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Using the information from problem 4, scientists do a further testcross using a heterozygote for height and nose morphology. The offspring are tall upturned snout, 40; dwarf upturned snout, 9; dwarf downturned snout, 42; tall downturned snout, 9. Calculate the recombination frequency from these data, and then use your answer from problem 4 to determine the correct order of the three linked genes.

Short Answer

Expert verified

18% is the frequency of recombination between the genes for height tall (T) and an upturned snout (S).

The correct order of the three genes on the chromosome is T-A-S.

Step by step solution

01

Recombination frequency

Recombinant frequency measures the proportion of recombinant offspring obtained when parents with specific traits are crossed.It represents the chances of recombination that occurs between the two genes in a chromosome.

Thus, recombinant frequencies between the genes help to calculate the distance between the genes on the chromosome.

The recombinant frequency between two genes is calculated using the following formula:

Recombinationfrequency=NumberofrecombinantsTotalnumberofoffspringsร—100

02

Explanation for the recombinant frequency between genes for height and nose morphology

Four types of offspring were obtained in the testcross using heterozygote for height and tall morphology. The testcross using heterozygote with tall and an upturned snout produced four types of offspring.

The tall upturned snout (40) and dwarf downturned snout (42) were wild-type offspring, while dwarf upturned snout (9) and tall downturned snout (9) were recombinant offspring.

The total number of offspring produced in the cross is 40+9+42+9=100

The total number of recombinants is 9+9=18.

The recombination frequency is calculated by substituting the values into the following equation:

lRecombinationfrequency=18100ร—100Recombinationfrequency=18%

Thus,the recombination frequency for the genes between tall (T) and an upturned snout (A) is 18%.

03

To determine the order of the genes on the chromosome  

From question four, the recombination frequency for the genes between tall (T) and antennae (A) obtained was 12%. The recombination frequency for the genes between antennae (A) and an upturned snout obtained was 5%. While the recombination frequency for the genes between tall (T) and an upturned snout (A) is 18%.

From the recombinant frequencies obtained from three crosses, it is inferred that the distance between the genes for height (T) and nose morphology (S) is the highest, that is, 18%. In comparison, the recombinant frequency between the genes for antennae (A) and nose morphology (S) is the least, that is, 5%.

The data indicate that genes for antennae and nose morphology are located nearer than the genes for height and nose morphology. This exhibits that the order of the genes on the chromosomes must beT-A-S.

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Most popular questions from this chapter

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.)

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?

About 5% individuals with Down syndrome have a chromosomal translocation in which a third copy of chromosome 21 is attached to chromosome 14. If this translocation occurred in a parentโ€™s gonad, how could it lead to Down syndrome in a child?

Theฯ‡2value means nothing on its own- it is used to find the probability that, assuming the hypothesis is true, the observed data set could have resulted from random fluctuations. A low probability suggests that the observed data are consistent with the hypothesis, and thus the hypothesis should be rejected, A standard cutoff point used by biologists is a probability of 0.05(5%). If the probability corresponding to theฯ‡2value is 0.05or considered statistically significant, the hypothesis (that the genes are unlinked) should be rejected. If the probability is above 0.05, the results are not statistically significant: the observed data are consistent with the hypothesis.

To find the probability, locate yourฯ‡2value in theฯ‡2Distribution table in Appendix F. The โ€œdegree of freedomโ€ (pdf) of your data set is the number of categories (here,4 phenotypes), minus 1, so df=3.

(a). Determines which values on the df =3 line of the table your calculatedฯ‡2value lies between.

(b). The column headings for these values show the probability range for yourฯ‡2number. Based on whether there is non-significant (pโ‰ค0.05) or significant (p>0.05) difference between the observed and expected values, are the data consistent with the hypothesis that the two genes are unlinked and assorting independently, or is there enough evidence to reject this hypothesis?

Crossing over is thought to be evolutionarily advantageous because it continually shuffles genetic alleles into novel combinations. Until recently, it was thought that the genes on the Y chromosome might degenerate because they lack homologous genes on the X chromosome with which to pair up prior to crossing over. However, when the Y chromosome was sequenced, eight large regions were found to be internally homologous to each other, and quite a few of the 78 genes represent duplicates. (Y chromosome researcher David Page has called it a "hall of mirrors.โ€). Explain what might be a benefit of these regions.

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