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Botany · Ch 5 — Taxonomy and Systematic Botany

Molecular taxonomy (molecular systematics / molecular phylogenetics)

5.11.5

Molecular taxonomy (molecular systematics / molecular phylogenetics)

Molecular taxonomy (molecular systematics / molecular phylogenetics) is the branch of phylogeny that analyses hereditary molecular differences - mainly in DNA sequences - to gain information and establish genetic relationships between members of different taxonomic categories, with results expressed as a phylogenetic tree. The advent of DNA cloning and sequencing methods has driven the field forward hugely.

A range of molecular markers is used: allozyme electrophoresis (detects variation at the enzyme level); mitochondrial DNA markers (non-nuclear, non-recombining, so homologous markers); microsatellites (short, highly variable tandem-repeat DNA sequences); RFLP - Restriction Fragment Length Polymorphism (identifies taxa from unique patterns of restriction sites, i.e. differences in the LENGTHS of DNA fragments after cutting with restriction enzymes); RAPD - Random Amplified Polymorphic DNA (uses a randomly synthesised primer to amplify unknown regions of DNA; useful within and between closely related species, though results are hard to replicate); AFLP - Amplified Fragment Length Polymorphism (similar to RFLP but the fragments each terminate in a characteristic sequence; used in population genetics and higher-level cladistic analysis); SNPs - Single Nucleotide Polymorphisms (the most abundant genome polymorphism, arising from single-nucleotide substitutions/insertions/deletions, detected via PCR, microchip arrays or fluorescence); and DNA microarrays/chips (immobilised DNA fragments on a slide/chip that match a known probe against an unknown sample, useful for species-specific identification). …

Table 5.7Molecular markers used in molecular taxonomy
MarkerDescription
Allozyme electrophoresisIdentifies genetic variation at the level of enzymes directly encoded by DNA
Mitochondrial DNA markersNon-nuclear DNA in mitochondria; the entire genome transcribes as one unit; not subject to recombination, so homologous markers
MicrosatelliteA simple DNA sequence repeated several times (usually 2-5 bp) across various points in the genome; highly variable, used as markers (e.g. TGTGTG tandem repeat)
Single Nucleotide Polymorphism (SNP)Arises from single nucleotide substitutions or insertions/deletions; the most abundant polymorphism type; detected by PCR, microchip arrays or fluorescence technology
DNA microarray / DNA chipSmall glass slides, silicon chips or nylon membranes with many immobilised DNA fragments; matches a known probe against DNA from an unknown sample; used for species identification
Arbitrary markers (RAPD, AFLP)Target a segment of DNA of unknown function to amplify unknown regions