Liqiang Zhu, Lina Hu, Aifang Li, Shuxuan Li, Yalan Li, Qianqian Wang, Yu Huang, Yanxia Feng, Qinghua Li, Shuying Feng
Background: Eukaryotic flagellum is highly conserved in basic structure and biogenesis, and defects in ciliary assembly or function lead to a wide range of human disease symptoms. The alga Dunaliella salina (D. salina), provides an excellent model for investigating flagellar/ciliary system. However, the genome it carries is unpublished. Results: To In this study, using high-throughput illumina RNA sequencing, the transcriptomes from flagella-assembling D. salina were analyzed firstly at an unprecedented depth. About 4 giga bases of raw sequence data were generated and 197,295 uni-genes were annotated with gene descriptions, conserved protein domains, or gene ontology terms against public databases. Among the annotated uni-genes, 25,412 uni-genes were differentially expressed during flagella regeneration, including 9,988 up-regulated uni-genes and 15,407 down-regulated unigenes. Moreover, to functionally categorize the D. salina uni-genes, the differentially expressed unigenes distributed into the category of biological process, molecular function and cellular component. These transcriptome datasets might reveal the mechanism of flagella assembly in D. salinacells, and serve as a public information platform for D. salina functional genomics and proteomics analysis. Furthermore, the differentially expressed unigenes involved in different signaling pathways of D. salina flagella assembly and human diseases were screened respectively.
Conclusion: These pathway-based results not only provide a further understanding to specific processes of ciliogenesis and ciliopathies, but also offer a cue to mechanism of human diseases.
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