Which technique analyzes DNA fragment lengths after restriction enzyme digestion?

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Multiple Choice

Which technique analyzes DNA fragment lengths after restriction enzyme digestion?

Explanation:
RFLP analyzes DNA fragment lengths after restriction enzyme digestion by focusing on how sequence differences alter where a DNA molecule is cut. When a genome is treated with restriction enzymes, the DNA is cut at specific short sequences, producing fragments whose sizes depend on where those sites occur. If an individual has a polymorphism that changes a restriction site or the distance between sites, the lengths of the resulting fragments differ. Running these fragments on a gel reveals a pattern of bands whose presence or absence and sizes reflect the underlying genetic variation. This approach relies on comparing fragment-length patterns across samples to detect polymorphisms. Other techniques don’t center on this kind of fragment-length analysis after digestion: PCR amplifies a targeted region to copy it, rather than assessing the entire digest pattern; RAPD uses random primers to generate fingerprint fragments without relying on known restriction sites; Sanger sequencing determines the exact nucleotide sequence rather than comparing fragment lengths after digestion.

RFLP analyzes DNA fragment lengths after restriction enzyme digestion by focusing on how sequence differences alter where a DNA molecule is cut. When a genome is treated with restriction enzymes, the DNA is cut at specific short sequences, producing fragments whose sizes depend on where those sites occur. If an individual has a polymorphism that changes a restriction site or the distance between sites, the lengths of the resulting fragments differ. Running these fragments on a gel reveals a pattern of bands whose presence or absence and sizes reflect the underlying genetic variation. This approach relies on comparing fragment-length patterns across samples to detect polymorphisms.

Other techniques don’t center on this kind of fragment-length analysis after digestion: PCR amplifies a targeted region to copy it, rather than assessing the entire digest pattern; RAPD uses random primers to generate fingerprint fragments without relying on known restriction sites; Sanger sequencing determines the exact nucleotide sequence rather than comparing fragment lengths after digestion.

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