Skip to main content
Genetics logoLink to Genetics
. 2004 Jul;167(3):1281–1291. doi: 10.1534/genetics.103.026120

The genetic covariance among clinal environments after adaptation to an environmental gradient in Drosophila serrata.

Carla M Sgrò 1, Mark W Blows 1
PMCID: PMC1470939  PMID: 15280242

Abstract

We examined the genetic basis of clinal adaptation by determining the evolutionary response of life-history traits to laboratory natural selection along a gradient of thermal stress in Drosophila serrata. A gradient of heat stress was created by exposing larvae to a heat stress of 36 degrees for 4 hr for 0, 1, 2, 3, 4, or 5 days of larval development, with the remainder of development taking place at 25 degrees. Replicated lines were exposed to each level of this stress every second generation for 30 generations. At the end of selection, we conducted a complete reciprocal transfer experiment where all populations were raised in all environments, to estimate the realized additive genetic covariance matrix among clinal environments in three life-history traits. Visualization of the genetic covariance functions of the life-history traits revealed that the genetic correlation between environments generally declined as environments became more different and even became negative between the most different environments in some cases. One exception to this general pattern was a life-history trait representing the classic trade-off between development time and body size, which responded to selection in a similar genetic fashion across all environments. Adaptation to clinal environments may involve a number of distinct genetic effects along the length of the cline, the complexity of which may not be fully revealed by focusing primarily on populations at the ends of the cline.

Full Text

The Full Text of this article is available as a PDF (139.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barton N. H. Clines in polygenic traits. Genet Res. 1999 Dec;74(3):223–236. doi: 10.1017/s001667239900422x. [DOI] [PubMed] [Google Scholar]
  2. Bohren B. B., Hill W. G., Robertson A. Some observations on asymmetrical correlated responses to selection. Genet Res. 1966 Feb;7(1):44–57. doi: 10.1017/s0016672300009460. [DOI] [PubMed] [Google Scholar]
  3. Calboli Federico C. F., Kennington W. Jason, Partridge Linda. QTL mapping reveals a striking coincidence in the positions of genomic regions associated with adaptive variation in body size in parallel clines of Drosophila melanogaster on different continents. Evolution. 2003 Nov;57(11):2653–2658. doi: 10.1111/j.0014-3820.2003.tb01509.x. [DOI] [PubMed] [Google Scholar]
  4. Cortese Marcelo D., Norry Fabian M., Piccinali Romina, Hasson Esteban. Direct and correlated responses to artificial selection on developmental time and wing length in Drosophila buzzatii. Evolution. 2002 Dec;56(12):2541–2547. doi: 10.1111/j.0014-3820.2002.tb00179.x. [DOI] [PubMed] [Google Scholar]
  5. Gockel J., Robinson S. J. W., Kennington W. J., Goldstein D. B., Partridge L. Quantitative genetic analysis of natural variation in body size in Drosophila melanogaster. Heredity (Edinb) 2002 Aug;89(2):145–153. doi: 10.1038/sj.hdy.6800121. [DOI] [PubMed] [Google Scholar]
  6. Hallas Rebecca, Schiffer Michele, Hoffmann Ary A. Clinal variation in Drosophila serrata for stress resistance and body size. Genet Res. 2002 Apr;79(2):141–148. doi: 10.1017/s0016672301005523. [DOI] [PubMed] [Google Scholar]
  7. Hoffmann A. A., Sgrò C. M., Lawler S. H. Ecological population genetics: the interface between genes and the environment. Annu Rev Genet. 1995;29:349–370. doi: 10.1146/annurev.ge.29.120195.002025. [DOI] [PubMed] [Google Scholar]
  8. Hoffmann AA, Merilä J. Heritable variation and evolution under favourable and unfavourable conditions. Trends Ecol Evol. 1999 Mar;14(3):96–101. doi: 10.1016/s0169-5347(99)01595-5. [DOI] [PubMed] [Google Scholar]
  9. Hoffmann Ary A., Shirriffs Jennifer. Geographic variation for wing shape in Drosophila serrata. Evolution. 2002 May;56(5):1068–1073. doi: 10.1111/j.0014-3820.2002.tb01418.x. [DOI] [PubMed] [Google Scholar]
  10. James A. C., Azevedo R. B., Partridge L. Cellular basis and developmental timing in a size cline of Drosophila melanogaster. Genetics. 1995 Jun;140(2):659–666. doi: 10.1093/genetics/140.2.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kingsolver J. G., Gomulkiewicz R., Carter P. A. Variation, selection and evolution of function-valued traits. Genetica. 2001;112-113:87–104. [PubMed] [Google Scholar]
  12. Kirkpatrick M., Bataillon T. Artificial selection on phenotypically plastic traits. Genet Res. 1999 Dec;74(3):265–270. doi: 10.1017/s0016672399004115. [DOI] [PubMed] [Google Scholar]
  13. Kirkpatrick M., Lofsvold D., Bulmer M. Analysis of the inheritance, selection and evolution of growth trajectories. Genetics. 1990 Apr;124(4):979–993. doi: 10.1093/genetics/124.4.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Lansing E, Justesen J, Loeschcke V., V Variation in the expression of Hsp70, the major heat-shock protein, and thermotolerance in larval and adult selection lines of Drosophila melanogaster. J Therm Biol. 2000 Dec 1;25(6):443–450. doi: 10.1016/s0306-4565(00)00008-5. [DOI] [PubMed] [Google Scholar]
  15. Loeschcke V., Bundgaard J., Barker J. S. Variation in body size and life history traits in Drosophila aldrichi and D. buzzatii from a latitudinal cline in eastern Australia. Heredity (Edinb) 2000 Nov;85(Pt 5):423–433. doi: 10.1046/j.1365-2540.2000.00766.x. [DOI] [PubMed] [Google Scholar]
  16. Sgrò Carla M., Blows Mark W. Evolution of additive and nonadditive genetic variance in development time along a cline in Drosophila serrata. Evolution. 2003 Aug;57(8):1846–1851. doi: 10.1111/j.0014-3820.2003.tb00592.x. [DOI] [PubMed] [Google Scholar]
  17. Stratton D. A. Reaction norm functions and QTL-environment interactions for flowering time in Arabidopsis thaliana. Heredity (Edinb) 1998 Aug;81(Pt 2):144–155. doi: 10.1046/j.1365-2540.1998.00369.x. [DOI] [PubMed] [Google Scholar]
  18. Sørensen J. G., Michalak P., Justesen J., Loeschcke V. Expression of the heat-shock protein HSP70 in Drosophila buzzatii lines selected for thermal resistance. Hereditas. 1999;131(2):155–164. doi: 10.1111/j.1601-5223.1999.00155.x. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES