ArticleTheScientificWorldJournal2014
Expression profiles of 12 late embryogenesis abundant protein genes from Tamarix hispida in response to abiotic stress.
Article in TheScientificWorldJournal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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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.
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Who cites it
3 citing papers in PubMed.
- Conferring of Drought and Heat Stress Tolerance in Wheat (Nanomaterials (Basel, Switzerland) · 2023Article
- Physical state of the culture medium triggers shift in morphogenetic pattern from shoot bud formation to somatic embryo inPhysiology and molecular biology of plants : an international journal of functional plant biology · 2018Article
- Making Plants Break a Sweat: the Structure, Function, and Evolution of Plant Salt Glands.Frontiers in plant science · 2017Review
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Authors and funding
5 authors.
Funding
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Abstract
Twelve embryogenesis abundant protein (LEA) genes (named ThLEA-1 to -12) were cloned from Tamarix hispida. The expression profiles of these genes in response to NaCl, PEG, and abscisic acid (ABA) in roots, stems, and leaves of T. hispida were assessed using real-time reverse transcriptase-polymerase chain reaction (RT-PCR). These ThLEAs all showed tissue-specific expression patterns in roots, stems, and leaves under normal growth conditions. However, they shared a high similar expression patterns in the roots, stems, and leaves when exposed to NaCl and PEG stress. Furthermore, ThLEA-1, -2, -3, -4, and -11 were induced by NaCl and PEG, but ThLEA-5, -6, -8, -10, and -12 were downregulated by salt and drought stresses. Under ABA treatment, some ThLEA genes, such as ThLEA-1, -2, and -3, were only slightly differentially expressed in roots, stems, and leaves, indicating that they may be involved in the ABA-independent signaling pathway. These findings provide a basis for the elucidation of the function of LEA genes in future work.
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