The expression of the six rice ASR genes is differentially regulated in a tissue-dependent manner according to environmental conditions and reproductive stages. OsASR1 and OsASR3 are the most abundant and are found in most tissues; they are enriched in the leaves and roots, respectively. Coexpression analysis of OsASR1 and OsASR3 and a comparison of the cis-acting elements upstream of OsASR1 and OsASR3 suggested that their expression is regulated in common by abiotic stresses but differently regulated by hormone and sugar signals. The results of quantitative real-time PCR analyses of OsASR1 and OsASR3 expression under various conditions further support this model. The expression of both OsASR1 and OsASR3 was induced by drought stress, which is a major regulator of the expression of all ASR genes in rice. In contrast, ABA is not a common regulator of the expression of these genes. OsASR1 transcription was highly induced by ABA, whereas OsASR3 transcription was strongly induced by GA. In addition, OsASR1 and OsASR3 expression was significantly induced by sucrose and sucrose/glucose treatments, respectively. The induction of gene expression in response to these specific hormone and sugar signals was primarily observed in the major target tissues of these genes (i.e., OsASR1 in leaves and OsASR3 in roots). Our data also showed that the overexpression of either OsASR1 or OsASR3 in transgenic rice plants increased their tolerance to drought and cold stress. Taken together, our results revealed that the transcriptional control of different rice ASR genes exhibit different tissue-dependent sugar and hormone-sensitivities.

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Abiotic stresses such as drought, high salinity, and cold are key factors in determining crop yield. Rice is a notoriously drought-susceptible crop due in part to its small root system. Abscisic acid (ABA) involves in abiotic stress resistance in plants. The basic leucine zipper (bZIP) transcription factors play important roles in the ABA signaling pathway in plants. OsbZIP12 is a member of the group E bZIP transcription factor family in rice (Oryza sativa). Expression of OsbZIP12 is induced by abiotic stresses and ABA as well as sugar in rice. It is rapidly and strongly induced by drought stress. Corresponding with expression patterns, several stress and sugar-associated cis-acting elements were found in the OsbZIP12 promoter region. Transgenic rice overexpressing OsbZIP12 showed significantly improved drought tolerance and hypersensitivity to ABA. The elevated levels of expression of the ABA responding LEA3 and Rab16 genes in transgenic rice may enhance drought tolerance. These results indicate that OsbZIP12 is a positive regulator of ABA signaling and drought stress tolerance in rice and that OsbZIP12 could be involved in crosstalk among stress, hormone, and sugar signaling. We propose that OsbZIP12 is an important player in rice for conferring ABA-dependent drought tolerance and has high potential for use in the genetic improvement of stress tolerance.

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Plant-specific ethylene response factors (ERFs) play important roles in abiotic and biotic stress responses in plants. Using a transgenic approach, we identified two rice ERF genes, OsERF4a and OsERF10a, which conferred drought stress tolerance. In particular, OsERF4a contains a conserved ERF-associated amphiphilic repression (EAR) motif in its C-terminal region that has been shown to function as a transcriptional repression domain. Expression profiling of transgenic rice plants over-expressing OsERF4a using either a constitutively active or an ABA-inducible promoter identified 45 down-regulated and 79 up-regulated genes in common. The increased stress tolerance by over-expression of the EAR domain-containing protein OsERF4a could result from suppression of a repressor of the defense response. Expression of the putative silent information regulator 2 (Sir2) repressor protein was repressed, and expression of several stress-response genes were induced by OsERF4a over-expression. The Sir2 and 7 out of 9 genes that were down-regulated by OsERF4a over-expression were induced by high salinity and drought treatments in non-transgenic control plants. Genes that were down- and up-regulated by OsERF4a over-expression were highly biased toward chromosome 11. Rice chromosome 11 has several large clusters of disease-resistance and defense-response genes. Taken together, our results suggest that OsERF4a is a positive regulator of shoot growth and water-stress tolerance in rice during early growth stages. We propose that OsERF4a could work by suppressing a repressor of the defense responses and/or by controlling the expression of a large number of genes located on chromosome 11.