The Ca 21-binding protein calmodulin mediates cellular Ca 21 signals in response to a wide array of stimuli in higher eukaryotes. Plants express numerous CaM isoforms. Transcription of one soybean (Glycine max) CaM isoform, SCaM-4, is dramatically induced within 30 min of pathogen or NaCl stresses. To characterize the cis-acting element(s) of this gene, we isolated an approximately 2-kb promoter sequence of the gene. Deletion analysis of the promoter revealed that a 130-bp region located between nucleotide positions 2858 and 2728 is required for the stressors to induce expression of SCaM-4. A hexameric DNA sequence within this region, GAAAAA (GT-1 cis-element), was identified as a core cis-acting element for the induction of the SCaM-4 gene. The GT-1 cis-element interacts with an Arabidopsis GT-1-like transcription factor, AtGT-3b, in vitro and in a yeast selection system. Transcription of AtGT-3b is also rapidly induced within 30 min after pathogen and NaCl treatment. These results suggest that an interaction between a GT-1 cis-element and a GT-1-like transcription factor plays a role in pathogen-and salt-induced SCaM-4 gene expression in both soybean and Arabidopsis.Plant cells, like animal cells, elevate their cytosolic free-calcium levels ([Ca 21 ] cyt ) with varying amplitude, frequency, and duration in response to a variety of external stimuli (Thomas et al., 1996; Berridge, 1997;McAinsh and Hetherington, 1998 -bound CaM transduces the signals into many cellular processes through modulation of a variety of CaM-binding proteins, including enzymes such as kinases, phosphatases, and nitric-oxide synthase, as well as receptors, ion channels, G-proteins, and transcription factors (Liao et al., 1996;Snedden and Fromm, 1998;Lee et al., 1999a;Zuhlke et al., 1999).In plant cells, in contrast to mammalian cells, multiple CaM genes code for a number of CaM isoforms. This has been shown in wheat (Triticum aestivum; Yang et al., 1996), potato (Solanum tuberosum; Takezawa et al., 1995;Poovaiah et al., 1996), and soybean (Glycine max; Lee et al., 1995a), among others. Over 30 genes encoding CaM isoforms are found in the Arabidopsis genome (The Arabidopsis Genome Initiative, 2000). We have recently cloned five CaM isoforms from soybean (SCaM-1-5). Although SCaM-1-3 are more than 90% identical to mammalian CaM, SCaM-4 and SCaM-5 exhibit only a 78% homology with SCaM-1 and are therefore the most divergent isoforms reported thus far in the plant and animal kingdoms. SCaM-4 is considered to be a bona fide CaM isoform based on the following characteristics. In its primary protein structure, SCaM-4 has four conserved putative EF-hands and a central linker region, hallmark structural features of CaM (Lee et al., 1995a). In addition, most of the nonconsensus amino acids occur outside the EF-hands, and the total number of Article, publication date, and citation information can be found at www.plantphysiol.org/cgi

The Ca 2؉ signal is essential for the activation of plant defense responses, but downstream components of the signaling pathway are still poorly defined. Here we demonstrate that specific calmodulin (CaM) isoforms are activated by infection or pathogen-derived elicitors and participate in These results suggest that specific CaM isoforms are components of a SA-independent signal transduction chain leading to disease resistance.

Sessile plants have developed a very delicate system to sense diverse kinds of endogenous developmental cues and exogenous environmental stimuli by using a simple Ca2+ ion. Calmodulin (CaM) is the predominant Ca2+ sensor and plays a crucial role in decoding the Ca2+ signatures into proper cellular responses in various cellular compartments in eukaryotes. A growing body of evidence points to the importance of Ca2+ and CaM in the regulation of the transcriptional process during plant responses to endogenous and exogenous stimuli. Here, we review recent progress in the identification of transcriptional regulators modulated by Ca2+ and CaM and in the assessment of their functional significance during plant signal transduction in response to biotic and abiotic stresses and developmental cues.

