Answered: Sketch the chromosome pairing and the…

Sketch the chromosome pairing and the different segregation patterns that can arise in an individual heterozygous for a reciprocal translocation.

Human Biology (MindTap Course List)

11th Edition

ISBN:9781305112100

Author:Cecie Starr, Beverly McMillan

Publisher:Cecie Starr, Beverly McMillan

Chapter20: Chromosomes And Human Genetics

Section: Chapter Questions

Problem 10SQ

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Concept explainers

Genetic Recombination

Recombination is crucial to this process because it allows genes to be reassorted into diverse combinations. Genetic recombination is the process of combining genetic components from two different origins into a single unit. In prokaryotes, genetic recombination takes place by the unilateral transfer of deoxyribonucleic acid. It includes transduction, transformation, and conjugation. The genetic exchange occurring between homologous deoxyribonucleic acid sequences (DNA) from two different sources is termed general recombination. For this to happen, an identical sequence of the two recombining molecules is required. The process of genetic exchange which occurs in eukaryotes during sexual reproduction such as meiosis is an example of this type of genetic recombination.

Microbial Genetics

Genes are the functional units of heredity. They transfer characteristic information from parents to the offspring.

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Sketch the chromosome pairing and the different segregation patterns
that can arise in an individual heterozygous for a reciprocal
translocation.

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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.
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. Diagram the alternate, adjacent-1, and adjacent-2 segregation patterns in anaphase I of meiosis.
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.
Define reciprocal translocations
Draw a Punnett square for the dihybrid cross. There are two known alleles of gene occupying a specific locus in the X chromosome. The gene in question codes for a transcription factor involved in digit development. The mutant allele is dominant and gives rise to an additional but non-functioning little finger (polydactyly) on both hands. A couple have had their DNA sequenced at the region of interest, the male exhibits polydactyly because of the mutation, the female is homozygous wild type at the same locus and therefore has the wild type phenotype. Both have green eyes. In this story; eye colour shows a monogenic autosomal inheritance pattern and the allele for brown eyes shows incomplete dominance with that for blue eyes, the heterozygote phenotype is green eyes. The genes for eye colour and polydactyly show no linkage.
Explain why heterozygotes for inversions and translocations have low fertility.
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 the products of alternate, adjacent-1, and adjacent-2 segregations.
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 Xa. Draw the pairing arrangement of these chromosomes in prophase 1 of meiosis. Mention their gametic composition. b. Draw the alternate, adjacent I, and adjacent II segregation patterns in anaphase I of meiosis. Mention their gametic composition.
crossing over within a pericentric inversion produces chromosomes that have extra copies of some genes and no copies of other genes. The fertilization of gametes containing chromosomes with duplications or deletions often result in children with syndromes characterized by developmental delay, intellectual disability, abnormal development of organ systems, and early death. Maarit Jaarola and colleagues examined individual sperm cells of a male who was heterozygous for a pericentric inversion on chromosome 8 and determined that crossing over took place within the pericentric inversion in 26% of the meiotic divisions (M. Jaarola, R. H. Martin, and T. Ashley. 1998. American Journal of Human Genetics 63:218–224). Assume that you are a genetic counselor and that a couple seeks counseling from you. Both the man and the woman are phenotypically normal, but the woman is heterozygous for a pericentric inversion on chromosome 8. The man is karyotypically normal. What is the probability that this…
A normal mother has translocations on chromosomes 14:21. With respect to chromosomes 14:21, how many combinations of chromosomes are possible? How many gametes are viable? If the woman has children with an normal father, what is the probability that there is a daughter with Down Syndrome or a son with an unaffected phenotype?
Consider and individual with 3 pairs of homologous chromosomes labeled as: A/a B/b D/d(where the slash line separates one chromosome from its homologues). How many differentmeiotic products (sperm or egg) can this individual produce? What are these?
Contrast the genetic composition of gametes derived from tetrads of inversion heterozygotes where crossing over occurs within a paracentric versus a pericentric inversion.Contrast the genetic composition of gametes derived from tetrads of inversion heterozygotes where crossing over occurs within a paracentric versus a pericentric inversion.