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Characterization of Phaseolus Vulgaris CDNA Clones Responsive to Water Deficit: Identification of a Novel Late Embryogenesis Abundant-like Protein

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Journal Plant Mol Biol
Date 1998 Feb 12
PMID 9349263
Citations 22
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Abstract

Six cDNA clones from Phaseolus vulgaris, whose expression is induced by water deficit and ABA treatment (rsP cDNAs) were identified and characterized. The sequence analyses of the isolated clones suggest that they encode two types of late-embryogenesis abundant (LEA) proteins, a class-1 cytoplasmic low-molecular-weight heat shock protein (lmw-HSP), a lipid transfer protein (LTP), and two different proline-rich proteins (PRP). One of the putative LEA proteins identified corresponds to a novel 9.3 kDa LEA-like protein. During the plant response to a mild water deficit (psi w = -0.35 MPa) all genes identified present a maximal expression at around 16 or 24 h of treatment, followed by a decline in expression levels. Rehydration experiments revealed that those genes encoding PRPs and LTP transiently re-induce or maintain their expression when water is added to the soil after a dehydration period. This is not the case for the lea genes whose transcripts rapidly decrease, reaching basal levels a few hours after rehydration (4 h). Under water deficit and ABA treatments, the highest levels of expression for most of the genes occur in the root, excluding the ltp gene whose maximum expression levels are found in the aerial regions of the plant. This indicates that for these genes, both water deficit and ABA-dependent expression are under organ-specific control. The data presented here support the importance of these proteins during the plant response to water deficit.

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References
1.
Frensch J, Hsiao T . Rapid Response of the Yield Threshold and Turgor Regulation during Adjustment of Root Growth to Water Stress in Zea mays. Plant Physiol. 1995; 108(1):303-312. PMC: 157335. DOI: 10.1104/pp.108.1.303. View

2.
Raschke E, Baumann G, Schoffl F . Nucleotide sequence analysis of soybean small heat shock protein genes belonging to two different multigene families. J Mol Biol. 1988; 199(4):549-57. DOI: 10.1016/0022-2836(88)90300-2. View

3.
Niu X, Bressan R, Hasegawa P, Pardo J . Ion Homeostasis in NaCl Stress Environments. Plant Physiol. 1995; 109(3):735-742. PMC: 161372. DOI: 10.1104/pp.109.3.735. View

4.
Almoguera C, Jordano J . Developmental and environmental concurrent expression of sunflower dry-seed-stored low-molecular-weight heat-shock protein and Lea mRNAs. Plant Mol Biol. 1992; 19(5):781-92. DOI: 10.1007/BF00027074. View

5.
Church G, Gilbert W . Genomic sequencing. Proc Natl Acad Sci U S A. 1984; 81(7):1991-5. PMC: 345422. DOI: 10.1073/pnas.81.7.1991. View