Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide

The genome size of coffee trees (Coffea sp.) was assessed using flow cytometry. Nuclear DNA was stained with two dyes (4',6-diamino-2-phenylindole dihydrochloride hydrate (DAPI) and propidium iodide (PI)). Fluorescence in coffee tree nuclei (C-PI orC-DAPI) was compared with that of the standard, petunia (P-PI or P-DAPI). If there is no stoichiometric error, then the ratio between fluorescence of the target nuclei and that of the standard nuclei (R-PI or R-DAPI) is expected to be proportional to thegenome size. Between-tree differences in target:standard fluorescence ratios were noted in Coffea liberica var. dewevrei using propidium iodide and DAPI. For both dyes, between-tree differences were due to a lack of proportionality when comparing locations of the coffee peak and the petunia peak. Intraspecific genome size variations clearly cannot explain variations in the target: standard fluorescence ratio. The origin of the lack of proportionality between target and standard fluorescences differed for the two dyes. With propidium iodide, there was a regression line convergence point, and no between-tree differences were noted in this respect, whereas there was no such convergence with DAPI. An accurate estimate of genome size can thus be obtained with PI. Implications with respect to accessibility and binding mode are discussed.

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Main Authors: 99614 Noirot, M., 46618 Barre, P., 87745 Louarn, J., 63686 Duperray, C., 75866 Hamon, S.
Format: biblioteca
Published: 2002
Subjects:COFFEA, COFFEA LIBERICA, PETUNIA, HIBRIDOS, CAFE, ADN, GENOMAS, ACIDOS NUCLEICOS,
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spelling KOHA-OAI-BVE:891722020-02-03T21:57:02ZConsequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide 99614 Noirot, M. 46618 Barre, P. 87745 Louarn, J. 63686 Duperray, C. 75866 Hamon, S. 2002The genome size of coffee trees (Coffea sp.) was assessed using flow cytometry. Nuclear DNA was stained with two dyes (4',6-diamino-2-phenylindole dihydrochloride hydrate (DAPI) and propidium iodide (PI)). Fluorescence in coffee tree nuclei (C-PI orC-DAPI) was compared with that of the standard, petunia (P-PI or P-DAPI). If there is no stoichiometric error, then the ratio between fluorescence of the target nuclei and that of the standard nuclei (R-PI or R-DAPI) is expected to be proportional to thegenome size. Between-tree differences in target:standard fluorescence ratios were noted in Coffea liberica var. dewevrei using propidium iodide and DAPI. For both dyes, between-tree differences were due to a lack of proportionality when comparing locations of the coffee peak and the petunia peak. Intraspecific genome size variations clearly cannot explain variations in the target: standard fluorescence ratio. The origin of the lack of proportionality between target and standard fluorescences differed for the two dyes. With propidium iodide, there was a regression line convergence point, and no between-tree differences were noted in this respect, whereas there was no such convergence with DAPI. An accurate estimate of genome size can thus be obtained with PI. Implications with respect to accessibility and binding mode are discussed.The genome size of coffee trees (Coffea sp.) was assessed using flow cytometry. Nuclear DNA was stained with two dyes (4',6-diamino-2-phenylindole dihydrochloride hydrate (DAPI) and propidium iodide (PI)). Fluorescence in coffee tree nuclei (C-PI orC-DAPI) was compared with that of the standard, petunia (P-PI or P-DAPI). If there is no stoichiometric error, then the ratio between fluorescence of the target nuclei and that of the standard nuclei (R-PI or R-DAPI) is expected to be proportional to thegenome size. Between-tree differences in target:standard fluorescence ratios were noted in Coffea liberica var. dewevrei using propidium iodide and DAPI. For both dyes, between-tree differences were due to a lack of proportionality when comparing locations of the coffee peak and the petunia peak. Intraspecific genome size variations clearly cannot explain variations in the target: standard fluorescence ratio. The origin of the lack of proportionality between target and standard fluorescences differed for the two dyes. With propidium iodide, there was a regression line convergence point, and no between-tree differences were noted in this respect, whereas there was no such convergence with DAPI. An accurate estimate of genome size can thus be obtained with PI. Implications with respect to accessibility and binding mode are discussed.COFFEACOFFEA LIBERICAPETUNIAHIBRIDOSCAFEADNGENOMASACIDOS NUCLEICOSAnnals of Botany (RU)
institution IICA
collection Koha
country Costa Rica
countrycode CR
component Bibliográfico
access En linea
databasecode cat-sibiica
tag biblioteca
region America Central
libraryname Sistema de Bibliotecas IICA/CATIE
topic COFFEA
COFFEA LIBERICA
PETUNIA
HIBRIDOS
CAFE
ADN
GENOMAS
ACIDOS NUCLEICOS
COFFEA
COFFEA LIBERICA
PETUNIA
HIBRIDOS
CAFE
ADN
GENOMAS
ACIDOS NUCLEICOS
spellingShingle COFFEA
COFFEA LIBERICA
PETUNIA
HIBRIDOS
CAFE
ADN
GENOMAS
ACIDOS NUCLEICOS
COFFEA
COFFEA LIBERICA
PETUNIA
HIBRIDOS
CAFE
ADN
GENOMAS
ACIDOS NUCLEICOS
99614 Noirot, M.
46618 Barre, P.
87745 Louarn, J.
63686 Duperray, C.
75866 Hamon, S.
Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
description The genome size of coffee trees (Coffea sp.) was assessed using flow cytometry. Nuclear DNA was stained with two dyes (4',6-diamino-2-phenylindole dihydrochloride hydrate (DAPI) and propidium iodide (PI)). Fluorescence in coffee tree nuclei (C-PI orC-DAPI) was compared with that of the standard, petunia (P-PI or P-DAPI). If there is no stoichiometric error, then the ratio between fluorescence of the target nuclei and that of the standard nuclei (R-PI or R-DAPI) is expected to be proportional to thegenome size. Between-tree differences in target:standard fluorescence ratios were noted in Coffea liberica var. dewevrei using propidium iodide and DAPI. For both dyes, between-tree differences were due to a lack of proportionality when comparing locations of the coffee peak and the petunia peak. Intraspecific genome size variations clearly cannot explain variations in the target: standard fluorescence ratio. The origin of the lack of proportionality between target and standard fluorescences differed for the two dyes. With propidium iodide, there was a regression line convergence point, and no between-tree differences were noted in this respect, whereas there was no such convergence with DAPI. An accurate estimate of genome size can thus be obtained with PI. Implications with respect to accessibility and binding mode are discussed.
format
topic_facet COFFEA
COFFEA LIBERICA
PETUNIA
HIBRIDOS
CAFE
ADN
GENOMAS
ACIDOS NUCLEICOS
author 99614 Noirot, M.
46618 Barre, P.
87745 Louarn, J.
63686 Duperray, C.
75866 Hamon, S.
author_facet 99614 Noirot, M.
46618 Barre, P.
87745 Louarn, J.
63686 Duperray, C.
75866 Hamon, S.
author_sort 99614 Noirot, M.
title Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
title_short Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
title_full Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
title_fullStr Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
title_full_unstemmed Consequences of stoichiometric error on nuclear DNA content evaluation in Coffea liberica var. dewevrei using DAPI and propidium iodide
title_sort consequences of stoichiometric error on nuclear dna content evaluation in coffea liberica var. dewevrei using dapi and propidium iodide
publishDate 2002
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