ETEXT CAMPBELL BIOLOGY IN FOCUS INSTANT
3rd Edition
ISBN: 9780135964422
Author: Urry
Publisher: PEARSON
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Chapter 12, Problem 11TYU
FOCUS ON EVOLUTION
Crossing over is thought to be evolutionarily advantageous because it continually shuffles genetic alleles into novel combinations. Until recently, it was thought that Y-linked genes might degenerate because they lack homologous genes on the X chromosome with which to recombine. However, when the Y chromosome was sequenced, eight large regions were found to be internally homologous to each other, and quite a few of the 78 genes represent duplicates. Explain how this might be beneficial.
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EVOLUTION CONNECTION Crossing over is thought to beevolutionarily advantageous because it continually shufflesgenetic alleles into novel combinations. Until recently, it wasthought that the genes on the Y chromosome might degenerate because they lack homologous genes on the X chromosomewith which to pair up prior to crossing over. However, when theY chromosome was sequenced, eight large regions were foundto be internally homologous to each other, and quite a few ofthe 78 genes represent duplicates. (Y chromosome researcherDavid Page has called it a “hall of mirrors.”) Explain what mightbe a benefit of these regions.
Cat fur coat color genetics is interesting. Orange fur is dominant (''B'') to black fur (''b'') and piebald, which is white spotting, is dominant (''S'') to non-white-spotted (''s''). Both of those genes are located on the X chromosome. In addition, in cats, somatic cells exhibit X-inactivation randomly, which explains why there are tortoiseshell cats (when heterozygous, have orange and black spots) as well as calico cats (orange and black but also with white spots). An orange and white spotted male is mated with a tortoiseshell female.
Draw a dihybrid Punnet square to show the possible offspring:
Item 10
10 of 15
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A cross in Drosophila melanogaster involved the recessive X-linked genes for white eye (w), yellow body (y), and cut wings (c). A wild-type tri-hybrid female was crossed with wild-type males and
only the male offspring were tallied. On the basis of the results shown below, which of the choices shown best represents the genetic map of the three loci on the X-chromosome?
Phenotype
Male Offspring
+у ct
63
W + +
60
w y ct
16
+ + +
11
+ + ct
4
w y +
+ у +
247
w + ct
197
5.5 mu
21.5 mu
><
ct
5.5 mu
21.5 mu
y
ct
21.5 mu
5.5 mu
ct
4.5 mu
20.5 mu
y
ct
20.5 mu
4.5 mu
ct
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Chapter 12 Solutions
ETEXT CAMPBELL BIOLOGY IN FOCUS INSTANT
Ch. 12.1 - Which one of Mendels laws relates to the...Ch. 12.1 - MAKE CONNECTIONS Review the description of meiosis...Ch. 12.1 - WHAT IF? Propose a possible reason that the first...Ch. 12.2 - A white-eyed female Drosophila is mated with a...Ch. 12.2 - Neither Tim nor Rhoda has Duchenne muscular...Ch. 12.2 - MAKE CONNECTIONS Consider what you learned about...Ch. 12.3 - When two genes are located on the same chromosome,...Ch. 12.3 - For each type of offspring of the testcross in...Ch. 12.3 - WHAT IF? Genes A, B, and C are located on the same...Ch. 12.4 - About 5% of individuals with Down syndrome have a...
Ch. 12.4 - WHAT IF? The ABO blood type locus has been mapped...Ch. 12.4 - MAKE CONNECTIONS The gene that is activated on the...Ch. 12.4 - Women born with an extra X chromosome (XXX) are...Ch. 12 - A man with hemophilia (a recessive, sex-linked...Ch. 12 - Pseudohypertrophic muscular dystrophy is an...Ch. 12 - A space probe discovers a planet inhabited by...Ch. 12 - Using the information from problem 3, scientists...Ch. 12 - A man with red-green color blindness (a recessive,...Ch. 12 - You design Drosophila crosses to provide...Ch. 12 - A wild-type fruit fly (heterozygous for gray body...Ch. 12 - Assume that genes A and B are 50 map units apart...Ch. 12 - Prob. 9TYUCh. 12 - SCIENTIFIC INQUIRY DRAW IT Assume you are mapping...Ch. 12 - FOCUS ON EVOLUTION Crossing over is thought to be...Ch. 12 - FOCUS ON INFORMATION The continuity of life is...Ch. 12 - SYNTHESIZE YOUR KNOWLEDGE Butterflies have an X-Y...
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- Cat fur coat color genetics is interesting. Orange fur is dominant (''B'') to black fur (''b'') and piebald, which is white spotting, is dominant (''S'') to non-white-spotted (''s''). Both of those genes are located on the X chromosome. In addition, in cats, somatic cells exhibit X-inactivation randomly, which explains why there are tortoiseshell cats (when heterozygous, have orange and black spots) as well as calico cats (orange and black but also with white spots). An orange and white spotted male is mated with a tortoiseshell female. State the genotype of the male and the female.arrow_forwardIt is also note that Chimpanzee has a chromosomal complement of 2N = 48, whereas human has 2N = 46. Interestingly, chromosomal banding patterns have revealed that the chromosome 12 and 13 of chimp show homology with human chromosome 2 (see figure for the alignment of human and chimp banding patterns). This is a good example of chromosomal aberration in evolution. What type of chromosomal rearrangement is likely explained the evolution of human chromosome 2 from the two chromosomes of chimpanzee? A. Translocation B. Duplication C. Inversion D. Deletionarrow_forwardIn Drosophila the genes forked bristles (f and f+) and vermilion eyes (v and v+) are ~24 m.u. apart on the X chromosome. From a cross of f v / f+ v+ females with f v / y males, what % of the progeny do you expect to have the f+ v+ phenotypes? (Don’t let the X chromosome throw you off – this question is essentially asking what % of the female’s gametes will be f+ v+).arrow_forward
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- . Genomes A, B, and C all have basic chromosomenumbers (x) of nine. These genomes were derivedoriginally from plant species that had diverged from each other sufficiently far back in the evolutionarypast that the chromosomes from one genome can nolonger pair with the chromosomes from any other genome. For plants with the following kinds of euploidchromosome complements, (i) state the number ofchromosomes in the organism; (ii) provide terms thatdescribe the individual’s genetic makeup as accurately as possible; (iii) state whether or not it is likelythat this plant will be fertile, and if so, give the number of chromosomes (n) in the gametes.a. AABBCb. BBBBc. CCCd. BBCCe. ABCf. AABBCCarrow_forwardIn humans, chromosome 16 sometimes has a heavily stained area near the centromere. This feature can be seen in a microscope, but otherwise has no effect on the phenotype of the person carrying it. When such a “blob" exists on a given copy of chromosome 16, it is a constant feature of that chromosome and is inherited. A couple conceived a child, but the fetus had multiple abnormalities and was miscarried. e.g., The fetus had three copies of chromosome 16, where 2 of the 3 copies of chromosome 16 had large blobs. Both of the mother's copies of chromosome 16 lacked blobs, but the father was heterozygous for blobs. The fetus was formed from a fertilization event that included a gamete produced by the in which nondisjunction occurred during the meiotic division. Select an answer and submit. For keyboard navigation, use the up/down arrow keys to select an answer. a mother; first. mother; second. father; first. C Your answer d father; second. E3 Fullso L e Insufficient information is provided…arrow_forwardWhy do some genes express themselves later in life? Why not earlier? How many chromosomes in a human that has trisomy-15? How many chromosomes in a human that is triploid?arrow_forward
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