
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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Transcribed Image Text:QUESTION 15
Chromosomal rearrangements can be caused crossing over between repetitive (duplicated) DNA segments in a process called non-allelic homologous recombination (NAHR). Match the recombination event with the
NAHR indicated in the picture.
2 3
4
2
3
O A. Translocation
O B. Iversion
OC. Deletion
O D. Deletion and duplication
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- A chromosome initially has the following segments:A B • C D E F G Draw the chromosome, identifying its segments, that would result from the following mutations. Q. Paracentric inversion that includes DEFGarrow_forward1. Which changes in chromosome structure cause a change in the total amount of genetic material, and which do not? 2. How does a chromosomal duplication occur? 3. An inversion heterozygote has the following inverted chromosome: B What would be the products if a crossover occurred between the genes F and E on the inverted chromosome and the normal chromosome? 4. An individual has the following reciprocal translocation: с D Centromere A B JI HGF ED CKLM Inverted region с D What would be the outcome of alternate segregation, adjacent -1 segregation and adjacent-2 segregation? 5. Two phenotypically unaffected parents produce two children with familial Down syndrome. Regarding chromosome 14 and 21, what are the chromosomal composition of the parents? 6. Explain how aneuploidy, deletions and duplications cause genetic imbalances. 7. Why do you think that deletions and monosomies are more detrimental than duplications and trisomies? 8. Describe some of the advantages of polyploid plants. 9.…arrow_forwardA chromosome initially has the following segments:A B • C D E F G Draw the chromosome, identifying its segments, that would result from the following mutations. Q.Deletion of FGarrow_forward
- What kind of chromosome rearrangement (shown as ?) is represented below? a. insertion b. Pericentric inversion c. Robersonian translocation d. Paracentric inversion e. balanced translocationarrow_forwardThe normal sequence of nine genes on a certainDrosophila chromosome is 123 • 456789, where the dotrepresents the centromere. Some fruit flies were foundto have aberrant chromosomes with the followingstructures:a. 123 • 476589 c. 1654 • 32789b. 123 • 46789 d. 123 • 4566789Name each type of chromosomal rearrangement, anddraw diagrams to show how each would synapse withthe normal chromosome.arrow_forwardConsider the following two wild type chromosomes: AB•CDEFGH I•JKLMN What kind of rearrangement is observed in the mutated chromosomes below? AB•CLMN I•JKDEFGH A. non-reciprocal translocation B. tandem duplication C. reciprocal translocation D. displaced duplication E. deletionarrow_forward
- Part A Diagram A represents a chromosomal inversion event. A, B, C, D, E, F, are chromosomal loci. Represents a centromere. Diagram B shows a crossing over event between non-sister chromatids (darker vs. lighter lines) during meiosis I. A A Which of the following represents a recombinant chromosome resulting from the cross-over event shown in diagram B? E F MARK ALL THE ANSWES THAT APPLY. Inversion A E C B B EEEEarrow_forwardContrast the outcomes of homologous recombinationand nonhomologous end-joining mechanisms for therepair of double-strand breaks.arrow_forwardAn organism described as 2n=4 has the chromosomes below with genes indicated by letters and centromeres indicated by periods. Select the BEST description of the chromosome aberration present in this organism. HJM.NPQ HJM.NPQ S.TVXZ S.TVXXVZ Select one: 0 a. Paracentric Inversion O b. Reverse Tandem Duplication Oc. Robertsonian Translocation Od. Terminal Deletion e. Tandem Duplication Of. Nonreciprocal Translocation g. Interstitial Deletion Oh. Pericentric Inversion Homobrachial Displaced Duplication Oj. Heterobrachial Displaced Duplication Ok. Reciprocal Translocationarrow_forward
- Which of these changes in chromosome structure alter the total amount of genetic material?arrow_forward1.Describe the rearrangement in chromosomes A-C. indicate the specific markers genes flanking the crossover/breakage points (e.g., a translocation with breakpoints between markers X and Z). 2.Chromosome rearrangements can be caused by crossing over between repetitive DNA sequences. Draw a picture similar to Figure showing how crossovers between repetitive sequences could have produced chromosome rearrangement A. indicate the location and orientation of the repetitive DNA segments relative to the marker genes.arrow_forwardDescribe how non-allelic recombination can change the genome Describe how recombination can result in loss of heterozygosityarrow_forward
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