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Ch. 7 - Linkage and Chromosome Mapping in Eukaryotes
Klug - Essentials of Genetics 10th Edition
Klug10th EditionEssentials of GeneticsISBN: 9780135588789Not the one you use?Change textbook
Chapter 7, Problem 24

DNA markers have greatly enhanced the mapping of genes in humans. What are DNA markers, and what advantage do they confer?

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1
Understand that DNA markers are specific sequences in the genome that can be easily identified and tracked across generations. They serve as landmarks on chromosomes.
Recognize that DNA markers are often polymorphic, meaning they vary between individuals, which makes them useful for distinguishing different genetic regions.
Learn that DNA markers do not necessarily have to be genes themselves; they can be any identifiable DNA sequence such as microsatellites or single nucleotide polymorphisms (SNPs).
Explore how DNA markers help in gene mapping by allowing researchers to track the inheritance of nearby genes through linkage analysis, even if the gene itself is not directly observable.
Identify the advantage of DNA markers as they enable more precise and efficient mapping of genes associated with traits or diseases, speeding up the discovery process and improving genetic studies.

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Key Concepts

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

DNA Markers

DNA markers are specific sequences in the genome that vary among individuals and can be easily identified. They serve as landmarks on chromosomes, helping researchers track the inheritance of nearby genes. Common types include microsatellites and single nucleotide polymorphisms (SNPs).
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Gene Mapping

Gene mapping involves determining the location of genes on chromosomes. DNA markers facilitate this by acting as reference points, allowing scientists to associate particular markers with traits or diseases through linkage analysis.
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Advantages of DNA Markers in Genetics

DNA markers provide a precise and efficient way to identify genetic variations linked to diseases or traits. They enable high-resolution mapping, reduce reliance on phenotypic traits, and accelerate the discovery of gene-disease associations.
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