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比较转录组分析鉴定与海参棘皮动物海地瓜发育相关的基因。

Comparative transcriptome analysis identifies genes associated with papilla development in the sea cucumber Apostichopus japonicus.

机构信息

Key Laboratory of Mariculture & Stock Enhancement in North China's Sea, Ministry of Agriculture and Rural Affairs, Dalian Ocean University, Dalian, Liaoning 116023, PR China.

School of Life Science and Biotechnology, Dalian University of Technology, Dalian, Liaoning 116023, PR China.

出版信息

Comp Biochem Physiol Part D Genomics Proteomics. 2019 Mar;29:255-263. doi: 10.1016/j.cbd.2018.12.009. Epub 2018 Dec 28.

DOI:10.1016/j.cbd.2018.12.009
PMID:30634154
Abstract

To explore the molecular mechanisms underlying the initial differentiation and formation of papillae in sea cucumbers, the transcriptomes of Apostichopus japonicus pentactulae (without papillae) were compared to those of A. japonicus juveniles (with papillae). From the RNA of the three pentactula libraries and the three juvenile libraries, we obtained 41-46 million raw reads, yielding 39-45 million clean reads. From these, we generated 599,673 transcripts and identified 230,604 unigenes. Across all six transcriptomes, we identified 246,207 single nucleotide polymorphisms (SNPs) and 80,455 single sequence repeats (SSRs). There were more transition SNPs (60.74%) than transversion SNPs (39.26%). The mononucleotide repeat was the most abundant SSR motif. We identified 7965 differentially expressed unigenes (DEGs) in the juveniles and the pentactulae; 2421 DEGs were expressed only in the juveniles, and 1238 were expressed only in the pentactulae. Of all DEGs, 5215 were significantly upregulated and 2750 were significantly downregulated in the juveniles as compared to the pentactulae. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses indicated that the DEGs were primarily enriched in ribosome synthesis, cell proliferation, tight junction formation, collagen fibrillogenesis, and neurogenesis.

摘要

为了探究海参初期乳头状形成的分子机制,我们比较了无乳头状的五触手幼体和有乳头状的幼体的转录组。从三个五触手文库和三个幼体文库的 RNA 中,我们获得了 4100 万到 4600 万条原始读段,生成了 3900 万到 4500 万条清洁读段。在此基础上,我们生成了 599673 条转录本并鉴定了 230604 个基因。在这六个转录组中,我们鉴定出了 246207 个单核苷酸多态性(SNP)和 80455 个单核苷酸重复(SSR)。转换 SNP(60.74%)多于颠换 SNP(39.26%)。单核苷酸重复是最丰富的 SSR 基序。我们在幼体和五触手幼体中鉴定出了 7965 个差异表达基因(DEGs);2421 个 DEGs 仅在幼体中表达,1238 个仅在五触手幼体中表达。所有 DEGs 中,有 5215 个在幼体中显著上调,2750 个在幼体中显著下调。基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析表明,DEGs 主要富集于核糖体合成、细胞增殖、紧密连接形成、胶原纤维生成和神经发生等过程。

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引用本文的文献

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