The genetic difference between two Drosophila species, D. heteroneura and D. silvestris, as measured by nucleotide diversity, is about 1.8 percent. The difference between chimpanzees (Pan troglodytes) and humans (H. sapiens) is about the same, yet the latter species is classified in a different genera. Y Part A Is this valid? Drag the terms on the left to the appropriate blanks on the right to complete the sentences. Not all terms will be used. empirical data are reproductively isolated molecular data the Hardy-Weinberg law share a common ancestor Submit traditions The classification of organisms into different species is based on evidence that they Classifications above the species level are not based on arbitrary and based on that extend far beyond DNA sequence information. evious Answers Request Answer Reset Help Pearson. Indeed, it is somewhat

The genetic difference between two Drosophila species, D. heteroneura and D. silvestris, as measured by nucleotide diversity, is about 1.8 percent. The difference between chimpanzees (Pan troglodytes) and humans (H. sapiens) is about the same, yet the latter species is classified in a different genera. Y Part A Is this valid? Drag the terms on the left to the appropriate blanks on the right to complete the sentences. Not all terms will be used. empirical data are reproductively isolated molecular data the Hardy-Weinberg law share a common ancestor Submit traditions The classification of organisms into different species is based on evidence that they Classifications above the species level are not based on arbitrary and based on that extend far beyond DNA sequence information. evious Answers Request Answer Reset Help Pearson. Indeed, it is somewhat

Biology: The Unity and Diversity of Life (MindTap Course List)

14th Edition

ISBN:9781305073951

Author:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Publisher:Cecie Starr, Ralph Taggart, Christine Evers, Lisa Starr

Chapter26: Human Evolution

Section: Chapter Questions

Problem 2DAA: Neanderthal Hair Color The MCIR gene regulates pigmentation in humans (Sections 14.1 and 15.l...

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Neanderthal Hair Color The MC1R gene regulates pigmentation in humans (Sections 14.1 and 15.1 revisited), so loss-of-function mutations in this gene affect hair and skin color. A person with two mutated alleles for this gene makes more of the reddish melanin than the brownish melanin, resulting in red hair and pale skin. DNA extracted from two Neanderthal fossils contains a mutated MC1R allele that has not yet been found in humans. To see how the Neanderthal mutation affects the function of the MC1R gene. Carles Lalueza-Fox and her team introduced the allele into cultured monkey cells (FIGURE 26.16). FIGURE 26.16 MC1R activity in monkey cells transgenic for an unmutated MC1R gene, the Neanderthal MC1R allele, or the gene for green fluorescent protein (GFP). GFP is not related to MC1R. 1. How did MCR1 activity in monkey cells with the mutant allele differ from that in cells with the normal allele?
Neanderthal Hair Color The MCIR gene regulates pigmentation in humans (Sections 14.1 and 15.l revisited), .so loss-of-function mutations in this gene affect hair and .skin color. A person with two mutated alleles for this gene makes more of the reddish melanin than the brownish melanin, resulting in red hair and pa le skin. DNA extracted from two Neanderthal fossils contains a mutated MC1R allele that has not yet been found in humans, To see how the. Neanderthal mutation affects the function of the MC1R gene, Carles Lalueza-Fox and her team introduced the allele into cultured monkey cells (FIGURE 26.1 6). FIGURE 26.16 MC1R activity in monkey cells transgenic for an unmutated MClR gene, the Neanderthal MC1R allele or the gene for green fluorescent protein (GFP). GFP is- not related to MC1R. 2. What does this imply about the mutations effect on Neanderthal hair color?
Neanderthal Hair Color The MCIR gene regulates pigmentation in humans (Sections 14.1 and 15.l revisited), .so loss-of-function mutations in this gene affect hair and .skin color. A person with two mutated alleles for this gene makes more of the reddish melanin than the brownish melanin, resulting in red hair and pa le skin. DNA extracted from two Neanderthal fossils contains a mutated MC1R allele that has not yet been found in humans, To see how the. Neanderthal mutation affects the function of the MC1R gene, Carles Lalueza-Fox and her team introduced the allele into cultured monkey cells (FIGURE 26.1 6). FIGURE 26.16 MC1R activity in monkey cells transgenic for an unmutated MClR gene, the Neanderthal MC1R allele or the gene for green fluorescent protein (GFP). GFP is- not related to MC1R. What purpose do the cells with the gene for green fluorescent protein serve in this experiment?
Explain why we use both Giemsa and DAPI when studying human genetics, and not just one or the other. How are they similar, and how are they different?
. Peas (Pisum sativum) are diploid and 2n = 14. In Neurospora, the haploid fungus, n = 7. If you were to isolategenomic DNA from both species and use electrophoresisto separate DNA molecules by size, how many distinctDNA bands would be visible in each species?
Tiny foxes live on the Channel Islands off the coastof Southern California; the adults weigh less than3 lbs. These so-called island foxes (Urocyon littoralis) derived from the mainland gray fox (Urocyoncinereoargenteus). Analysis of genome sequencesrevealed that unlike the mainland foxes, the foxeson a single island have shockingly little geneticdiversity.a. The genome of only one fox from each island wassequenced. How would the lack of genetic diversitybe evident in a single genome sequence?b. The populations of the foxes on each island aresmall. How might the low diversity have occurred?c. Why is low genetic diversity thought to lead tospecies extinction?d. Hypothesize as to why the Channel Island foxesare thriving without human assistance despite theirlack of genome sequence diversity
Length of snakes can vary between 0.8m and 2.3 m long. In a large population of snakes there were just 2 of 2.3m length out of 560 snakes. How many genes are involved in determining this character?
. a. If you found a zinc-finger domain (which facilitates DNA binding) in a newly identified gene,what kinds of hypotheses could you make aboutthe gene’s function?b. Suppose that this newly identified gene shares ahigh percentage of similarity throughout its lengthwith a previously characterized gene in the sameorganism. What does this fact suggest about the origin of the two genes? Would you categorize thesegenes as being: (i) homologous, (ii) paralogous, or(iii) orthologous? (More than one answer may apply.)
A recent study examining the mutation rates of 5669 mammalian genes (17,208 sequences) indicates that, contrary to popular belief, mutation rates among lineages with vastly different generation lengths and physiological attributes are remarkably constant [Kumar, S., and Subramanian, S. (2002). Proc. Natl. Acad. Sci. USA 99:803–808]. The average rate is estimated at 12.2 * 10-9 per bp per year. What is the significance of this finding in terms of mammalian evolution?
The total number of genes in human is far less than the previous estimate.Comment?
In a study of a muscle disorder, several affected families exhibitedvision problems, muscle weakness, and deafness (M. Zeviani et al. 1990.American Journal of Human Genetics 47:904–914). Analysis of themtDNA from affected members of these families revealed that largenumbers of their mtDNA molecules possessed deletions of varyinglengths. Different members of the same family and even differentmitochondria from the same person possessed deletions of differentsizes, so the underlying defect appeared to be a tendency for the mtDNAof affected persons to have deletions. A pedigree of one of the familiesstudied is shown below. The researchers concluded that this disorder isinherited as an autosomal dominant trait, and they mapped the diseasecausinggene to a position on chromosome 10 in the nucleus.a. What characteristics of the pedigree rule out inheritance of a traitencoded by a gene in the mtDNA as the cause of this disorder?b. Explain how a mutation in a nuclear gene might lead to deletions…
What are molecular homologies used for ? Answe in simple terms