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恶性疟原虫红细胞内新型中等大小非编码RNA的深度分析。

Deep profiling of the novel intermediate-size noncoding RNAs in intraerythrocytic Plasmodium falciparum.

作者信息

Wei Chunyan, Xiao Tengfei, Zhang Peng, Wang Zhensheng, Chen Xiaowei, Zhang Lianhui, Yao Meixue, Chen Runsheng, Wang Heng

机构信息

Department of Microbiology and Parasitology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medicine, Peking Union Medical College, Beijing, China.

Laboratory of Bioinformatics and Noncoding RNA, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

出版信息

PLoS One. 2014 Apr 8;9(4):e92946. doi: 10.1371/journal.pone.0092946. eCollection 2014.

DOI:10.1371/journal.pone.0092946
PMID:24713982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3979661/
Abstract

Intermediate-size noncoding RNAs (is-ncRNAs) have been shown to play important regulatory roles in the development of several eukaryotic organisms. However, they have not been thoroughly explored in Plasmodium falciparum, which is the most virulent malaria parasite infecting human being. By using Illumina/Solexa paired-end sequencing of an is-ncRNA-specific library, we performed a systematic identification of novel is-ncRNAs in intraerythrocytic P. falciparum, strain 3D7. A total of 1,198 novel is-ncRNA candidates, including antisense, intergenic, and intronic is-ncRNAs, were identified. Bioinformatics analyses showed that the intergenic is-ncRNAs were the least conserved among different Plasmodium species, and antisense is-ncRNAs were more conserved than their sense counterparts. Twenty-two novel snoRNAs were identified, and eight potential novel classes of P. falciparum is-ncRNAs were revealed by clustering analysis. The expression of randomly selected novel is-ncRNAs was confirmed by RT-PCR and northern blotting assays. An obvious different expressional profile of the novel is-ncRNA between the early and late intraerythrocytic developmental stages of the parasite was observed. The expression levels of the antisense RNAs correlated with those of their cis-encoded sense RNA counterparts, suggesting that these is-ncRNAs are involved in the regulation of gene expression of the parasite. In conclusion, we accomplished a deep profiling analysis of novel is-ncRNAs in P. falciparum, analysed the conservation and structural features of these novel is-ncRNAs, and revealed their differential expression patterns during the development of the parasite. These findings provide important information for further functional characterisation of novel is-ncRNAs during the development of P. falciparum.

摘要

中等大小的非编码RNA(is-ncRNAs)已被证明在几种真核生物的发育中发挥重要的调控作用。然而,在恶性疟原虫(Plasmodium falciparum)中,它们尚未得到充分研究,恶性疟原虫是感染人类的最具毒性的疟原虫。通过对一个is-ncRNA特异性文库进行Illumina/Solexa双末端测序,我们对红细胞内的恶性疟原虫3D7株中的新型is-ncRNAs进行了系统鉴定。共鉴定出1198个新型is-ncRNA候选物,包括反义、基因间和内含子is-ncRNAs。生物信息学分析表明,基因间is-ncRNAs在不同疟原虫物种中保守性最低,反义is-ncRNAs比其正义对应物更保守。鉴定出22个新型snoRNAs,聚类分析揭示了8种潜在的新型恶性疟原虫is-ncRNAs类别。通过RT-PCR和Northern印迹分析证实了随机选择的新型is-ncRNAs的表达。观察到该寄生虫红细胞内发育早期和晚期新型is-ncRNA的表达谱明显不同。反义RNA的表达水平与其顺式编码的正义RNA对应物的表达水平相关,表明这些is-ncRNAs参与了该寄生虫基因表达的调控。总之,我们完成了对恶性疟原虫新型is-ncRNAs的深度分析,分析了这些新型is-ncRNAs的保守性和结构特征,并揭示了它们在寄生虫发育过程中的差异表达模式。这些发现为进一步研究恶性疟原虫发育过程中新型is-ncRNAs的功能特性提供了重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/825ab5847c14/pone.0092946.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/089dbda4634c/pone.0092946.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/fad422de29dd/pone.0092946.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/4f52a3027817/pone.0092946.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/6a490fcd26eb/pone.0092946.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/825ab5847c14/pone.0092946.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/089dbda4634c/pone.0092946.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/fad422de29dd/pone.0092946.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/4f52a3027817/pone.0092946.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/6a490fcd26eb/pone.0092946.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbae/3979661/825ab5847c14/pone.0092946.g005.jpg

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