Biology: The Unity and Diversity of Life (MindTap Course List)
14th Edition
ISBN: 9781305073951
Author: Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr
Publisher: Cengage Learning
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Chapter 14, Problem 10SQ
Expression of the SRY gene on the Y chromosome gives rise to the male
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Males 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…
Let’s suppose that a gene affecting pigmentation is found on the Xchromosome (in mammals or insects) or the Z chromosome (inbirds) but not on the Y or W chromosome. It is found on an autosome in bees. This gene exists in two alleles: D (dark) is dominant tod (light). What would be the phenotypic results of crosses betweentrue-breeding dark females and true-breeding light males and of thereciprocal crosses involving true-breeding light females and truebreeding dark males for each of the following species?A. Birds C. BeesB. Fruit flies D. Humans
What is a Barr body?
How many Barr bodies in a person with genotype XXXXX?
How is the structure of a Barr body different from that of other chromosomes in the cell?
How does the structure of a Barr body affect gene expression?
Color-blindness is an X-linked recessive trait. Heterozygous females are not color blind but they can sometimes have partial color blindness. Explain how this can occur.
Chapter 14 Solutions
Biology: The Unity and Diversity of Life (MindTap Course List)
Ch. 14 - Constructing a pedigree is particularly useful...Ch. 14 - Prob. 2SQCh. 14 - Prob. 3SQCh. 14 - Prob. 4SQCh. 14 - Prob. 5SQCh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ______ inheritance....Ch. 14 - A female child inherits one X chromosome from her...Ch. 14 - Prob. 1DAACh. 14 - Prob. 2DAA
Ch. 14 - Prob. 3DAACh. 14 - Prob. 9SQCh. 14 - Expression of the SRY gene on the Y chromosome...Ch. 14 - Prob. 11SQCh. 14 - Prob. 12SQCh. 14 - Prob. 13SQCh. 14 - Prob. 14SQCh. 14 - Match the chromosome terms appropriately. ____...Ch. 14 - Prob. 1GPCh. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes (XX); males...Ch. 14 - A mutated allele responsible for Marfan syndrome...Ch. 14 - The somatic cells of most individuals with Down...Ch. 14 - Mutations in the genes for clotting factor VIII...
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- Human sex chromosomes are XX for females and XY for males. a. With respect to an X-linked gene, how many different types of gametes can a male produce? b. If a female is homozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele? c. If a female is heterozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele?arrow_forwardWhat evidence indicates that a trait is coded by a dominant allele on an autosome?arrow_forwardHuman females have two X chromosomes XX; males have one X and one Y chromosome XY. a. With respect to X-linked alleles, how many different types of gametes can a male produce? b. A female homozygous for an X-linked allele can produce how many types of gametes with respect to that allele? c. A female heterozygous for an X-linked allele can produce how many types of gametes with respect to that allele?arrow_forward
- Let’s suppose that a gene affecting pigmentation is found on the Xchromosome (in mammals or insects) or the Z chromosome (in birds)but not on the Y or W chromosome. It is found on an autosome inbees. This gene exists in two alleles: D (dark) is dominant to d (light).What would be the phenotypic results of crosses between true-breedingdark females and true-breeding light males, and the reciprocal crossesinvolving true-breeding light females and true-breeding dark males,in the following species? Refer back to Figures 4.1 and 4.2 for themechanism of sex determination in these species.A. BirdsB. Fruit fliesC. BeesD. Humansarrow_forwardDefine the Random Monoallelic Expression: Inactivation of the X Chromosome ?arrow_forwardIn humans color vision is X-linked, the gene for color vision is located on the X chromosome but is absent on the Y chromosome. Normal color vision (XN) is dominant over colorblindness (Xn). Suppose a colorblind man fathers the children of a woman with genotype XNXN. What is the genotype of the father? What proportion of daughters will be colorblind? What proportion of the sons will be colorblind?arrow_forward
- Let’s say there is an organism with two pairs of alleles, W/w and Z/z, each pair is located on a different pair of chromosomes in the organism’s somatic cells. During Metaphase, what will you observe in the somatic cells?arrow_forwardBow-legs is hypothesized to be X-linked recessive trait in Drosophila melanogaster. The P1 virgin females were, once again, homozygous wild type but the males were bow-legged. There were 52 wild type males and 67 wild type females in the F1 generation. The F2 generation contained 30 wild type males, 75 wild type females, 40 bow-legged males and no bow-legged females. Is this what is to be expected? Use chi-square to prove your position.arrow_forwardIn humans, one of the genes determining color vision islocated on the X chromosome. The dominant form (C )produces normal color vision; red-green color deficiency(c) is recessive. If a man with normal color visionmarries a color-deficient woman, what is the probabilityof them having a color-deficient son? A color-deficientdaughter?arrow_forward
- A company that offers PGD terms an embryo “normal and healthy” if it has 46 chromosomes. Why is this statement misleading? , Two famous male actors had twins using a surrogate mother who carried two embryos that hadbeen fertilized in vitro, one with one man’s sperm and the other with the other man’s sperm. In terms of genetics, how closely are the babies, a boy and a girl, related to each other if they have different fathers?arrow_forwardHumans have two different sex chromosomes, X and Y. Figure 4 below shows the inheritance of sex in humans. Figure 4 Mother Father XX XX Y XY XY a) Copy the diagram into your answer booklet and draw a circle on the part of Figure 4 that shows an egg cell. b) What is the genotype of the male offspring? c) A man and a woman have two sons. The woman is pregnant with a third child. What is the chance that this child will also be a boy?arrow_forwardIn humans, color vision depends on genes encoding three pigments. The R (red pigment) and G (green pigment) genes are close together on the X chromosome, whereas the B (blue pigment) gene is autosomal. A recessive mutation in any one of these genes can cause color blindness. Suppose that a color-blind man married a woman with normal color vision. The four sons from this marriage were color-blind, and the five daughters were normal. Specify the most likely genotypes of both parents and their children, explaining your reasoning. (A pedigree drawing will probably be helpful.) (Problem 50 is by Rosemary Redfield.)arrow_forward
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