Yield gains in extra-early maize cultivars of three breeding eras under multiple environments

Open Access JournalAvailability of extra-early maize cultivars has facilitated the expansion of maize production into savannas of West and Central Africa (WCA). Fifty-six extra-early maize cultivars of three breeding eras;1995 to 2000, 2001 to 2006, and 2007 to 2012 were evaluated for 2 yr under 24 multiple-stress and 28 non-stress environments in WCA. Objectives of the study were to determine genetic improvement in grain yield of cultivars developed during the breeding eras, and identify high-yielding and s multiple-stress and non-stress environments. Yield gains from era 1 to era 3 under multiple stresses was associated with increased days to anthesis, reduced stalk lodging, and improved husk cover. Cultivars 2004 TZEE-Y Pop STR C4, TZEE-W Pop STR QPM C0, and TZEE-W Pop STR BC2 C0 of era 2; and TZEE-W STR 107 BC1, TZEE-W Pop STR C5, and 2012 TZEE-Y DT STR C5 of era 3 were high-yielding and stable across multiple-stress environments while 98 Syn EE-W from era 1, FERKE TZEE-W STR, TZEE-W Pop STR C3, and TZEE-Y Pop STR QPM C0 from era 2, and TZEE-W Pop STR C5, 2009 TZEE-OR2 STR QPM, 2009 TZEE-W STR, TZEE-Y STR 106, and TZEE-W DT C0 STR C5 from era 3 were outstanding across non-stress environments and should be tested extensively and commercialized. Considerable improvement has been made in breeding for multiple-stress tolerant extra-early maize cultivars

Over-expression of AhR (aryl hydrocarbon receptor) induces neural differentiation of Neuro2a cells: neurotoxicology study

BACKGROUND: Dioxins and related compounds are suspected of causing neurological disruption in human and experimental animal offspring following perinatal exposure during development and growth. The molecular mechanism(s) of the actions in the brain, however, have not been fully investigated. A major participant in the process of the dioxin-toxicity is the dioxin receptor, namely the aryl hydrocarbon receptor (AhR). AhR regulates the transcription of diverse genes through binding to the xenobiotic-responsive element (XRE). Since the AhR has also been detected in various regions of the brain, the AhR may play a key role in the developmental neurotoxicity of dioxins. This study focused on the effect of AhR activation in the developing neuron. METHODS: The influence of the AhR on the developing neuron was assessed using the Neuro2a-AhR transfectant. The undifferentiated murine neuroblastoma Neuro2a cell line (ATCC) was stably transfected with AhR cDNA and the established cell line was named N2a-Rα. The activation of exogenous AhR in N2a-Rα cells was confirmed using RNAi, with si-AhR suppressing the expression of exogenous AhR. The neurological properties of N2a-Rα based on AhR activation were evaluated by immunohistochemical analysis of cytoskeletal molecules and by RT-PCR analysis of mRNA expression of neurotransmitter-production related molecules, such as tyrosine hydroxylase (TH). RESULTS: N2a-Rα cells exhibited constant activation of the exogenous AhR. CYP1A1, a typical XRE-regulated gene, mRNA was induced without the application of ligand to the culture medium. N2a-Rα cells exhibited two significant functional features. Morphologically, N2a-Rα cells bore spontaneous neurites exhibiting axon-like properties with the localization of NF-H. In addition, cdc42 expression was increased in comparison to the control cell line. The other is the catecholaminergic neuron-like property. N2a-Rα cells expressed tyrosine hydroxylase (TH) mRNA as a functional marker of catecholaminergic neurotransmitter production. Thus, exogenous AhR induced catecholaminergic differentiation in N2a-Rα cells. CONCLUSION: The excessive activation of AhR resulted in neural differentiation of Neuro2a cells. This result revealed that dioxins may affect the nervous system through the AhR-signaling pathway. Activated AhR may disrupt the strictly regulated brain formation with irregular differentiation occurring rather than cell death