Overexpression of the plastidial pseudo‐protease AtFtsHi3 enhances drought tolerance while sustaining plant growth

突变体 耐旱性 脱落酸 拟南芥 生物 蛋白酶 野生型 蛋白酵素 基因 叶绿体 细胞生物学 拟南芥 表型 植物 生物化学
作者
Laxmi Mishra,Sam David Cook,Sunita Kushwah,Hanna Isaksson,Isabella R. Straub,Miriam Abele,Sanatkumar Mishra,Christina Ludwig,Eric Libby,Christiane Funk
出处
期刊:Physiologia Plantarum [Wiley]
卷期号:176 (3)
标识
DOI:10.1111/ppl.14370
摘要

Abstract With climate change, droughts are expected to be more frequent and severe, severely impacting plant biomass and quality. Here, we show that overexpressing the Arabidopsis gene AtFtsHi3 ( FtsHi3OE) enhances drought‐tolerant phenotypes without compromising plant growth. AtFtsHi3 encodes a chloroplast envelope pseudo‐protease; knock‐down mutants ( ftshi3‐1 ) are found to be drought tolerant but exhibit stunted growth. Altered AtFtsHi3 expression therefore leads to drought tolerance, while only diminished expression of this gene leads to growth retardation. To understand the underlying mechanisms of the enhanced drought tolerance, we compared the proteomes of ftshi3‐1 and pFtsHi3‐FtsHi3OE (pFtsHi3‐OE) to wild‐type plants under well‐watered and drought conditions. Drought‐related processes like osmotic stress, water transport, and abscisic acid response were enriched in pFtsHi3‐OE and ftshi3‐1 mutants following their enhanced drought response compared to wild‐type. The knock‐down mutant ftshi3‐1 showed an increased abundance of HSP90, HSP93, and TIC110 proteins, hinting at a potential downstream role of AtFtsHi3 in chloroplast pre‐protein import. Mathematical modeling was performed to understand how variation in the transcript abundance of AtFtsHi 3 can, on the one hand, lead to drought tolerance in both overexpression and knock‐down lines, yet, on the other hand, affect plant growth so differently. The results led us to hypothesize that AtFtsHi3 may form complexes with at least two other protease subunits, either as homo‐ or heteromeric structures. Enriched amounts of AtFtsH7/9, AtFtsH11, AtFtsH12, and AtFtsHi4 in ftshi3‐1 suggest a possible compensation mechanism for these proteases in the hexamer.
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