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It can be speculated that the glabrous phenotype of Yunnan Nuda rice results from epigenetic variations, such as DNA methylation.
Overexpression of miR160a or miR398b in transgenic rice results in increased H2O2 accumulation at the infection site and up-regulation of defence gene expression (i.e. PR1 and PR10) and enhanced resistance to M. oryzae (Li et al. 2013).
Failure to express OsPDIL1 1 in rice results in a floury endosperm and an endoplasmic reticulum stress response in rice (Satoh-Cruz et al., [2010]; Han et al., [2012]).
Similarly, the coleoptiles of the rice Osjar1 mutant grew longer than those of the wild-type under continuous far red light, indicating that interference of the JA pathway in rice results in an altered sensitivity to far red light (Riemann et al. 2008).
Blocking either BR biosynthesis or its signal transduction pathway in rice results in erect leaves.
Studies have shown that overexpression of a homologue of mammalian selenium binding protein in rice results in enhanced resistance to blast fungus and bacterial blight [ 97].
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From these sites, only nine have evidence of rice resulting from flotation and an additional eight from phytolith analysis.
Over expression of OsIRT and MxIRT gene in rice resulted in increased Fe and Zn concentration in rice grains (Lee and An 2009; Tan et al. 2015).
It is therefore unlikely that Jpn1 is the progeny of weedy rice resulting from crossing between Australian wild rice and Asian cultivars.
Several traits such as resistance to abiotic and biotic stresses have been successfully introgressed from wild species into cultivated rice, resulting in improved cultivated varieties (Vaughan 1994).
Consistently, insertional activation of OsCKX2 in transgenic rice resulted in increased expression of OsCKX2 with the plants showing a decreased tiller number phenotype.
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