Chapter 9: Problem 10
A male mouse from a true-breeding strain of hyperactive animals is crossed
with a female mouse from a true-breeding strain of lethargic animals. (These
are both hypothetical strains.) All the progeny are lethargic. In the
Chapter 9: Problem 10
A male mouse from a true-breeding strain of hyperactive animals is crossed
with a female mouse from a true-breeding strain of lethargic animals. (These
are both hypothetical strains.) All the progeny are lethargic. In the
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Get started for freeWhy is the rate of mutation in mitochondrial DNA higher than that in nuclear DNA but the incidence of genetic diseases caused by mutations in mitochondrial DNA relatively low?
Compare the molecular organization in mitochondrial DNA with that in chloroplast DNA.
Mutations in mitochondrial DNA appear to be responsible for a number of neurological disorders, including myoclonic epilepsy and ragged-red fiber disease, Leber's hereditary optic neuropathy, and Kearns-Sayre syndrome. In each case, the disease phenotype is expressed when the ratio of mutant to wild-type mitochondria exceeds a threshold peculiar to each disease, but usually in the 60 to 95 percent range. (a) Given that these are debilitating conditions, why has no cure been developed? Can you suggest a general approach that might be used to treat, or perhaps even cure, these disorders? (b) Compared with the vast number of mitochondria in an embryo, the number of mitochondria in an ovum is relatively small. Might such an ooplasmic mitochondrial bottleneck present an opportunity for therapy or cure? Explain.
In this chapter, we focused on extranuclear inheritance and how traits can be determined by genetic information contained in mitochondria and chloroplasts, and we discussed how expression of maternal genotypes can affect the phenotype of an organism. At the same time, we found many opportunities to consider the methods and reasoning by which much of this information was acquired. From the explanations given in the chapter, what answers would you propose to the following fundamental questions? (a) How was it established that particular phenotypes are inherited as a result of genetic information present in the chloroplast rather than in the nucleus? (b) How did the discovery of three categories of petite mutations in yeast lead researchers to postulate extranuclear inheritance of colony size? (c) What observations support the endosymbiotic theory? (d) What key observations in crosses between dextrally and sinistrally coiled snails support the explanation that this phenotype is the result of maternal- effect inheritance? (e) What findings demonstrate a maternal effect as the basis of a mode of inheritance?
What three criteria must a human disorder fulfill to be classified as a hereditary mitochondrial disease?
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