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Ch. 8 - Chromosome Mutations: Variation in Number and Arrangement
Klug - Concepts of Genetics  12th Edition
Klug12th EditionConcepts of Genetics ISBN: 9780135564776Not the one you use?Change textbook
Chapter 8, Problem 13

Discuss Ohno's hypothesis on the role of gene duplication in the process of evolution. What evidence supports this hypothesis?

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Ohno's hypothesis, proposed by Susumu Ohno, suggests that gene duplication is a major driver of evolutionary innovation. When a gene is duplicated, one copy retains the original function while the other copy is free to accumulate mutations, potentially leading to new functions or regulatory patterns.
Explain that gene duplication can occur through mechanisms such as unequal crossing over during meiosis, retrotransposition, or whole-genome duplication events. These processes create additional copies of genes in the genome.
Discuss the potential fates of duplicated genes: (1) nonfunctionalization, where one copy becomes a pseudogene; (2) subfunctionalization, where the two copies divide the original function; or (3) neofunctionalization, where one copy evolves a new function.
Provide evidence supporting Ohno's hypothesis, such as the presence of gene families (e.g., the globin gene family) that arose through duplication and subsequent divergence. These gene families often show functional specialization, supporting the idea of evolutionary innovation.
Highlight examples of whole-genome duplication events in evolutionary history, such as those in plants (e.g., polyploidy in wheat) and vertebrates, which have contributed to increased genetic complexity and the emergence of novel traits.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Ohno's Hypothesis

Ohno's hypothesis, proposed by Susumu Ohno in 1970, suggests that gene duplication is a key mechanism in evolution, allowing for genetic redundancy. This redundancy enables one copy of a gene to maintain its original function while the other can acquire mutations that may lead to new functions, contributing to evolutionary innovation and complexity.
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03:13
Translation:Wobble Hypothesis

Gene Duplication

Gene duplication is a process where a segment of DNA is copied, resulting in two identical or similar genes. This can occur through various mechanisms, such as unequal crossing over during meiosis or retrotransposition. The duplicated genes can diverge over time, leading to functional specialization, which is crucial for the evolution of new traits and adaptations.
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Evidence Supporting Ohno's Hypothesis

Evidence supporting Ohno's hypothesis includes comparative genomic studies that show higher rates of gene duplication in species with complex traits. Additionally, examples of gene families, such as the globin gene family, illustrate how duplicated genes can evolve new functions. Phylogenetic analyses also reveal patterns of gene duplication and subsequent divergence across different lineages, reinforcing the role of duplication in evolutionary processes.
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03:13
Translation:Wobble Hypothesis
Related Practice
Textbook Question

Inversions are said to 'suppress crossing over.' Is this terminology technically correct? If not, restate the description accurately.

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Textbook Question

Contrast the genetic composition of gametes derived from tetrads of inversion heterozygotes where crossing over occurs within a paracentric versus a pericentric inversion.

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Textbook Question

Human adult hemoglobin is a tetramer containing two alpha (α) and two beta (β) polypeptide chains. The α gene cluster on chromosome 16 and the β gene cluster on chromosome 11 share amino acid similarities such that 61 of the amino acids of the α-globin polypeptide (141 amino acids long) are shared in identical sequence with the β-globin polypeptide (146 amino acids long). How might one explain the existence of two polypeptides with partially shared function and structure on two different chromosomes?

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Textbook Question
What roles have inversions and translocations played in the evolutionary process?
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Textbook Question

The primrose, Primula kewensis, has 36 chromosomes that are similar in appearance to the chromosomes in two related species, P. floribunda (2n=18) and P. verticillata (2n=18). How could P. kewensis arise from these species? How would you describe P. kewensis in genetic terms?

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Textbook Question

Certain varieties of chrysanthemums contain 18, 36, 54, 72, and 90 chromosomes; all are multiples of a basic set of nine chromosomes. How would you describe these varieties genetically? What feature do the karyotypes of each variety share? A variety with 27 chromosomes has been discovered, but it is sterile. Why?

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