@ARTICLE{TreeBASE2Ref16524,
author = {J. F. Manen and C. Habashi and Daniel Jeanmonod and J. M. Park and Gerald M. Schneeweiss},
title = {Phylogeny and intraspecific variability of holoparasitic Orobanche (Orobanchaceae) inferred from plastid rbcL sequences},
year = {2004},
keywords = {},
doi = {},
url = {},
pmid = {},
journal = {Molecular Phylogenetics and Evolution},
volume = {33},
number = {},
pages = {482--500},
abstract = {The rbcL sequences of 106 specimens representing 28 species of the four recognized sections of Orobanche were analyzed and compared. Most sequences represent pseudogenes with high rates of non-synonymous substitutions and indel formation. This study confirms that the American lineage (sects. Gymnocaulis and Myzorrhiza) contains potentially functional rbcL-copies with intact open reading frames and low rate of non-synonymous substitutions. For the first time, this is also shown for a member of the Eurasian lineage, O. coerulescens of sect. Orobanche, while all other investigated species of sects. Orobanche and Trionychon contain pseudogenes with distorted reading frames and significantly higher rates of non-synonymous substitutions. Phylogenetic analyses of the rbcL sequences indicate that the genus Orobanche is not monophyletic, and that the American lineage might be more closely related to Boschniakia and Cistanche than to the other sections of Orobanche. Additionally, species of sect. Trionychon phylogenetically nest in sect. Orobanche. This is in concordance with results from other plastid markers (rps2 and matK), but in disagreement with other molecular (nuclear ITS), morphological, and karyological data. This might indicate that the ancestor of sect. Trionychon has captured the plastid genome or aprts of it of a member of sect. Orobanche. Apart from the phylogenetically problematic position of sect. Trionychon, the phylogenetic relationships within sect. Orobanche are similar to those inferred from nuclear ITS data and are close to the traditional groupings traditionally recognized based on morphology. The intraspecific variation of rbcL is low and is neither correlated with intraspecific morphological variability nor with host range. Ancestral character reconstruction using parsimony suggests that the ancestor of O. sect. Orobanche had a narrow host range.}
}
Taxa for tree 128793 of Study 2044

Citation title:
"Phylogeny and intraspecific variability of holoparasitic Orobanche (Orobanchaceae) inferred from plastid rbcL sequences".

This study was previously identified under the legacy study ID S2043
(Status: Published).
Taxa
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ID |
Taxon Label |
NCBI taxid |
uBIO namebankID |
4364861 |
Cryptosphaeria ligniota KT425233_CBS273.87 |
140168
|
3092641
|
4364816 |
Cryptosphaeria multicontinentalis KT425237_NSW03PO |
|
|
4364844 |
Cryptosphaeria pullmanensis KT425235_ATCC_52655 |
140169
|
3023782
|
4364499 |
Cryptovalsa ampelina GQ293908_DMO100 |
245560
|
1449019
|
4364220 |
Cryptovalsa ampelina HQ692558_HVVIT04 |
245560
|
1449019
|
4364688 |
Cryptovalsa ampelina KY752771_STEU_5947 |
245560
|
1449019
|
4364640 |
Cryptovalsa ampelina KY752772_STEU_6087 |
245560
|
1449019
|
4364653 |
Cryptovalsa ampelina KY752773_STEU_7942 |
245560
|
1449019
|
4364098 |
Cryptovalsa rabenhorstii HQ692620_WA07CO |
|
|
4364793 |
Diatrypaceae sp. 2905 ITS 1 1.ab1 F02 |
|
|
4364497 |
Diatrypaceae sp. 3071 ITS 1 1.ab1 G07 |
|
|
4364794 |
Diatrypaceae sp. ITS4 CS025 ID318 |
|
|
4364356 |
Diatrypaceae sp. ITS4 CS30 CSN1924 |
|
|
4364166 |
Eutypa consobrina AJ302447_E38M |
140182
|
3046075
|
4364524 |
Eutypa cremea KY111656_STEU_8082 |
|
|
4364597 |
Eutypa cremea KY752761_STEU_7945 |
|
|
4364587 |
Eutypa cremea KY752762_STEU_5832 |
|
|
4364714 |
Eutypa cremea KY752763_STEU_6085 |
|
|
4364882 |
Eutypa cremea KY752764_STEU_8139 |
|
|
4364230 |
Eutypa cremea KY752765_STEU_8410 |
|
|
4364616 |
Eutypa crustata AJ302448_E39C |
140189
|
3918770
|
4364481 |
Eutypa laevata HM164737_CBS291.87 |
140190
|
2414899
|
4364760 |
Eutypa lata aceri HM164734_CBS217.87 |
|
|
4364644 |
Eutypa lata HM164730_EAMS100 |
97096
|
3052741
|
4364106 |
Eutypa lata HQ692616_SAPN01 |
97096
|
3052741
|
4364704 |
Eutypa lata KY752766_STEU_6082 |
97096
|
3052741
|
4364908 |
Eutypa lata KY752767_STEU_6083 |
97096
|
3052741
|
4364229 |
Eutypa lata KY752768_STEU_6081 |
97096
|
3052741
|
4364556 |
Eutypa lata KY752769_STEU_6084 |
97096
|
3052741
|
4364500 |
Eutypa lata KY752770_STEU_8411 |
97096
|
3052741
|
4364899 |
Eutypa lejoplaca AY684221_020202_5 |
289310
|
5979730
|
4364554 |
Eutypa leptoplaca AY684225_CBS_286.87 |
140184
|
3046076
|
4364361 |
Eutypa leptoplaca AY684226_CBS_287.87 |
140184
|
3046076
|
4364217 |
Eutypa leptoplaca AY684227_CBS_288.87 |
140184
|
3046076
|
4364366 |
Eutypa petrakii petrakii HM164735_CBS244.87 |
|
|
4364234 |
Eutypa sparsa AY684219_3802_3a |
289311
|
3121595
|
4364879 |
Eutypa tetragona DQ006923_CBS_284.87 |
289312
|
3918302
|
4364295 |
Eutypella australiensis HM581945_CNP03 |
|
|
4364676 |
Eutypella citricola HQ692579_HVVIT07 |
|
3126723
|
4364845 |
Eutypella citricola HQ692581_HVOT01 |
|
3126723
|
4364134 |
Eutypella citricola HQ692589_HVGRF01 |
|
3126723
|
4364370 |
Eutypella citricola KY752777_STEU_7944 |
|
3126723
|
4364592 |
Eutypella citricola KY752778_STEU_5948 |
|
3126723
|
4364646 |
Eutypella citricola KY752779_STEU_7943 |
|
3126723
|
4364403 |
Eutypella citricola KY752780_STEU_8412 |
|
3126723
|
4364395 |
Eutypella citricola KY752781_STEU_8249 |
|
3126723
|
4364901 |
Eutypella microtheca HQ692560_ADEL300 |
|
|
4364624 |
Eutypella microtheca HQ692566_T2R2S7 |
|
|
4364186 |
Eutypella microtheca HQ692569_HVGRF02 |
|
|
4364417 |
Eutypella microtheca KY752774_STEU_6086 |
|
|
4364670 |
Eutypella microtheca KY752775_STEU_7941 |
|
|
4364437 |
Eutypella microtheca KY752776_STEU_5949 |
|
|
4364381 |
Eutypella vitis AJ302466_EL57A |
140563
|
3038164
|
4364185 |
Eutypella vitis DQ006943_MSUELM13 |
140563
|
3038164
|