A New Protein Phosphatase 2C (FsPP2C1) Induced by Abscisic Acid Is Specifically Expressed in Dormant Beechnut Seeds

Author:

Lorenzo Oscar1,Rodrı́guez Dolores1,Nicolás Gregorio1,Rodrı́guez Pedro L.2,Nicolás Carlos1

Affiliation:

1. Departamento de Fisiologı́a Vegetal, Facultad de Biologı́a, Universidad de Salamanca, Plaza de los Doctores de la Reina s/n. 37007–Salamanca, Spain (O.L., D.R., G.N., C.N.); and

2. Instituto de Biologı́a Molecular y Celular de Plantas, Universidad Politécnica-Consejo Superior de Investigaciones Cientı́ficas, Camino de la Vera, 46022–Valencia, Spain (P.L.R.)

Abstract

Abstract An abscisic acid (ABA)-induced cDNA fragment encoding a putative protein phosphatase 2C (PP2C) was obtained by means of differential reverse transcriptase-polymerase chain reaction approach. The full-length clone was isolated from a cDNA library constructed using mRNA from ABA-treated beechnut (Fagus sylvatica) seeds. This clone presents all the features of plant type PP2C and exhibits homology to members of this family such as AthPP2CA (61%), ABI1 (48%), or ABI2 (47%), therefore it was named FsPP2C1. The expression of FsPP2C1 is detected in dormant seeds and increases after ABA treatment, when seeds are maintained dormant, but it decreases and tends to disappear when dormancy is being released by stratification or under gibberellic acid treatment. Moreover, drought stress seems to have no effect on FsPP2C1 transcript accumulation. The FsPP2C1 transcript expression is tissue specific and was found to accumulate in ABA-treated seeds rather than in other ABA-treated vegetative tissues examined. These results suggest that the corresponding protein could be related to ABA-induced seed dormancy. By expressing FsPP2C1 inEscherichia coli as a histidine tag fusion protein, we have obtained direct biochemical evidence supporting Mg2+-dependent phosphatase activity of this protein.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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