Chapter 14: Problem 6
Why are organisms that have a haploid life cycle valuable tools for mutagenesis studies?
Chapter 14: Problem 6
Why are organisms that have a haploid life cycle valuable tools for mutagenesis studies?
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It has been noted that most transposons in humans and other organisms are located in noncoding regions of the genomeregions such as introns, pseudogenes, and stretches of particular types of repetitive DNA. There are several ways to interpret this observation. Describe two possible interpretations. Which Interpretation do you favor? Why?
Two related forms of muscular dystrophy-Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD)-are both recessive, X-linked, single-gene conditions caused by point mutations, deletions, and insertion in the dystrophin gene. Bach mutated form of dystrophin is one allele. Of the two diseases, DMD is much more severe. Given your knowledge of mutations, the genetic code, and translation, propose an explanation for why the two disorders differ greatly in severity.
In this chapter, we focused on how gene mutations arise and how cells repair DNA damage. In particular, we discussed spontaneous and induced mutations, DNA repair methods, and transposable elements, Based on your knowledge of these topics, answer several fundamental questions: (a) How do we know that mutations occur spontaneously? (b) How do we know that certain chemicals and wavelengths of radiation induce mutations in DNA? (c) How do we know that DNA repair mechanisms detect and correct the majority of spontaneous and induced mutations?
A number of different types of mutations in the HBB gene can cause human \(\beta\) -thalassemla, a disease characterized by various levels of anemia. Many of these mutations occur within introns or in upstream noncoding sequences. Explain why mutations in these regions often lead to severe disease, although they may not directly alter the coding regions of the gene.
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