1. The Chromosomal Basis of Mendel’s Laws

2. Mendel’s “principle of segregation” a.pairs of genes on homologous chromosomes separate gamete (meiosis) during gamete formation (meiosis) and end up in different gametes. gametes b.the fusion of gametes at fertilization pairs genes once again. Ex: The alleles for height in Mendel’s pea plants end up in separate gametes. Tt X Tt could yield four the offspring: TT, Tt, Tt, tt.

3. Mendel’s “principle of independent assortment”Mendel’s “principle of independent assortment” a.each pair of alleles on nonhomologous chromosomes segregates independently of other pairs during gamete formation Ex: When Mendel crossed F1 plants that were heterozygous for round yellow peas, some F2 plants did not resemble the parent plants.

4. Morgan’s First Mutant

5. Sex-linked Inheritance

6. Drosophila Testcross Black and Vestigial Wild Type (Gray and Normal) Gray and Normal Black and Vestigial

7. Evidence for linked genes in Drosophila Non-Parental Phenotype

8. Recombination Due to Crossing Over

10. If the two genes were on different chromosomes, the alleles from the F1 dihybrid would sort into gametes independently, and we would expect to see equal numbers of the four types of offspring. Since most offspring had a parental phenotype it can be concluded that the genes for body color and wing size are located on the same chromosome.

11. Linked genes tend to be inherited together because they are located near each other on the same chromosome. Recombinants have different phenotypes than the parents.

12. Morgan, who discovered that genes were located on chromosomes, proposed that some process must occasionally break the physical connection between genes on the same chromosome. This is now called crossing over, which accounts for the recombination of linked genes.

13. Sturdevant, a student of Morgan’s, devised a way to construct genetic maps, an ordered list of the genetic loci along a particular chromosome. He predicted that the further apart two genes are on a chromosome, the higher the probability that crossing over will occur.

14. Using recombination frequencies to construct a genetic map 1 map unit is equal to 1% recombination frequency a second crossover would cancel out the first and reduce the observed b-vg recomb. frequency

15. A genetic map based on recombination frequencies is called a linkage map and is based on the assumption that the probability of a crossover between two genetic loci is based on the distance separating the loci. The distances between genes are expressed as map units, with one map unit equivalent to a 1% recombination frequency.

16. Partial Genetic Map of a Drosophila Chromosome The numbers represent the distance between that locus and the locus for aristae length.

17. Investigators performed crosses that indicated bar-eye and garnet-eye alleles are 13 map units apart, scallop-wing and bar-eye alleles are 6 units apart, and garnet-eye and scallop-wing alleles are 7 units apart. What is the order of these alleles on the chromosome?

18. Given the following recombination frequencies, what is the correct order of the genes on the chromosome? A-B, 8 map units; A-C, 28 map units; A-D, 25 map units; B-C, 20 map units; B-D, 33 map units a)A-B-C-Dd) B-A-C-D b)D-C-A-Be) D-A-B-C c)A-D-C-B

19. Suppose alleles M and n are linked on one chromosome, and m and N are linked on the homologous chromosome. Individuals homozygous for M and n are mated with individuals homozygous for m and N. Their offspring are crossed with homozygous recessive individuals, and the following results are recorded: Mn/mn232mN/mn 240 MN/mn 15 mn/mn 13 How many units apart are these genes on the chromosome?

20. The frequency of crossing over between linked genes A and B is 35 percent; between B and C, 10 percent; between C and D, 15 percent; between C and A, 25 percent; between D and B, 25 percent. The sequence of the genes on the chromosome is: a. ACDBb. ACDB c. ABDCd. ABCD e. ADCB

21. Some Chromosomal Systems of Sex Determination Males have 1 X Sex Chromosome present in ovum Unfertilized males; fertilized females

22. Although female mammals, including humans, inherit two X chromosomes, one X chromosome in each cell becomes almost completely inactivated during embryonic development. The inactive X in each cell of a female condenses into a compact object called a Barr body, which lies along the inside of the nuclear envelope.

23. If a female is heterozygous for a sex-linked trait, about half her cells will express one allele, while the others will express the alternate allele.

24. X inactivation and the Tortoiseshell Cat

25. Calico Cat The white areas are determined by yet another gene.

26. Meiotic Nondisjunction

27. Translocation

28. Alterations of Chromosome Structure

29. Down Syndrome/Trisomy 21

30. Klinefelter Syndrome Male with at least 1 extra X chromosome

31. XYY Karyotype or Jacob Syndrome

32. Testing a Fetus for Genetic Disorders