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1 F, an S-locus F-box gene of Petunia inflata (Solanaceae).
2 -cherry), a member of the nightshade family (Solanaceae).
3 ts: Solanum dulcamara and Solanum rostratum (Solanaceae).
4 alpighiales (Erythroxylaceae) and Solanales (Solanaceae).
5 formance on a novel host, Physalis angulata (Solanaceae).
6 plant families (Asteraceae, Brassicaceae and Solanaceae).
7 h (tolerance) traits in Solanum carolinense (Solanaceae).
8 solanums) of the species-rich genus Solanum (Solanaceae).
9 play a role in MITE siRNA generation in the Solanaceae.
10 cies within the Cucurbitaceae, Fabaceae, and Solanaceae.
11 its loss is irreversible in the plant family Solanaceae.
12 psicum and Lycopersicon, both members of the Solanaceae.
13 ry mechanism for chromosome evolution in the Solanaceae.
14 ent that occurred prior to speciation of the Solanaceae.
15 homologues of the tomato kinases from other Solanaceae.
16 he two Rosaceae species as compared with the Solanaceae.
17 sylgalactosides are conserved throughout the Solanaceae.
18 ngerminated and germinated seeds, except for Solanaceae.
19 dium chain acylsugar accumulation across the Solanaceae.
20 es in controlling chlorophyll content in the Solanaceae.
21 es in potato, tomato, and other crops of the Solanaceae.
22 echanisms driving acylsugar evolution in the Solanaceae.
23 ive barriers (IRBs) are related to SI in the Solanaceae.
24 nctional homologs of systemin outside of the Solanaceae.
25 site of tropane alkaloid biosynthesis in the Solanaceae.
26 r gene regulation and pathogen resistance in Solanaceae.
27 on is conserved from the Brassicaceae to the Solanaceae.
28 mportant tropane alkaloids in species of the Solanaceae.
29 LAP-A) are expressed only in a subset of the Solanaceae.
30 ction and evolution of miR4376 in the family Solanaceae.
33 nach and Chlamydomonas reinhardtii), and non-Solanaceae activase fails to activate Solanaceae Rubisco
34 tology encompass terms relevant to Fabaceae, Solanaceae, additional cereal crops, and poplar (Populus
36 ed by an as yet unidentified receptor in the Solanaceae, although it has an FLS2-dependent virulence
37 fied taxonomically as Nicotiana benthamiana (Solanaceae), an accession of which, typically referred t
38 Gametophytic SI is well characterized for Solanaceae and although balancing selection is hypothesi
39 um pox virus and turnip mosaic virus in both Solanaceae and Brassicaceae systems, demonstrating poten
41 ch occupy a key evolutionary position in the Solanaceae and capture understudied variation in traits
42 ncestral Rubiscos of the (nightshade) family Solanaceae and characterized their kinetics after coexpr
43 y root disease (HRD) on hydroponically grown Solanaceae and Cucurbitaceae crops, besides being widely
44 eudicot families including the Brassicaceae, Solanaceae and Fabaceae, our work in eudicots supports a
45 g plants from three species of two families, Solanaceae and Fabaceae, results in the accumulation of
47 study of gene expression in tobacco and the Solanaceae and helps to fill a current gap in studies of
48 to extensive trait and phylogenetic data in Solanaceae and investigate how speciation and extinction
49 Utilizing a whole-genome phylogeny of 92 Solanaceae and its sister clade species, we employ an ev
51 nfant diet and they can be contaminated with Solanaceae and other plants containing tropane alkaloids
52 ncompatibility responses, such as S-RNase in Solanaceae and PrsS-PrpS in Papaveraceae, as well as the
53 ology between Sly-miR4376, a miRNA common to Solanaceae and reported to target autoinhibited Ca(2+) -
54 ll separated from the S-RNase sequences from Solanaceae and Rosaceae, and also from most known "S-lik
55 hat gave rise to the core euasterid families Solanaceae and Rubiaceae had a basic chromosome number o
56 ontaining biological data for species in the Solanaceae and their close relatives, with data types ra
57 es at the self-incompatibility locus ( S) of Solanaceae and their extraordinary spectrum of sequence
59 aena odorata (Asteraceae) Datura stramonium (Solanaceae), and Xanthium strumarium (Asteraceae), compa
60 s also functional in a family other than the Solanaceae, and could be considered for canker control.
