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香蕉(AAA品种Borjahaji)茎尖分生组织冷冻保存连续阶段的转录组分析

Transcriptome Profiling during Sequential Stages of Cryopreservation in Banana ( AAA cv Borjahaji) Shoot Meristem.

作者信息

Htwe Chaw Su Su, Rajkumar Subramani, Pathania Pooja, Agrawal Anuradha

机构信息

ICAR-National Bureau of Plant Genetic Resources, Pusa Campus, New Delhi 110012, India.

Division of Plant Genetic Resources, ICAR-Indian Agricultural Research Institute, Pusa Campus, New Delhi 110012, India.

出版信息

Plants (Basel). 2023 Mar 3;12(5):1165. doi: 10.3390/plants12051165.

Abstract

Cryopreservation approaches have been implemented in gene banks as a strategy to back up plant genetic resource collections that are vegetatively propagated. Different strategies have been employed to effectively cryopreserve plant tissue. There is little information on the cellular processes and molecular adjustments that confer resilience to the multiple stresses imposed during a cryoprotocol. In the present work, the cryobionomics of banana ( sp.), a non-model species, was investigated through the transcriptomic approach using RNA-Seq. Proliferating meristems of in vitro explants ( AAA cv 'Borjahaji') were cryopreserved using the droplet-vitrification technique. Transcriptome profiling analysis of eight cDNA libraries including the bio-replicates for T0 (stock cultures (control tissue), T1 (high sucrose pre-cultured), T2 (vitrification solution-treated) and T3 (liquid nitrogen-treated) meristem tissues was carried out. The raw reads obtained were mapped with a reference genome sequence. A total of 70 differentially expressed genes (DEGs) comprising 34 upregulated and 36 downregulated were identified in all three phases as compared to control (T0). Among the significant DEGs (>log FC 2.0), during sequential steps, 79 in T1, 3 in T2 and the 4 in T3 were upregulated and 122 in T1, 5 in T2 and 9 in T3 were downregulated. Gene ontology (GO) enrichment analysis showed that these significant DEGs were involved in the upregulation of biological process (BP-170), cellular component (CC-10) and molecular function (MF-94) and downregulation of biological process (BP-61), cellular component (CC-3) and molecular function (MF-56). The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that DEGs were involved in the biosynthesis of secondary metabolites, glycolysis/gluconeogenesis, MAPK signaling, EIN 3-lke 1 protein, 3-ketoacy-CoA synthase 6-like, and fatty acid elongation during cryopreservation. For the first time, a comprehensive transcript profiling during four stages of cryopreservation in banana were carried out, which will pave the way for devising an effective cryopreservation protocol.

摘要

冷冻保存方法已在基因库中实施,作为一种备份无性繁殖的植物遗传资源收集品的策略。人们采用了不同的策略来有效地冷冻保存植物组织。关于赋予植物组织在冷冻保存方案中承受多种胁迫能力的细胞过程和分子调节的信息很少。在本研究中,通过使用RNA测序的转录组学方法研究了非模式物种香蕉(品种)的低温生物学。使用液滴玻璃化技术对体外外植体(AAA品种‘Borjahaji’)的增殖分生组织进行冷冻保存。对包括T0(库存培养物(对照组织))、T1(高蔗糖预培养)、T2(玻璃化溶液处理)和T3(液氮处理)分生组织组织的生物重复样本在内的八个cDNA文库进行了转录组分析。获得的原始读数与参考基因组序列进行比对。与对照(T0)相比,在所有三个阶段共鉴定出70个差异表达基因(DEG),其中34个上调,36个下调。在显著的差异表达基因(>log FC 2.0)中,在连续步骤中,T1中有79个上调,T2中有3个上调,T3中有4个上调,T1中有122个下调,T2中有5个下调,T3中有9个下调。基因本体(GO)富集分析表明,这些显著的差异表达基因参与了生物过程(BP-170)、细胞成分(CC-10)和分子功能(MF-94)的上调以及生物过程(BP-61)、细胞成分(CC-3)和分子功能(MF-56)的下调。京都基因与基因组百科全书(KEGG)通路分析表明,差异表达基因在冷冻保存过程中参与次生代谢物的生物合成、糖酵解/糖异生、MAPK信号传导、EIN 3样1蛋白、3-酮酰基辅酶A合酶6样和脂肪酸延长。首次对香蕉冷冻保存四个阶段的综合转录谱进行了分析,这将为设计有效的冷冻保存方案铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a33d/10005800/3ee3fce31f94/plants-12-01165-g001.jpg

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