This study aimed to survey the expression of genes involved in rice N uptake and aasimilatory network and to understand the potential molecular mechanisms responsible for the NO3^-enhanced NH4^＋ uptake. By using quantitative real-time polymerase chain reaction （PCR）, the genes related to N nutrition, including ammonium transporters （AMTs） and ammonium assimilatory enzymes （GS and GOGAT）, were transcriptionally analyzed in rice plants grown in the absence and presence of NO4^- in the NH4^＋-containing medium. The results showed that NH4^＋ uptake by rice was enhanced by the NO3^- supply to the medium. At the same time and in parallel, the amount of transcripts of seven genes （OsAMT1;1, OsAMT1;2, OsAMT4;1, OsGLNP, OsGLU1, OsGLT1, and OsGLTP） was increased in rice roots, but the expression of two genes （OsGLN1;1 and OsGLN1;P） was decreased and that of OsAMT1;3 remained without change. Up- or downregulation of these genes involved in NH4^＋ uptake and assimilation correlated with the increase in NH4^＋ uptake in the presence of NO3^- in rice roots.
Post-anthesis photoassimilation is very important for wheat （Triticum aestivum L.） grain filling. The aim of the present study was to map quantitative trait loci （QTL） for post-anthesis dry matter accumulation （DMA）. A set of 120 doubled haploid （DH） lines, derived from winter wheat varieties Hanxuan 10 and Lumai 14, was grown under field conditions in two consecutive growing seasons during 2002-2004 in Beijing. Post-anthesis DMA per culm and related traits, including flag leaf greenness （FLG） and flag leaf weight （FLW; dry weight per flag leaf） at flowering, and grain weight per ear （GWE） were investigated. All traits segregated continuously in the DH population in both trials. The DMA was significantly and positively correlated with GWE, with the correlation coefficients being 0.79 and 0.66 in the 2002-2003 and 2003-2004 growing seasons （both P〈0.01）, suggesting the importance of DMA in grain filling. Further correlation analysis showed that FLW was more closely correlated with DMA and GWE than FLG in both growing seasons, indicating that FLW was more important than FLG in influencing DMA and GWE. In total, 30 QTLs for these four traits were mapped and distributed on 10 chromosomes. Phenotypic variations explained by an individual QTL were in the range 5.8%-21.3%, 5.9%-17.2%, 5.1%-18.1%, and 5.6%-16.2% for FLG, FLW, DMA, and GWE, respectively. Eight QTLs for DMA were detected, of which four （on chromosome arms 2AS, 4BL, 5AS, and 7AS） were linked with QTLs for GWE; two （on chromosome arms 5BL and 7BL） coincided with QTLs for FLW. These results may provide useful information for developing marker-assisted selection for the improvement of DMA.
Jun-Ying SuYi-Ping TongQuan-You LiuBin LiRui-Lian JingJi-Yun LiZhen-Sheng Li
Nitrate is a major nitrogen （N） source for most crops. Nitrate uptake by root cells is a key step of nitrogen metabolism and has been widely studied at the physiological and molecular levels. Understanding how nitrate uptake is regulated will help us engineer crops with improved nitrate uptake efficiency. The present study investigated the regulation of the high-affinity nitrate transport system （HATS） by exogenous abscisic acid （ABA） and glutamine （Gin） in wheat （Triticum aestivum L.） roots. Wheat seedlings grown in nutrient solution containing 2 mmol/L nitrate as the only nitrogen source for 2weeks were deprived of N for 4d and were then transferred to nutrient solution containing 50 μmol/L ABA, and 1 mmol/L Gin in the presence or absence of 2 mmol/L nitrate for 0, 0.5, 1, 2, 4, and 8 h. Treated wheat plants were then divided into two groups. One group of plants was used to investigate the mRNA levels of the HATS components NRT2 and NAR2 genes in roots through semi-quantitative RT-PCR approach, and the other set of plants were used to measure high-affinity nitrate influx rates in a nutrient solution containing 0.2 mmol/L ^15N-labeled nitrate. The results showed that exogenous ABA induced the expression of the TaNRT2.1, TaNRT2.2, TaNRT2.3, TaNAR2.1, and TaNAR2.2 genes in roots when nitrate was not present in the nutrient solution, but did not further enhance the induction of these genes by nitrate. Glutamine, which has been shown to inhibit the expression of NRT2 genes when nitrate is present in the growth media, did not inhibit this induction. When Gin was supplied to a nitrate-free nutrient solution, the expression of these five genes in roots was induced. These results imply that the inhibition by Gin of NRT2 expression occurs only when nitrate is present in the growth media. Although exogenous ABA and Gin induced HATS genes in the roots of wheat, they did not induce nitrate influx.
Chao CaiXue-Qiang ZhaoYong-Guan ZhuBin LiYi-Ping TongZhen-Sheng Li
