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BioMed Central Page 1 of 3 (page number not for citation purposes) BMC Evolutionary Biology Open Access Correction Evolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscura Pedro Simões* 1 , Marta Pascual 2 , Josiane Santos 1 , Michael R Rose 3 and Margarida Matos 1 Address: 1 Universidade de Lisboa, Faculdade de Ciências da Universidade de Lisboa, Centro de Biologia Ambiental, Departamento de Biologia Animal, Campo Grande, 1749-016 Lisboa, Portugal, 2 Department of Genetics, Faculty of Biology, University of Barcelona, 08028 Barcelona, Spain and 3 Department of Ecology and Evolutionary Biology, University of California, Irvine, California 92697-2525, USA Email: Pedro Simões* - [email protected]; Marta Pascual - [email protected]; Josiane Santos - [email protected]; Michael R Rose - [email protected]; Margarida Matos - [email protected] * Corresponding author Abstract Here we present a correction to our article "Evolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscura". We have recently detected an error concerning the application of the Ln RH formula – a test to detect positive selection – to our microsatellite data. Here we provide the corrected data and discuss its implications for our overall findings. The corrections presented here have produced some changes relative to our previous results, namely in a locus (dsub14) that presents indications of being affected by positive selection. In general, our populations present less consistent indications of positive selection for this particular locus in both periods studied – between generations 3 and 14 and between generation 14 and 40 of laboratory adaptation. Despite this, the main findings of our study regarding the possibility of positive selection acting on that particular microsatellite still hold. As previously concluded in our article, further studies should be performed on this specific microsatellite locus (and neighboring areas) to elucidate in greater detail the evolutionary forces acting on this specific region of the O chromosome of Drosophila subobscura. Correction We have recently detected an error in our article [1], con- cerning the application of the Ln RH formula to our mic- rosatellite data. This necessitates some changes in the results and figures presented in the "Testing for positive selection during laboratory adaptation" results section. Here we provide the corrected data and discuss its implications for our overall findings. Corrected Ln RH values comparing generations 3 and 14 remain significantly different between loci in both TW and AR populations (one-way ANOVA; p < 0.001). Stand- ardized Ln RH values for microsatellite locus dsub14 fall outside the 95% confidence interval of the standard nor- mal distribution for AR 1 (p < 0.03). AR 2 and AR 3 popula- tions show a marginally significant deviation from expectation of neutrality (p < 0.06 for AR 2 ; p < 0.07 for AR 3 ). But AR populations present less consistent indica- tions of positive selection between generations 3 and 14 than previously indicated [1]. In addition, standardized Ln RH values for dsub14 between generations 3 and 14 in TW populations no longer differ significantly from neu- Published: 12 June 2009 BMC Evolutionary Biology 2009, 9:133 doi:10.1186/1471-2148-9-133 Received: 9 February 2009 Accepted: 12 June 2009 This article is available from: http://www.biomedcentral.com/1471-2148/9/133 © 2009 Simões et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Page 1: Evolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscura

BioMed CentralBMC Evolutionary Biology

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Open AcceCorrectionEvolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscuraPedro Simões*1, Marta Pascual2, Josiane Santos1, Michael R Rose3 and Margarida Matos1

Address: 1Universidade de Lisboa, Faculdade de Ciências da Universidade de Lisboa, Centro de Biologia Ambiental, Departamento de Biologia Animal, Campo Grande, 1749-016 Lisboa, Portugal, 2Department of Genetics, Faculty of Biology, University of Barcelona, 08028 Barcelona, Spain and 3Department of Ecology and Evolutionary Biology, University of California, Irvine, California 92697-2525, USA

Email: Pedro Simões* - [email protected]; Marta Pascual - [email protected]; Josiane Santos - [email protected]; Michael R Rose - [email protected]; Margarida Matos - [email protected]

* Corresponding author

AbstractHere we present a correction to our article "Evolutionary dynamics of molecular markers duringlocal adaptation: a case study in Drosophila subobscura". We have recently detected an errorconcerning the application of the Ln RH formula – a test to detect positive selection – to ourmicrosatellite data. Here we provide the corrected data and discuss its implications for our overallfindings. The corrections presented here have produced some changes relative to our previousresults, namely in a locus (dsub14) that presents indications of being affected by positive selection.In general, our populations present less consistent indications of positive selection for thisparticular locus in both periods studied – between generations 3 and 14 and between generation14 and 40 of laboratory adaptation. Despite this, the main findings of our study regarding thepossibility of positive selection acting on that particular microsatellite still hold. As previouslyconcluded in our article, further studies should be performed on this specific microsatellite locus(and neighboring areas) to elucidate in greater detail the evolutionary forces acting on this specificregion of the O chromosome of Drosophila subobscura.

