期刊文献+

火龙果转录组测序、基因表达与功能分析 被引量:5

De novo assembly and transcriptome analysis of Hylocereus undulatus during development
下载PDF
导出
摘要 利用高通量测序技术对火龙果(Hylocereus undulatus Britt)红肉品种‘大红二号’的花芽、果实和枝条不同发育阶段的基因表达进行研究。结果显示,转录组测序共获得468.68 Gb原始数据(Raw data),从头组装获得239 152条转录本和162 519条unigene,约53.74%的unigene得到注释。分别在43 506条和16 251条unigene中检测到600 283个SNP位点和56 147个SSR位点。基因表达分析结果表明,在火龙果不同组织Fl510、Fl513、Fl514、Fl518、F711、F715、S513、S419中分别有31、7、5、152、17、63、17、8个特异表达的unigene。通过GO和KEGG富集分析,发现了一些组织特异的GO条目和代谢通路,如在Fl510中富集的类萜骨架生物合成代谢通路等。本研究还对参与花发育的候选基因进行了鉴定和表达分析,他们包括COL基因、FT-like基因、分生组织决定基因和器官决定基因等。 High-throughput sequencing was used to analyze the gene expression of the reproductive buds, fruits, and shoots of Hylocereus undulatus Britt ‘Dahong2’ at different developmental stages. In total, 468. 68 Gb of raw data were generated and de novo assembled into 239 152 transcripts and 162 519 unigenes. Approximately 53. 74% of all unigenes were annotated based on seven public databases. In total, 600 283 SNPs and 56147 SSRs were identified from 43 506 and 16 251 unigenes, respectively. Gene expression analysis showed that 31, 7, 5, 152, 17, 63, 17, and 8 unigenes were specifically expressed in Fl510, Fl513, Fl514, Fl518, F711, F715, S513, and S419, respectively. Through GO and KEGG enrichment analyses, several unique GO terms and metabolic pathways in different tissues were identified;for example, terpenoid backbone biosynthesis (ko00900) showed significant enrichment in Fl510. We also focused on the molecular mechanism of H.undulatus ‘Dahong2’ flower development and identified a suite of unigenes involved in floral development, including COL , FT - like , meristem identity, and organ identity genes.
作者 魏开发 李艺宣 Wei Kai-Fa;Li Yi-Xuan(School of Biological Sciences and Biotechnology ,Minnan Normal University ,Zhangzhou,Fujian 363000,China)
出处 《植物科学学报》 CAS CSCD 北大核心 2019年第2期198-210,共13页 Plant Science Journal
基金 福建省产业技术开发与应用计划对外合作项目(2015I0006)~~
关键词 火龙果 转录组测序 生长 花发育 基因表达 Hylocereus undulatus Transcriptome sequencing Growth Floral development Gene expression
  • 相关文献

参考文献2

二级参考文献181

  • 1Mandel M A;Gustafson-Brown C;Savidge B;Yanofsky M F.Molecular characterization of the Arabidopsis floral homeotic gene APETALA1,1992.
  • 2Lohmann J U,Hong R L,Hobe M,et al.A molecular link between stem cell regulation and floral patterning in Arabidopsis[].Cell.2001
  • 3Molinero-Rosales N,Jamilena M,Zurita S,et al.FALSIFLORA, the tomato orthologue of FLORICAULA and LEAFY, controls flowering time and floral meristem identity[].Plant Journal The.1999
  • 4Pellegrini L,Tan S,Richmond TJ.Structure of serum response factor core bound to DNA[].Nature.1995
  • 5Putterill J,Robson F,Lee K,Simon R,Coupland G.The CONSTANS gene of Arabidopsis promotes flowering and encodes a protein showing similarities to zinc finger transcription factors[].Cell.1995
  • 6Ruiz-Garcia L,Madueno F,Wilkinson M,et al.Different roles of flowering-time genes in the activation of floral Initiation genes in Arabidopsis[].Plant Cell The.1997
  • 7Abe, M., Kobayashi, Y., Yamamoto, S., Daimon, Y., Yamaguchi, A., Ikeda, Y., Ichinoki, H., Notaguchi, M., Goto, K., and Araki, T. (2005). FD, a bZlP protein mediating signals from the floral pathway integrator FT at the shoot apex. Science 309:1052-1056.
  • 8Adrian, J., Farrona, S., Reimer, J.J., Albani, M.C., Coupland, G., and Turck, F. (2010). cis-Regulatory elements and chromatin state coordinately control temporal and spatial expression of FLOWERING LOCUS T in Arabidopsis. Plant Cell 22:1425-1440.
  • 9Aguilar-Martinez, J.A., Poza-Carri6n, C., and Cubas, P. (2007). Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds. Plant Cell 19:458-472.
  • 10Ahn, J.H., Miller, D., Winter, V,J., Banfield, M.J., Lee, J.N., Yoo, S.Y., Henz, S.R., Brady, R.L., and Weigel, D. (2006). A divergent external loop confers antagonistic activity on floral regulators FT and TFL1. EMBO J. 25:605-614.

共引文献57

同被引文献92

引证文献5

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部