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Genetic modification in plants leads to change in morphology.
CeO2 nanoparticles may induce modification in plants at molecular levels [35, 75, 76].
The most prominent morphological modification in plants induced by both HS and DEB includes the promotion of lateral roots emergence (Fig. 2A).
It might be possible that STT3A and STT3B act differently on the substrate selection and even the occurrence of N-linked protein modification in plants, which conferred different types of N-glycans on the substrate peptides.
Genome editing (GE) tools ensure targeted mutagenesis and sequence-specific modification in plants using a wide resource of customized endonucleases; namely, zinc-finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), and the CRISPR (clustered regularly interspaced short palindromic repeats)/Cas (CRISPR-associated protein) system.
In this review, we describe the different approaches that can be tested to improve the efficiency of CRISPR induced gene modification in plants, which include the use of optimal transformation and regeneration protocols, the design of appropriate guide RNAs and donor templates and the choice of nucleases and means of delivery.
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The whole genome based concept described herein should be useful for both detection and characterization of known as well as unknown genetic modifications in plants.
We have developed a high resolution microarray-based method for the detection of both known and unknown genetic modifications in plants.
The method is PCR-independent, applies direct hybridization of total genomic DNA and takes advantage of the high degree of recycling and sequence similarity between elements commonly used in genetic modifications in plants.
Land use intensification often results in modification in plant cover and nutrient inputs with subsequent potential effects on composition and structure of soil microbial community and fractions.
The role of histone modification in plant geminivirus infection needs futher investigation.
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