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转录组学和 iTRAQ 蛋白质组学方法揭示了日本鳗鲡(Anguilla japonica)鳃中新型短期高渗胁迫响应蛋白。

Transcriptomic and iTRAQ proteomic approaches reveal novel short-term hyperosmotic stress responsive proteins in the gill of the Japanese eel (Anguilla japonica).

机构信息

Department of Biology, Hong Kong Baptist University, Hong Kong.

出版信息

J Proteomics. 2013 Aug 26;89:81-94. doi: 10.1016/j.jprot.2013.05.026. Epub 2013 Jun 2.

Abstract

UNLABELLED

Osmoregulation is critical for the survival of fishes that migrate between freshwater (FW) and seawater (SW). The eel, as a catadromous fish, has been studied for decades to reveal the mechanisms of osmoregulation. These studies, however, have been limited by the lack of a genomic database to decipher the mechanism of osmoregulation at a molecular level. In this study, using high-throughput transcriptomic and proteomic technologies, we have provided the first genome-wide study to identify hyperosmotic responsive proteins in the gills of the Japanese eel. Deep sequencing using the 454 platform produced over 660,000 reads with a mean length of 385 bp. For the proteomic study, we collected gill samples from three different treatment groups of fish that had fully adapted to FW/SW or were transferred from FW to SW for 6h. The respective group of gill proteins were extracted and labeled using an isobaric tag for relative and absolute quantitation (iTRAQ) using LTQ-Orbitrap, a high resolution mass spectrometer. Among the 1519 proteins identified from the gill samples, 96 proteins were differentially expressed between FW and SW adapted fish. Nineteen hyperosmotic responsive proteins were detected (10 up-regulated and 9 down-regulated proteins) after 6h post FW to SW transfer.

BIOLOGICAL SIGNIFICANCE

The study has provided the most comprehensive, targeted investigation of eel gill proteins to date, and shown the powerfulness of combining transcriptomic and proteomic approaches to provide molecular insights of osmoregulation mechanisms in a non-model organism, eel.

摘要

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渗透压调节对于在淡水 (FW) 和海水 (SW) 之间洄游的鱼类的生存至关重要。鳗鲡作为一种溯河洄游鱼类,已经被研究了几十年,以揭示其渗透压调节机制。然而,这些研究受到缺乏基因组数据库的限制,无法从分子水平上破译渗透压调节机制。在这项研究中,我们使用高通量转录组学和蛋白质组学技术,首次进行了全基因组研究,以鉴定日本鳗鲡鳃中的高渗响应蛋白。使用 454 平台进行深度测序产生了超过 660,000 条平均长度为 385bp 的reads。对于蛋白质组学研究,我们从已经完全适应 FW/SW 或从 FW 转移到 SW 6 小时的三组鱼中收集了鳃样本。使用等重标记相对和绝对定量 (iTRAQ) 技术,从 LTQ-Orbitrap 高分辨率质谱仪中提取和标记相应组的鳃蛋白。在从鳃样本中鉴定的 1519 种蛋白质中,有 96 种蛋白质在 FW 和 SW 适应的鱼之间表达差异。在 FW 到 SW 转移后 6 小时检测到 19 种高渗响应蛋白(10 种上调蛋白和 9 种下调蛋白)。

生物学意义

该研究提供了迄今为止对鳗鲡鳃蛋白最全面、有针对性的调查,并展示了结合转录组学和蛋白质组学方法的强大功能,为非模式生物鳗鲡的渗透压调节机制提供了分子见解。

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