Literature DB >> 15375684

Highly polymorphic DNA markers to specify strains of the ectomycorrhizal basidiomycete Tricholoma matsutake based on sigmamarY1, the long terminal repeat of gypsy-type retroelement marY1.

Hitoshi Murata1, Katsuhiko Babasaki, Akiyoshi Yamada.   

Abstract

The ectomycorrhizal basidiomycete Tricholoma matsutake produces commercially valuable fruit bodies--matsutake--in Pinus sp. forest. Here we report that PCR with outward facing primers designed based on sequences comprising sigma(marY1), the long terminal repeat of the gypsy-type retroelement marY1, specifies strains of T. matsutake. PCR with a primer based on the 22-bp sequence conserved at the 5'-end of sigma(marY1) conferred 73 reliable bands overall whose profiles depend upon strains of T. matsutake and T. magnivelare, the latter known as 'American matsutake'. This PCR system gave no detectable band in any other species of Tricholoma tested, including T. bakamatsutake and T. fulvocastaneum, symbionts closely related to T. matsutake, as well as a host plant, Pinus densiflora. Similarly, PCR with a set of primers based on 26-bp and 28-bp sequences at bp 48-73 and bp 281-308 of sigma(marY1), internal regions that are mutated in a variant of marY1, conferred 90 reliable bands only in strains of T. matsutake. Theoretically, PCR with the 22-bp primer would allow generation of 2(73), or 9.4x10(21), types of polymorphism, and PCR with a combination of 26- and 28-bp primers, 2(90), or 1.2x10(27) types. The probability of falsely specifying two different isolates as the same strain is <1/10(21). While polymorphisms conferred by the primer based on the 5' end of sigma(marY1) rather exhibit genetic conservation of a group of T. matsutake, those resulting from primers based on the internal sequences more clearly demonstrate intra-specific diversification. Both systems revealed that T. matsutake is divergent within the species. Ectomycorrhizas formed between P. densiflora and T. matsutake were identified by the PCR systems developed in the present study. This method, using sigma(marY1) as a genetic marker, is useful in analyzing the diversity of T. matsutake, monitoring the behavior of individual mycorrhizas, and specifying the ecological background of fruit bodies traded in markets.

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Year:  2004        PMID: 15375684     DOI: 10.1007/s00572-004-0319-0

Source DB:  PubMed          Journal:  Mycorrhiza        ISSN: 0940-6360            Impact factor:   3.387


  20 in total

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Journal:  Nucleic Acids Res       Date:  1990-11-25       Impact factor: 16.971

2.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools.

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Journal:  Nucleic Acids Res       Date:  1997-12-15       Impact factor: 16.971

3.  Molecular evidence from retroposons that whales form a clade within even-toed ungulates.

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Journal:  Nature       Date:  1997-08-14       Impact factor: 49.962

4.  Identification of Ty1-copia retrotransposons in three ectomycorrhizal basidiomycetes: evolutionary relationships and use as molecular markers.

Authors:  Jesús Díez; Thierry Béguiristain; François Le Tacon; Josep M Casacuberta; Denis Tagu
Journal:  Curr Genet       Date:  2003-02-04       Impact factor: 3.886

5.  marY1, a member of the gypsy group of long terminal repeat retroelements from the ectomycorrhizal basidiomycete Tricholoma matsutake.

Authors:  H Murata; A Yamada
Journal:  Appl Environ Microbiol       Date:  2000-08       Impact factor: 4.792

6.  Expression of marY1, a gypsy-type LTR-retroelement from the ectomycorrhizal homobasidiomycete Tricholoma matsutake, in the budding yeast Saccharomyces cerevisiae.

Authors:  H Murata; Y Miyazaki
Journal:  Biosci Biotechnol Biochem       Date:  2001-04       Impact factor: 2.043

7.  Host species-specific conservation of a family of repeated DNA sequences in the genome of a fungal plant pathogen.

Authors:  J E Hamer; L Farrall; M J Orbach; B Valent; F G Chumley
Journal:  Proc Natl Acad Sci U S A       Date:  1989-12       Impact factor: 11.205

8.  Molecular genetic analysis of the rice blast fungus, magnaporthe grisea.

Authors:  B Valent; F G Chumley
Journal:  Annu Rev Phytopathol       Date:  1991       Impact factor: 13.078

9.  Pot2, an inverted repeat transposon from the rice blast fungus Magnaporthe grisea.

Authors:  P Kachroo; S A Leong; B B Chattoo
Journal:  Mol Gen Genet       Date:  1994-11-01

10.  Grasshopper, a long terminal repeat (LTR) retroelement in the phytopathogenic fungus Magnaporthe grisea.

Authors:  K F Dobinson; R E Harris; J E Hamer
Journal:  Mol Plant Microbe Interact       Date:  1993 Jan-Feb       Impact factor: 4.171

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  12 in total

1.  Ectomycorrhizal symbiosis in vitro between Tricholoma matsutake and Pinus densiflora seedlings that resembles naturally occurring 'shiro'.