61 lucosinolates in Brassicaceae, acylsugars in Solanaceae, and flavour compounds in apple, indicate tha
62 s tested, even including some members of the Solanaceae, and it is therefore unlikely that Chi2;1 is
63 latory pairs and R-type defense genes in the Solanaceae, and provided a genomic basis for the lack of
65 hree flowering plant families, including the Solanaceae, and this self/non-self recognition mechanism
66 We show that diversification patterns in Solanaceae are better explained by breeding system and a
68 ily, termed TNACS, appears restricted to the Solanaceae, as they are absent from currently sequenced
69 novel Ascomycete PAMP, RcCDI1, recognized by Solanaceae but not by monocots, which activates cell dea
70 ibited PAMP activity, inducing cell death in Solanaceae but not in other families of dicots or monoco
71 emin regulates antiherbivore defenses in the Solanaceae, but in other plant families, peptides with a
72 e trend strengthened when we weighted edible Solanaceae by nicotine concentration (ptrend = 0.004).
73 capable of inducing alkalinization in other Solanaceae cell types (or species), indicating that stru
74 complements of the key founders of the main Solanaceae clades and the rearrangements that led to the
75 ing fruit ripening is conserved in different Solanaceae clades, and that climacteric fruit ripening i
76 ly associated with consumption of all edible Solanaceae combined (relative risk [RR] = 0.81, 95% conf
77 ealed that transgenic expression of AtEFR in Solanaceae confers elf18 responsiveness and broad-spectr
78 er of genes in tomato (Solanum lycopersicum; Solanaceae) contains genes for terpene synthases (TPSs)
80 ) -mediated response in tomato and two other Solanaceae crops is distinct from that in Arabidopsis th
81 ) -mediated response in tomato and two other Solanaceae crops is distinct from that in Arabidopsis th
82 steroidal glycoalkaloids (SGAs) produced in Solanaceae crops, including tomato, are antinutritional
83 ) soil effectively protects tomato and other Solanaceae crops, pepper (Capsicum annuum) and eggplant
86 ely related to a tobacco (Nicotiana tabacum; Solanaceae) diterpene synthase encoding Z-abienol syntha
87 has been previously reported, the N-terminal Solanaceae domain (SD) of Sw-5b also interacts with NSm
89 shared with most Eudicots, and a more recent Solanaceae event that is shared with tomato and other so
94 ynthesized in the glandular trichomes of the Solanaceae family and are implicated in protection again
96 l hundreds of acylsugars produced across the Solanaceae family and even within a single plant, built
97 ly evolved before the diversification of the Solanaceae family and underwent lineage-specific diversi
98 ted to AtRTE1, we report that members of the Solanaceae family contain two phylogenetically distinct
105 hole genome data for an increasing number of Solanaceae family members including tomato, potato, pepp
106 ME8) cytochrome P450 hydroxylases across the Solanaceae family revealed two distinct clades producing
108 ypSys gene family to be found outside of the Solanaceae family, and its encoded peptide precursor is
109 titute the largest monophyletic group in the Solanaceae family, but a high-quality genome assembly fr
110 ion in fruit morphology among members of the Solanaceae family, fine-tuning regulation of gene expres
111 lanum rostratum Dunal), which belongs to the Solanaceae family, is a worldwide noxious invasive weed
112 f adaptation and phenotypic diversity in the Solanaceae family, other species in the Asterid clade su
113 pepper (Capsicum annuum), all members of the Solanaceae family, using reverse-transcription polymeras
114 g comparative resource for the plants of the Solanaceae family, which includes important crop and mod
115 erated, we investigated the evolution of the Solanaceae family-specific, trichome-localized acylsugar
128 ty (SI) for a population of Lycium parishii (Solanaceae) from Organ Pipe National Monument, Arizona.
129 ene fossil berries of the nightshade family (Solanaceae) from the Esmeraldas Formation in Colombia an
130 -MiS22) and found abundant MiS insertions in Solanaceae genomic DNA and expressed sequence tags (EST)
133 he results suggest that domestication of the Solanaceae has been driven by mutations in a very limite
134 gender dimorphism in North American Lycium (Solanaceae) has evolved in polyploid, self-compatible ta
135 uctive barriers between even closely related Solanaceae have precluded a genetic dissection, we captu
136 omato species (Solanum section Lycopersicon (Solanaceae)) have been described as polymorphic for mati
139 sized in the roots of specific genera of the Solanaceae in a multistep pathway that is only partially
140 olanum lycopersicum) is a model organism for Solanaceae in both molecular and agronomic research.
