转录组分析揭示干旱胁迫下不同耐旱皂荚幼苗的调控机制

IF 1.9 Q3 GENETICS & HEREDITY BMC genomic data Pub Date : 2024-03-13 DOI:10.1186/s12863-024-01216-y
Fuhua Liu, Yang Zhao, Xiurong Wang, Biao Wang, Feng Xiao, Kequan He
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引用次数: 0

摘要

背景:从生态和经济角度来看,中华皂荚(Gleditsia sinensis)都是重要的树种。然而,幼苗期的暂时干旱阻碍了其生长,从而阻碍了中华皂角产业的发展。采用人工模拟控水方法对半年生盆栽幼苗进行干旱胁迫和补水。对干旱胁迫和补水过程中五个不同阶段的高抗性(HR)和高感性(HS)苗系叶片进行 RNA 测序(RNA-seq)分析,研究其基因表达模式:结果表明:在G. sinensis HR和HS家系中,差异表达基因主要富集在 "叶绿体"(GO:0009507)、"光合作用"(GO:0015979)、"植物激素信号转导"(map04075)、"类黄酮生物合成"(map00941)、"胁迫响应"、"对活性氧(ROS)的响应"(GO:0000302)、"信号转导"(GO:0007165)等相关通路中。sinensis HR 和 HS 家族中的 "胁迫响应"、"活性氧(ROS)响应"(GO:0000302)和 "信号转导"(GO:0007165)。此外,与 "植物激素信号转导"(map04075)和渗透调节相关的通路也被富集。中药材两个科耐旱性的差异可能与 "跨膜转运体活性"(GO:0022857)、"胁迫响应"、"激素和信号转导"(GO:0007165)、"角质素、亚精胺和蜡的生物合成"(map00073)、"核糖体"(map03010)、"光合作用"(map00195)、"糖代谢 "等有关。对严重干旱胁迫下 DEGs 的富集分析表明,两个家族的耐旱性可能与 "水溶性维生素代谢过程"(GO:0006767)、"光合作用"(map00195)、"植物激素信号转导"(map04075)、"淀粉和蔗糖代谢"(map00500)以及 "半乳糖代谢"(map00052)有关。与渗透调节相关的基因,如δ-1-吡咯啉-5-羧酸合成酶(P5CS)、氨基酸渗透酶(AAP)、氨基酸渗透酶 2(AAP2)和三卤糖-磷酸合成酶(TPS),以及抗氧化酶 L-抗坏血酸过氧化物酶 6(APX6),可能是涉及中华鹅掌楸耐旱性的重要基因。研究随机选择了五个基因,利用实时定量 PCR(RT-qPCR)对 RNA-seq 结果进行了验证,结果表明转录组数据是可靠的:本研究揭示了中华皂角耐旱机制的分子调控信息,为进一步研究中华皂角耐旱育种的分子机制提供了参考。
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Transcriptome analysis reveals regulatory mechanisms of different drought-tolerant Gleditsia sinensis seedlings under drought stress.

Background: Gleditsia sinensis is a significant tree species from both ecological and economic perspectives. However, its growth is hampered by temporary droughts during the seedling stage, thereby impeding the development of the G. sinensis industry. Drought stress and rehydration of semi-annual potted seedlings using an artificial simulated water control method. RNA sequencing (RNA-seq) analyses were conducted on leaves collected from highly resistant (HR) and highly susceptible (HS) seedling families at five different stages during the process of drought stress and rehydration to investigate their gene expression patterns.

Results: The differentially expressed genes (DEGs) were predominantly enriched in pathways related to "chloroplast" (GO:0009507), "photosynthesis" (GO:0015979), "plant hormone signal transduction" (map04075), "flavonoid biosynthesis" (map00941), "stress response", "response to reactive oxygen species (ROS)" (GO:0000302), "signal transduction" (GO:0007165) in G. sinensis HR and HS families exposed to mild and severe drought stress. Additionally, the pathways related to "plant hormone signal transduction" (map04075), and osmoregulation were also enriched. The difference in drought tolerance between the two families of G. sinensis may be associated with "transmembrane transporter activity" (GO:0022857), "stress response", "hormones and signal transduction" (GO:0007165), "cutin, suberine and wax biosynthesis" (map00073), "ribosome" (map03010), "photosynthesis" (map00195), "sugar metabolism", and others. An enrichment analysis of DEGs under severe drought stress suggests that the drought tolerance of both families may be related to "water-soluble vitamin metabolic process" (GO:0006767), "photosynthesis" (map00195), "plant hormone signal transduction" (map04075), "starch and sucrose metabolism" (map00500), and "galactose metabolism" (map00052). Osmoregulation-related genes such as delta-1-pyrroline-5-carboxylate synthase (P5CS), Amino acid permease (AAP), Amino acid permease 2 (AAP2) and Trehalose-phosphate synthase (TPS), as well as the antioxidant enzyme L-ascorbate peroxidase 6 (APX6), may be significant genes involved in drought tolerance in G. sinensis. Five genes were selected randomly to validate the RNA-seq results using quantitative real-time PCR (RT-qPCR) and they indicated that the transcriptome data were reliable.

Conclusions: The study presents information on the molecular regulation of the drought tolerance mechanism in G. sinensis and provides a reference for further research on the molecular mechanisms involved in drought tolerance breeding of G. sinensis.

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