Biology
5th Edition
ISBN: 9781260487947
Author: BROOKER
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 18, Problem 5TY
Summary Introduction
Introduction: According Lyon hypothesis the dosage compensation that takes place in mammals is a result of inactivation of the X-chromosome in cells. He explained his hypothesis with the example of patchwork pattern on calico cat.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Give typing answer with explanation and conclusion to all parts
The chromosomes drawn below are found in a human skin cell. The lines represent the chromosomes themselves. The letters indicate the location of a particular version of a gene.
a) T/F An individual’s offspring are more likely to inherit a D1 and R together than a D1 and T9 together.
b) T/F About 50% of the egg cells from this individual will have both T9 and BA5.
c) T/F Because r is recessive, the frequency at which the r version of the gene occurs in a population is lower than the frequency at which the R version occurs in the population.
d) T/F If the protein produced by the BA gene is involved in the formation of ovaries, then the BA gene is likely located on a sex chromosome.
e) T/F Because the genes shown here are found in skin cells, these genes code for proteins required for skin cell function.
In a female human cell, what would be the effect on X inactivation if
SİRNAS that eliminate the products of the Tsix gene are added?
Select one:
a. One of the two X chromosomes would become inactivated.
b. Both of the X chromosomes would become inactivated.
c. Neither of the X chromosomes would become inactivated.
d. Only the maternal X chromosome would become inactivated.
e. Only the paternal X chromosome would become inactivated.
Which of the following statements is FALSE about x chromosome inavtivation in mammals?
A. It relies on chromatic remodeling
B. It leads to the formation of Barr body.
C. It only occurs in males.
D. It involves histone modification
Chapter 18 Solutions
Biology
Ch. 18.2 - Prob. 1CCCh. 18.3 - Prob. 1CCCh. 18.3 - Prob. 1CSCh. 18.5 - Prob. 1CSCh. 18.5 - Prob. 1CCCh. 18.6 - Prob. 1EQCh. 18.6 - Prob. 2EQCh. 18.6 - Prob. 3EQCh. 18.6 - Prob. 1CCCh. 18.6 - Prob. 2CC
Ch. 18 - Which of the following is an example of an...Ch. 18 - Prob. 2TYCh. 18 - A female mouse that is Igf2 Igf2 is crossed to a...Ch. 18 - Prob. 4TYCh. 18 - Prob. 5TYCh. 18 - Prob. 6TYCh. 18 - Prob. 7TYCh. 18 - Prob. 8TYCh. 18 - Based on the ideas proposed by Morgan, which of...Ch. 18 - Extranuclear inheritance occurs because a. certain...Ch. 18 - Define epigenetics. Are all epigenetic changes...Ch. 18 - What is a Barr body? How is its structure...Ch. 18 - Core Concept: Information A core concept of...Ch. 18 - Prob. 1COQCh. 18 - Mendel studied seven traits in garden pea plants,...
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
- Which of the following situations does not describes a chromosomal mutation? Select one: a. A cytosine nucleotide is substituted for thymine nucleotide in a gene. b. A portion of Chromosome 4 is deleted during interphase of meiosis. c. The sister chromatids of Chromosome 18 do not separate during anaphase II. d. A section of Chromosome 17 is duplicated leading to problems in the peripheral nervous system.arrow_forwardIn the lab, you discover two yeast haploid mutants that cannot produce arginine. You cross them together and the resulting diploid produces arginine. If producing arginine is the wild type phenotype, what can you definitively conclude? A.The haploid strains have identical mutations in the same genes. B.The haploid strains have identical mutations in different genes. C.The haploid strains have mutations in different genes. D.The haploid strains have mutations in the same gene. E.The haploid strains must belong to the complementation group encoding the first enzyme in the biosynthetic pathway.arrow_forwardCan chromosome duplications cause negative effects to an organism? Why or why not? A. No. Duplicated regions of chromosomes are quickly lost by looping out during meiosis. B. Yes. Duplicated regions increase gene dosage, which affects processes like development that require specific amounts of protein. C. No. Cells with duplications function even more efficiently than those without duplications. D. No. Duplicated regions of chromosomes cannot affect gene dosage because the cell can always compensate for extra copies of genes. E. Yes. Duplicated regions require DNA to be replicated, which delays the cell cycle and wastes energy.arrow_forward
- For the Igf2 gene, where do de novo methylation and maintenancemethylation occur?a. De novo methylation occurs in sperm, and maintenancemethylation occurs in egg cells.b. De novo methylation occurs in egg cells, and maintenancemethylation occurs in sperm cells.c. De novo methylation occurs in sperm, and maintenancemethylation occurs in somatic cells of offspring.d. De novo methylation occurs in egg cells, and maintenancemethylation occurs in somatic cells of offspring.arrow_forwardThe chromosomes drawn below are found in a human skin cell. The lines represent the chromosomes themselves. The letters indicate the location of a particular version of a gene. d) T/F If the protein produced by the BA gene is involved in the formation of ovaries, then the BA gene is likely located on a sex chromosome. e) T/F Because the genes shown here are found in skin cells, these genes code for proteins required for skin cell function.arrow_forwardIn this image of the human karyotype: A. The sister chromatids have separated B. There are 46 pairs of chromosomes C. The DNA has already been replicated D. There are 23 pairs of autosomes E. None are true.arrow_forward