141 gene duplicate function have occurred in the Solanaceae, in that individual gene roles are distinct,
142 d portions of the plant in contrast with the Solanaceae, in which tropane alkaloid biosynthesis occur
143 me sequencing of PacBio for 18 accessions in Solanaceae, including 15 accessions of five wild tomato
147 c self-incompatibility (SI) possessed by the Solanaceae is controlled by a highly polymorphic locus c
148 that TA biosynthesis in Erythroxylaceae and Solanaceae is polyphyletic and that independent recruitm
149 rd distinct type of cyclotide precursor, and Solanaceae is the fourth phylogenetically disparate plan
155 The potentially protective effect of edible Solanaceae largely occurred in men and women who had nev
156 We identified 22 families of MITEs in the Solanaceae (MiS1-MiS22) and found abundant MiS insertion
158 urces and findings elevate Physalis to a new Solanaceae model system and establish a paradigm in the
159 rescences of tomato and related nightshades (Solanaceae), new lateral inflorescence branches develop
161 mal glandular secreting trichomes across the Solanaceae (nightshade) family is ideal for investigatin
162 Across a phylogeny of 56 wild species of Solanaceae (nightshades), we show here that the repeated
165 nces obtained by RT-PCR from five species of Solanaceae now reveal a picture of conspicuous inter-spe
166 common evolutionary pathway to polyploidy in Solanaceae occurs via direct breakdown of self-incompati
167 bacco (Nicotiana tabacum) is a member of the Solanaceae, one of the agronomically most important grou
168 is of TFs has been made from a member of the Solanaceae, one of the most important families of vascul
169 ly prior to or after the radiation of either Solanaceae or Rubiaceae as has been recently suggested.
173 gth regulator alone in groundcherry, another Solanaceae plant, also enabled engineering to a compact
174 tobacco) fails to activate Rubisco from non-Solanaceae plants (e.g. spinach and Chlamydomonas reinha
176 tritional steroidal glycoalkaloids (SGAs) in Solanaceae plants have provided deep insights into their
179 mato plants and many of its relatives in the Solanaceae produce a mixture of O-acyl sugars that contr
180 lanum lycopersicum) and other species in the Solanaceae produce and secrete a mixture of O-acylsugars
181 sicum) and many other species throughout the Solanaceae produce and secrete mixtures of sugar esters
182 mes of many plants in the nightshade family (Solanaceae) produce O-acylsugars, and in cultivated and
186 te 2006, interest and participation from the Solanaceae research community has been strong and growin
187 ) was formed as an umbrella organization for Solanaceae research in over 30 countries to address impo
188 air of congeners from each of five genera in Solanaceae reveals extensive transgeneric evolution of L
193 dings from various plant families, including Solanaceae, Rosaceae, Papaveraceae, and Brassicaceae, an
196 persicum) model system Micro-Tom (MT) by the Solanaceae (S)-biotype of Moniliophthora perniciosa, whi
199 neralist Trichoplusia ni and the facultative Solanaceae-specialist Manduca sexta, was significantly i
200 notable differences between tobacco and non-Solanaceae species in TF family size and evidence for bo
204 the whole-genome triplication identified in Solanaceae species such as tomato, the genome includes s
206 SGN currently houses map and marker data for Solanaceae species, a large expressed sequence tag colle
207 ly from Fabaceae, Brassicaceae, Poaceae, and Solanaceae species, but also from representatives of oth
208 se/oxygenase (Rubisco, EC 4.1.1.39) from non-Solanaceae species, including the green alga Chlamydomon
212 owever, that in the nightshade plant family (Solanaceae), species with functional self-incompatibilit
213 hich half the annotated NLRs were targets of Solanaceae-specific and conserved miRNAs, at the NB subd
214 in genes in various eudicots show that three Solanaceae-specific CUL1 genes share a common origin, wi
216 lutionarily conserved sORFs, we uncovered 96 Solanaceae-specific sORFs, revealing the importance of s
218 ato and feeds on several wild species in the Solanaceae, such as S. eleagnifolium and S. rostratum Du
219 ited resistance in both the Brassicaceae and Solanaceae suggests that this trait may be more widely d
220 reductase in yeast engineered to express the Solanaceae TA pathway enables the production of a hybrid
221 pecies - Jaltomata sinuosa and J. umbellata (Solanaceae) - that have divergent suites of floral trait
222 hat allow plants to avoid inbreeding--in the Solanaceae (the nightshade family) is controlled by a po
223 umbers fall within the range observed in the Solanaceae, the only other family with RNase-based incom
228 a positional candidate gene approach in the Solanaceae, these genes were genetically mapped in peppe
233 ns of red flower color in the tomato family, Solanaceae, using large-scale data mining and new sequen
235 nt genomes, indicating that evolution of the Solanaceae was not associated with the gain or loss of T
236 in the ground cherry, Physalis crassifolia (Solanaceae), was surveyed in a natural population occurr
237 y in the asterid core eudicot genus Petunia (Solanaceae), we carried out global and fine-scale gene e
238 omatillo genus, these findings indicate that Solanaceae were distributed at least from southern South
239 ion of these early Eocene fossils shows that Solanaceae were well diversified long before final Gondw
241 ter to the well-documented phenomenon in the Solanaceae where SC accompanying polyploidization is fre
242 phosphate synthase, previously only found in Solanaceae, which is likely involved in the biosynthesis
244 es similar biology with other members of the Solanaceae, yet has features unique within the family, s