Population genetics of the yellow fever mosquito in Trinidad: comparisons of amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers
G. Yan et al., Population genetics of the yellow fever mosquito in Trinidad: comparisons of amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers, MOL ECOL, 8(6), 1999, pp. 951-963
Recent development of DNA markers provides powerful tools for population ge
netic analyses. Amplified fragment length polymorphism (AFLP) markers resul
t from a polymerase chain reaction (PCR)-based DNA fingerprinting technique
that can detect multiple restriction fragments in a single polyacrylamide
gel, and thus are potentially useful for population genetic studies. Becaus
e AFLP markers have to be analysed as dominant loci in order to estimate po
pulation genetic diversity and genetic structure parameters, one must assum
e that dominant (amplified) alleles are identical in state, recessive (unam
plified) alleles are identical in state, AFLP fragments segregate according
to Mendelian expectations and that the genotypes of an AFLP locus are in H
ardy-Weinberg equilibrium (HWE), The HWE assumption is untestable for natur
al populations using dominant markers. Restriction fragment length polymorp
hism (RFLP) markers segregate as codominant alleles, and can therefore be u
sed to test the HWE assumption that is critical for analysing AFLP data. Th
is study examined whether the dominant AFLP markers could provide accurate
estimates of genetic variability for the Aedes aegypti mosquito populations
of Trinidad, West Indies, by comparing genetic structure parameters using
AFLP and RFLP markers. For AFLP markers, we tested a total of five primer c
ombinations and scored 137 putative loci. For RFLP, we examined a total of
eight mapped markers that provide a broad coverage of mosquito genome. The
estimated average heterozygosity with AFLP markers was similar among the po
pulations (0.39), and the observed average heterozygosity with RFLP markers
varied from 0.44 to 0.58. The average F-ST (standardized among-population
genetic variance) estimates were 0.033 for AFLP and 0.063 for RFLP markers.
The genotypes at several RFLP loci were not in HWE, suggesting that the as
sumption critical for analysing AFLP data was invalid for some loci of the
mosquito populations in Trinidad. Therefore, the results suggest that, comp
ared with dominant molecular markers, codominant DNA markers provide better
estimates of population genetic variability, and offer more statistical po
wer for detecting population genetic structure.