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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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 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).
Two nonhomologous chromosomes have the following segments, where * represents the centromere: *ABCDEFG , *RSTUVWX. Name the type of chromosomal rearrangements that would produce each of the following chromosomes. *ABABCDEFG , *ABCD , GFEDCBA*RSTUVWX , *RSWVUTX , *ABCWX , *RSTUVDEFG . Which of these types of abnormalities are most likely embryonic lethal and which ones are not usually a problem for the individual carrying them? Briefly explain why.
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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- Here is a depiction of the position of several genes on 2 chromosomes, with a dash "-" depicting the position of the centromere. Chromosome A has genes ABCD-EFGHIJ Chromosome B has genes 1234-56789. Please name the kind of rearrangement that would result in the following derivative chromosomes: 12D-EFGHIJ AB4-56789 O Unbalanced reciprocal translocation Unbalanced nonreciprocal translocation Balanced reciprocal translocation Balanced nonreciprocal translocationarrow_forwardA diploid individual is heterozygous for a chromosome rearrangement. The original chromosome and its rearranged homolog have the following segments, where ∙ represents a centromere: A B ∙ C D E F G A B ∙ C F E D G While paired in prophase I, a single crossing-over occurs between segment E and segment D of the paired chromosomes. Describe the unusual crossing-over structure that forms as a result.What gamete types will result from crossing over when meiosis is complete? please asaparrow_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
- 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…arrow_forwardAssume that the diploid number of a certain species is four chromosomes, two large and two small (2n=4). a) Of the following figures, which represents a 3n (triploid) cell in mitotic metaphase? b) For each of the wrong answers from part (a) above, explain briefly why it cannot represent a triploid cell in mitotic metaphase.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_forward
- L, R, P and D are four genes located on the same chromosome in a diploid organism. Map distances between different pairs of genes were determined and the following results obtained. Based on these data, what is the order of the genes on the chromosome? D-R: 35 CM P-D: 5 CM L-R: 10 CM D-P: 30 CM D-L 25 CM P-R: 40 CM Note that only one orientation of the order is given as an answer choice. For example: ABCD has the same order as DCBA, but only ABCD would be listed as a possible answer. So be sure to check both orientations when comparing your gene order to the possible answer choices. D-L-P-R P-D-L-R P-R-D-L L-P-R-D R-L-D-Parrow_forwardConsider the true diploid plant cell (2n=2x=6) below wherein the light blue chromosomes A, B, C (from largest to smallest) are paternally derived. These chromosomes contain the same gene pattern and structural features as maternally-derived purple chromosomes A’, B’, and C’, respectively. Draw and label the chromosomes as observed in the following stages Anaphase (c.1), Anaphase I (c.2), and Anaphase II (c.3). Assume no crossing-over events occurred at Meiosis.arrow_forwardTwo 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
- Two phenotypically normal parents produce a phenotypicallyabnormal child in which chromosome 5 is missing part of its longarm but has a piece of chromosome 7 attached to it. The child alsohas one normal copy of chromosome 5 and two normal copies ofchromosome 7. With regard to chromosomes 5 and 7, what do youthink are the chromosomal compositions of the parents?arrow_forwardGiven the following genetic map, predict the chance an offspring would inherit the exact same haplotypes that the parents had. Assume interference in this area of the chromosome is 5%. Please report your value as a percent (%). A |-- 3 mu -- |-- 12 mu -- | Parent 1 Haplotypes: A1 B6 C14/A5 B1 C3 Parent 2 Haplotypes: A8 B3 C2 / A7 B2 C5arrow_forwardIn the classic "X" figure of the chromosome, is the whole X from one parent, or is one side of the X from the mother and the other side from the father?arrow_forward
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