Study Guide for Campbell Biology
11th Edition
ISBN: 9780134443775
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Jane B. Reece, Martha R. Taylor, Michael A. Pollock
Publisher: PEARSON
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Chapter 15, Problem 7IQ
Summary Introduction
To determine: The chromosome alterations on the first chromosome of the daughter cells which produced a gene sequence of A-B-C-O-P-Q-G-J-I-H
Introduction: The errors during the process of meiosis or mutagens such as radiation can cause four types of changes in a chromosome structure. A deletion occurs due to chromosomal breakage and an entire chromosomal fragment is lost. The chromosomal fragment may attach as an extra segment to a sister chromatid or a non-sister chromatid called duplication. Inversion is the reattachment of the fragment to the original chromosome in reverse orientation. Translocation is when the chromosomal fragment becomes attached to a non-homologous chromosome.
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A phenotypically abnormal individual has a phenotypically normalfather with an inversion on one copy of chromosome 7 and a phenotypicallynormal mother without any changes in chromosomestructure. The orders of genes along the two copies of chromosome7 in the father are as follows:
R T D M centromere P U X Z C (normal chromosome 7)R T D U P centromere M X Z C (inverted chromosome 7)
The phenotypically abnormal offspring has a chromosome 7 withthe following order of genes:
R T D M centromere P U D T R
Using a sketch, explain how this chromosome was formed. In youranswer, explain where the crossover occurred (i.e., between whichtwo genes).
A wild-type chromosome has the following segments:
A B C • D E F G H I
Researchers have found individuals that are heterozygous for each of the following chromosome mutations. For each mutation, sketch how the wild-type and mutated chromosomes would pair in prophase I of meiosis, showing all chromosome strands.
Q. A B C • D H I
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. Give the products that result from alternate, adjacent-1, and adjacent-2 segregation.
Chapter 15 Solutions
Study Guide for Campbell Biology
Ch. 15 - Complete the following summary of Morgans crosses...Ch. 15 - Two normal color-sighted individuals have two...Ch. 15 - In a testcross between a heterozygote tall,...Ch. 15 - With unlinked genes, an equal number of parental...Ch. 15 - The following recombination frequencies have been...Ch. 15 - a. What is the difference between an organism with...Ch. 15 - Prob. 7IQCh. 15 - Prob. 8IQCh. 15 - Mendels law of independent assortment applies to...Ch. 15 - You have found a new mutant phenotype in fruit...
Ch. 15 - Prob. 3SYKCh. 15 - Prob. 4SYKCh. 15 - Thomas Hunt Morgan firmly established the location...Ch. 15 - Prob. 2TYKCh. 15 - Sex-linked traits a. are coded for by genes...Ch. 15 - Prob. 4TYKCh. 15 - Prob. 5TYKCh. 15 - Prob. 6TYKCh. 15 - Prob. 7TYKCh. 15 - Prob. 8TYKCh. 15 - Prob. 9TYKCh. 15 - Prob. 10TYKCh. 15 - Consider three genes on the X chromosome: A, B,...Ch. 15 - Prob. 12TYKCh. 15 - Genomic imprinting a. explains cases in which the...Ch. 15 - Prob. 14TYKCh. 15 - Prob. 15TYKCh. 15 - Suppose that alleles for an X-linked character for...Ch. 15 - Some girls who fail to undergo puberty are found...Ch. 15 - Prob. 18TYKCh. 15 - The genetic event that results in Turner syndrome...Ch. 15 - Prob. 20TYKCh. 15 - Prob. 1GPCh. 15 - Prob. 2GPCh. 15 - Prob. 3GPCh. 15 - Prob. 4GPCh. 15 - Prob. 5GPCh. 15 - Red-green color blindness is caused by a...
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- A chromosome with the following gene order has a paracentric inversion of BCDE. A B C D E F • G H If a cross-over occurred between C and D, what would the resulting chromosomes look like?arrow_forwardAn 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.arrow_forwardAn 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.arrow_forward
- 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 a. Draw the pairing arrangement of these chromosomes in prophase I of meiosis. b. Diagram the alternate, adjacent-1, and adjacent-2 segregation patterns in anaphase I of meiosis. c. Give the products that result from alternate, adjacent-1, and adjacent-2 segregation.arrow_forwardAn individual that is heterozygous for an inversion has the following chromosomes(∗ is the centromere):M N O P Q • R S T Um n o t s r • q p u Assume that a crossover occurred between P and Q. Starting with “M” allele, list the remaining genes in order (NO spaces between the letters) of the chromosome resulting from crossing over. You must use upper and lower-case letters correctly and the * symbol for the centromere(s).arrow_forwardAn 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. Explain why the fertility of this individual is likely to be less than the fertility of an individual without a translocation.arrow_forward
- Two phenotypically normal parents produce a phenotypically abnormal child in which chromosome 5 is missing part of its long arm but has a piece of chromosome 7 attached to it. The child also has one normal copy of chromosome 5 and two normal copies of chromosome 7. With regard to chromosomes 5 and 7, what do you think are the chromosomal compositions of the parents? Would it most likely be reciprocal translocation? It wouldn't be simple translocation because then the child would have the entirety of one chromosome and only some of the other, but in this case, there is only partial chromosome 5 and chromosome 7?arrow_forward. In a diploid organism of 2n = 10, assume that you canlabel all the centromeres derived from its female parentand all the centromeres derived from its male parent.When this organism produces gametes, how many maleand female-labeled centromere combinations are possible in the gametes?arrow_forwardWhy are the X and Y chromosomes not considered homologous even though they recombine at the PAR region?arrow_forward
- In a haploid fungus, the genes al-2 and arg-6 are 30 m.u.apart on chromosome 1, and the genes lys-5 and met-1are 20 m.u. apart on chromosome 6. In a crossal-2 + ; + met-1 × + arg-6 ; lys-5 +what proportion of progeny would be prototrophic + + ;+ +?arrow_forwardAn 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.arrow_forwardAn initial crossover event will occur between A and B, as indicated in the corresponding image. After this initial event occurs, a second cross over event occurs (not illustrated) involving the products of the first crossover event. Given the chromosome organization below, which two chromatids of the bivalent were involved and between which genes did the second crossover event occur to produce the indicated chromosomes? a. A B c, A b c, a B C, and a b C b. A B C, A B C, a b c, and a b c (return to the original crossover depicted in the image, and then determine how the second crossover event produced this arrangementarrow_forward
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