Evidence map›Paper›PMID 21653253›Full record

ArticleMolecular & cellular proteomics : MCP2011

A novel late embryogenesis abundant like protein associated with chilling stress in Nicotiana tabacum cv. bright yellow-2 cell suspension culture.

Ying-Ping Gai, Xian-Ling Ji, Wei Lu, Xue-Juan Han, Guo-Dong Yang, Cheng-Chao Zheng

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Article in Molecular & cellular proteomics : MCP, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

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0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Ornamental plants adapted to urban ecosystem pollution: lawn grasses tolerating deicing reagents.Environmental science and pollution research international · 2022
    Article
  3. Genomic Analysis of Soybean PP2A-BFrontiers in plant science · 2021
    Article
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ying-Ping GaiState Key Laboratory of Crop Biology, Shandong Agricultural University, Taian, Shandong, 271018, PR China.
Xian-Ling Ji
Wei Lu
Xue-Juan Han
Guo-Dong Yang
Cheng-Chao Zheng

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low temperature is one of the major abiotic stresses limiting the productivity and geographical distribution of many important crops. To identify proteins associated with chilling stress in Nicotiana tabacum cv. bright yellow-2 (BY-2) cell suspension culture, we utilized a proteomic approach with two-dimensional electrophoresis to compare proteins from samples of treated with or without chilling treatment at 4 °C. One protein specifically more abundant in chilling treated sample was identified and designated as NtLEA7-3. Rapid amplification of cDNA ends gave rise to a full-length NtLEA7-3 cDNA with a complete open reading frame of 1267 bp, encoding a 322 amino acid polypeptide. Homology search and sequence multi-alignment demonstrated that the deduced NtLEA7-3 protein sequence shared a high identity with LEA-like proteins from other plants. Subcellular localization analysis indicated that the NtLEA7-3 was localized exclusively in the nucleus. When the gene was overexpressed in bright yellow-2 cells, the transgenic bright yellow-2 cells show more resistant to chilling stress than the wild-type cells. In addition, transgenic Arabidopsis plants overexpressing the NtLEA7-3 are much more resistant to cold, drought, and salt stresses. Interestingly, the expression of NtLEA7-3 in tobacco was not tissue-specific and induced by chilling, drought and salt stresses. All of these, taken together, suggest that NtLEA7-3 is worthwhile to elucidate the contribution of the proteins to the tolerance mechanism to chilling stress, and can be considered as a potential target for crop genetic improvement in the future.

Indexed as

Stress, PhysiologicalAmino Acid SequenceCell Culture TechniquesCold TemperatureGene ExpressionMolecular Sequence DataNicotianaPlant ProteinsPlant RootsProteomeSeedsSequence Homology, Amino Acidlate embryogenesis abundant protein, plantPlant ProteinsProteome

Identifiers

PMID21653253
PMCPMC3226408

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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.