华北农学报 ›› 2019, Vol. 34 ›› Issue (4): 53-61. doi: 10.7668/hbnxb.201751584

所属专题: 生物技术

• 作物遗传育种·种质资源·生物技术 • 上一篇    下一篇

利用转录组测序分析茄子萼片刺相关差异基因

潜宗伟, 陈海丽, 崔彦玲   

  1. 北京市农林科学院 蔬菜研究中心, 农业部华北地区园艺作物生物学与种质创制重点实验室, 蔬菜种质改良北京市重点实验室, 北京 100097
  • 收稿日期:2018-11-21 出版日期:2019-08-28
  • 通讯作者: 崔彦玲(1965-),女,河北行唐人,研究员,硕士,主要从事蔬菜遗传育种研究。
  • 作者简介:潜宗伟(1982-),男,湖北枣阳人,硕士,助理研究员,主要从事蔬菜遗传育种研究。
  • 基金资助:
    国家重点研发资助项目(2017YFD0101901);北京市农林科学院青年基金资助项目(QNJJ201602);北京市创新团队资助项目(GCTDZJ2014033002);北京市农林科学院创新项目(KJCX20170102)

Analysis of Prickle Development Genes in Eggplant Calyx via Transcriptome Sequencing

QIAN Zongwei, CHEN Haili, CUI Yanling   

  1. Vegetable Research Center, Beijing Academy of Agricultural and Forestry Sciences, Key Laboratory of Biology and Genetic Improvement of Horticultural Crops(North China), Ministry of Agriculture, P. R. China, Beijing Key Laboratory of Vegetable Germplasm Improvement, Beijing 100097, China
  • Received:2018-11-21 Published:2019-08-28

摘要: 为了发掘茄子萼片刺形成的相关基因,为茄子萼片刺形成的机理和基因定位奠定基础,以萼片有刺和萼片无刺的2个自交系1607和1608为材料,构建了F2遗传分离群体,利用新一代高通量测序手段对双亲和2个混池的转录组进行了测序分析。通过转录组分析,共获得409 363 358个干净的高通量序列,其中比对到参考基因组的序列共有311 756 616个,比对效率均大于75.00%。发掘24 310个新基因,其中获得注释信息的新基因总数为1 540个。对转录组测序获得的全部基因表达量进行了分析,在双亲中共得到2 438个差异表达基因,其中97个差异基因在2个混池中同时存在。通过对差异基因的注释分析,富集到了可能与茄子萼片刺形成的相关的候选基因3个:SmCKXEggplant_newGene_1802)、SmSTSSme2.5_09750.1_g00002)和SmFAREggplant_newGene_4241)。SmCKX是一个茄子细胞分裂素氧化酶/脱氢酶相关基因,与番茄的Solyc04g080820.2Solyc04g080810.3,拟南芥的AtCKX6具有同源性。SmSTS是茄子水苏糖合成酶相关的基因,与番茄的Solyc01g079300.3基因和拟南芥的AT4G01970.1基因同源性较高。SmFAR是一个脂肪酰辅酶A还原酶相关基因,与番茄Solyc11g067180.2基因(FARx相关基因)同源。以上同源基因参与了植物角质,小檗碱和蜡生物合成途径、细胞分裂素合成途径和水苏糖代谢途径,因此,茄子萼片刺的形成可能具有相同的代谢调控途径。

关键词: 茄子, 萼片刺, 转录组, 基因

Abstract: To explore genes involved in prickle development in eggplant calyx and provide the basic knowledge for the mechanism and gene mapping of prickle development in eggplant calyx, two inbred lines, of which 1607 is the line with prickles while 1608 is not, were used to construct the F2 population. The two parental lines and two separate pools were then used for RNA sequencing. A total of 409 363 358 clean reads were obtained, of which 311 756 616 were aligned to the eggplant reference genome, with the alignment efficiency over 75.00%. A total of 24 310 new transcripts were found and 1 540 of them were annotated. 2 438 genes were differentially expressed between the two parental lines and the two pools, of which 97 were also shared between the two pools. Based on gene annotation, three genes might be involved in the formation of prickle:SmCKX (Eggplant_newGene_1802), SmSTS (Sme2.5_09750.1_g00002)and SmFAR (Eggplant_newGene_4241). SmCKX is acytokinin oxidase/dehydrogenase, SmSTS is a stachyose synthase, and SmFAR is a fatty acyl-CoA reductase. Their homologues function in cytokinin synthesis, stachyose metabolism and wax biosynthesis pathways, individually, indicated that the development of prickle in eggplant calyx might be also affected by the aforementioned signaling.

Key words: Eggplant, Prickle in eggplant calyx, Transcriptome, Gene

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引用本文

潜宗伟, 陈海丽, 崔彦玲. 利用转录组测序分析茄子萼片刺相关差异基因[J]. 华北农学报, 2019, 34(4): 53-61. doi: 10.7668/hbnxb.201751584.

QIAN Zongwei, CHEN Haili, CUI Yanling. Analysis of Prickle Development Genes in Eggplant Calyx via Transcriptome Sequencing[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2019, 34(4): 53-61. doi: 10.7668/hbnxb.201751584.

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