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Registro Completo |
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Biblioteca(s): |
Embrapa Florestas. |
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Data corrente: |
31/03/1999 |
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Data da última atualização: |
14/08/2012 |
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Autoria: |
MAZZA, M. C. M. |
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Afiliação: |
Pesquisadora da Embrapa-CNPF. |
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Título: |
Use of rapd markers in the study of genetic diversity of Araucaria angustifolia (Bert.) populations in Brazil. |
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Ano de publicação: |
1997 |
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Fonte/Imprenta: |
In: INTERNATIONAL FOUNDATION SCIENCE (Stockholm, Sweden). Recent advances in biotechnology for tree conservation and management: Proceedings of an INF Workshop, Florianopolis, Brazil, 15-19 september 1997. Stockholm: IFS / UFSC, 1997. |
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Páginas: |
p. 103-111 |
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ISBN: |
9185798-460 |
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Idioma: |
Inglês |
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Conteúdo: |
The araucaria forest (mixed ombrophilous forest with Araucaria angustifolia Bertoloni or the subtropical evergreen seasonal conifer forest) is one of the most important biomes that originally covered a large part of Southerm Brazil. With human population growth and expansion of agriculture, this forest was cut extensively and currently occupies less than 3% of its original area. large continuous forests wer also fragmented during this process and A. angustifolia populations are scattered in islands. This deforestation process probably ressulted in genetic erosion of A. angustifolia. Knowledge of diversity and distribution of genes within species and their local populations is an essential tool for the management and conservation of that species and biome. The aim of the present study was to analyse the genetic variability and differentiation among five populations of A. angustifolia through RAPD markers. Eleven DNA extraction protocols were tested in a factorial design, including use of different types of deproteinizing and antioxidant agents and detergents. Good quality DNA from buds of adult A. angustifolia trees was obtained only with a complex treatment which included addition of sarcosil to the extraction buffer, additional steps of phenol treatments, chloroform-isoamyl alcohol and low concentration-NaCl 1% CTAB reprecipitation. Other methods wer evalueted in attempts to simplify the process, increase yield and quality of DNA, and to decrease costs. The trial includes the determination of the leaf maturity stage from which good quality DNA could be obtained in large quantity. Quantity of DNA varied in the range of 20-1000 ng/ul, with higher values for buds and terminal needles. One hundred twenty random ten-base primers are being evaluated in five provenances, using bulking strategy, to determinate polymorphic and reproducible RAPD markers. Analysis of genetic structure in remnants of araucaria forests with the use of RAPD markers and gene flow between islands with the use of microsatellite markers will follow. MenosThe araucaria forest (mixed ombrophilous forest with Araucaria angustifolia Bertoloni or the subtropical evergreen seasonal conifer forest) is one of the most important biomes that originally covered a large part of Southerm Brazil. With human population growth and expansion of agriculture, this forest was cut extensively and currently occupies less than 3% of its original area. large continuous forests wer also fragmented during this process and A. angustifolia populations are scattered in islands. This deforestation process probably ressulted in genetic erosion of A. angustifolia. Knowledge of diversity and distribution of genes within species and their local populations is an essential tool for the management and conservation of that species and biome. The aim of the present study was to analyse the genetic variability and differentiation among five populations of A. angustifolia through RAPD markers. Eleven DNA extraction protocols were tested in a factorial design, including use of different types of deproteinizing and antioxidant agents and detergents. Good quality DNA from buds of adult A. angustifolia trees was obtained only with a complex treatment which included addition of sarcosil to the extraction buffer, additional steps of phenol treatments, chloroform-isoamyl alcohol and low concentration-NaCl 1% CTAB reprecipitation. Other methods wer evalueted in attempts to simplify the process, increase yield and quality of DNA, and to decrease costs. The trial includes t... Mostrar Tudo |
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Palavras-Chave: |
Araucaraia angustifolia; Conservacao genetica; Estrutura genetica; Genetica de populacao; Genetics structure; Marcadores RAPD; Nature conservation. |
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Thesaurus Nal: |
genetic markers; population genetics. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02975nam a2200241 a 4500
001 1303551
005 2012-08-14
008 1997 bl uuuu u00u1 u #d
020 $a9185798-460
100 1 $aMAZZA, M. C. M.
245 $aUse of rapd markers in the study of genetic diversity of Araucaria angustifolia (Bert.) populations in Brazil.
260 $aIn: INTERNATIONAL FOUNDATION SCIENCE (Stockholm, Sweden). Recent advances in biotechnology for tree conservation and management: Proceedings of an INF Workshop, Florianopolis, Brazil, 15-19 september 1997. Stockholm: IFS / UFSC$c1997
300 $ap. 103-111
520 $aThe araucaria forest (mixed ombrophilous forest with Araucaria angustifolia Bertoloni or the subtropical evergreen seasonal conifer forest) is one of the most important biomes that originally covered a large part of Southerm Brazil. With human population growth and expansion of agriculture, this forest was cut extensively and currently occupies less than 3% of its original area. large continuous forests wer also fragmented during this process and A. angustifolia populations are scattered in islands. This deforestation process probably ressulted in genetic erosion of A. angustifolia. Knowledge of diversity and distribution of genes within species and their local populations is an essential tool for the management and conservation of that species and biome. The aim of the present study was to analyse the genetic variability and differentiation among five populations of A. angustifolia through RAPD markers. Eleven DNA extraction protocols were tested in a factorial design, including use of different types of deproteinizing and antioxidant agents and detergents. Good quality DNA from buds of adult A. angustifolia trees was obtained only with a complex treatment which included addition of sarcosil to the extraction buffer, additional steps of phenol treatments, chloroform-isoamyl alcohol and low concentration-NaCl 1% CTAB reprecipitation. Other methods wer evalueted in attempts to simplify the process, increase yield and quality of DNA, and to decrease costs. The trial includes the determination of the leaf maturity stage from which good quality DNA could be obtained in large quantity. Quantity of DNA varied in the range of 20-1000 ng/ul, with higher values for buds and terminal needles. One hundred twenty random ten-base primers are being evaluated in five provenances, using bulking strategy, to determinate polymorphic and reproducible RAPD markers. Analysis of genetic structure in remnants of araucaria forests with the use of RAPD markers and gene flow between islands with the use of microsatellite markers will follow.
650 $agenetic markers
650 $apopulation genetics
653 $aAraucaraia angustifolia
653 $aConservacao genetica
653 $aEstrutura genetica
653 $aGenetica de populacao
653 $aGenetics structure
653 $aMarcadores RAPD
653 $aNature conservation
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