Helicobacter pylori is a causative agent of gastritis and peptic ulcer. cagA ؉ H. pylori strains are more virulent than cagA ؊ strains and are associated with gastric carcinoma. The cagA gene product, CagA, is injected by the bacterium into gastric epithelial cells and subsequently undergoes tyrosine phosphorylation. The phosphorylated CagA specifically binds SHP-2 phosphatase, activates the phosphatase activity, and thereby induces morphological transformation of cells. CagA proteins of most Western H. pylori isolates have a 34-amino acid sequence that variably repeats among different strains. Here, we show that the repeat sequence contains a tyrosine phosphorylation site. CagA proteins having more repeats were found to undergo greater tyrosine phosphorylation, to exhibit increased SHP-2 binding, and to induce greater morphological changes. In contrast, predominant CagA proteins specified by H. pylori strains isolated in East Asia, where gastric carcinoma is prevalent, had a distinct tyrosine phosphorylation sequence at the region corresponding to the repeat sequence of Western CagA. This East Asian-specific sequence conferred stronger SHP-2 binding and morphologically transforming activities to Western CagA. Finally, a critical amino acid residue that determines SHP-2 binding activity among different CagA proteins was identified. Our results indicate that the potential of individual CagA to perturb host-cell functions is determined by the degree of SHP-2 binding activity, which depends in turn on the number and sequences of tyrosine phosphorylation sites. The presence of distinctly structured CagA proteins in Western and East Asian H. pylori isolates may underlie the strikingly different incidences of gastric carcinoma in these two geographic areas.

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Floral induction is a crucial developmental step in higher plants. Florigen, a mobile floral activator that is synthesized in the leaf and transported to the shoot apex, was recently identified as a protein encoded by FLOWERING LOCUS T (FT) and its orthologs; the rice florigen is Heading date 3a (Hd3a) protein. The 14-3-3 proteins mediate the interaction of Hd3a with the transcription factor OsFD1 to form a ternary structure called the florigen activation complex on the promoter of OsMADS15, a rice APETALA1 ortholog. However, crucial information, including the spatiotemporal overlap among FT-like proteins and the components of florigen activation complex and downstream genes, remains unclear. Here, we confirm that Hd3a coexists, in the same regions of the rice shoot apex, with the other components of the florigen activation complex and its transcriptional targets. Unexpectedly, however, RNA-sequencing analysis of shoot apex from wild-type and RNA-interference plants depleted of florigen activity revealed that 4,379 transposable elements (TEs; 58% of all classifiable rice TEs) were expressed collectively in the vegetative and reproductive shoot apex. Furthermore, in the reproductive shoot apex, 214 TEs were silenced by florigen. Our results suggest a link between floral induction and regulation of TEs.floral transition | FT-like proteins | shoot apical meristem | transposable elements | rice F loral induction has been studied extensively over the years, and the use of molecular genetics in the model species Arabidopsis thaliana has been particularly successful in identifying genes and genetic pathways that are involved in flower development (1-3). Several key flowering genes sense environmental conditions and activate the proper expression of genes that are essential for floral induction. Once floral induction occurs, further key genes positively and negatively regulate each other in the shoot apex and activate flower identity genes, eventually leading to the formation of flowers (1-3).One of the critical molecules for floral induction is florigen, a mobile floral activator that is produced in leaves and transported to the shoot apex. Many studies now indicate that proteins encoded by Arabidopsis FLOWERING LOCUS T (FT) and its orthologs in other species are florigens (4-8). Transcription of florigen genes is tightly regulated by environmental conditions, and florigen protein is transported from leaves to the shoot apex where it induces the expression of downstream genes to ensure proper flower development. Despite its important role in floral induction, many questions about florigen remain unresolved. They include its molecular function, mechanism of transport, localization in the shoot apex, and the identities of its downstream genes.Rice is a short-day (SD) plant and has two florigens, Heading date 3a (Hd3a) and RICE FLOWERING LOCUS T1 (RFT1), which predominate, respectively, under SD and long-day (LD) conditions (7, 9). When GFP fusions of Hd3a and RFT1 are expressed under their own promoters, GFP fluorescence...

Proanthocyanidins, which are oligomers and polymers of flavan-3-ol units (e.g., (+)-catechin and (−)-epicatechin), are important components of grapes for red winemaking. Flavan-3-ols are biosynthesized by the catalysis of anthocyanidin reductase (ANR) and leucoanthocyanidin reductase (LAR). In this study, we investigated the effect of shading on proanthocyanidin biosynthesis in berries of Vitis vinifera 'Cabernet Sauvignon'. Shading of the berries reduced the accumulation of proanthocyanidins and the transcription of ANR and LAR genes in the skins during berry development, while no significant effect was observed in the seeds. Because the proanthocyanidins significantly decreased in the skins and seeds of the control berries during ripening, the levels of proanthocyanidins were similar in the shaded and control berries at the harvest stage.

Use of a 2-ethynylaniline having an alkyl or aryl group on the terminal alkyne selectively produced a variety of polyfunctionalized indole derivatives in moderate to excellent yields via indium-catalyzed intramolecular cyclization of the corresponding alkynylaniline. In contrast, employment of a substrate with a trimethylsilyl group or with no substituent group on the terminal triple bond, exclusively afforded polysubstituted quinoline derivatives in good yields via indium-promoted intermolecular dimerization of the ethynylaniline. This indium catalytic system successfully accommodated the intramolecular cyclization of other arylalkyne skeletons involving a carboxylic acid and an amide group.