畜牧兽医学报 ›› 2017, Vol. 48 ›› Issue (2): 235-242.doi: 10.11843/j.issn.0366-6964.2017.02.006

• 遗传育种 • 上一篇    下一篇

不同生长时期梅花鹿鹿茸转录组分析

张然然,刘华淼,王磊,邢秀梅*,苏伟林,高兵   

  1. (中国农业科学院特产研究所 特种经济动物分子生物重点实验室,长春 130112)
  • 收稿日期:2016-08-11 出版日期:2017-02-23 发布日期:2017-02-23
  • 通讯作者: 邢秀梅,研究员,E-mail: xingxiumei2004@126.com
  • 作者简介:张然然(1990-),女,河北深州人,硕士,主要从事特种经济动物种质资源保护与遗传育种研究,E-mail: heavenranran@163.com
  • 基金资助:

    特种动物遗传资源创新团队(CAAS-ASTIP-201X-ISAPS)

Transcriptome Analysis of Sika Deer Antlers at Different Stages

ZHANG Ran-ran, LIU Hua-miao, WANG Lei, XING Xiu-mei*, SU Wei-lin, GAO Bing   

  1. (State Key Laboratory of Special Economic Animal Molecular Biology, Institute of Special Animal and Plant Sciences of Chinese Academy of Agricultural Sciences, Changchun 130112, China)
  • Received:2016-08-11 Online:2017-02-23 Published:2017-02-23

摘要:

本研究旨在探究不同生长时期梅花鹿鹿茸的转录组差异,丰富梅花鹿鹿茸转录组信息。选取5个生长时期(10、20、28、44、66 d)的梅花鹿鹿茸组织作为试验样品,利用Illumina HiSeqTM 2500高通量测序,并用测序评估、基因注释等生物信息学方法进行分析。结果,经过测序、转录本拼接获得了375 657 条contigs,平均长度为688 bp,329 946个unigenes,平均长度为534 bp。通过比对Nr、Nt、Pfam、KOG/COG、Swiss-prot、KEGG、GO 等7大数据库,90.07% unigenes得到了成功注释。其中39 674个(12.02%)基因成功注释到GO数据库,在level 2水平上共分为41个类别;17 732个(5.37%)基因成功注释到将 KOG 的26个类别中。对5个生长时期的鹿茸转录本文库进行比较分析,共发现了509个差异基因,其中407个差异表达基因成功注释到GO数据库中,主要为信号转导、氧化还原、转录调节、蛋白酶降解等生物学过程。其中转录调节基因PER1、EGR1的表达随着鹿茸的生长而增加,而GAS1则相反,随着鹿茸的生长而降低,推测PER1、EGR1、GAS1等转录因子在鹿茸生长过程中可能起着重要的调节作用。本研究利用高通量测序技术对不同生长时期的梅花鹿鹿茸组织进行了转录组测序和分析,筛选到了梅花鹿鹿茸在不同生长时期下的差异表达基因,并获得了差异表达基因的功能。

关键词: 梅花鹿, 鹿茸, 转录组, 差异表达基因

Abstract:

The objective of this study was to find the transcriptome differences of sika deer antlers at different stages, and enrich the sika deer antler transcriptome data. The sika deer antlers aged 10, 20, 28, 44 and 66 d were selected as experimental material,then the transcriptome libraries of antlers were constructed by using Illumina HiSeqTM 2500 platform, and the transcriptome data were analyzed by bioinformatics methods, such as sequencing assess and gene annotation. The results showed that a total of 375 657 contigs with an average length of 688 bp were generated, from which 329 946 unigenes with an average length of 534 bp were defined. 90.07% of the 297 198 unigenes were annotated in public databases of Nr,Nt,Pfam,KOG/COG,Swiss-prot,KEGG and GO. Through annotation classification, a total of 39 674(12.02%) genes were divided into 41 GO function categories at level 2, and 17 732 (5.37%) genes were annotated in 26 KOG categories. Comparative analysis of differentially expressed genes in sika deer antler at 5 different stages, and 509 differentially expressed genes were screened, from which 407 genes were annotated in GO database including signal transduction, oxidation-reduction process, regulation of transcription, proteolysis, and so on. And the expression of PER1 and EGR1 (transcription regulation gene) increased with the growth of antlers, on the contrary, the expression of GAS1 decreased. It indicates that PER1, EGR1, GAS1 may have important role in regulation of antler growth. The transcriptome study of the antler tissue in the different growth period revealed the number of differentially expressed genes by using high-throughput sequencing technology, obtained the function of differentially expressed genes.

Key words: sika deer, antler, transcriptome, differentially expressed genes

中图分类号: