gene sequence. Can be good or bad.

  28. Chromosome Map

  29. Trisomy 21

  30. Great Apes Karyotype

  31. Mutations Cont. • Chromosome Mutations • Deletion- loss of part of a chromosome. • Inversion- break off and reattach in reverse. • Translocation- break off and attaches to another chromosome.

  32. Gene Mutations • Point Mutation- substitution, addition, or removal of a single nucleotide. • Ex sickle cell anemia (A for T) • Substitution- nucleotides switch • Frame Shift- caused by deletion or addition.

  33. Ways to detect genetic Disorders. • Genetic Screening • Genetic Counseling • Amniocentesis • Chorionic villi sampling • Pedigrees

  34. Genetic Traits and Disorders • Huntington’s Disease- (single allele) • Blood Type- (multiple alleles) • Skin Color- (polygenic alleles) • Non-disjunction (addition or subtraction of chromosomes) • Monosomy- One chromosome • Trisomy- Three chromosomes • Trisomy-21 – Down Syndrome

  35. Huntington’s Disease

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