Comparison between cell wall integrity (CWI) maintenance mechanisms in (A) Saccharomyces cerevisiae and (B) Arabidopsis thaliana. In both organisms, mechanosensitive ion channels and receptors trigger signal transduction processes involving Ca2+ influx into the cytoplasm and the activation of cascades including calcium-dependent protein kinases (CDPKs), guanosine nucleotide exchange factors (GEFs) and mitogen-activated protein kinases (MAPKs) that eventually activate transcription factors. In A. thaliana, the processes are regulated in a more intricate manner, exemplified by the complex interconnected networks regulated by jasmonic acid (JA), salicylic acid (SA), and abscisic acid (ABA). The processes enable the regulation of gene expression in a tightly controlled and highly adaptive manner, allowing specific changes in cell wall and cellular metabolism to maintain cell wall integrity. Arrows are connecting elements belonging to the same pathway. ROS: reactive oxygen species; PTI: PAMP-triggered immunity; CRD: cysteine-rich domain; NGN: N-glycosilated asparagine; TM: transmembrane domain; GPI: glycosylphosphatidylinositol; STR: serine-/threonine-rich; STE: signal transduction element; LRR: leucine-rich repeat domain; LysM: lysin-motif-containing ectodomain; RALF: rapid alkalinization factor peptide; OGs: oligogalacturonides; TF: transcription factor; EGF-like: epidermal-growth-factor-like ectodomain.