Kuliev and Verlinsky (2004) state that there was a relatively high number of separation errors at meiosis I. In these cases the centromere underwent a premature division, occurring at meiosis I rather than meiosis II. Regarding chromosome 21, what would you expect to be the chromosome 21 complement in the secondary oocyte in which you saw a single chromatid (monad) for chromosome 21 in the first polar body? If this secondary oocyte was involved in fertilization, what would be the expected consequences?

Kuliev and Verlinsky (2004) state that there was a relatively high number of separation errors at meiosis I. In these cases the centromere underwent a premature division, occurring at meiosis I rather than meiosis II. Regarding chromosome 21, what would you expect to be the chromosome 21 complement in the secondary oocyte in which you saw a single chromatid (monad) for chromosome 21 in the first polar body? If this secondary oocyte was involved in fertilization, what would be the expected consequences?

Name: Kuliev and Verlinsky (2004) state that there was a relatively high num
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: Kuliev and Verlinsky (2004) state that there was a relatively high number of separation errors at meiosis I. In these cases the centromere underwent a premature division, occurring at meiosis I rather than meiosis II. Regarding chromosome 21, what wo

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 16QP: Assume that a meiotic-nondisjunction event causes trisomy 8 in a newborn. If two of the three copies...

See similar textbooks

Similar questions

Variations in Chromosome NumberAneuploidy Describe the process of nondisjunction and explain when it takes place during cell division.
Meiosis is characterized by the pairing of homologouschromosomes during prophase I. In many species, an elaboratestructure called the synaptonemal complex forms betweenhomologues. During this pairing, homologues may exchangechromosomal material at sites called chiasmata. In meiosis I, thehomologues separate from each other, reducing the chromosomenumber to the haploid state (thus the reductive division). It isfollowed by a second division without replication, during whichsister chromatids become separated. The result of meiosis I and IIis four haploid cells. If sister chromatids separated at the first division, would meiosis still work?
A diploid organism produces four gametes from one parent cell through the process of meiosis. Two gametes are found to have 7 chromosomes and two gametes are found to have 5 chromosomes. A) Is this the expected number of chromosomes that would be found in each gamete following a normal cycle of meiosis? If yes, explain why. If no, explain why not and describe how the gamete situation described above occurred. B) Determine the number of homologous chromosome pairs that the original parent cell contained, before meiosis began. Explain how you determined this value.
During metaphase I of meiosis, tetrads align along the metaphase plate independently of each other. Therefore, there is a random “shuffle” of maternal and paternal chromosomes in the resulting gametes.The following diagram demonstrates how this works in a diploid cell with four chromosomes (2n=4) . Because there are two pairs of chromosomes and each pair can align in one of two ways during metaphase I, the number of possible variations in the gametes produced is 22 or 4.For an organism that is , there are three pairs of chromosomes, so the number of possible variations in the gametes produced due to independent assortment in metaphase I is 23 or 8. In an organism with a haploid number of 7, how many possible combinations of maternal and paternal chromosomes can occur in its gametes? a. 72=49 b. 27=128 c.17=1 d. 214=16 384
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?
If nondisjunction occurs in humans for one pair of homologous chromosomes during meiosis I. The other pairs segregate normally. a) Will any normal gametes result? b) How many chromosomes will each human gamete have? If nondisjunction occurs in humans for sister chromatids during meiosis II. The other pairs segregate normally. a) Will any normal gametes result? b) How many chromosomes will each human gamete have?
During metaphase I of meiosis, tetrads align along the metaphase plate independently of each other. Therefore, there is a random “shuffle” of maternal and paternal chromosomes in the resulting gametes.The following diagram demonstrates how this works in a diploid cell with four chromosomes . Because there are two pairs of chromosomes and each pair can align in one of two ways during metaphase I, the number of possible variations in the gametes produced is , or .For an organism that is , there are three pairs of chromosomes, so the number of possible variations in the gametes produced due to independent assortment in metaphase I is , or . In an organism with a haploid number of , how many possible combinations of maternal and paternal chromosomes can occur in its gametes? Select one: a. 72=49 b. 27=128 c.17=1 d. 214=16 384
Assume that you were examining a first polar body and noted that it had one copy (dyad) of each chromosome except chromosome 21. Chromosome 21 was completely absent. What would you expect to be the chromosome 21 complement (only with respect to chromosome 21) in the secondary oocyte? What consequences are likely in the resulting zygote if the secondary oocyte was fertilized?
A diploid cell has 15 picograms of DNA in G₁ phase. If this cell is a germ line cell that undergoes meiosis, how much DNA will each daughter cell contain at the end of meiosis I? How much DNA will each daughter cell contain at the end of meiosis II? MI = 30 pg: MII = 15 pg O MI = 15 pg; MII = 15 pg MI = 7.5 pg; MII = 15 pg O MI = 15 pg: MII = 7.5 pg
If nondisjunction occurs in humans for one pair of homologous chromosomes during meiosis I. The other pairs segregate normally. a) Will any normal gametes result? b) How many chromosomes will each human gametehave? If nondisjunction occurs in humans for sister chromatids during meiosis II. The other pairs segregate normally. a) Will any normal gametes result? b) How many chromosomes will each human gamete have?
A diploid species has 3 pairs of chromosomes in its somatic cells. In males, the first pair is large submetacentric[1]; the second is medium acrocentric[2], and the third is small telocentric[3]. In females, the first two pairs are like those of the males while the third is large metacentric[4][5], with satellite4 Illustrate the karyograms (drawing/picture of the chromosome) of the following: A triploid cell in females tetrasomic cell in males tetraploid cell in females [1] submetacentric --centrosome is just above the middle of the chromosome [2] acrocentric --centrosome is much higher location than submetacentric so that the “p” arm of the chromosome is much shorter than the q arm [3] telocentric --the centromere is at the end of the chromosome [4] metacentric --centrosome is in the middle of the chromosome; thus the “p-arm” and the “q-arm” or both arms of the chromosome are equal in length [5] satellite-a constriction in an arm of a chromosome, aside…
Match the following: A duplicated chromosome is made of 2.A maternal and paternal chromosome present together, each with two sister chromatids 3.Semi-condensed DNA made up of coiled nucleosomes. 4.Super-coiled DNA strands. 5.Contains only one copy of each chromosome. 6.Name of an error during meiosis resulting in fewer chromosomes than normal in a zygote or individual (2n-1) 7.General term for an error resulting in the incorrect number of chromosomes in a gamete after meiosis 8.A specific version of a gene, such as blue eye colour 9.A region on a chromosome that codes for a protein 10.Region where chromosomes are attached 11.None of the above (should be selected more than once) with monosomy trisomy aneuploidy centromere gene sister chromatids diploid Haploid tetrad telomere Chromosomes Chromatin allele