BackgroundNa+ exclusion from leaf blades is one of the key mechanisms for glycophytes to cope with salinity stress. Certain class I transporters of the high-affinity K+ transporter (HKT) family have been demonstrated to mediate leaf blade-Na+ exclusion upon salinity stress via Na+-selective transport. Multiple HKT1 transporters are known to function in rice (Oryza sativa). However, the ion transport function of OsHKT1;4 and its contribution to the Na+ exclusion mechanism in rice remain to be elucidated.ResultsHere, we report results of the functional characterization of the OsHKT1;4 transporter in rice. OsHKT1;4 mediated robust Na+ transport in Saccharomyces cerevisiae and Xenopus laevis oocytes. Electrophysiological experiments demonstrated that OsHKT1;4 shows strong Na+ selectivity among cations tested, including Li+, Na+, K+, Rb+, Cs+, and NH4+, in oocytes. A chimeric protein, EGFP-OsHKT1;4, was found to be functional in oocytes and targeted to the plasma membrane of rice protoplasts. The level of OsHKT1;4 transcripts was prominent in leaf sheaths throughout the growth stages. Unexpectedly however, we demonstrate here accumulation of OsHKT1;4 transcripts in the stem including internode II and peduncle in the reproductive growth stage. Moreover, phenotypic analysis of OsHKT1;4 RNAi plants in the vegetative growth stage revealed no profound influence on the growth and ion accumulation in comparison with WT plants upon salinity stress. However, imposition of salinity stress on the RNAi plants in the reproductive growth stage caused significant Na+ overaccumulation in aerial organs, in particular, leaf blades and sheaths. In addition, 22Na+ tracer experiments using peduncles of RNAi and WT plants suggested xylem Na+ unloading by OsHKT1;4.ConclusionsTaken together, our results indicate a newly recognized function of OsHKT1;4 in Na+ exclusion in stems together with leaf sheaths, thus excluding Na+ from leaf blades of a japonica rice cultivar in the reproductive growth stage, but the contribution is low when the plants are in the vegetative growth stage.Electronic supplementary materialThe online version of this article (doi:10.1186/s12870-016-0709-4) contains supplementary material, which is available to authorized users.
Every mission into deep space has a communications system to carry commands and other information from Earth to a spacecraft or to a remote planet and to return scientific data to Earth [1]. Communications systems are central to the success of space missions. Large amounts of data need to be transferred (for example, nearly 25 TB in 2013 concerning the Mars Reconnaissance Orbiter (MRO)), and the demand will grow in the future [1] because of the employment of more sophisticated instruments that will generate more data. This will require the availability of high network transfer rates. Satellite systems already have to cope with difficult communication challenges: long round trip times (RTTs); the likelihood of data loss due to errors on the communication link; possible channel disruptions; and coverage issues at high latitudes and in challenging terrain. These problems are magnified in space communications characterized by huge distances among network nodes, which imply extremely long delays and intermittent connectivity. At the same time, a space communications system must be reliable over time due to the long duration of space missions. Moreover, the importance of enabling Internet-like communications with space vehicles is increasing, realizing the concept of extended Future Internet, an IP (Internet Protocol) pervasive network of networks including interplanetary communication [2], where a wide variety of science information values are acquired through sensors and transmitted.The Delay-and Disruption Tolerant Network (DTN) architecture [3] introduces an overlay protocol that interfaces with either the transport layer or lower layers. Each node of the DTN architecture can store information for a long time before forwarding it. Thanks to these features, a DTN is particularly suited to cope with the challenges imposed by space communication. As summarized in [4], the origin of the DTN concept lies in a generalization of requirements identified for interplanetary networking (IPN), where latencies that may reach the order of tens of minutes, as well as limited and highly asymmetric bandwidth, must be faced.However, other scenarios in planetary networking, called "challenged networks," such as military tactical networking, sparse sensor networks, and networking in developing or otherwise communications-challenged regions, can also benefit from the DTN solution. Delays and disruptions can be handled at each DTN hop in a path between a sender and a destination. Nodes on the path can provide the storage necessary for data in transit before forwarding it to the next node on the path. In consequence, the contemporaneous end-to-end connectivity that Transmission Control Protocol (TCP) and other standard Internet transport protocols require in order to reliably transfer application data is not required.In practice, in standard TCP/IP networks, ABSTRACTDelay-and Disruption Tolerant Networks (DTNs) are based on an overlay protocol and on the store-carry-forward paradigm. In practice, each DTN node can store information for a...
The neural basis of functional lateralization in language processing is a fundamental issue in systems neuroscience. We used functional MRI (fMRI) to examine hemispheric dominance during the processing of signed and spoken sentences. By using tasks involving comprehension of sentences (Sc) and sentential non-word detection (Sn), we compared different groups and stimulus conditions. Under the sign condition with sentence stimuli in Japanese Sign Language (JSL), we tested two groups of subjects: Deaf signers (Deaf) of JSL, and hearing bilinguals (children of Deaf adults, CODA) of JSL and Japanese (JPN). Under the speech condition, we tested hearing monolinguals (Mono) of JPN with auditory JPN stimuli alone (AUD), or with an audiovisual presentation of JPN and JSL stimuli (A&V). We found that the overall bilateral activation patterns under the four experimental conditions of Deaf, CODA, AUD and A&V were almost identical, despite differences in stimuli (JSL and JPN) and groups (Deaf, CODA and Mono). Moreover, consistently left-dominant activations involving frontal and temporo-parietal regions were observed across all four conditions. Furthermore, irrespective of the modalities of sign and speech, the main effects of task (Sc-Sn) were found primarily in the left regions: the ventral part of the inferior frontal gyrus (F3t/F3O), the precentral sulcus, the superior frontal gyrus, the middle temporal gyrus, the angular gyrus and the inferior parietal gyrus. Among these regions, only the left F3t/F3O showed no main effects of modality condition. These results demonstrate amodal commonality in the functional dominance of the left cortical regions for comprehension of sentences, as well as the essential and universal role of the left F3t/F3O in processing linguistic information from both signed and spoken sentences.
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