Evidence map›Paper›PMID 23300689›Full record

ArticlePloS one2012

Development of transcriptomic resources for interrogating the biosynthesis of monoterpene indole alkaloids in medicinal plant species.

Elsa Góngora-Castillo, Kevin L Childs, Greg Fedewa, John P Hamilton, David K Liscombe, Maria Magallanes-Lundback, Kranthi K Mandadi, Ezekiel Nims, Weerawat Runguphan, Brieanne Vaillancourt and 5 more

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

65 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Critical parameters for robustPlant direct · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Ancestral Sequence Reconstruction for Exploring Alkaloid Evolution.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  20. Article

5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Elsa Góngora-CastilloDepartment of Plant Biology, Michigan State University, East Lansing, Michigan, United States of America.
Kevin L Childs
Greg Fedewa
John P Hamilton
David K Liscombe
Maria Magallanes-Lundback
Kranthi K Mandadi
Ezekiel Nims
Weerawat Runguphan
Brieanne Vaillancourt
Marina Varbanova-Herde
Dean Dellapenna
Thomas D McKnight
Sarah O'Connor
C Robin Buell

Funding

Advancing Drug Development from Medicinal Plants using Transcriptomics and MetaboRC2GM092521 · NIGMS · UNIVERSITY OF KENTUCKY · PI CHAPPELL, JOE, DELLAPENNA, DEAN · 2009 to 2010
$6.0M
Biotechnology and Biological Sciences Research Council BBS/E/J/000C0654NIGMS NIH HHS 1RC2GM092521NIGMS NIH HHS RC2 GM092521
6 · The paper itself

Abstract

The natural diversity of plant metabolism has long been a source for human medicines. One group of plant-derived compounds, the monoterpene indole alkaloids (MIAs), includes well-documented therapeutic agents used in the treatment of cancer (vinblastine, vincristine, camptothecin), hypertension (reserpine, ajmalicine), malaria (quinine), and as analgesics (7-hydroxymitragynine). Our understanding of the biochemical pathways that synthesize these commercially relevant compounds is incomplete due in part to a lack of molecular, genetic, and genomic resources for the identification of the genes involved in these specialized metabolic pathways. To address these limitations, we generated large-scale transcriptome sequence and expression profiles for three species of Asterids that produce medicinally important MIAs: Camptotheca acuminata, Catharanthus roseus, and Rauvolfia serpentina. Using next generation sequencing technology, we sampled the transcriptomes of these species across a diverse set of developmental tissues, and in the case of C. roseus, in cultured cells and roots following elicitor treatment. Through an iterative assembly process, we generated robust transcriptome assemblies for all three species with a substantial number of the assembled transcripts being full or near-full length. The majority of transcripts had a related sequence in either UniRef100, the Arabidopsis thaliana predicted proteome, or the Pfam protein domain database; however, we also identified transcripts that lacked similarity with entries in either database and thereby lack a known function. Representation of known genes within the MIA biosynthetic pathway was robust. As a diverse set of tissues and treatments were surveyed, expression abundances of transcripts in the three species could be estimated to reveal transcripts associated with development and response to elicitor treatment. Together, these transcriptomes and expression abundance matrices provide a rich resource for understanding plant specialized metabolism, and promotes realization of innovative production systems for plant-derived pharmaceuticals.

Indexed as

Gene Expression ProfilingConserved SequenceHigh-Throughput Nucleotide SequencingHumansMagnoliopsidaPlants, MedicinalRNA, MessengerSecologanin Tryptamine AlkaloidsSequence Homology, Nucleic AcidRNA, MessengerSecologanin Tryptamine Alkaloids

Identifiers

PMID23300689
PMCPMC3530497

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.