Field performance of transgenic elite commercial hybrid rice expressing Bacillus thuringiensis δ-endotoxin

Here we describe development of transgenic elite rice lines expressing a Bt fusion gene derived from cryIA(b) and cryIA(c) under the control of rice actinI promoter. The lines used in the study were indica CMS restorer line of Minghui 63 and its derived hybrid rice Shanyou 63. The level of Bt fusion protein CryIA(b)/CryIA(c) detected in Minghui 63 (T51-1) plants was 20 ng/mg soluble protein. The Bt Shanyou 63 was field-tested in natural and repeated heavy manual infestation of two lepidopteran insects, leaffolder and yellow stem borer. The transgenic hybrid plants showed high protection against both insect pests without reduced yield

Site-independently integrated transgenes in the elite restorer rice line Minghui 63 allow removal of a selectable marker from the gene of interest by self-segregation

In this study, we have demonstrated that two independent loci are involved in the integration of the insecticidal protein gene cryIAb/cryIAc and selectable marker gene hph in the recipient genome of the elite Chinese CMS restorer line Minghui 63. We have also documented the structural organization of these transgenes in each locus by restriction enzyme digestion and Southern blot analysis. The independent locus integration of different transgenes allowed us to remove the selectable marker gene hph from the gene of interest simply by self-segregation. Not having the selectable marker gene will enhance the commercial value of our transgenic line TT51-1, which showed a consistently high level of resistance against repeated infestations of yellow stem borers and natural outbreaks of leaf-folders, without a reduction in yield potential

The Rice Eukaryotic Translation Initiation Factor 3 Subunit e (OseIF3e) Influences Organ Size and Pollen Maturation

Eukaryotic translation initiation factor 3 (eIF3) is a large protein complex that participates in most translation initiation processes. While eIF3 has been well characterized, less is known about the roles of individual eIF3 subunits, particularly in plants. Here, we identified and characterized OseIF3e in rice (Oryza sativa L.). OseIF3e was constitutively expressed in various tissues, but most strongly in vigorously growing organs. Transgenic OseIF3e-silenced rice plants showed inhibited growth in seedling and vegetative stages. Repression of OseIF3e led to defects in pollen maturation but did not affect pollen mitosis. In rice, eIF3e interacted with eIF3 subunits b, d, e, f, h, and k, and with eIF6, forming homo- and heterodimers to initiate translation. Furthermore, OseIF3e was shown by yeast two-hybrid assay to specifically bind to interactors of cyclin-dependent kinases 1, 5, and 6. This interaction was mediated by the sequence of amino acid residues at positions 118–138, which included a conserved motif (IGPEQIETLYQFAKF). These results suggested although OseIF3e is not a functional core subunit of eIF3, it still plays crucial roles in rice growth and development, in combination with other factors. We proposed a pathway by which OseIF3e influence organ size and pollen maturation in rice, providing an opportunity to optimize plant architecture for crop breeding

OseIF3h Regulates Plant Growth and Pollen Development at Translational Level Presumably through Interaction with OsMTA2

The initiation stage of protein biosynthesis is a sophisticated process tightly regulated by numerous initiation factors and their associated components. However, the mechanism underlying translation initiation has not been completely understood in rice. Here, we showed knock-out mutation of the rice eukaryotic translation initiation factor 3 subunit h (OseIF3h) resulted in plant growth retardation and seed-setting rate reduction as compared to the wild type. Further investigation demonstrated an interaction between OseIF3h and OsMTA2 (mRNA adenosine methylase 2), a rice homolog of METTL3 (methyltransferase-like 3) in mammals, which provided new insight into how N6-methyladenosine (m6A) modification of messenger RNA (mRNA) is engaged in the translation initiation process in monocot species. Moreover, the RIP-seq (RNA immunoprecipitation sequencing) data suggested that OseIF3h was involved in multiple biological processes, including photosynthesis, cellular metabolic process, precursor metabolites, and energy generation. Therefore, we infer that OseIF3h interacts with OsMTA2 to target a particular subset of genes at translational level, regulating plant growth and pollen development

Expression and function of a hybrid Bt toxin gene in the transgenic rice conferring resistance to insect pests

A hybrid Bt toxin gene was made from cryIA(b) and cryIA(c) after optimization of their codon usage to meet high G+C content in rice and placed under control of the rice Actin I promoter along with its first intron. This hybrid Bt toxin gene was introduced into the genome of an elite indica rice cultivar IR72 through biolistic method. Five independent transformants were identified out of 27 transgenic plants obtained. The level of the hybrid Bt toxin was estimated to be 0.01%-0.20% of the total soluble protein in leaf or stem tissue of the transgenic plants. This considerable range of expression levels was studied for a strong insecticidal effect. As demonstrated by insect bioassay, neonate larva mortality rates of yellow stem borer (Scirpophaga incertulas) (YSB) for selected T0 transgenic rice plants as well as T2 homozygous lines were 100%. This is the first report of a hybrid Bt toxin gene [cryIA (b) and cryIA(c)] driven by rice Actin I promoter in any cereal crop including rice conferring resistance to insect pest. The present hybrid Bt toxin gene deployment strategy will provide sustainable insect pest resistance in rice

Additional file 4: Figure S1. of Development of high-lysine rice via endosperm-specific expression of a foreign LYSINE RICH PROTEIN gene

Amino acid content in T14 generation of PA110 and PA64S. (JPG 1752 kb

Nuphar japonicum DC.

原著和名: カハホネ科名: スイレン科 = Nymphaeaceae採集地: 茨城県 牛久沼 (茨城県 牛久沼)採集日:採集者: 櫻井 宏整理番号: JH045478国立科学博物館整理番号: TNS-VS-99547