Evidence map›Paper›PMID 19283408›Full record

ArticlePlanta2009

Cloning and characterization of a squalene synthase gene from a petroleum plant, Euphorbia tirucalli L.

Hidenobu Uchida, Hirofumi Yamashita, Masataka Kajikawa, Kiyoshi Ohyama, Osamu Nakayachi, Ryuji Sugiyama, Katsuyuki T Yamato, Toshiya Muranaka, Hideya Fukuzawa, Miho Takemura and 1 more

Abstract read
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Article in Planta, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.5field-weighted citation impact, top 19% of its field
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

24 citing papers in PubMed, 55 citations in OpenAlex.

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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

11 authors at 7 institutions in 1 country.

Hidenobu UchidaResearch Institute for Bioresources and Biotechnology, Ishikawa Prefectural University, Ishikawa, 921-8836, Japan.
Hirofumi Yamashita
Masataka Kajikawa
Kiyoshi Ohyama
Osamu Nakayachi
Ryuji Sugiyama
Katsuyuki T Yamato
Toshiya Muranaka
Hideya Fukuzawa
Miho Takemura
Kanji Ohyama
Ishikawa Prefectural University · JPKyoto University · JPKyoto Prefectural University · JPNara Institute of Science and Technology · JPRIKEN Center for Sustainable Resource Science · JPUniversity of Toyama · JPYokohama City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Euphorbia tirucalli L., which is also known as a petroleum plant, produces a large amount of phytosterols and triterpenes. During their biosynthesis, squalene synthase converts two molecules of the hydrophilic substrate farnesyl diphosphate into a hydrophobic product, squalene. An E. tirucalli cDNA clone of a putative squalene synthase gene (EtSS) was isolated by RT-PCR followed by 5'- and 3'-RACE. The restriction fragment polymorphisms revealed by Southern blot analysis suggest that EtSS is a single copy gene. The glycine at the 287th residue from the N-terminal end of domain C has replaced alanine, which is conserved among all the other SS sequences deposited in the Genbank database. The N-terminal 380 residues of the hydrophilic sequence was expressed as a peptide-tagged protein in E. coli, and the resultant bacterial crude extract was incubated with farnesyl diphosphate and NADPH. GC-MS analysis showed that squalene was detected in the in vitro reaction mixture. E. tirucalli transgenic callus lines, in which EtSS was overexpressed, accumulated increased amounts of phytosterols as compared with that of wild type callus. RT-PCR analysis of wild type E. tirucalli plants revealed that the EtSS transcript accumulated in almost equal amounts in the stems and the leaves with a stalk, while a lower amount was detected in the roots. In situ hybridization analysis revealed that prominent antisense-probe signal was detected in the cambia within bundle sheathes. These results indicate that EtSS functions prominently in cambia, which are located adjacent to conductive tubes, and that this gene plays important roles in phytosterol accumulation in petroleum plants.

Indexed as

Amino Acid SequenceCloning, MolecularDNA, ComplementaryEuphorbiaFarnesyl-Diphosphate FarnesyltransferaseGas Chromatography-Mass SpectrometryGene Expression Regulation, EnzymologicGene Expression Regulation, PlantIn Situ HybridizationMolecular Sequence DataNADPPhytosterolsPlant ProteinsPlants, Genetically ModifiedPolyisoprenyl PhosphatesRecombinant ProteinsDNA, ComplementaryFarnesyl-Diphosphate Farnesyltransferasefarnesyl pyrophosphateNADPPhytosterolsPlant ProteinsPolyisoprenyl PhosphatesRecombinant ProteinsSesquiterpenesSqualene

Identifiers

PMID19283408
OpenAlexW2042085131

What OpenQuestion holds

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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.