日本医蛭唾液腺对饥饿胁迫响应的转录组比较
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Q786;S917.4

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国家自然科学基金(31440030)


Comparative transcriptome analysis of salivary glands of Hirudo nipponia in response to starvation
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National Natural Science Foundation of China (31440030)

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    摘要:

    为了探究饥饿胁迫对日本医蛭唾液腺基因表达水平的影响,本实验通过Illumina Hiseq 2500高通量测序平台分别对饥饿30 d处理组(D30)和饥饿0 d (D0)对照组的日本医蛭的唾液腺组织进行双端测序,对获得的原始数据进行质量控制及从头组装,获得145 981个unigenes,平均长度为675 bp,N50为1 127 bp。针对CDD、KOG、COG、NR、NT、PFAM、Swissprot、TrEMBL、GO和KEGG等数据库的序列比对分析,145 981个unigenes均能得到注释。通过引入TPM(transcripts per million)来估算基因表达水平,并通过DEGseq进行基因表达差异分析。以饥饿0 d为对照组,显著差异基因筛选条件设置为Q value<0.05且差异倍数|Fold Change| > 2,获得2 650个差异基因,其中667个基因显著上调,1 983个基因显著下调。选取日本医蛭唾液腺4个重要功能基因进行荧光定量PCR(qRT-PCR)验证,结果证明转录组测序分析可靠。将所有差异表达基因进行GO功能富集分析,显著富集到175条途径,其中胞质核糖体途径富集程度最为显著,核糖体途径次之,且参与这些途径的差异基因基本均下调。KEGG通路富集分析进一步证明,差异基因在核糖体通路中富集程度最为显著。此外,差异基因中4个基因被预测参与抗凝、抗血栓、抗菌、抗炎和抗肿瘤过程,这可能在各种疾病的治疗中发挥重要作用。参与核糖体通路的基因表达量显著降低,表明日本医蛭唾液腺通过降低蛋白质代谢以应对饥饿环境。该实验结果为深入研究日本医蛭唾液腺饥饿胁迫适应的分泌调控机制以及药用价值基因的发掘提供了重要的参考材料,并为其他医学蛭类研究提供参考依据。

    Abstract:

    In order to investigate the variations of gene expression of salivary gland in Hirudo nipponia under starvation stress, two libraries of starvation treatment group (D30) and control group (D0) were constructed and sequenced using the Illumina HiSeq 2500 platform (paired-end). After stringent quality control of raw data, 145 981 unigenes were obtained using de novo assembly. The average length of unigenes was 675 bp and N50 length was 1 127 bp. And then all of unigenes were annotated via sequence alignment analysis in CDD, KOG, COG, NR, NT, PFAM, Swissprot, TrEMBL, GO and KEGG databases. The amount of gene expression was also estimated according to TPM (transcripts per million). By comparing the transcriptome data of D30 sample and D0 sample, the differentially expressed genes (DEGs) were screened out with a threshold criteria Q value<0.05 and |Fold Change| > 2. Totally 2 650 DEGs were identified under starvation stress, among which 667 genes were up-regulated and 1 983 genes were down-regulated. Four functional DEGs were selected for qRT-PCR analysis, and the results confirmed that the transcriptome analysis was reliable. In addition, 175 pathways were significantly enriched when all the DEGs were subject to GO enrichment analysis. The results showed that most of the DEGs were involved in cytoplasmic ribosome pathway and ribosome pathway was second. The DEGs were almost down-regulated in these pathways. It was also proved in KEGG enrichment analysis that most DEGs were involved in ribosome pathway was second. The DEGs down-regulated in ribosome pathway can indicate that it reduces protein metabolism under starvation stress. Futhermore, 4 genes were predicted to be involved in anticoagulatory, antithrombotic, antibacterial, anti-inflammatory and antitumor processes, which might play important roles in the treatment of various diseases. The results above mentioned provide important reference information for further study on the molecular mechanism of starvation tolerance of salivary gland and the discovery of pharmaceutical value genes in H. nipponia, and also provide reference for other medicinal leeches.

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邢月婷,管峰,李诗语,张世雄,罗媛媛.日本医蛭唾液腺对饥饿胁迫响应的转录组比较[J].水产学报,2020,44(5):754~766

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  • 收稿日期:2018-12-19
  • 最后修改日期:2019-10-13
  • 录用日期:2019-10-24
  • 在线发布日期: 2020-04-28
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