The transforming growth factors-β (TGF-β1 through -β5) are a family of homodimeric cytokines that regulate proliferation and function in many cell types. Family members have 66 to 80% sequence identity and nine strictly conserved cysteines. A crystal structure of a member of this family, TGF-β2, has been determined at 2.1 angstrom (Å) resolution and refined to an R factor of 0.172. The monomer lacks a well-defined hydrophobic core and displays an unusual elongated nonglobular fold with dimensions of approximately 60 Å by 20 Å by 15 Å. Eight cysteines form four intrachain disulfide bonds, which are clustered in a core region forming a network complementary to the network of hydrogen bonds. The dimer is stabilized by the ninth cysteine, which forms an interchain disulfide bond, and by two identical hydrophobic interfaces. Sequence profile analysis of other members of the TGF-β superfamily, including the activins, inhibins, and several developmental factors, imply that they also adopt the TGF-β fold.
Plant architecture is determined by genetic and developmental programs as well as by environmental factors. Sessile plants have evolved a subtle adaptive mechanism that allows them to alter their growth and development during periods of stress. Phytohormones play a central role in this process; however, the molecules responsible for integrating growth-and stressrelated signals are unknown. Here, we report a gain-of-function rice (Oryza sativa) mutant, tld1-D, characterized by (and named for) an increased number of tillers, enlarged leaf angles, and dwarfism. TLD1 is a rice GH3.13 gene that encodes indole-3-acetic acid (IAA)-amido synthetase, which is suppressed in aboveground tissues under normal conditions but which is dramatically induced by drought stress. The activation of TLD1 reduced the IAA maxima at the lamina joint, shoot base, and nodes, resulting in subsequent alterations in plant architecture and tissue patterning but enhancing drought tolerance. Accordingly, the decreased level of free IAA in tld1-D due to the conjugation of IAA with amino acids greatly facilitated the accumulation of late-embryogenesis abundant mRNA compared with the wild type. The direct regulation of such drought-inducible genes by changes in the concentration of IAA provides a model for changes in plant architecture via the process of drought adaptation, which occurs frequently in nature.
The involvement of calcium and calcium-activated calmodulin (Ca 2ϩ -CaM) in heat shock (HS) signal transduction in wheat (Triticum aestivum) was investigated. Using Fluo-3/acetoxymethyl esters and laser scanning confocal microscopy, it was found that the increase of intracellular free calcium ion concentration started within 1 min after a 37°C HS. The levels of CaM mRNA and protein increased during HS at 37°C in the presence of Ca 2ϩ . The expression of hsp26 and hsp70 genes was up-regulated by the addition of CaCl 2 and down-regulated by the calcium ion chelator EGTA, the calcium ion channel blockers LaCl 3 and verapamil, or the CaM antagonists N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide and chlorpromazine. Treatment with Ca 2ϩ also increased, and with EGTA, verapamil, chlorpromazine, or trifluoperazine decreased, synthesis of HS proteins. The temporal expression of the CaM1-2 gene and the hsp26 and hsp70 genes demonstrated that up-regulation of the CaM1-2 gene occurred at 10 min after HS at 37°C, whereas that of hsp26 and hsp70 appeared at 20 min after HS. A 5-min HS induced expression of hsp26 after a period of recovery at 22°C after HS at 37°C. Taken together, these results indicate that Ca 2ϩ -CaM is directly involved in the HS signal transduction pathway. A working hypothesis about the relationship between upstream and downstream of HS signal transduction is presented.Organisms have developed a diverse array of mechanisms for adapting to environmental changes. One of the best characterized responses is the induction of heat shock proteins (HSPs). The heat shock (HS) response has been found in almost every organism studied to date. The HSPs are synthesized by cells in response to elevated temperature but are also induced by other environmental stresses (Noven et al., 1992; Kilstrup et al., 1997) and play an important role in the thermotolerance of plants (Queitsch et al., 2000; Burke, 2001). A connection between HS response and oxidative stress has been observed (Gong et al., 1997a;Lee et al., 2000;Larkindale and Knight, 2002; Panchuk et al., 2002). The HSPs are divided into several families based on their molecular mass, and most have molecular chaperones functions (for review, see Boston et al., 1996;Miernyk, 1999). Angiosperms synthesize more small HSPs (smHSPs) than other organisms. These smHSPs are likely critical for survival of heat stress and for specific developmental processes in plants (Waters et al., 1996).The changes in cytoplasmic calcium levels act as a ubiquitous signal in eukaryotic cells. HS induced a large increase in intracellular free calcium ion concentration ([Ca 2ϩ ] i ) in Chinese hamster (Cricetulus barabensis) HA-1 fibroblasts (Calderwood et al., 1988). In plants, Gong et al. (1998) observed that HS caused a transient increase in [Ca 2ϩ ] i . The change in [Ca 2ϩ ] i is also involved in regulating the binding activity of the HS transcription factor (HSF) to the HS element (Mosser et al., 1990), the synthesis of HSPs (Kiang et al., 1994;Kuznetsov et al., 1998), and...
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