We say that genes that are close together on the same chromosome are linked. What does that mean? Imag- ine that in a diploid nucleus, one chromosome has the allele R and right next to it on the same chromosome is the allele T for a different gene. Are these linked? Imag- ine that r is right next to t on the homologous chro- mosome. If this cell never undergoes meiosis, does this matter at all? If it does undergo meiosis, what are the two genotypes that the gametes are most likely to have? Look at Figure 16-17 for help if you need it.

We say that genes that are close together on the same chromosome are linked. What does that mean? Imag- ine that in a diploid nucleus, one chromosome has the allele R and right next to it on the same chromosome is the allele T for a different gene. Are these linked? Imag- ine that r is right next to t on the homologous chro- mosome. If this cell never undergoes meiosis, does this matter at all? If it does undergo meiosis, what are the two genotypes that the gametes are most likely to have? Look at Figure 16-17 for help if you need it.

Name: Think about the same two genes that were mentioned in Question 23—R an
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Description: Think about the same two genes that were mentioned in Question 23—R and T, present in the heterozygous condition as R and r, T and t. Now imagine that the gene for flower color (the alleles R and r) is not on the same chromosome as the gene for plant

Human Heredity: Principles and Issues (MindTap Course List)

11th Edition

ISBN:9781305251052

Author:Michael Cummings

Publisher:Michael Cummings

Chapter6: Cytogenetics: Karyotypes And Chromosome Aberrations

Section: Chapter Questions

Problem 3QP: A colleague e-mails you saying that she has identified an interesting chromosome variation at 21q13....

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A colleague e-mails you saying that she has identified an interesting chromosome variation at 21q13. In discussing this discovery with a friend who is not a cytogeneticist, explain how you would describe this location, defining each term in the chromosome address 21q13.
in the experiment of following chromosomal dna mvement througgh meiosis, why. do you use non-sister chromatids to demobstrate crossing over? what combinatiobns of alleles could result from a crossover between BD and bd chromosomes? Identify two ways that meiosis contributes to genetic recombination. Why is it necessary to reduce the number of chromosomes in gametes, but not in other cell?
Suppose that meiosis occurs in the transient diploid stageof the cycle of a haploid organism of chromosome number n. What is the probability that an individual haploidcell resulting from the meiotic division will have a complete parental set of centromeres (that is, a set all fromone parent or all from the other parent)?
A sexually reproducing organism has the following phenotype DdEeAaTt: The D and E loci are on the same arm of a metacentric chromosome in cis configuration. The A locus is on the long arm of an acrocentric chromosome and the T locus is on a telocentric chromosome. There are no other chromosomes. Using diagrams, show a cell at metaphase of mitosis and show the results of mitosis. Ensure you show the location of the gene loci on the different chromosomes.
A chromosome that was involved in a reciprocal translocation alsohas an inversion. In addition, the cell contains two normalchromosomes.Make a drawing that shows how these chromosomes will pair duringmetaphase of meiosis I.
Somatic cells in organisms of a particular diploidplant species normally have 14 chromosomes. Thechromosomes in the gametes are numbered from 1through 7. Rarely, zygotes are formed that containmore or fewer than 14 chromosomes. For each of thezygotes below, (i) state whether the chromosomecomplement is euploid or aneuploid; (ii) provideterms that describe the individual’s genetic makeupas accurately as possible; and (iii) state whether ornot the individual will likely develop through theembryonic stages to make an adult plant, and if so,whether or not this plant will be fertile.a. 11 22 33 44 5 66 77b. 111 22 33 44 555 66 77c. 111 222 333 444 555 666 777d. 1111 2222 3333 4444 5555 6666 7777
An individual is heterozygous for a reciprocal translocation, with the following chromosomes: A • B C D E F A • B C V W X R ST • U D E F R ST • U V W X Q. Draw a picture of these chromosomes pairing in prophase I of meiosis.
Meiotic nondisjunction is much more likely than mitotic nondisjunction.Based on this observation, would you conclude that meioticnondisjunction is usually due to nondisjunction during meiosisI or meiosis II? Explain your reasoning?
An individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B • C D E F G A B • C D V W X R S • T U E F G R S • T U V W X Q. Draw the pairing arrangement of these chromosomes in prophase I of meiosis.
A sexually reproducing organism has the following phenotype DdEeAaTt. The D and E loci are on the same arm of a metacentric chromosome in the cis configuration. The A locus is on the long arm of an acrocentric chromosome and the T locus is on a telocentric chromosome. There are no other chromosomes. Show a diagram of the cell in metaphase of mitosis and the result of mitosis.
During a practical, a group of biology students are tasked to study the cell cycle of an insect. This insect has the karyotype 2n=6, with genotype Ff Gg Hh KK. The students must draw a cell at the end of telophase of mitosis, using red lines for maternal chromosomes, blue lines for paternal chromosomes and black dots to represent centromeres. The drawing provided by the students is shown below. kt a) Identify three mistakes the students made when producing this diagram. In your answer only refer to elements already present in the figure. b) This fly is used in a testcross. What is the probability of producing a fly with genotype ff Gg hh Kk?
On rare occasions, an organism may have three copies of achromosome and therefore has three copies of the genes on thatchromosome (instead of the usual number of two copies). Forsuch a rare organism, the alleles for each gene usually segregateso that a gamete will contain one or two copies of the gene. Let’ssuppose that a rare pea plant has three copies of the chromosomethat carries the height gene. Its genotype is TTt. The plant is alsoheterozygous for the seed color gene, Yy, which is found on adifferent chromosome. With regard to both genes, how manytypes of gametes can this plant make, and in what proportions?(Assume that it is equally likely that a gamete will contain oneor two copies of the height gene.)