Biology: The Unity and Diversity of Life (MindTap Course List)
15th Edition
ISBN: 9781337408332
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Chapter 41, Problem 4DAA
Summary Introduction
To explain: The percentage of sperm from a heterozygous man that would carry the del allele.
Concept introduction: The epididymis is a part of the male reproductive system. Through the epididymis, the sperm travel from the testis to the vas deferens.
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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…
Butterflies 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.
Which findings support the fact that the presence of the Y-
chromosome rather than the lack of a second X-chromosome
determines the development of maleness in mammals?
A transgenic mouse with two X-chromosomes and the SRY gene from
the Y-chromosome develops male sex organs.
A human with an XXXY genotype (Klinefelter syndrome) is
phenotypically male.
A human with an XO genotype (Turner syndrome) is phenotypically
female.
a and b, but not c
a, b, and c
Chapter 41 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 41 - Stuck Sperm Cells lining the epididymis secrete a...Ch. 41 - Prob. 2DAACh. 41 - Prob. 3DAACh. 41 - Prob. 4DAACh. 41 - Sexual reproduction ___ . a. requires formation of...Ch. 41 - The ___ is a genetic dead end. a. polar body b....Ch. 41 - Prob. 3SQCh. 41 - Prob. 4SQCh. 41 - During a menstrual cycle, a midcycle surge of...Ch. 41 - Prob. 6SQ
Ch. 41 - Prob. 7SQCh. 41 - Male germ cells divide by meiosis inside the...Ch. 41 - A male attains an erection when ___ . a. muscles...Ch. 41 - Prob. 10SQCh. 41 - Prob. 11SQCh. 41 - Prob. 12SQCh. 41 - Match each disease with the type of organism that...Ch. 41 - Match each structure with its description. ____...Ch. 41 - Match each hormone with its source. ____ FSH and...Ch. 41 - Prob. 1CTCh. 41 - Fraternal twins are nonidentical siblings that...Ch. 41 - Some sperm mitochondria enter an egg during...Ch. 41 - Occasionally more than one sperm penetrates and...
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- Albinism is caused by an autosomal recessive allele that interferes with skin pigmentation in mammals. Two normally pigmented human parents already have an albino boy. They plan to continue to have children until they get a girl. Some or all of this information is important for each of the questions below. a) What is the probability that their next child (currently unborn) will be a girl with albinism? Explain your reasoning. b) What is the probability their first female child will be albino? Explain your reasoning. c) The answer to part (b) is different (and, yes, the answer is different) from the answer to part (a). Explain why. (Hint: it has something to do with the underlined words.)arrow_forwardThe introduction to this chapter described the search for genes that determine pattern baldness in humans. In 1916, Dorothy Osborn suggested that pattern baldness is a sex-influenced trait that is dominant in males and recessive in females. More research suggested that pattern baldness is an X-linked recessive trait. Would you expect to see independent assortment between genetic markers on the X chromosome and pattern baldness if (a) pattern baldness is sexinfluenced and (b) if pattern baldness is X-linked recessive? Explain your answer.arrow_forwardBarr 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 ?arrow_forward
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