Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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How does X inactivation contribute to a person’s
a. It controls the number and kind of genes inherited on an X
chromosome.
b. It determines which X chromosome is expressed in a male.
c. It allows for the expression of either the maternal or the paternal X
in different cells.
d. It enhances the expression of Y-linked genes in males.
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- You examine a maternal effect protein that regulates cell division. Will a mutation in this gene display a defect in the mother with the mutation, or in her offspring who have not inherited the mutation?arrow_forwardThere is a protein called neurogenin that stimulates neuronal cells to differentiate. In order to determine what kind of receptor neurogenin binds to, you add a general phosphatase (one that can remove phosphates from any substrate) to neural cells when you add neurogenin, and you discover that this inhibits differentiation. Furthermore, in the presence of this phosphatase, you find that not even a G protein is activated in response to neurogenin. 1. With this information, what kind of receptor does neurogenin bind to? 2. In a normal cell, how does the G protein in this pathway get activated? 3. In a normal cell, why does the response to neurogenin cease over time?arrow_forwardWhat are X-inactivation and Barr body?arrow_forward
- If a Drosophila female that is homozygous for an X-linked recessive mutation is bred with a male that carries the corresponding wild-type allele, the offspring will..... a. show the mutant phenotype in all individuals. b. be uniform wild-type. c. show a phenotype intermediate to the parents' phenotype. d. show the mutant phenotype in all males and the wild-type phenotype in all females. e. have mutant and wild-type males and mutant and wild-type females.arrow_forwardIn 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.arrow_forwardWhich of the following is a FALSE statement? A) An individual with two X chromosomes and one Y chromosome has testes. B. The human female determines the sex of her offspring. (C) Genomic imprinting allows for differential expressions of an allele. D. Epigenetic changes can be passed on to a zygote. Deletion of the SRY gene would cause male fetuses to develop as females.arrow_forward
- Which of the following statements is TRUE? Overexpression of the X-chromosome in the somatic cells of males a. leads to the formation of a Barr body in male cells' nuclei. b. leads to cellular mosaicism in males hemizygous for an X-linked gene. c. is characteristic of all XY systems of sex determination. d. is the mechanism in flies to compensate for the higher dosage of X-linked genes in females as compared to males. e. None of the abovearrow_forwardColor blindness in humans is an X-linked recessive trait. This means that... O a. Females are more likely to be color blind than males b. The gene associated with color blindness is found on the X chromosome, and an individual must have one (in males) or two (in females) mutant copies of the allele in order to be diagnosed as being color blindarrow_forward
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