Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis. / Tsaballa, Aphrodite; Nikolaidis, Alexandros; Trikka, Foteini; Ignea, Codruta; Kampranis, Sotirios C.; Makris, Antonios M.; Argiriou, Anagnostis.

I: BMC Genomics, Bind 16, 504, 2015.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Tsaballa, A, Nikolaidis, A, Trikka, F, Ignea, C, Kampranis, SC, Makris, AM & Argiriou, A 2015, 'Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis', BMC Genomics, bind 16, 504. https://doi.org/10.1186/s12864-015-1738-3

APA

Tsaballa, A., Nikolaidis, A., Trikka, F., Ignea, C., Kampranis, S. C., Makris, A. M., & Argiriou, A. (2015). Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis. BMC Genomics, 16, [504]. https://doi.org/10.1186/s12864-015-1738-3

Vancouver

Tsaballa A, Nikolaidis A, Trikka F, Ignea C, Kampranis SC, Makris AM o.a. Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis. BMC Genomics. 2015;16. 504. https://doi.org/10.1186/s12864-015-1738-3

Author

Tsaballa, Aphrodite ; Nikolaidis, Alexandros ; Trikka, Foteini ; Ignea, Codruta ; Kampranis, Sotirios C. ; Makris, Antonios M. ; Argiriou, Anagnostis. / Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis. I: BMC Genomics. 2015 ; Bind 16.

Bibtex

@article{bb8b2033cdbd42ddb9b8706b8123ea34,
title = "Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis",
abstract = "BACKGROUND: Solanum elaeagnifolium, an invasive weed of the Solanaceae family, is poorly studied although it poses a significant threat to crops. Here the analysis of the transcriptome of S. elaeagnifolium is presented, as a means to explore the biology of this species and to identify genes related to its adaptation to environmental stress. One of the basic mechanisms by which plants respond to environmental stress is through the synthesis of specific secondary metabolites that protect the plant from herbivores and microorganisms, or serve as signaling molecules. One important such group of secondary metabolites are terpenes.RESULTS: By next-generation sequencing, the flower/leaf transcriptome of S. elaeagnifolium was sequenced and de novo assembled into 75,618 unigenes. Among the unigenes identified, several corresponded to genes involved in terpene biosynthesis; these included terpene synthases (TPSs) and genes of the mevalonate (MVA) and the methylerythritol phosphate (MEP) pathways. Functional characterization of two of the TPSs showed that one produced the sesquiterpene (E)-caryophyllene and the second produced the monoterpene camphene. Analysis of wounded S. elaeagnifolium leaves has shown significant increase of the concentration of (E)-caryophyllene and geranyl linalool, two terpenes implicated in stress responses. The increased production of (E)-caryophyllene was matched to the induced expression of the corresponding TPS gene. Wounding also led to the increased expression of the putative 1-deoxy-D-xylulose-5-phosphate synthase 2 (DXS2) gene, a key enzyme of the MEP pathway, corroborating the overall increased output of terpene biosynthesis.CONCLUSIONS: The reported S. elaeagnifolium de novo transcriptome provides a valuable sequence database that could facilitate study of this invasive weed and contribute to our understanding of the highly diverse Solanaceae family. Analysis of genes and pathways involved in the plant's interaction with the environment will help to elucidate the mechanisms that underly the intricate features of this unique Solanum species.",
keywords = "Alkyl and Aryl Transferases, Amino Acid Sequence, Flowers, Gene Expression Profiling, Gene Expression Regulation, Plant, Molecular Sequence Data, Monoterpenes, Plant Leaves, Plant Proteins, Sequence Alignment, Silver, Solanum, Stress, Physiological, Terpenes, Transcriptome, Wounds and Injuries",
author = "Aphrodite Tsaballa and Alexandros Nikolaidis and Foteini Trikka and Codruta Ignea and Kampranis, {Sotirios C.} and Makris, {Antonios M.} and Anagnostis Argiriou",
year = "2015",
doi = "10.1186/s12864-015-1738-3",
language = "English",
volume = "16",
journal = "BMC Genomics",
issn = "1471-2164",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis

AU - Tsaballa, Aphrodite

AU - Nikolaidis, Alexandros

AU - Trikka, Foteini

AU - Ignea, Codruta

AU - Kampranis, Sotirios C.

AU - Makris, Antonios M.

