@ARTICLE{TreeBASE2Ref15344,
author = {Esra Einax and Kerstin Voigt},
title = {Oligonucleotide primers for the universal amplification of beta-tubulin genes facilitate analyses among the regnum FUNGI.},
year = {2003},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Organisms Diversity & Evolution},
volume = {3},
number = {3},
pages = {185--194},
abstract = {Among genes coding for proteins with basic structural functions in all eukaryotes, the highly conserved and functionally essential gene for beta-tubulin is receiving increasing attention in the reconstruction of phylogenies within a broad organismic range. We therefore constructed a set of twelve universally applicable primers that allow reliable amplification of beta-tubulin genes among all major eukaryotic kingdoms including fungi (Eumycota), animals (Metazoa) and green plants (Viridiplantae). For primer design, the amino acid sequences of 35 beta-tubulin genes from Ascomycota, Basidiomycota, Chytridiomycota, Zygomycota, Metazoa, Oophyta and Viridiplantae were aligned and used for the definition of four well-conserved regions. These are suitable priming sites in PCR amplification experiments. Out of these amino acid regions twelve primers were designed, which initiate the amplification of beta-tubulin genes from a wide range of eukaryotic organisms with special emphasis on fungi. In four pair-wise primer applications gene fragments of up to 1,500 bp in size could be isolated, which comprise nearly complete beta-tubulin genes from twelve representative species of the Eumycota. The sequences of 7 beta-tubulin fragments were obtained from Allomyces moniliformis, A. neomoniliformis, Blastocladiella britannica, Chytridium confervae, Mortierella isabellina and Trametes versicolor. Reliable amplification of beta-tubulin over a broad spectrum of organisms provides a strong basis for the establishment of both deep level phylogenies and studies of complex species groups based on beta-tubulin gene trees.}
}
Citation for Study 973
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Citation title:
"Oligonucleotide primers for the universal amplification of beta-tubulin genes facilitate analyses among the regnum FUNGI.".
![About](/treebase-web/images/icons/information.png)
This study was previously identified under the legacy study ID S857
(Status: Published).
Citation
Einax E., & Voigt K. 2003. Oligonucleotide primers for the universal amplification of beta-tubulin genes facilitate analyses among the regnum FUNGI. Organisms Diversity & Evolution, 3(3): 185-194.
Authors
Abstract
Among genes coding for proteins with basic structural functions in all eukaryotes, the highly conserved and functionally essential gene for beta-tubulin is receiving increasing attention in the reconstruction of phylogenies within a broad organismic range. We therefore constructed a set of twelve universally applicable primers that allow reliable amplification of beta-tubulin genes among all major eukaryotic kingdoms including fungi (Eumycota), animals (Metazoa) and green plants (Viridiplantae). For primer design, the amino acid sequences of 35 beta-tubulin genes from Ascomycota, Basidiomycota, Chytridiomycota, Zygomycota, Metazoa, Oophyta and Viridiplantae were aligned and used for the definition of four well-conserved regions. These are suitable priming sites in PCR amplification experiments. Out of these amino acid regions twelve primers were designed, which initiate the amplification of beta-tubulin genes from a wide range of eukaryotic organisms with special emphasis on fungi. In four pair-wise primer applications gene fragments of up to 1,500 bp in size could be isolated, which comprise nearly complete beta-tubulin genes from twelve representative species of the Eumycota. The sequences of 7 beta-tubulin fragments were obtained from Allomyces moniliformis, A. neomoniliformis, Blastocladiella britannica, Chytridium confervae, Mortierella isabellina and Trametes versicolor. Reliable amplification of beta-tubulin over a broad spectrum of organisms provides a strong basis for the establishment of both deep level phylogenies and studies of complex species groups based on beta-tubulin gene trees.
About this resource
- Canonical resource URI:
http://purl.org/phylo/treebase/phylows/study/TB2:S973
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- Show BibTeX reference
@ARTICLE{TreeBASE2Ref15344,
author = {Esra Einax and Kerstin Voigt},
title = {Oligonucleotide primers for the universal amplification of beta-tubulin genes facilitate analyses among the regnum FUNGI.},
year = {2003},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Organisms Diversity & Evolution},
volume = {3},
number = {3},
pages = {185--194},
abstract = {Among genes coding for proteins with basic structural functions in all eukaryotes, the highly conserved and functionally essential gene for beta-tubulin is receiving increasing attention in the reconstruction of phylogenies within a broad organismic range. We therefore constructed a set of twelve universally applicable primers that allow reliable amplification of beta-tubulin genes among all major eukaryotic kingdoms including fungi (Eumycota), animals (Metazoa) and green plants (Viridiplantae). For primer design, the amino acid sequences of 35 beta-tubulin genes from Ascomycota, Basidiomycota, Chytridiomycota, Zygomycota, Metazoa, Oophyta and Viridiplantae were aligned and used for the definition of four well-conserved regions. These are suitable priming sites in PCR amplification experiments. Out of these amino acid regions twelve primers were designed, which initiate the amplification of beta-tubulin genes from a wide range of eukaryotic organisms with special emphasis on fungi. In four pair-wise primer applications gene fragments of up to 1,500 bp in size could be isolated, which comprise nearly complete beta-tubulin genes from twelve representative species of the Eumycota. The sequences of 7 beta-tubulin fragments were obtained from Allomyces moniliformis, A. neomoniliformis, Blastocladiella britannica, Chytridium confervae, Mortierella isabellina and Trametes versicolor. Reliable amplification of beta-tubulin over a broad spectrum of organisms provides a strong basis for the establishment of both deep level phylogenies and studies of complex species groups based on beta-tubulin gene trees.}
}
- Show RIS reference
TY - JOUR
ID - 15344
AU - Einax,Esra
AU - Voigt,Kerstin
T1 - Oligonucleotide primers for the universal amplification of beta-tubulin genes facilitate analyses among the regnum FUNGI.
PY - 2003
UR -
N2 - Among genes coding for proteins with basic structural functions in all eukaryotes, the highly conserved and functionally essential gene for beta-tubulin is receiving increasing attention in the reconstruction of phylogenies within a broad organismic range. We therefore constructed a set of twelve universally applicable primers that allow reliable amplification of beta-tubulin genes among all major eukaryotic kingdoms including fungi (Eumycota), animals (Metazoa) and green plants (Viridiplantae). For primer design, the amino acid sequences of 35 beta-tubulin genes from Ascomycota, Basidiomycota, Chytridiomycota, Zygomycota, Metazoa, Oophyta and Viridiplantae were aligned and used for the definition of four well-conserved regions. These are suitable priming sites in PCR amplification experiments. Out of these amino acid regions twelve primers were designed, which initiate the amplification of beta-tubulin genes from a wide range of eukaryotic organisms with special emphasis on fungi. In four pair-wise primer applications gene fragments of up to 1,500 bp in size could be isolated, which comprise nearly complete beta-tubulin genes from twelve representative species of the Eumycota. The sequences of 7 beta-tubulin fragments were obtained from Allomyces moniliformis, A. neomoniliformis, Blastocladiella britannica, Chytridium confervae, Mortierella isabellina and Trametes versicolor. Reliable amplification of beta-tubulin over a broad spectrum of organisms provides a strong basis for the establishment of both deep level phylogenies and studies of complex species groups based on beta-tubulin gene trees.
L3 -
JF - Organisms Diversity & Evolution
VL - 3
IS - 3
SP - 185
EP - 194
ER -