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Protein tyrosine phosphatases (PTPs) are essential regulators of signal transduction pathways, and control, together with protein tyrosine kinases (PTKs), the reversible phosphorylation of tyrosine residues.
Autonomous extra-SCN clocks in the forebrain and peripheral organs are synchronized via humoral and neuronal pathways and control the tissue and cell-type specific rhythmic expression of target genes [2], [3].
Rho GTPases function as molecular switches in many different signaling pathways and control a wide range of cellular processes.
FAK and PYK2 are closely related non-receptor tyrosine kinases, participating in diverse signaling pathways and control a number of cellular processes (Mitra et al., 2005; Schaller, 2010).
Further studies have shown that B3-domain transcription factors are important nodes in hormone signaling pathways and control important steps in hormone biosynthesis.
Transcription factors are also important downstream integrators of signaling pathways and control gene expression to generate responses to nutrient limitation [ 34].
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The cell cycle machinery receives signals transduced by various growth factor pathways and controls cellular quiescence, proliferation, differentiation, senescence, and apoptosis [32], [33].
Recently, NBS-LRR genes were implicated in having a dual role in both regulating developmental pathways and controlling resistance to fungal pathogens [ 75].
rasl11b cDNA has been isolated from a subtractive library between embryos expressing a constitutively activated Nodal signaling pathway and control embryos [42].
All factors operate at different levels of the pathway and control the spontaneous activity of C3 convertase [ 2, 3].
Whether there is a mechanistic connection between nutrient control of the PKA pathway and control of fermentative growth remains to be elucidated.
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