Analysis of the microRNA transcriptome and expression of different isomiRs in human peripheral blood mononuclear cellsReportar como inadecuado

Analysis of the microRNA transcriptome and expression of different isomiRs in human peripheral blood mononuclear cells - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

BMC Research Notes

, 6:390

First Online: 28 September 2013Received: 03 October 2012Accepted: 17 September 2013DOI: 10.1186-1756-0500-6-390

Cite this article as: Vaz, C., Ahmad, H.M., Bharti, R. et al. BMC Res Notes 2013 6: 390. doi:10.1186-1756-0500-6-390


BackgroundMicroRNAs miRNAs have been recognized as one of the key regulatory non-coding RNAs that are involved in a number of basic cellular processes. miRNA expression profiling helps to identify miRNAs that could serve as biomarkers. Next generation sequencing NGS platforms provide the most effective way of miRNA profiling, particularly as expression of different isoforms of miRNA IsomiRs can be estimated by NGS. Therefore, it is now possible to discern the overall complexity of miRNA populations that participate in gene regulatory networks. It is thus important to consider different isoforms of miRNA as part of total profiling in order to understand all aspects of the biology of miRNAs.

ResultsHere next generation sequencing data of small RNAs derived from normal peripheral blood mononuclear cells PBMC and Chronic myeloid leukemia CML patients has been used to generate miRNA profiles using a computation pipeline which can identify isomiRs that are natural variants of mature miRNAs. IsomiR profiles have been generated for all the 5p and 3p miRNAs previously known as major mature miRNA and minor or miRNA* and the data has been presented as a composite total miRNA transcriptome. The results indicated that the most abundant isomiR sequence of about 68% miRNAs, did not match the reference miRNA sequence as entered in the miRBase and that there is a definite pattern in relative concentration of different isomiRs derived from same precursors. Finally, a total of 17 potential novel miRNA sequences were identified suggesting that there are still some new miRNAs yet to be discovered.

ConclusionsInclusion of different isoforms provides a detailed miRnome of a cell type or tissues. Availability of miRnome will be useful for finding biomarkers of different cell types and disease states. Our results also indicate that the relative expression levels of different isoforms of a miRNA are likely to be dynamic and may change with respect to changes in the cell or differentiation status.

KeywordsMicroRNA Next generation sequencing Normalization IsomiR miRnome Peripheral blood mononuclear cells PBMC Chronic myeloid leukemia CML Electronic supplementary materialThe online version of this article doi:10.1186-1756-0500-6-390 contains supplementary material, which is available to authorized users.

Download fulltext PDF

Autor: Candida Vaz - Hafiz M Ahmad - Richa Bharti - Priyatama Pandey - Lalit Kumar - Ritu Kulshreshtha - Alok Bhattacharya


Documentos relacionados