@ARTICLE{TreeBASE2Ref15828,
author = {David S. Hibbett and Yukitaka Fukumasa-Nakai and Akihiko Tsuneda and Michael J Donoghue},
title = {Phylogenetic diversity in shiitake inferred from nuclear ribosomal DNA sequences.},
year = {1995},
keywords = {biogeography; conservation; edible fungi; ITS; Lentinula; phylogeny; shiitake ; },
doi = {},
url = {http://www.jstor.org/stable/3760806},
pmid = {},
journal = {Mycologia},
volume = {87},
number = {},
pages = {618--638},
abstract = {Phylogenetic relationships of the edible shiitake mushroom (Lentinula, Tricholomataceae) were studied using DNA sequences from the internal transcribed spacers (ITS) of nuclear ribosomal DNA. The ingroup consisted of seven isolates of L. edodes from Japan and Thailand, nine isolates of L. lateritia from Borneo, Papua New Guinea, and Tasmania, and five isolates of L. novaezelandieae from New Zealand. These species designations are based on morphological species concepts in Lentinula. However, because Lentinula isolates from throughout Asia-Australasia are mating compatible, some authors treat all of these as belonging to L. edodes. The outgroup included two isolates of L. boryana from Mexico. Parsimony, distance, and maximum likelihood analyses were performed, with various combinations of taxa, characters, and character codings, and bootstrap and decay index measures of robustncss. Alternate topologies were evaluated in terms of tree lengths, maximum likelihood ratios, and Templeton's nonparametric test of parsimony. Results suggest that there are four independent lineages of shiitake in Asia-Australasia, which provides partial support for the morphologically based species concepts. Lentinula novaezelandieae and L. edodes sensu stricto were supported as monophyletic, but L. lateritia appears to be paraphyletic. A corollary of this is that the morphology of L. laleritia should be plesiomorphic for shiitake, which seems plausible based on outgroup comparison. In general, there is a strong correlation between the geographic origins of the isolates and the lineages supported. Biogeographic interpretation of ITS trees suggests that the ancestral area for shiitake in Asia-Australasia is in the South Pacific, which was the most phylogenetically diverse area examined. Phylogenetic analyses including previously published ITS2 sequences of three shiitake isolates of unknown origin placed the unknown isolates in a group of L. edodes sensu stricto isolates from Japan and Thailand, which suggests that the unknown isolates are from northeast or continental Asia. ITS-based cladograms have points of agreement as well as disagreement with previously published mitochondrial DNA-based dendrograms from a subset of the isolates used in this study. Discrepancies between the ITS and mtDNA trees could mean that the nuclear ITS and the mttDA have different evolutionary histories. However, comparison of mtDNA and ITS data are complicated by the fact that the mtDNA data are based on pairwise distances, whereas the ITS data are discrete. Practical implica- tions of the results for shiitake breeding and conservation are discussed.}
}
Matrix 2845 of Study 288

Citation title:
"Phylogenetic diversity in shiitake inferred from nuclear ribosomal DNA sequences.".

This study was previously identified under the legacy study ID S3x30x98c12c42c56
(Status: Published).
Matrices
Title: Fig. 1 ITS
Description: Legacy TreeBASE Matrix ID = M197c3x30x98c13c32c09
Rows
Taxon Label |
Row Segments |
Characters 1?–30 |
Letinula boryana MEX1 |
(none)
|
----GAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula boryana MEX2 |
(none)
|
----GAG?AAAAGTCGTAACAAGGTTTCCG |
Letinula edodes JPN1 |
(none)
|
--------------------------TCCG |
Letinula edodes JPN2 |
(none)
|
---------------------------CCG |
Letinula edodes JPN6 |
(none)
|
----GA-TATAAGTCGTAACAAGGTTTCCG |
Letinula edodes JPN4 |
(none)
|
--GGGAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula edodes JPN5 |
(none)
|
--------------------------TCCG |
Letinula edodes JPN3 |
(none)
|
------G-AAAAGTCGTAACA-GG-TTCCG |
Letinula lateritia PNG5 |
(none)
|
--GGGAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula lateritia PNG6 |
(none)
|
----GAGTAAAAGTCGTAACGAGGTTTCCG |
Letinula lateritia PNG7 |
(none)
|
---G?AGTAAAAGTC?TAGCAAGGTTTCCG |
Letinula lateritia PNG8 |
(none)
|
TGGG?AGTAAAAGTCGTAACAAGGTTTCCG |
Letinula lateritia BOR |
(none)
|
--GGAAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula lateritia PNG1 |
(none)
|
-----------------------????CCG |
Letinula lateritia PNG2 |
(none)
|
------------GTCGTAAC?AGGCCGCCG |
Letinula lateritia PNG3 |
(none)
|
-----------AGTCGTACCAAGGTTTCCG |
Letinula lateritia PNG4 |
(none)
|
----GAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula edodes THL |
(none)
|
------GAGAAA?TC?TAACCAGGTTTCCG |
Letinula lateritia TAS |
(none)
|
---GAAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula novaezelandieae NZL5 |
(none)
|
---GAAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula novaezelandieae NZL3 |
(none)
|
-TGGGAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula novaezelandieae NZL4 |
(none)
|
--GGGAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula novaezelandieae NZL2 |
(none)
|
---GGAGTAAAAGTCGTAACAAGGTTTCCG |
Letinula novaezelandieae NZL1 |
(none)
|
-TGGGAGTAAAAGTCGTAACAAGGTTTCCG |
Columns
Column |
Character Description |
879
|
indel.88
|
880
|
indel.93-97
|
881
|
indel.103
|
882
|
indel.125
|
883
|
indel.127
|
884
|
indel.158-159
|
885
|
indel.166-168
|
886
|
indel.172
|
887
|
indel.177
|
888
|
indel.180
|
889
|
indel.183
|
890
|
indel.189
|
891
|
indel.197
|
892
|
indel.198
|
893
|
indel.204
|
894
|
indel.206
|
895
|
indel.211
|
896
|
indel.212-216
|
897
|
indel.229
|
898
|
indel.241
|
899
|
indel.278
|
900
|
indel.486
|
901
|
indel.495-497
|
902
|
indel.518
|
903
|
indel.537
|
904
|
indel.540
|
905
|
indel.568-569
|
906
|
indel.570-571
|
907
|
indel.572
|
908
|
indel.580
|
909
|
indel.590
|
910
|
indel.591
|
911
|
indel.598-599
|
912
|
indel.623
|
913
|
indel.627
|
914
|
indel.628
|
915
|
indel.629-644
|
916
|
indel.645-647
|
917
|
indel.648-659
|
918
|
indel.660-708
|
919
|
indel.724
|
920
|
indel.728-733
|
921
|
indel.772-773
|
922
|
indel.775-776
|
923
|
indel.777
|
924
|
indel.778
|
925
|
indel.779
|
926
|
indel.798-799
|
927
|
indel.811-812
|
928
|
indel.814-815
|
929
|
indel.821-824
|
930
|
mtDNA TYPE
|
931
|
distribution
|