CorrectionWe have recently detected an error in our article [1], con-cerning the application of the Ln RH formula to our mic-rosatellite data. This necessitates some changes in theresults and figures presented in the "Testing for positiveselection during laboratory adaptation" results section. Herewe provide the corrected data and discuss its implicationsfor our overall findings.

Corrected Ln RH values comparing generations 3 and 14remain significantly different between loci in both TW

and AR populations (one-way ANOVA; p < 0.001). Stand-ardized Ln RH values for microsatellite locus dsub14 falloutside the 95% confidence interval of the standard nor-mal distribution for AR1 (p < 0.03). AR2 and AR3 popula-tions show a marginally significant deviation fromexpectation of neutrality (p < 0.06 for AR2; p < 0.07 forAR3). But AR populations present less consistent indica-tions of positive selection between generations 3 and 14than previously indicated [1]. In addition, standardizedLn RH values for dsub14 between generations 3 and 14 inTW populations no longer differ significantly from neu-

Published: 12 June 2009

BMC Evolutionary Biology 2009, 9:133 doi:10.1186/1471-2148-9-133

Received: 9 February 2009Accepted: 12 June 2009

This article is available from: http://www.biomedcentral.com/1471-2148/9/133

© 2009 Simões et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Page 2: Evolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscura

BMC Evolutionary Biology 2009, 9:133 http://www.biomedcentral.com/1471-2148/9/133

tral expectation, despite the fact that the Ln RH values forthese populations remain high (Fig. 1).

Between generations 14 and 40, corrected Ln RH valuesare not significantly different across loci either for TW orAR populations (one-way ANOVA; p > 0.05), though theywere significant in our previous analysis for the AR data.Standardized Ln RH values for dsub14 fall outside the 95%confidence interval for AR2 (p < 0.04) and outside the 90%marginal confidence interval for AR1 (p < 0.06) – see Fig.

2, in contrast with the significant deviations previouslyreported for all AR populations [1].

A new analysis that includes the wider range of genera-tions analyzed (40 versus 3, Fig. 3) indicates a significantdeviation pattern for locus dsub14 in all AR populations (p< 0.02 for AR1; p < 0.03 for AR2 and AR3), the TW3 popu-lation (p < 0.03), and a marginally significant deviationfor TW1 (p < 0.07). Furthermore, as we already stated inour paper, the high Ln RH values in locus dsub14 were

Standardized Heterozygosity ratios (Ln RH) between generations 14 and 40Figure 2Standardized Heterozygosity ratios (Ln RH) between generations 14 and 40. Ln RH ratios (H40/H14) for AR (Fig. 2A) and TW (Fig. 2B) populations. Dashed lines represent the 95% confidence interval of the standardized normal distribution.

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Standardized Heterozygosity ratios (Ln RH) between generations 3 and 14Figure 1Standardized Heterozygosity ratios (Ln RH) between generations 3 and 14. Ln RH ratios (H14/H3) for AR (Fig. 1A) and TW (Fig. 1B) populations. Dashed lines represent the 95% confidence interval of the standardized normal distribution.

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Page 3: Evolutionary dynamics of molecular markers during local adaptation: a case study in Drosophila subobscura

BMC Evolutionary Biology 2009, 9:133 http://www.biomedcentral.com/1471-2148/9/133

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caused by the increase of an initially low-frequency allelein all populations analyzed, which is an observation infavour of positive selection acting near this marker.

In general, we conclude that our main findings regardingthe action of positive selection in our study hold, sinceour data is still suggestive of a deviation from neutralexpectations in locus dsub14, although the signal is lesspronounced than reported before. Nevertheless, as previ-ously concluded [1], more studies should be conducted inthis specific microsatellite locus (and neighboring areas)to further elucidate the evolutionary forces acting on thisspecific region of the O chromosome.

We regret any inconvenience that this error in our datamight have caused the readers.

References1. Simões P, Pascual M, Santos J, Rose MR, Matos M: Evolutionary

dynamics of molecular markers during local adaptation: acase study in Drosophila subobscura. BMC Evol Biol 2008, 8:66.

Standardized Heterozygosity ratios (Ln RH) between generations 3 and 40Figure 3Standardized Heterozygosity ratios (Ln RH) between generations 3 and 40. Ln RH ratios (H40/H3) for AR (Fig. 3A) and TW (Fig. 3B) populations. Dashed lines represent the 95% confidence interval of the standardized normal distribution.

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