Authors:  Akiyoshi Yamada; Ken Maeda; Hisayasu Kobayashi; Hitoshi Murata
Journal:  Mycorrhiza       Date:  2005-11-05       Impact factor: 3.387

2.  Genetic mosaics in the massive persisting rhizosphere colony "shiro" of the ectomycorrhizal basidiomycete Tricholoma matsutake.

Authors:  Hitoshi Murata; Akira Ohta; Akiyoshi Yamada; Maki Narimatsu; Norihiro Futamura
Journal:  Mycorrhiza       Date:  2005-04-14       Impact factor: 3.387

3.  Spore germination and ectomycorrhizae formation of Tricholoma matsutake on pine root systems with previously established ectomycorrhizae from a dikaryotic mycelial isolate of T. matsutake.

Authors:  Yuka Horimai; Hiroki Misawa; Kentaro Suzuki; Yu Tateishi; Hitoshi Furukawa; Takashi Yamanaka; Shozo Yamashita; Toshiharu Takayama; Masaki Fukuda; Akiyoshi Yamada
Journal:  Mycorrhiza       Date:  2021-03-24       Impact factor: 3.387

4.  Intra- and inter-specific variations in the copy number of two types of retrotransposons from the ectomycorrhizal basidiomycete Tricholoma matsutake.

Authors:  Hitoshi Murata; Katsuhiko Babasaki
Journal:  Mycorrhiza       Date:  2005-06-07       Impact factor: 3.387

5.  Traceability of Asian Matsutake, specialty mushrooms produced by the ectomycorrhizal basidiomycete Tricholoma matsutake, on the basis of retroelement-based DNA markers.

Authors:  Hitoshi Murata; Katsuhiko Babasaki; Tomoki Saegusa; Kenji Takemoto; Akiyoshi Yamada; Akira Ohta
Journal:  Appl Environ Microbiol       Date:  2008-02-15       Impact factor: 4.792

6.  Mobile DNA distributions refine the phylogeny of "matsutake" mushrooms, Tricholoma sect. Caligata.

Authors:  Hitoshi Murata; Yuko Ota; Muneyoshi Yamaguchi; Akiyoshi Yamada; Shinichiro Katahata; Yuichiro Otsuka; Katsuhiko Babasaki; Hitoshi Neda
Journal:  Mycorrhiza       Date:  2013-02-26       Impact factor: 3.387

7.  In vitro ectomycorrhizal specificity between the Asian red pine Pinus densiflora and Tricholoma matsutake and allied species from worldwide Pinaceae and Fagaceae forests.

Authors:  Akiyoshi Yamada; Hisayasu Kobayashi; Hitoshi Murata; Erbil Kalmiş; Fatih Kalyoncu; Masaki Fukuda
Journal:  Mycorrhiza       Date:  2009-11-26       Impact factor: 3.387

8.  Heavy-ion beam mutagenesis of the ectomycorrhizal agaricomycete Tricholoma matsutake that produces the prized mushroom "matsutake" in conifer forests.

Authors:  Hitoshi Murata; Tomoko Abe; Hiroyuki Ichida; Yoriko Hayashi; Takashi Yamanaka; Tomoko Shimokawa; Ko Tahara
Journal:  Mycorrhiza       Date:  2017-11-21       Impact factor: 3.387

9.  A qPCR assay that specifically quantifies Tricholoma matsutake biomass in natural soil.

Authors:  Muneyoshi Yamaguchi; Maki Narimatsu; Toru Fujita; Masataka Kawai; Hisayasu Kobayashi; Akira Ohta; Akiyoshi Yamada; Norihisa Matsushita; Hitoshi Neda; Tomoko Shimokawa; Hitoshi Murata
Journal:  Mycorrhiza       Date:  2016-07-01       Impact factor: 3.387

10.  Tmt1: the first LTR-retrotransposon from a Tuber spp.

Authors:  Claudia Riccioni; Andrea Rubini; Beatrice Belfiori; Valentina Passeri; Francesco Paolocci; Sergio Arcioni
Journal:  Curr Genet       Date:  2007-10-31       Impact factor: 2.695

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