Consider a true-breeding plant, AABBCC, crossed with another true-breeding plant, aabbcc, whose resulting offspring are AaBbCc. If you cross the F₁ generation, and independent assortment is operational, the expected fraction of offspring in each phenotypic class is given by the expression N!/M!(N−M)! where N is the total number of alleles (six in this example) and M is the number of uppercase alleles. In a cross of AaBbCc×AaBbCc, what proportion of the offspring would be expected to contain two uppercase alleles?

A dark-red strain and a white strain of wheat are crossed and produce an intermediate, medium-red F₁. When the F₁ plants are interbred, an F₂ generation is produced in a ratio of 1 dark-red: 4 medium-dark-red: 6 medium-red: 4 light-red: 1 white. Further crosses reveal that the dark-red and white F₂ plants are true breeding

How many additive alleles are needed to produce each possible phenotype?

A dark-red strain and a white strain of wheat are crossed and produce an intermediate, medium-red F₁. When the F₁ plants are interbred, an F₂ generation is produced in a ratio of 1 dark-red: 4 medium-dark-red: 6 medium-red: 4 light-red: 1 white. Further crosses reveal that the dark-red and white F₂ plants are true breeding

Based on the ratios in the F₂ population, how many genes are involved in the production of color?

The use of nucleotide sequence data to measure genetic variability is complicated by the fact that the genes of many eukaryotes are complex in organization and contain 5' and 3' flanking regions as well as introns. Researchers have compared the nucleotide sequence of two cloned alleles of the γ-globin gene from a single individual and found a variation of 1 percent. Those differences include 13 substitutions of one nucleotide for another and three short DNA segments that have been inserted in one allele or deleted in the other. None of the changes takes place in the gene's exons (coding regions). Why do you think this is so, and should it change our concept of genetic variation?

List as many human traits as you can that are likely to be under the control of a polygenic mode of inheritance.

Floral traits in plants often play key roles in diversification, in that slight modifications of those traits, if genetically determined, may quickly lead to reproductive restrictions and evolution. Insight into genetic involvement in flower formation is often acquired through selection experiments that expose realized heritability. Lendvai and Levin (2003) conducted a series of artificial selection experiments on flower size (diameter) in Phlox drummondii. Data from their selection experiments are presented in the following table in a modified form and content.

Considering that differences in control values represent year-to-year differences in greenhouse conditions, calculate (in mm) the average response to selection over the three-year period