Evidence map›Paper›PMID 19967454›Full record

ArticleMolecular biology reports2010

Isolation and characterization of a Glutamate decarboxylase (GAD) gene and their differential expression in response to abiotic stresses from Panax ginseng C. A. Meyer.

Jung-Hye Lee, Yu-Jin Kim, Dae-Young Jeong, Gayathri Sathiyaraj, Rama Krishna Pulla, Ju-Sun Shim, Jun-Gyo In, Deok-Chun Yang

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Article in Molecular biology reports, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

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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

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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

16 citing papers in PubMed, 41 citations in OpenAlex.

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  6. γ-Aminobutyric Acid Alleviates Programmed Cell Death in TwoInternational journal of molecular sciences · 2024
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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

8 authors at 1 institution in 1 country.

Jung-Hye LeeKorean Ginseng Center for Most Valuable Products and Ginseng Genetic Resource Bank, Kyung Hee University, Seocheon, Giheung-gu, Yongin-si, Gyunggi-do, 449-701, Republic of Korea.
Yu-Jin Kim
Dae-Young Jeong
Gayathri Sathiyaraj
Rama Krishna Pulla
Ju-Sun Shim
Jun-Gyo In
Deok-Chun Yang
Kyung Hee University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glutamate decarboxylase (GAD) catalyzes the conversion of L-glutamate to γ-aminobutyric acid (GABA). A full-length cDNA encoding GAD (designated as PgGAD) was isolated and characterized from the root of Panax ginseng C. A. Meyer. The length cDNA of PgGAD was 1881 bp and contained a 1491 bp open reading frame (ORF) encoding a glutamate decarboxylase protein of 496 amino acids, possessing a Ser-X-X-Lys active site, which belongs to the GAD group. The deduced amino acid sequence of the PgGAD was classified in the plant GAD family and has 76-85% high similarity with other plants as like petunia, Arabidopsis, tomato. Secondary structure of PgGAD was predicted by using SOPMA software program. Southern blot analysis of genomic DNA suggests that, there is more than one copy of the PgGAD gene. The organ specific gene expression pattern also studied in P. ginseng seedlings, in which the stem showed elevated expression than root, leaf, bud and rhizomes. Along with this, we also confirmed the gene expression of PgGAD under various abiotic stresses like temperature stress, osmotic stress, anoxia, oxidative stress, and mechanical damage. Temporal analysis of gene expression except exposure of oxidative stress revealed an enhanced expression after each stresses. The enzyme activity of PgGAD was stimulated to 2-fold under cold stress.

Indexed as

Gene Expression Regulation, PlantBlotting, SouthernCloning, MolecularCold TemperatureDNA, ComplementaryEnzyme AssaysGene Expression ProfilingGene Expression Regulation, EnzymologicGenes, PlantGlutamate DecarboxylasePanaxProtein Structure, SecondaryRegulatory Sequences, Nucleic AcidRNA, MessengerSequence Analysis, DNASequence Homology, Amino AcidDNA, ComplementaryGlutamate DecarboxylaseRNA, Messenger

Identifiers

PMID19967454
OpenAlexW2029616336

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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.