首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >De novo transcriptomic analysis to identify differentially expressed genes during the process of aerenchyma formation in Typha angustifolia leaves
【24h】

De novo transcriptomic analysis to identify differentially expressed genes during the process of aerenchyma formation in Typha angustifolia leaves

机译:DE Novo转录组分析在Typha angustifolia叶片中腾飞症形成过程中鉴定差异表达基因

获取原文
获取原文并翻译 | 示例
           

摘要

Lysigenous aerenchyma is formed through programmed cell death (PCD) in Typha angustifolia leaves. However, the genome and transcriptome data for this species are unknown. To further elucidate the molecular basis of PCD during aerenchyma formation in T. angustifolia leaves, transcriptomic analysis of T. angustifolia leaves was performed using Illumina sequencing technology, revealing 73,821 unigenes that were produced by assembly of the reads in T1, T2 and T3 samples. The important pathways, such as programmed cell death (PCD), aerenchyma formation, and ethylene responsiveness were regulated by these unigenes. 1-aminocyclopropane-l-carboxylate synthase (ACS) and 1-aminocyclopropane-l-carboxylate oxidase (ACO) were highly up-regulated as key enzymes for ethylene synthesis, along with respiratory burst oxidase homolog (RBOH), metallothionein, calmodulin-like protein (CML), and polygalacturonase (PG), may collectively explain the PCD involved in T. angustifolia aerenchyma formation. We hypothesize that fermentation, metabolism and glycolysis generate ATP for PCD. We searched the 73,821 unigenes against protein databases, and 24,712 were annotated. Based on sequence homology, 16,012 of the 73,821 annotated unigenes were assigned to one or more Gene Ontology (GO) terms. Meanwhile, a total of 9537 unigenes were assigned to 126 pathways in the KEGG database. In summary, this investigation provides important guidelines for exploring the molecular mechanisms of aerenchyma formation in aquatic plants.
机译:通过Typha Angustifolia叶中的编程细胞死亡(PCD)形成溶滤雾膜。然而,该物种的基因组和转录组数据是未知的。为了进一步阐明在T.Angustifolia叶片的灌冻血症形成期间PCD的分子基础,使用Illumina测序技术进行Angustifolia叶片的转录组分析,揭示了通过组装T1,T2和T3样品中的读取产生的73,821个unigenes。通过这些unigenes调节重要的途径,例如编程细胞死亡(PCD),雾藻形成和乙烯反应性。 1-氨基环丙烷-1-羧酸盐合酶(ACS)和1-氨基环丙烷-1-羧酸氧化酶(ACO)被高度上调作为乙烯合成的关键酶,以及呼吸爆发氧化酶同源物(RBOH),金属硫蛋白,钙调蛋白样蛋白质(CML)和PolyGalactuRonase(PG)可以共同解释涉及T.Angustifolia雾藻形成的PCD。我们假设发酵,代谢和糖酵解产生ATP的PCD。我们在针对蛋白质数据库的73,821个未成年人搜查,24,712人被注释。基于序列同源性,将73,821个注释的未经成果中的16,012分配给一种或多种基因本体学(GO)术语。同时,共有9537个未在Kegg数据库中分配126个途径。总之,本调查提供了探索水生植物中的灌冻室的分子机制的重要指导。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号