Senescence is a necessary part of most complex organisms that controlled by many complicated genetic programs. However, unlike animals and humans, leaf senescence has a great impact on nutrient recycling from source to sink to promote reproductive success, thus has strong adaptive advantages in plants [1,2]. Therefore, from the agricultural point of view, understanding the process of leaf senescence is extremely important for the breeding of higher-yielding crop with optimized nutritional qualities.Onset and progression of leaf senescence is controlled primarily by developmental age, and it is also influenced by a number of endogenous and external factors that are integrated into the developmental age. Abscisic acid (ABA), a plant hormone identified in the 1960s [3], has been regarded as an important regulator in promoting leaf senescence. During leaf senescence, a dramatic increase in endogenous ABA levels is found in many plants, concomitantly with upregulation of a subset of ABA signaling genes and senescence-associated genes (SAGs), and exogenously applied ABA also induces expression of several SAGs which accelerate leaf senescence. In addition, a variety of biotic and abiotic stresses also elevate the ABA level and activate signaling pathways leading to senescence. These indicate that ABA plays a key role in regulating initiation and progression of leaf senescence; however, molecular basis of ABA-mediated leaf senescence signaling pathway is still largely unknown. Very recently, several components in two model plant species Arabidopsis and rice were identified, providing mechanistic insights into ABA-mediated leaf senescence signaling [2,46].Receptor protein kinase 1 (RPK1) is an age-dependent action of an ABA-inducible receptor kinase, and acts as a positive regulator of leaf senescence in Arabidopsis [4].RPK1 encodes a membrane-bound protein that contains a leucine-rich repeat domain at its N-terminus. Conditional overexpression of RPK1 at the mature stage significantly promoted leaf senescence, whereas RPK1 knockout mutant exhibited reduced sensitivity to ABA-induced senescence. Consistently, RPK1 is an upstream component of ABA signaling and its expression is increased in an ABA-dependent manner throughout the progression of leaf senescence. However, induction of RPK1 expression in young plants leads to retarded growth but does not trigger the senescence symptoms, suggesting that function of RPK1 in ABAinduced leaf senescence is dependent on the developmental age.Senescence-associated gene113 (SAG113) is a negative regulator of ABA signaling controlling water loss during senescence in Arabidopsis [5]. SAG113 encodes a Golgi-localized PP2C family protein phosphatase, which is able to complement the yeast PP2C-deficient ptd1 mutant, confirming that SAG113 is the functional ortholog of PTC1.SAG113 is induced by ABA in senescing leaves and its expression is significantly repressed in both ABA biosynthesis and signaling mutant aba2-1 and abi4-1. The loss-offunction mutants of SAG113 display a delay in leaf ...