Investigation on the causes of stoichiometric error in genome size estimation using heat experiments: consequences on data interpretation.

BACKGROUND AND AIMS In microdensitometry and flow cytometry, estimation of nuclear DNA content in a sample requires a standard with a known nuclear DNA content. It is assumed that dye accessibility to DNA is the same in the sample and standard nuclei. Stoichiometric error arises when dye accessibility is not proportional between the sample and standard. The aim of the present study was to compare the effects of standardization (external-internal) on nuclear fluorescence of two Coffea species and petunia when temperature increases, and the consequences on genome size estimation. METHODS Two coffee tree taxa, C. liberica subsp dewevrei (DEW) and C. pseudozanguebarieae (PSE), and Petunia hybrida were grown in a glasshouse in Montpellier, France. Nuclei were extracted by leaf chopping and at least 2 h after nuclei extraction they were stained with propidium iodide for approx. 3 min just before cytometer processing. In the first experiment, effects of heat treatment were observed in mixed (DEW + petunia) and unmixed extracts (petunia and DEW in separate extracts). Nine temperature treatments were carried out (21, 45, 55, 60, 65, 70, 75, 80 and 85 degrees C). In a second experiment, effects of heating on within-species genome size variations were investigated in DEW and PSE. Two temperatures (21 and 70 degrees C) were selected as representative of the maximal range of chromatin decondensation. KEY RESULTS AND CONCLUSIONS In coffee trees, sample and standard nuclei reacted differently to temperature according to the type of standardization (pseudo-internal vs. external). Cytosolic compounds released in the filtrate would modify chromatin sensitivity to decondensation. Consequently, the 'genome size' estimate depended on the temperature. Similarly, intraspecific variations in genome size changed between estimations at 21 degrees C and 70 degrees C. Consequences are discussed and stoichiometric error detection methods are proposed, along with proposals for minimizing them.

[1]  Jaroslav Dolezel,et al.  Plant DNA flow cytometry and estimation of nuclear genome size. , 2005, Annals of botany.

[2]  J. Greilhuber “Self-tanning”—a new and important source of stoichiometric error in cytophotometric determination of nuclear DNA content in plants , 2004, Plant Systematics and Evolution.

[3]  P. Barre,et al.  Effects of caffeine and chlorogenic acid on propidium iodide accessibility to DNA: consequences on genome size evaluation in coffee tree. , 2003, Annals of botany.

[4]  P. Barre,et al.  Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide. , 2002, Annals of botany.

[5]  H. Price,et al.  Sunflower (Helianthus annuus) Leaves Contain Compounds that Reduce Nuclear Propidium Iodide Fluorescence , 2000 .

[6]  S. Hamon,et al.  Nucleus–Cytosol Interactions—A Source of Stoichiometric Error in Flow Cytometric Estimation of Nuclear DNA Content in Plants , 2000 .

[7]  H. Price,et al.  ENVIRONMENTALLY CORRELATED VARIATION IN 2C NUCLEAR DNA CONTENT MEASUREMENTS IN HELIANTHUS ANNUUS L. , 1998 .

[8]  H. Price,et al.  ENVIRONMENTALLY INDUCED NUCLEAR 2C DNA CONTENT INSTABILITY IN HELIANTHUS ANNUUS (ASTERACEAE) , 1996 .

[9]  P. Barre,et al.  Reliable flow cytometric estimation of nuclear DNA content in coffee trees. , 1996, Cytometry.

[10]  W. Göhde,et al.  Sex determination in dioecious plants Melandrium album and M. rubrum using high-resolution flow cytometry. , 1995, Cytometry.

[11]  D. Marie,et al.  A cytometric exercise in plant DNA histograms, with 2C values for 70 species , 1993, Biology of the cell.

[12]  J. Doležel Flow cytometric analysis of nuclear DNA content in higher plants , 1991 .

[13]  F Otto,et al.  DAPI staining of fixed cells for high-resolution flow cytometry of nuclear DNA. , 1990, Methods in cell biology.

[14]  T R Tiersch,et al.  Reference standards for flow cytometry and application in comparative studies of nuclear DNA content. , 1989, Cytometry.

[15]  J. Greilhuber Severely distorted Feulgen-DNA amounts in Pinus (Coniferophytina) after nonadditive fixations as a result of meristematic self-tanning with vacuole contents , 1986 .

[16]  D. Galbraith,et al.  Rapid Flow Cytometric Analysis of the Cell Cycle in Intact Plant Tissues , 1983, Science.

[17]  I J Christensen,et al.  Standardization of high-resolution flow cytometric DNA analysis by the simultaneous use of chicken and trout red blood cells as internal reference standards. , 1983, Cytometry.

[18]  D. E. Koeppe,et al.  The relationship of tissue chlorogenic acid concentrations and leaching of phenolics from sunflowers grown under varying phosphate nutrient conditions , 1976 .

[19]  Y. Cohen,et al.  Changes in phenolic compounds of sunflowers infected by Plasmopara halstedii , 1975 .

[20]  M. Melamed,et al.  Thermal denaturation of DNA in situ as studied by acridine orange staining and automated cytofluorometry. , 1975, Experimental cell research.