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具有不同愈伤能力的马铃薯品种中创伤栓质化沉积的转录调控。

Transcriptional regulation of wound suberin deposition in potato cultivars with differential wound healing capacity.

机构信息

Department of Biochemistry and Molecular Biology, The University of Nevada, Reno, NV, 89557, USA.

State Key Laboratory of Biocatalysis and Enzyme Engineering, School of Life Sciences, Hubei University, Wuhan, 430062, China.

出版信息

Plant J. 2021 Jul;107(1):77-99. doi: 10.1111/tpj.15275. Epub 2021 May 18.

Abstract

Wounding during mechanical harvesting and post-harvest handling results in tuber desiccation and provides an entry point for pathogens resulting in substantial post​-harvest crop losses. Poor wound healing is a major culprit of these losses. Wound tissue in potato (Solanum tuberosum) tubers, and all higher plants, is composed of a large proportion of suberin that is deposited in a specialized tissue called the wound periderm. However, the genetic regulatory pathway controlling wound-induced suberization remains unknown. Here, we implicate two potato transcription factors, StMYB102 (PGSC0003DMG400011250) and StMYB74 (PGSC0003DMG400022399), as regulators of wound suberin biosynthesis and deposition. Using targeted metabolomics and transcript profiling from the wound healing tissues of two commercial potato cultivars, as well as heterologous expression, we provide evidence for the molecular-genetic basis of the differential wound suberization capacities of different potato cultivars. Our results suggest that (i) the export of suberin from the cytosol to the apoplast and ligno-suberin deposition may be limiting factors for wound suberization, (ii) StMYB74 and StMYB102 are important regulators of the wound suberization process in tubers, and (iii) polymorphisms in StMYB102 may influence cultivar-specific wound suberization capacity. These results represent an important step in understanding the regulated biosynthesis and deposition of wound suberin and provide a practical foundation for targeted breeding approaches aimed at improving potato tuber storage life.

摘要

在机械收获和收获后处理过程中造成的创伤会导致块茎干枯,并为病原体提供入口,从而导致大量收获后作物损失。伤口愈合不良是造成这些损失的主要原因。马铃薯(Solanum tuberosum)块茎和所有高等植物的伤口组织主要由称为伤口周皮的特殊组织中沉积的大量角质素组成。然而,控制伤口诱导角质化的遗传调控途径尚不清楚。在这里,我们认为两个马铃薯转录因子 StMYB102(PGSC0003DMG400011250)和 StMYB74(PGSC0003DMG400022399)是伤口角质素生物合成和沉积的调节剂。通过对两个商业马铃薯品种的伤口愈合组织进行靶向代谢组学和转录谱分析以及异源表达,我们为不同马铃薯品种伤口角质化能力的分子遗传基础提供了证据。我们的结果表明:(i)质外体中角质素的输出和木质素角质素的沉积可能是伤口角质化的限制因素,(ii)StMYB74 和 StMYB102 是块茎伤口角质化过程的重要调节剂,(iii)StMYB102 的多态性可能影响特定品种的伤口角质化能力。这些结果代表了理解伤口角质素的调控生物合成和沉积的重要一步,并为旨在提高马铃薯块茎贮藏寿命的靶向育种方法提供了实用基础。

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