AU - Argiriou, Anagnostis

PY - 2015

Y1 - 2015

N2 - BACKGROUND: Solanum elaeagnifolium, an invasive weed of the Solanaceae family, is poorly studied although it poses a significant threat to crops. Here the analysis of the transcriptome of S. elaeagnifolium is presented, as a means to explore the biology of this species and to identify genes related to its adaptation to environmental stress. One of the basic mechanisms by which plants respond to environmental stress is through the synthesis of specific secondary metabolites that protect the plant from herbivores and microorganisms, or serve as signaling molecules. One important such group of secondary metabolites are terpenes.RESULTS: By next-generation sequencing, the flower/leaf transcriptome of S. elaeagnifolium was sequenced and de novo assembled into 75,618 unigenes. Among the unigenes identified, several corresponded to genes involved in terpene biosynthesis; these included terpene synthases (TPSs) and genes of the mevalonate (MVA) and the methylerythritol phosphate (MEP) pathways. Functional characterization of two of the TPSs showed that one produced the sesquiterpene (E)-caryophyllene and the second produced the monoterpene camphene. Analysis of wounded S. elaeagnifolium leaves has shown significant increase of the concentration of (E)-caryophyllene and geranyl linalool, two terpenes implicated in stress responses. The increased production of (E)-caryophyllene was matched to the induced expression of the corresponding TPS gene. Wounding also led to the increased expression of the putative 1-deoxy-D-xylulose-5-phosphate synthase 2 (DXS2) gene, a key enzyme of the MEP pathway, corroborating the overall increased output of terpene biosynthesis.CONCLUSIONS: The reported S. elaeagnifolium de novo transcriptome provides a valuable sequence database that could facilitate study of this invasive weed and contribute to our understanding of the highly diverse Solanaceae family. Analysis of genes and pathways involved in the plant's interaction with the environment will help to elucidate the mechanisms that underly the intricate features of this unique Solanum species.

AB - BACKGROUND: Solanum elaeagnifolium, an invasive weed of the Solanaceae family, is poorly studied although it poses a significant threat to crops. Here the analysis of the transcriptome of S. elaeagnifolium is presented, as a means to explore the biology of this species and to identify genes related to its adaptation to environmental stress. One of the basic mechanisms by which plants respond to environmental stress is through the synthesis of specific secondary metabolites that protect the plant from herbivores and microorganisms, or serve as signaling molecules. One important such group of secondary metabolites are terpenes.RESULTS: By next-generation sequencing, the flower/leaf transcriptome of S. elaeagnifolium was sequenced and de novo assembled into 75,618 unigenes. Among the unigenes identified, several corresponded to genes involved in terpene biosynthesis; these included terpene synthases (TPSs) and genes of the mevalonate (MVA) and the methylerythritol phosphate (MEP) pathways. Functional characterization of two of the TPSs showed that one produced the sesquiterpene (E)-caryophyllene and the second produced the monoterpene camphene. Analysis of wounded S. elaeagnifolium leaves has shown significant increase of the concentration of (E)-caryophyllene and geranyl linalool, two terpenes implicated in stress responses. The increased production of (E)-caryophyllene was matched to the induced expression of the corresponding TPS gene. Wounding also led to the increased expression of the putative 1-deoxy-D-xylulose-5-phosphate synthase 2 (DXS2) gene, a key enzyme of the MEP pathway, corroborating the overall increased output of terpene biosynthesis.CONCLUSIONS: The reported S. elaeagnifolium de novo transcriptome provides a valuable sequence database that could facilitate study of this invasive weed and contribute to our understanding of the highly diverse Solanaceae family. Analysis of genes and pathways involved in the plant's interaction with the environment will help to elucidate the mechanisms that underly the intricate features of this unique Solanum species.

KW - Alkyl and Aryl Transferases

KW - Amino Acid Sequence

KW - Flowers

KW - Gene Expression Profiling

KW - Gene Expression Regulation, Plant

KW - Molecular Sequence Data

KW - Monoterpenes

KW - Plant Leaves

KW - Plant Proteins

KW - Sequence Alignment

KW - Silver

KW - Solanum

KW - Stress, Physiological

KW - Terpenes

KW - Transcriptome

KW - Wounds and Injuries

U2 - 10.1186/s12864-015-1738-3

DO - 10.1186/s12864-015-1738-3

M3 - Journal article

C2 - 26149407

VL - 16

JO - BMC Genomics

JF - BMC Genomics

SN - 1471-2164

M1 - 504

ER -

ID: 159084580