Changes in antioxidant system and sucrose metabolism in maize varieties exposed to Cd.

Different maize varieties respond differentially to cadmium (Cd) stress. However, the physiological mechanisms that determine the response are not well defined. Antioxidant systems and sucrose metabolism help plants to cope with abiotic stresses, including Cd stress. The relationship of these two systems in the response to Cd stress is unclear. Seed is sensitive to Cd stress during germination. In this study, we investigated changes in the antioxidant system, sucrose metabolism, and abscisic acid and gibberellin concentrations in two maize varieties with low (FY9) or high (SY33) sensitivities to Cd under exposure to CdCl2 (20 mg L-1) at different stages of germination (3, 6, and 9 days).The seed germination and seedling growth were inhibited under Cd stress. The superoxide, malondialdehyde, and proline concentrations, and the superoxide dismutase, peroxidase, catalase, and lipoxygenase activities increased compared with those of the control (CK; without Cd). The expression levels of three genes (ZmOPR2, ZmOPR5, and ZmPP2C6) responsive to oxidative stress increased differentially in the two varieties under Cd stress. The activity of the antioxidant system and the transcript levels of oxidative stress-responsive genes were higher in the Cd-tolerant variety, FY9, than in the sensitive variety, SY33. Sucrose metabolism was increased under Cd stress compared with that of the CK and was more active in the Cd-sensitive variety, SY33. These results suggest that the antioxidant system is the first response to Cd stress in maize, and that sucrose metabolism is cooperative and complementary under exposure to Cd.

Responses of maize hybrids with contrasting maturity to planting date in Northeast China.

Maize sowing in semi-humid region of Jilin province is often delayed beyond the optimum planting time window because of soil water stress typically occurring before or during the planting season. Research was conducted at Lishu city, in Jilin province from 2009 through 2010 to determine the responses of maize hybrids with contrasting maturity to planting date. Three popular hybrids with contrasting different maturity, short-season hybrid Jidan27, mid-season hybrid Xianyu335, and full-season hybrid Zhengdan958 were planted in early May and mid-May and thinned to populations of 67,500 plants ha-1. The results showed that durations from emergence to silking stage for all the hybrids consistently shortened as the planting delayed, but interaction effects of hybrids, planting date and year existed for the duration of silking to physiological maturity stage. The longer maturity hybrid usually had grain yield advantage over earlier maturity hybrid when planting at early May, but the earlier maturity hybrid often showed a greater yield than longer maturity hybrid when planting was delayed. The highest yield occurred at the treatment combination of the mid-season hybrid and delayed planting date, and the shorter season hybrid typically showed stable and higher grain yield across planting dates. Changes in grain volume per unit of land area among hybrids and planting date treatment combination were consistent with the changes in grain yields, indicating that the yield is determined usually by the sink capacity. Further research is needed to evaluate the effects of hybrids maturity and planting date on maize under different planting densities.

Genetic analysis of maize shank length by QTL mapping in three recombinant inbred line populations.

In maize, the shank is a unique tissue linking the stem to the ear. Shank length (SL) mainly affects the transport of photosynthetic products to the ear and the dehydration of kernels via regulated husk morphology. The limited studies on SL revealed it is a highly heritable quantitative trait controlled by significant additive and additive-dominance effects. However, the genetic basis of SL remains unclear. In this study, we analyzed three maize recombinant inbred line (RIL) populations to elucidate the molecular mechanism underlying the SL. The data indicated the SL varied among the three RIL populations and was highly heritable. Additionally, the SL was positively correlated with the husk length (HL), husk number (HN), ear length (EL), and ear weight (EW) in the BY815/K22 (BYK) and CI7/K22 (CIK) RIL populations, but was negatively correlated with the husk width (HW) in the BYK RIL population. Moreover, 10 quantitative trait loci (QTL) for SL were identified in the three RIL populations, five of which were large-effect QTL. The percentage of the total phenotypic variation explained by the QTL for SL was 13.67 %, 20.45 %, and 30.81 % in the BY815/DE3 (BYD), BYK, and CIK RIL populations, respectively. Further analyses uncovered some genetic overlap between SL and EL, SL and ear row number (ERN), SL and cob weight (CW), and SL and HN. Unlike the large-effect QTL qSL BYK-2-2, which spanned the centromere, the other four large-effect QTL were delimited to a single peak bin via bin map. Furthermore, 2, 5, 6, and 12 genes associated with SL were identified for qSL BYK-2-1, qSL CIK-2-1, qSL CIK-9-1, and qSL CIK-9-2, respectively. Five of the candidate genes for SL may contribute to the hormone metabolism and sphingolipid biosynthesis regulating cell elongation, division, differentiation, and expansion. These results may be relevant for future studies on the genetic basis of SL and for the molecular breeding of maize based on marker-assisted selection to develop new varieties with an ideal SL.