Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN: 9781305389892
Author: Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 13, Problem 9TYK
Summary Introduction
To review:
The reason behind different
Introduction:
Turner’s syndrome is the syndrome in which female individuals possess 45 chromosomes instead of 46 due to monosomy of the X chromosome. Klinefelter's syndrome occurs in males and these individuals have an extra copy of X chromosome and thus possess 47 chromosomes instead of 46.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Barr bodies are formed to adjust X chromosome dosage in species other than humans, such as Drosophila (fruit flies) and C. elegans (nematodes). True or False ?
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:
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.
Chapter 13 Solutions
Biology: The Dynamic Science (MindTap Course List)
Ch. 13.1 - You want to determine whether genes a and b are...Ch. 13.2 - You have a true-breeding strain of...Ch. 13.3 - What mechanisms are responsible for: (a)...Ch. 13.4 - A man has Simpson syndrome, an addiction to a...Ch. 13.4 - Prob. 2SBCh. 13.5 - Prob. 1SBCh. 13 - In humans, redgreen color blindness is an X-linked...Ch. 13 - The following pedigree shows the pattern of...Ch. 13 - Individuals affected by a condition known as...Ch. 13 - A number of genes carried on the same chromosome...
Ch. 13 - Prob. 5TYKCh. 13 - Discuss Concepts Can a linkage map be made for a...Ch. 13 - In Drosophila, two genes, one for body color and...Ch. 13 - Another gene in Drosophila determines wing length....Ch. 13 - Prob. 9TYKCh. 13 - You conduct a cross in Drosophila that produces...Ch. 13 - Discuss Concepts Crossing-over does not occur...Ch. 13 - Prob. 12TYKCh. 13 - Prob. 13TYKCh. 13 - Prob. 14TYKCh. 13 - Prob. 1ITDCh. 13 - Prob. 2ITDCh. 13 - Prob. 3ITDCh. 13 - Prob. 4ITD
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- XX individuals can be sex-reversed males if one of their X chromosomes contains a translocated portion of the Y chromosome that includes the SRY gene. In light of what you now know about X-chromosome inactivation, it seems that this karyotype might have more complex consequences. In fact, although most such males are completely sex-reversed, X-chromosome inactivation can cause some of these XX males to have varying degrees of residual female characteristics. a. X-chromosome inactivation in normal XX embryos occurs earlier in development than SRY production in normal XY embryos. When present on a translocation X chromosome, SRY is subject to inactivation. Formulate a hypothesis to explain why many XX individuals with a translocation X chromosome that includes the SRY gene are not completely sex-reversed (male). b. Based on your answer to part (a), why do you think some individuals with this karyotype are completely sex-reversed?arrow_forwardMales of many diploid species (like us) have X and Y sex chromosomes. They are hemizygous for most X- linked genes. Thus, males express most X-linked alleles, whether they are dominant or recessive in females. In the fruit fly Drosophila, it is common to achieve the equivalent of a test cross of X-linked genes in females by assessing the readily observed phenotypes of their male progeny. Since males do not receive X-linked genes from their father, sires of these crosses can be normal or wild-type flies. In fly genetics, it is conventional to name a gene after the mutant phenotype that enabled its discovery. Your challenge is to establish gene order and map distances between three X-linked genes in Drosophila. Each gene is represented by recessive mutant alleles that express rather distinctive phenotypes relative to their dominant wild-type alternative alleles. Flies expressing fruitless (f) are bisexual, lush (1) have a heightened responses to ethanol, and ken&barbie (kb) lack external…arrow_forward. Researchers discovered recently that the sole functionof the SRY protein is to activate an autosomal genecalled Sox9 in the presumptive gonad (before it has“decided” to become a testis or an ovary).a. What would be the sex of an XY individual homozygous for nonfunctional mutant alleles of Sox9?Explain.arrow_forward
- Hi! I would love to get some help on the box-and arrow model question! :) A male individual who is XYSRY has the following genotype for the AMH gene on chromosome 19: AMH1 AMH2. The AMH1 allele codes for a protein that is capable of binding to the receptor for AMH. The AMH2 allele codes for a protein that is unable to bind with the receptor for AMH. Based on your understanding of biology, what is the likely phenotype of this individual? Humans have 23 pairs of chromosomes of which 22 pairs are autosomal and the 23rd pair is sex-linked.In a human female, the sex chromosome pair is represented as XX, whereas, in a human male, it is represented as XY.AMH is an anti-Mullerin hormone produced by the Sertoli cells in males and helps in the development of the sex organs. Each pair of chromosomes has a pair of genes called alleles at the same loci representing a single character. Each gene of an allele represents the expression of the character.A gene can either show expression or…arrow_forwardHuman females who are heterozygous for an X-linked recessive allele