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对两种太平洋牡蛎的小RNA转录组进行高通量测序,鉴定出参与渗透应激反应的微小RNA。

High throughput sequencing of small RNAs transcriptomes in two Crassostrea oysters identifies microRNAs involved in osmotic stress response.

作者信息

Zhao Xuelin, Yu Hong, Kong Lingfeng, Liu Shikai, Li Qi

机构信息

Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao 266003, China.

The Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences and Program of Cell and Molecular Biosciences, Auburn University, Auburn, AL 36849, USA.

出版信息

Sci Rep. 2016 Mar 4;6:22687. doi: 10.1038/srep22687.

DOI:10.1038/srep22687
PMID:26940974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4778033/
Abstract

Increasing evidence suggests that microRNAs post-transcriptionally regulate gene expression and are involved in responses to biotic and abiotic stress. However, the role of miRNAs involved in osmotic plasticity remains largely unknown in marine bivalves. In the present study, we performed low salinity challenge with two Crassostrea species (C. gigas and C. hongkongensis), and conducted high-throughput sequencing of four small RNA libraries constructed from the gill tissues. A total of 202 and 87 miRNAs were identified from C. gigas and C. hongkongensis, respectively. Six miRNAs in C. gigas and two in C. hongkongensis were differentially expressed in response to osmotic stress. The expression profiles of these eight miRNAs were validated by qRT-PCR. Based on GO enrichment and KEGG pathway analysis, genes associated with microtubule-based process and cellular component movement were enriched in both species. In addition, five miRNA-mRNA interaction pairs that showed opposite expression patterns were identified in the C. hongkongensis, Differential expression analysis identified the miRNAs that play important regulatory roles in response to low salinity stress, providing insights into molecular mechanisms that are essential for salinity tolerance in marine bivalves.

摘要

越来越多的证据表明,微小RNA在转录后调控基因表达,并参与生物和非生物胁迫反应。然而,在海洋双壳贝类中,参与渗透可塑性的微小RNA的作用仍 largely unknown。在本研究中,我们对两种牡蛎(长牡蛎和香港牡蛎)进行了低盐度挑战,并对从鳃组织构建的四个小RNA文库进行了高通量测序。分别从长牡蛎和香港牡蛎中鉴定出202个和87个微小RNA。长牡蛎中的6个微小RNA和香港牡蛎中的2个微小RNA在渗透胁迫下差异表达。通过qRT-PCR验证了这8个微小RNA的表达谱。基于GO富集和KEGG通路分析,在两个物种中,与基于微管的过程和细胞成分运动相关的基因均被富集。此外,在香港牡蛎中鉴定出5对表达模式相反的微小RNA-信使RNA相互作用对。差异表达分析确定了在低盐度胁迫反应中起重要调控作用的微小RNA,为深入了解海洋双壳贝类耐盐性的分子机制提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/6519b0095d2e/srep22687-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/4035826be225/srep22687-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/ea122261b7d5/srep22687-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/5e37375f5ee3/srep22687-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/6519b0095d2e/srep22687-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/4035826be225/srep22687-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/ea122261b7d5/srep22687-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/5e37375f5ee3/srep22687-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/165a/4778033/6519b0095d2e/srep22687-f4.jpg

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