Researchers have exploited Minute mutations in order to study the
To circumvent the tiny clone problem, researchers generate GFP-marked homozygous l-/l- clones that are also M+/M+, in flies that are l-/l+ and M-/M+. The loss of the Minute mutation only in cells within the clone gives the l-/l- cells a growth advantage over their neighbors, enabling the mutant clone to grow large enough to study. Diagram chromosomes that could be used to generate such clones.
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Chapter 19 Solutions
Genetics: From Genes to Genomes
- In drosophila, a recessive mutation (m-) of a maternal effect gene results in an abnormalphenotype wherein homozygous (m-m-) females produce eggs that cannot support embryonicdevelopment. Homozygous (m-m-) males, however, can still produce viable sperm. Using m+ todenote a normal gene, determine the genotypes and phenotypes of the F1s produce by a crossbetween a heterozygous female and a recessive male. From the offspring, backcross the recessivefemale with the paternal strain. What are the genotypes and phenotypes of the F2s?arrow_forwardIn drosophila, a recessive mutation (m-) of a maternal effect gene results in an abnormal phenotype wherein homozygous (m-m-) females produce eggs that cannot support embryonic development. Homozygous (m-m-) males, however, can still produce viable sperm. (A) Using m+ to denote a normal gene, determine the genotypes and phenotypes of the F1s produce by a cross between a heterozygous female and a recessive male. (B) From the offspring, backcross the recessive female with the paternal strain. What are the genotypes and phenotypes of the F2s? (C) If m-m- females produce useless eggs, then how are m-m- produced?arrow_forwardThe GAL gene system in yeast is used to metabolize galactose. In the presence of galactose, the GAL genes are expressed; however, in the absence of galactose, the GAL genes are repressed. A yeast mutant is discovered that continuously expresses the GAL genes in the presence or absence of galactose. Which one of the following mutations is likely the cause of constitutively expressed GAL genes? deletion of GAL4 deletion of the UAS elements in the regulatory regions of GAL genes O deletion of GAL3 O deletion of GAL80arrow_forward
- The locations of six deletions have been mapped to a Drosophila chromosome, as shown in the following deletion map. Recessive mutations a, b, c, d, e, and f are known to be located in the same region as the deletions, but the order of the mutations on the chromosome is not known. (refer image for contination )arrow_forwardDrosophila females homozygous for loss-of-functionmutations in the gene aubergine are sterile. RNA-Seqexperiments show that in the ovaries of these females,the levels of RNAs for many kinds of transposable elements are more than 10× higher than in wild-type ovaries. The aubergine gene encodes a Piwi-family protein.a. Why do you think these females are sterile?b. Piwi proteins interact with piRNAs that are transcribed from piRNA gene clusters. Given that thelevels of many kinds of TEs are elevated in mutantovaries, what kinds of DNA sequences do youthink are located in these clusters?c. Many investigators think of piRNAs as a kind ofdefensive mechanism that protects organisms fromthe effects of new transposable elements that mightbe introduced into genomes, for example fromother species. Explainarrow_forwardThe Drosophila gene Sex lethal (Sxl) is deserving of itsname. Certain alleles have no effect on XY animals butcause XX animals to die early in development. Other alleles have no effect on XX animals but cause XY animals to die early in development. Thus, some Sxl allelesare lethal to females, while others are lethal to males.a. Would you expect a null mutation in Sxl to causelethality in males or in females? b. Why do Sxl alleles of either type cause lethality ina specific sex?The gene transformer (tra) gets its name from sexualtransformation, as some tra alleles can change XXanimals into morphological males, while other traalleles can change XY animals into morphologicalfemales.c. Which of these sex transformations would becaused by null alleles of tra and which would becaused by constitutively active alleles of tra?d. In contrast with Sxl, null tra mutations do notcause lethality either in XX or in XY animals.However, the Sxl protein regulates the productionof the Tra protein. Why…arrow_forward
- Leber Congenital Amaurosis (LCA) causes progressive vision loss due to defects in the gene that encodes RPE65 isomerase. Affected individuals are homozygous recessive for mutant alleles of the RPE65 gene. You are trying to determine the molecular nature of the mutations in three individuals with LCA. For ease of analysis, you may assume that each individual is homozygous for the same mutant allele (though the three individuals have different mutations than each other). You use the polymerase chain reaction to amplify DNA from each patient and you determine the sequence of the DNA and compare it to unaffected individuals. You identify the following differences. Note that the non-template strand of DNA is given and the changes are highlighted using red boldface. You can assume that the sequences are in the first reading frame (eg. the first three nucleotides of each sequence is a codon). The coding region of the gene is 1602 bp and the position of the sequences shown below is…arrow_forwardAPOE gene has been found to be a major contributor to sporadic Alzheimer's disease (AD), by acting as an age-of-onset modifier for the common relatively late-onset forms of the disease. Among four alleles causing early onset of AD, the epsilon4 allele (APOE4) disrupts this function. If you generate transgenic monkeys in which the normal allele of APOE gene is knocked out, what phenotype will you expect for those knockout monkeys? A. The APE mRNA expression will be completely suppressed. B. They slow down the development of AD. C. They develop AD early. D. They don't show any AD symptom.arrow_forwardA maternal effect gene in Drosophila, called torso, is found as a recessive allele that prevents the correct development of anterior- and posterior-most structures. A wild-type (homozygous) male iscrossed to a female of unknown genotype. This mating produces 100% larva that are missing theiranterior- and posterior-most structures and therefore die during early development. What is the genotype and phenotype of the female fly in this cross? What are the genotypes andphenotypes of the female fly’s parents? Show COMPLETE cross. Maternal genotype:Paternal genotype:F1 genotype:F1 phenotype:arrow_forward
- A maternal effect gene in Drosophila, called torso, is found as a recessive allele that prevents the correct development of anterior- and posterior-most structures. A wild-type (homozygous) male is crossed to a female of unknown genotype. This mating produces 100% larva that are missing their anterior- and posterior-most structures and therefore die during early development. What is the genotype and phenotype of the female fly in this cross? What are the genotypes and phenotypes of the female fly’s parents? Show COMPLETE cross.arrow_forwardIn humans, dosage compensation is accomplished by: inactivating one X chromosome in female somatic cells inactivating one homolog from each homologous pair of chromosomes in female somatic cells inactivating the Y chromosome in male somatic cells increasing gene expression from the X chromosome in male somatic cellarrow_forwardYou are interested in studying position effect variegation in Drosophila using the chromosome depicted below: Deactivation of the w+ gene gives a white eye phenotype and deactivation of the rst+ gene gives a rough eye phenotype; the normal phenotypes are red and smooth. Because the rst+ and w+ genes have now been placed close to a heterochromatic domain, some sections (or sectors) of the eye display mutant phenotypes due to gene deactivation while others display the normal, wild type phenotype. Which phenotype would you not expect to see rst w Inverted X chromosome white smooth eye sectors white rough eye sectors red smooth eye sectors red rough eye sectorsarrow_forward
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