Overexpression of the plastidal pseudo-proteaseAtFtsHi3confers drought tolerance without penalizing growth

Author:

Cook Sam D.,Mishra Laxmi S.ORCID,Isaksson HannaORCID,Straub Isabella R.,Abele MiriamORCID,Mishra Sanatkumar,Ludwig ChristinaORCID,Libby Eric,Funk ChristianeORCID

Abstract

AbstractDrought is one of the most severe environmental stresses affecting plant biomass production and quality, however, the molecular mechanisms of drought response in plants remain unclear. Here, we demonstrate that overexpression of the Arabidopsis gene FTSHi3 under the influence of its endogenous, or the 35S constitutive promoter results in drought-tolerant phenotypes without penalising plant growth. FTSHi3 encodes a pseudo-protease located in the chloroplast envelope and knock-down mutants (ftshi3-1) have previously been found to be drought tolerant, but highly reduced in growth. Changes in FtsHi3 transcript abundance therefore seems to induce drought tolerance inArabidopsis thaliana. Overexpression of FTSHi3 (pFTSHi3-OE) impacts leaf stomatal density, lowers stomatal conductance and increases water use efficiency. To explore the underlying mechanisms behind this, we compared the proteomes offtshi3-1andpFTSHi3-OEto wild type plants grown under drought and watered conditions. Under drought conditions, the drought related processes ‘osmotic stress’, ‘water transport’ and ‘response to abscisic acid’ were enriched, indicating thatpFtsHi3-OEandftshi3-1mutants are more active in their response to drought than the wild-type. The proteins HSP90, HSP93 and TIC110 were more abundant in the knock-down mutant, which suggests that FtsHi3 might play a downstream role in chloroplast pre-protein import. Increased abundance of FtsH7/9 and FtsH11, FtsH12 and FtsHi4 inftshi3-1combined with the fact that FtsH proteases function as homo- or heteromeric complexes suggests that these proteases may be possible interacting partners. To explore this, we constructed mathematical models that show FtsHi3 likely interacts with at least two other (pseudo-) proteases.

Publisher

Cold Spring Harbor Laboratory

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