- Which of the following statements is FALSE? Inactivation of one of the two X chromosomes in the somatic cells of mammalian females..... a. underlies the Calico phenotype in cats. b. leads to cellular mosaicism in females heterozygous for an X-linked gene. c. affects 75 % of the paternal and 25 % of the maternal X-chromosomes of a mammalian body. d. leads to the formation of a Barr body in female cells' nuclei. e. is the mechanism in mammals to compensate for the higher dosage of X-linked genes in females as compared to males.arrow_forwardColorblindness and hemophilia are both X-linked traits in humans. Explain how a female who has a defective color vision gene on one X chromosome and a defective blood clotting gene causing hemophilia on the other X chromosome can be neither a hemophiliac nor colorblind? Please discuss the effect of Gene dosage compensation in your answer and in your answer describe the molecular process by which this occurs.arrow_forwardWhy are multiple copies of the X chromosome tolerated? A. Genes on the X chromosome are not expressed during development. B. The extra copies of the X chromosome are inactivated. C. There are no genes on the X chromosome that are detrimental when present in multiple copies D. The X chromosome only encodes sex related genesarrow_forward
- Imagine a scenario in which prenatal testing of a human female fetus indicates that the baby will have a normal XX karyotype but is heterozygous for a mutation that inactivates the Xist promoter. Allele “Xr” represents the mutated version of the Xist promoter, and “XR” represents the normal version of the Xist promoter. How will this mutation affect the process of X inactivation?A. "X inactivation will still be random with both mutant and normal X chromosomes being randomly inactivated" B. "The chromosome with the mutant Xist promoter will always be active" C. "The chromosome with the mutant Xist promoter will always be inactivated" D. "The normal X chromosome (no mutation in Xist) will always be active" E. "The normal X chromosome (no mutation in Xist) will always be inactivated"arrow_forwardA typical egg cell of a female primate contains 23 chromosomes. How many chromosomes does a typical skin cell of a female primate contain? A) 12 chromosomes B) 23 chromosomes C) 46 chromosomes D) 92 chromosomes The karyotype shown would belong to A. Normal human male B. Normal human female C. Male with a chromosomal abnormality D. Female with a chromosomal abnormality 11 12arrow_forwardFor XCI to occur, where are the Xist and Tsix genes expressed?a. Xist is expressed only on Xa, and Tsix is expressed onlyon Xi.b. Xist is expressed only on Xi, and Tsix is expressed onlyon Xa.c. Xist is expressed only on Xa, and Tsix is expressed onlyon Xa.d. Xist is expressed only on Xi, and Tsix is expressed onlyon Xi.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Anatomy & Physiology (11th Edition)BiologyISBN:9780134580999Author:Elaine N. Marieb, Katja N. HoehnPublisher:PEARSON
Biology 2eBiologyISBN:9781947172517Author:Matthew Douglas, Jung Choi, Mary Ann ClarkPublisher:OpenStax
Anatomy & PhysiologyBiologyISBN:9781259398629Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa StouterPublisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)BiologyISBN:9780815344322Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter WalterPublisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & PhysiologyBiologyISBN:9781260159363Author:Martin, Terry R., Prentice-craver, CynthiaPublisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)BiologyISBN:9781260231700Author:Sylvia S. Mader, Michael WindelspechtPublisher:McGraw Hill Education
Human Anatomy & Physiology (11th Edition)
Biology
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:PEARSON
Biology 2e
Biology
ISBN:9781947172517
Author:Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher:OpenStax
Anatomy & Physiology
Biology
ISBN:9781259398629
Author:McKinley, Michael P., O'loughlin, Valerie Dean, Bidle, Theresa Stouter
Publisher:Mcgraw Hill Education,
Molecular Biology of the Cell (Sixth Edition)
Biology
ISBN:9780815344322
Author:Bruce Alberts, Alexander D. Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter
Publisher:W. W. Norton & Company
Laboratory Manual For Human Anatomy & Physiology
Biology
ISBN:9781260159363
Author:Martin, Terry R., Prentice-craver, Cynthia
Publisher:McGraw-Hill Publishing Co.
Inquiry Into Life (16th Edition)
Biology
ISBN:9781260231700
Author:Sylvia S. Mader, Michael Windelspecht
Publisher:McGraw Hill Education
Genetic Variation and Mutation | 9-1 GCSE Science Biology | OCR, AQA, Edexcel; Author: SnapRevise;https://www.youtube.com/watch?v=bLP8udGGfHU;License: Standard YouTube License, CC-BY