Mitogen-activated protein kinase (MAPK) cascades are known to transduce plant defense signals, but the downstream components of the MAPK have as yet not been elucidated. Here, we report an MAPK from rice (Oryza sativa), BWMK1, and a transcription factor, OsEREBP1, phosphorylated by the kinase. The MAPK carries a TDY phosphorylation motif instead of the more common TEY motif in its kinase domain and has an unusually extended C-terminal domain that is essential to its kinase activity and translocation to the nucleus. The MAPK phosphorylates OsEREBP1 that binds to the GCC box element (AGCCGCC) of the several basic pathogenesis-related gene promoters, which in turn enhances DNA-binding activity of the factor to the cis element in vitro. Transient co-expression of the BWMK1 and OsEREBP1 in Arabidopsis protoplasts elevates the expression of the ␤-glucuronidase reporter gene driven by the GCC box element. Furthermore, transgenic tobacco (Nicotiana tabacum) plants overexpressing BWMK1 expressed many pathogenesis-related genes at higher levels than wild-type plants with an enhanced resistance to pathogens. These findings suggest that MAPKs contribute to plant defense signal transduction by phosphorylating one or more transcription factors.Mitogen-activated protein kinase (MAPK) cascades are known to play essential roles in the signal transduction pathways involved in numerous eukaryotic cellular processes from cell division to cell death (Davis, 2000; Ligterink and Hirt, 2001). In the last few years, it has become apparent that MAPK cascades also play vital roles in signal transduction pathways of plants, including plant defense signaling (Innes, 2001; Tena et al., 2001; Zhang and Klessig, 2001). The Arabidopsis genome sequence has revealed the presence of 23 MAPK genes in the genome, which suggests that the MAPK cascades in plants may be quite complex.Accumulating lines of evidence indicate that plants rapidly activate MAPKs when exposed to a variety of abiotic and biotic stress stimuli (Ligterink et al., 1997; Zhang et al., 1998; Seo et al., 1999; Cardinale et al., 2000; Ichimura et al., 2000). These include pathogens, pathogen-derived elicitors, and defense-related second messengers. In tobacco (Nicotiana tabacum), two MAPKs, SIPK and WIPK, are activated by both various pathogen-related signals and diverse abiotic stresses, indicating that pathogen defense signaling is part of an integrated stress-signaling network in plants. Orthologs of SIPK and WIPK in Arabidopsis (AtMPK6 and AtMAPK3, respectively) and alfalfa (Medicago sativa; SIMK and SAMK, respectively) are also activated by both biotic and abiotic stresses (Seo et al., 1995; Zhang and Klessig, 1997; Nuhse et al., 2000). Recently, the MAPKK, NtMEK2, was identified to operate in the cascade upstream of SIPK and WIPK because a constitutively active NtMEK2 activates endogenous SIPK and WIPK molecules in transiently transformed tobacco cells. Furthermore, the constitutively active NtMEK2 induces hypersensitive cell death and the expression of defense genes (Yan...

Cellular Na+/K+ ratio is a crucial parameter determining plant salinity stress resistance. We tested the function of plasma membrane Na+/K+ cotransporters in the High-affinity K+ Transporter (HKT) family from the halophytic Arabidopsis (Arabidopsis thaliana) relative Thellungiella salsuginea. T. salsuginea contains at least two HKT genes. TsHKT1;1 is expressed at very low levels, while the abundant TsHKT1;2 is transcriptionally strongly up-regulated by salt stress. TsHKT-based RNA interference in T. salsuginea resulted in Na+ sensitivity and K+ deficiency. The athkt1 mutant lines overexpressing TsHKT1;2 proved less sensitive to Na+ and showed less K+ deficiency than lines overexpressing AtHKT1. TsHKT1;2 ectopically expressed in yeast mutants lacking Na+ or K+ transporters revealed strong K+ transporter activity and selectivity for K+ over Na+. Altering two amino acid residues in TsHKT1;2 to mimic the AtHKT1 sequence resulted in enhanced sodium uptake and loss of the TsHKT1;2 intrinsic K+ transporter activity. We consider the maintenance of K+ uptake through TsHKT1;2 under salt stress an important component supporting the halophytic lifestyle of T. salsuginea.