SlSGRL, a tomato SGR-like protein, promotes chlorophyll degradation downstream of the ABA signaling pathway

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Détails bibliographiques
Publié dans:Plant physiology and biochemistry : PPB. - 1991. - 157(2020) vom: 06. Dez., Seite 316-327
Auteur principal: Yang, Minmin (Auteur)
Autres auteurs: Zhu, Shaobo, Jiao, Baozhen, Duan, Ming, Meng, Qingwei, Ma, Nana, Lv, Wei
Format: Article en ligne
Langue:English
Publié: 2020
Accès à la collection:Plant physiology and biochemistry : PPB
Sujets:Journal Article ABI5 Abscisic acid Chlorophyll degradation SGRL Tomato Plant Proteins Chlorophyll 1406-65-1 Abscisic Acid 72S9A8J5GW
Description
Résumé:Copyright © 2020 Elsevier Masson SAS. All rights reserved.
Chlorophyll (chl) degradation plays a vital role during green plant growth and development, including nutrient metabolism, fruit and seed maturation, and phototoxic detoxification. STAY-GREEN (SGR) is a plant-specific regulator involved in chl degradation. Previous studies showed that SlSGR1 functioned in chl degradation and lycopene accumulation during fruit ripening of tomato (Solanum lycopersicum). However, little is known about SlSGR-LIKE (SlSGRL) gene, which is a homolog of SlSGR1. We cloned the SlSGRL gene and created transgenic tomato plants overexpressing (OE) SlSGRL. Expression analysis showed that SlSGRL was up-regulated by abscisic acid (ABA). Our data showed that SlSGRL-OE lines exhibited earlier leaf yellowing than wild-type (WT) lines under ABA treatment. Yeast two-hybrid (Y2H) assay revealed that SlSGRL interacted with pheophytin pheophorbide hydrolase (SlPPH) and light-harvesting complex a2 (SlLHCa2) to promote the chl degradation. Further analysis demonstrated that ABA-INSENSITIVE5 (SlABI5) and SlABI5-LIKE regulated SlSGRL expression by directly binding to the sequence (-611 to -582) of the SlSGRL promoter that included an ABRE cis-element. We proposed that SlSGRL, which was regulated by SlABI5/SlABI5-LIKE, mainly acted in ABA-induced chl degradation via interacting with SlPPH and SlLHCa2
Description:Date Completed 27.01.2021
Date Revised 07.12.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1873-2690
DOI:10.1016/j.plaphy.2020.10.028