sometimes exhibit mild expression of the trait. However, such mild expression of X-linked traits in females who are heterozygous for Xlinked alleles is not seen in Drosophila. What might cause this difference in the expression of X-linked genes between human females and female Drosophila? (Hint: In Drosophila, dosage compensation is accomplished by doubling the activity of genes on the X chromosome of males.)arrow_forwardButterflies have an X-Y sex-determination system that is different from that of flies or humans. Female butterflies may be either XY or X0, while butterflies with two or more X chromosomes are males. This photograph shows a tiger swallowtail gynandromorph, which is half male (left side) and half female (right side). Given that the first division of the zygote divides the embryo into the future right and left halves of the butterfly, propose a hypothesis that explains how nondisjunction during the first mitosis might have produced this unusual-looking butterfly. Question is also in the picture.arrow_forward
- In domesticated cats, the following are Independently assorting: 6. Normal ears (T) is dominant to tufted ears (t); Curved whiskers (C) is dominant to straight whiskers (c); The presence of six toes (S) is dominant to five toes (s); Gene for hair length is an X-linked codominant. The three phenotypes for hair length are long (XHXH), medium (X"X*), and short (X"Xh); medium is the heterozygous condition. Given two parents: TtccSSXHXh x TtCcSsXHY a) How many different gametes could be formed in the female cat with respect to these four traits? b) How many different phenotypes are possible in the offspring from this mating?arrow_forwardIn Drosophila melanogaster white (w) and miniature (m) wings are controlled by X-linked recessive genes with a recombination fruequency between them of approximately 38%. Show the sexes, phenotypes and proportions of offspring expected from the following mating:a. ++/wm female X wm maleb. +m/w+ female X w+ malec. w+/+m female X ++ maleIf we assume that white eyes and miniature wings are not x-linked but are linkedto the autosomal genes, what phenotypic frequencies would you expect from this cross: ++/wm female X ++/wm male?arrow_forwardYour internship with Dr. Nefario at Gru Industries is going well so far, but a recent mission to obtain a shrink ray requires a special kind of Minion. You identify that the ideal Minion phenotypes for this mission are two eyes, pale yellow, and short. From your previous work, you’ve found that:Two-eyed (D) is completely dominant over one-eyed (d)Yellow (Y) is incompletely dominant with white (y)Tall (T) is completely dominant over short (t) a. The only reproductive individuals you have at the moment (it was surprise mission!) are a true breeding two-eyed, yellow, short Minion and a one heterozygous for each trait. What genotypic ratios would you expect for this crossassuming that each locus is on a different chromosome? What total proportion would you expect to be the desired phenotype for the mission? b. The mission has since been delayed due to lack of financial support, so you’ve got some time. All the individuals from the F1 cross above are now reproductive. Which genotypes would…arrow_forward
- Red-green colorblindness is determined in humans by a single X-linked locus. Colorblind males are XbY, and males with normal vision are XBY. XB is dominant, so XBXB and XBXb females have normal vision, while XbXb females are colorblind. Typically, 8% of males are red-green colorblind. Assuming H-W equilibrium, what percentage of females is typically colorblind?arrow_forwardYou discover a new X-linked mutation for antenna shape in Drosophila (fruit flies) which produces long antennae. You call this new allele long (XL2), and discover it is incompletely dominant with the short antennae allele (XL1), so the heterozygotes (XL1XL2) have antennae that are intermediate in length (and XL2 homozygote females have long antennae). Males only have either long or short antennae. You cross a female with long antennae with a male with short antennae. What proportion of their male offspring do you expect to have short antennae? Group of answer choices 0.75 0.50 0 1.00 0.25arrow_forwardIn Drosophila sex determination (Check all that apply.) A) XY individuals transcribe the Sxl gene early but not late. B XX individuals carry the Sxl gene, XY individuals do not. XX individuals transcribe the Sxl gene, XY individuals do not. XX individuals express the Sxl protein, XY individuals do not. E) The Sxl transcript (Pre-MRNA) is spliced differently in XX compared to XY individuals.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Biology: The Dynamic Science (MindTap Course List)BiologyISBN:9781305389892Author:Peter J. Russell, Paul E. Hertz, Beverly McMillanPublisher:Cengage Learning
Human Biology (MindTap Course List)BiologyISBN:9781305112100Author:Cecie Starr, Beverly McMillanPublisher:Cengage Learning
Biology: The Dynamic Science (MindTap Course List)
Biology
ISBN:9781305389892
Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher:Cengage Learning
Human Biology (MindTap Course List)
Biology
ISBN:9781305112100
Author:Cecie Starr, Beverly McMillan
Publisher:Cengage Learning
Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY