For each type of offspring of the test-cross in Figure 15.9, explain the relationship between its phenotype and the alleles contributed by the female parent. (It will be useful to draw out the chromosomes of each fly and follow alleles throughout the cross.)

Short Answer

Expert verified

The female parent contributes the alleles, and the male parent contributes recessive alleles. The contribution made by the female parent determines the offspring's phenotype.

Step by step solution

01

Description of offspring

Offspring is the young one of the organism. In sexual reproduction, the fusion of male and female gametes results in the formation of gametes. The offspring produced from sexual reproduction tends to possess the character of parents.

02

Description of the dominant and recessive allele

An allele is a variant present in the gene. The recessive allele is the allele that masks its effect. The other type of allele is the dominant alleles that get expressed in the offspring.

03

Allelic expression in the phenotype

The phenotype of the test crossing produced offspring such as wild type (gray normal), black vestigial, gray vestigial, and black normal. Out of these offspring, only female characters are more prominently seen in these offspring.

The male characters are recessive alleles, so the expression is not prominent. The alleles that are found in the eggs are exposed to the phenotype of the organism.

Hence, the female characters are predominantly seen in the test cross.

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Most popular questions from this chapter

You design Drosophila crosses to provide recombination data for genes a, which is located on the chromosome shown in Figure 15.12. Gene a has recombination frequencies of 14% with the vestigial wing locus and 26% with the brown eye locus. Approximately where is a located along the chromosome?

Gene dosage—the number of copies of a gene that are actively being expressed—is important to proper development. Identify and describe two processes that establish the proper dosage of certain genes.

Assume that genes A and B are on the same chromosome and are 50 map units apart. An animal heterozygous at both loci is crossed with one that is homozygous recessive at both loci. What percentage of the offspring will show recombinant phenotypes resulting from crossover? Without knowing these genes are on the same chromosome, how would you interpret the results of this cross?

Consider what you learned about dominant and recessive alleles in Concept 14.1. If a disorder were caused by a dominant X-linked allele, how would the inheritance pattern differ from what we see for recessive X-linked disorders?

A wild-type fruit fly (heterozygous for the gray body color and red eyes) is mated with a black fruit fly with purple eyes. The offspring are wild-type, 721; black purple, 751; gray purple, 49; black red, 45. What is the recombination frequency between these genes for the body color and eye color? Using information for problem 3, what fruit flies (genotypes and phenotypes) would you mate to determine the order of the body color, wing size, and eye color genes on the chromosome?

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