CO2浓度升高和/或镉胁迫下水稻根系lncRNAs的鉴定及表达分析

IF 3.4 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Genomics Pub Date : 2025-01-01 DOI:10.1016/j.ygeno.2024.110980
Ziyuan Feng, Xiaoyu Wang, Zihan Luo, Aihua Liu, Caixia Wen, Qi Ma, Wenyong Liu, Xuemei Li, Lianju Ma, Yueying Li, Bin Yang, Lanlan Wang
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(2) MAPK signaling pathway-plant (relevant genes Os04g0534166, Os05g0399800 regulated by MSTRG.18576.11, MSTRG.20864.1) and diterpenoid biosynthesis (relevant genes Os12g0491800, Os02g0570400 regulated by MSTRG.8965.1, MSTRG.11509.1) were annotated in AC vs Cd; Under EC relative to AC, DE-lncRNAs were annotated significantly to the flavonoid biosynthesis (relevant genes Os10g0196100, Os10g0320100, Os11g0116300, Os03g0819600 regulated by MSTRG.4612.1, MSTRG.4668.1, MSTRG.6051.1, MSTRG.16669.1); Under composite treatments, relative to AC, DE-lncRNAs were mainly annotated in the plant hormone signal transduction pathway (relevant genes Os03g0180800, Os03g0180900, Os03g0181100 regulated by MSTRG.13776.1). 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引用次数: 0

摘要

CO2的逐渐升高是全球气候变化之一,Cd胁迫也是影响水稻(Oryza sativa L.)的主要非生物胁迫因子。水稻幼苗在2种CO2和2种CdCl2浓度下处理7 d(处理名称:400 ± 20 μmol mol-1 CO2和0 μmol L-1 CdCl2浓度,AC;400 ± 20 μmol mol-1 CO2和150 μmol L-1 CdCl2浓度,Cd;800 ± 20 μmol mol-1 CO2和0 μmol L-1 CdCl2浓度,EC;800 ± 20 μmol mol-1 CO2和150 μmol L-1 CdCl2浓度,EC + Cd)。利用高通量测序、靶基因注释和qRT-PCR分析技术对lncRNAs信息进行分析和挖掘,揭示高浓度CO2和/或Cd胁迫下水稻根系中lncRNAs的调控机制。结果表明:(1)共鉴定出326个(AC vs Cd)、331个(AC vs EC)、343个(AC vs EC + Cd)、112个(Cd vs EC + Cd) de - lncrna。(2)在AC vs Cd中标注了MAPK信号通路-植物(MSTRG.18576.11、MSTRG.20864.1调控的相关基因Os04g0534166、Os05g0399800)和二萜类生物合成(MSTRG.8965.1、MSTRG.11509.1调控的相关基因Os12g0491800、Os02g0570400);在EC相对于AC的条件下,DE-lncRNAs在类黄酮生物合成中有显著的注释(相关基因Os10g0196100、Os10g0320100、Os11g0116300、Os03g0819600由MSTRG.4612.1、MSTRG.4668.1、MSTRG.6051.1、MSTRG.16669.1调控);在复合处理下,相对于AC, de - lncrna主要在植物激素信号转导通路(MSTRG.13776.1调控的相关基因Os03g0180800、Os03g0180900、Os03g0181100)上有注释。联合处理下,CO2升高通过MSTRG调控的DE-lncRNAs(相关基因Os09g0419200)调控苯丙类生物合成,缓解Cd胁迫损伤。29573。1)。
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Identification and expression analysis of lncRNAs in rice roots (Oryza sativa L.) under elevated CO2 concentration and/or cadmium stress
The gradual rise of CO2 is one of the global climate changes, Cd stress is also a major abiotic stress factor that affects rice (Oryza sativa L.). The rice seedlings were treated under two CO2 concentrations and two CdCl2 concentrations for 7 days (treatments names: 400 ± 20 μmol mol−1 CO2 and 0 μmol L−1 CdCl2 concentrations, AC; 400 ± 20 μmol mol−1 CO2 and 150 μmol L−1 CdCl2 concentrations, Cd; 800 ± 20 μmol mol−1 CO2 and 0 μmol L−1 CdCl2 concentrations, EC; 800 ± 20 μmol mol−1 CO2 and 150 μmol L−1 CdCl2 concentrations, EC + Cd). The lncRNAs informations were analyzed and excavated using high-throughput sequencing, target genes annotation, and qRT-PCR analysis techniques so as to reveal the regulatory mechanism of lncRNAs in rice roots under high CO2 concentrations and/or Cd stress. The results show that: (1) 326 (AC vs Cd), 331 (AC vs EC), 343 (AC vs EC + Cd), 112 (Cd vs EC + Cd) DE-lncRNAs were identified. (2) MAPK signaling pathway-plant (relevant genes Os04g0534166, Os05g0399800 regulated by MSTRG.18576.11, MSTRG.20864.1) and diterpenoid biosynthesis (relevant genes Os12g0491800, Os02g0570400 regulated by MSTRG.8965.1, MSTRG.11509.1) were annotated in AC vs Cd; Under EC relative to AC, DE-lncRNAs were annotated significantly to the flavonoid biosynthesis (relevant genes Os10g0196100, Os10g0320100, Os11g0116300, Os03g0819600 regulated by MSTRG.4612.1, MSTRG.4668.1, MSTRG.6051.1, MSTRG.16669.1); Under composite treatments, relative to AC, DE-lncRNAs were mainly annotated in the plant hormone signal transduction pathway (relevant genes Os03g0180800, Os03g0180900, Os03g0181100 regulated by MSTRG.13776.1). Under combined treatment, elevated CO2 alleviates Cd stress damage by regulating phenylpropanoid biosynthesis through DE-lncRNAs (relevant genes Os09g0419200 regulated by MSTRG. 29,573.1).
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来源期刊
Genomics
Genomics 生物-生物工程与应用微生物
CiteScore
9.60
自引率
2.30%
发文量
260
审稿时长
60 days
期刊介绍: Genomics is a forum for describing the development of genome-scale technologies and their application to all areas of biological investigation. As a journal that has evolved with the field that carries its name, Genomics focuses on the development and application of cutting-edge methods, addressing fundamental questions with potential interest to a wide audience. Our aim is to publish the highest quality research and to provide authors with rapid, fair and accurate review and publication of manuscripts falling within our scope.
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