Literature DB >> 12231932

Characterization of the Early Stages of Genetic Salt-Stress Responses in Salt-Tolerant Lophopyrum elongatum, Salt-Sensitive Wheat, and Their Amphiploid.

A. F. Galvez1, P. J. Gulick, J. Dvorak.   

Abstract

Eleven unique cDNA clones corresponding to genes showing enhanced mRNA accumulation in the early stages of salt stress (early salt stress induced, ESI) were previously isolated. The accumulation of these mRNAs in Lophopyrum elongatum (Host) A. Love, salt-sensitive wheat (Triticum aestivum L.), and their amphiploid is compared. The accumulation of ESI mRNAs was much greater in the L. elongatum roots than in the shoots. Additionally, mRNA accumulation in the roots of the three genotypes showed a biphasic response. The first phase occurred within a few hours after the onset of stress and had a large osmotic shock component, as indicated by induction of the accumulation of these mRNAs by a nonsaline osmoticum. The ion-specific component, however, also played a role. External Ca2+ reduced this response. The second phase was characterized by either constantly elevated mRNA levels or gradually increasing mRNA levels. The same biphasic response was elicited by exogenous abscisic acid (ABA). The response of all mRNAs to ABA closely approximated the response to 250 mM NaCl treatment in all three genotypes. The differences among the three genotypes in response to NaCl and ABA treatments were largely confined to the first phase of the response, in which mRNA levels were highest in L. elongatum and lowest in wheat. The levels of ESI mRNAs in the amphiploid closely approximated levels calculated on the basis of the doses of wheat and L. elongatum genomes in the amphiploid, which indicated an additive contribution of the genomes to early salt stress response in the amphiploid. The inducer of the ESI mRNA accumulation in response to NaCl and other osmotica is produced in the stressed roots and shows only minor, if any, translocation. A putative candidate for this inducer is root ABA.

Entities:  

Year:  1993        PMID: 12231932      PMCID: PMC158971          DOI: 10.1104/pp.103.1.257

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  11 in total

1.  Differential mRNA transcription during salinity stress in barley.

Authors:  S Ramagopal
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

2.  Displacement of ca by na from the plasmalemma of root cells : a primary response to salt stress?

Authors:  G R Cramer; A Läuchli; V S Polito
Journal:  Plant Physiol       Date:  1985-09       Impact factor: 8.340

3.  Salt toleration by plants: enhancement with calcium.

Authors:  P A Lahaye; E Epstein
Journal:  Science       Date:  1969-10-17       Impact factor: 47.728

4.  A cDNA-based comparison of dehydration-induced proteins (dehydrins) in barley and corn.

Authors:  T J Close; A A Kortt; P M Chandler
Journal:  Plant Mol Biol       Date:  1989-07       Impact factor: 4.076

5.  A method for isolation of intact, translationally active ribonucleic acid.

Authors:  G Cathala; J F Savouret; B Mendez; B L West; M Karin; J A Martial; J D Baxter
Journal:  DNA       Date:  1983

6.  Characterization of a rice gene showing organ-specific expression in response to salt stress and drought.

Authors:  B Claes; R Dekeyser; R Villarroel; M Van den Bulcke; G Bauw; M Van Montagu; A Caplan
Journal:  Plant Cell       Date:  1990-01       Impact factor: 11.277

7.  On the evolution of the adaptation of Lophopyrum elongatum to growth in saline environments.

Authors:  J Dvorák; M Edge; K Ross
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

8.  Characterization of osmotin : a thaumatin-like protein associated with osmotic adaptation in plant cells.

Authors:  N K Singh; C A Bracker; P M Hasegawa; A K Handa; S Buckel; M A Hermodson; E Pfankoch; F E Regnier; R A Bressan
Journal:  Plant Physiol       Date:  1987-10       Impact factor: 8.340

9.  Coordinate Gene Response to Salt Stress in Lophopyrum elongatum.

Authors:  P J Gulick; J Dvorák
Journal:  Plant Physiol       Date:  1992-11       Impact factor: 8.340

10.  Abscisic acid and water-stress induce the expression of a novel rice gene.

Authors:  J Mundy; N H Chua
Journal:  EMBO J       Date:  1988-08       Impact factor: 11.598

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  22 in total

1.  Membrane hyperpolarization and salt sensitivity induced by deletion of PMP3, a highly conserved small protein of yeast plasma membrane.

Authors:  C Navarre; A Goffeau
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

Review 2.  Plant abiotic stress-related RCI2/PMP3s: multigenes for multiple roles.

Authors:  Pedro S C F Rocha
Journal:  Planta       Date:  2015-08-26       Impact factor: 4.116

3.  Chromosomal control of the tolerance of gradually and suddenly imposed salt stress in the Lophopyrum elongatum and wheat, Triticum aestivum L. genomes.

Authors:  G Y Zhong; J Dvorak
Journal:  Theor Appl Genet       Date:  1995-02       Impact factor: 5.699

4.  The salt stress-inducible protein kinase gene, Esi47, from the salt-tolerant wheatgrass Lophopyrum elongatum is involved in plant hormone signaling.

Authors:  W Shen; A Gómez-Cadenas; E L Routly; T H Ho; J A Simmonds; P J Gulick
Journal:  Plant Physiol       Date:  2001-03       Impact factor: 8.340

5.  ESI3, a stress-induced gene from Lophopyrum elongatum.

Authors:  P J Gulick; W Shen; H An
Journal:  Plant Physiol       Date:  1994-02       Impact factor: 8.340

6.  Molecular and physiological responses to abscisic acid and salts in roots of salt-sensitive and salt-tolerant Indica rice varieties.

Authors:  A Moons; G Bauw; E Prinsen; M Van Montagu; D Van der Straeten
Journal:  Plant Physiol       Date:  1995-01       Impact factor: 8.340

7.  The ionic environment controls the contribution of the barley HvHAK1 transporter to potassium acquisition.

Authors:  Fabiana R Fulgenzi; María Luisa Peralta; Silvina Mangano; Cristian H Danna; Augusto J Vallejo; Pere Puigdomenech; Guillermo E Santa-María
Journal:  Plant Physiol       Date:  2008-03-21       Impact factor: 8.340

8.  Comparison of the genetic organization of the early salt-stress-response gene system in salt-tolerant Lophopyrum elongatum and salt-sensitive wheat.

Authors:  J Dubcovsky; A F Galvez; J Dvořák
Journal:  Theor Appl Genet       Date:  1994-03       Impact factor: 5.699

9.  Overexpression of AlTMP2 gene from the halophyte grass Aeluropus littoralis in transgenic tobacco enhances tolerance to different abiotic stresses by improving membrane stability and deregulating some stress-related genes.

Authors:  Walid Ben-Romdhane; Rania Ben-Saad; Donaldo Meynard; Nabil Zouari; Ali Mahjoub; Lotfi Fki; Emmanuel Guiderdoni; Abdullah Al-Doss; Afif Hassairi
Journal:  Protoplasma       Date:  2018-02-15       Impact factor: 3.356

10.  Diversification of the barley and wheat blt101/wpi6 promoters by the Xumet element without affecting stress responsiveness.

Authors:  Michiya Koike; Hideki Kato; Ryozo Imai
Journal:  Mol Genet Genomics       Date:  2008-04-30       Impact factor: 3.291

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