Alternative Splicing at the Intersection of Biological Timing, Development, and Stress Responses[OPEN]

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Cyclic Nucleotide Monophosphates and Their Cyclases in Plant Signaling (2017, background): “…in splicing factors and spliceosomal proteins are predicted to modulate the circadian clock and the highly complex plant defense responses (e.g., Staiger and Brown, 2013) and that the phosphorylation status of spliceosome components can affect splicing (Feng et al., 2008; Lipp et al., 2015)…”
Complexity of the Alternative Splicing Landscape in Plants[C][W][OPEN] (2013, background): “There is an ever-growing body of literature on how alternative splicing (AS) influences important developmental and signaling pathways, and many important examples have been discussed in the accompanying review by Staiger and Brown (2013).”
Mechanism of Salinity Tolerance in Plants: Physiological, Biochemical, and Molecular Characterization (2014, background): “A nuclear coactivator, At-SKIP (Ski-interacting protein), expression was found to increase in response to salt, mannitol, and ABA treatment, and At-SKIP overexpression or antisense lines show altered tolerance to a plethora of abiotic stress factors [186], and it is likely that a role in alternative”
Araport11: a complete reannotation of the Arabidopsis thaliana reference genome (2016, background): “It has recently become apparent that the expression patterns of many transcript isoforms change with the developmental stages and/or environmental conditions (Staiger and Brown, 2013).”