Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Genome-wide profiling and differential expression of microRNA in rat pluripotent stem cells. / Sherstyuk, Vladimir V.; Medvedev, Sergey P.; Elisaphenko, Evgeniy A. и др.
в: Scientific Reports, Том 7, № 1, 2787, 05.06.2017, стр. 2787.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Genome-wide profiling and differential expression of microRNA in rat pluripotent stem cells
AU - Sherstyuk, Vladimir V.
AU - Medvedev, Sergey P.
AU - Elisaphenko, Evgeniy A.
AU - Vaskova, Evgeniya A.
AU - Ri, Maxim T.
AU - Vyatkin, Yuri V.
AU - Saik, Olga V.
AU - Shtokalo, Dmitry N.
AU - Pokushalov, Evgeniy A.
AU - Zakian, Suren M.
N1 - Publisher Copyright: © The Author(s) 2017.
PY - 2017/6/5
Y1 - 2017/6/5
N2 - MicroRNAs (miRNAs) constitute a class of small noncoding RNAs that plays an important role in the post-transcriptional regulation of gene expression. Much evidence has demonstrated that miRNAs are involved in regulating the human and mouse pluripotency. Nevertheless, to our knowledge, miRNAs in the pluripotent stem cells of one of the most commonly used model organisms - the Rattus norvegicus have not been studied. In the present study, we performed deep sequencing of small RNA molecules in the embryonic fibroblasts, embryonic stem cells, and induced pluripotent stem cells of laboratory rats. Bioinformatics analysis revealed 674 known miRNAs and 394 novel miRNA candidates in all of the samples. Expression of known pluripotency-associated miRNAs, such as the miR-290-295 and miR-183-96-182 clusters as well as members of the miR-200 family, was detected in rat pluripotent stem cells. Analysis of the targets of differentially expressed known and novel miRNAs showed their involvement in the regulation of pluripotency and the reprogramming process in rats. Bioinformatics and systems biology approaches identified potential pathways that are regulated by these miRNAs. This study contributes to our understanding of miRNAs in the regulation of pluripotency and cell reprogramming in the laboratory rat.
AB - MicroRNAs (miRNAs) constitute a class of small noncoding RNAs that plays an important role in the post-transcriptional regulation of gene expression. Much evidence has demonstrated that miRNAs are involved in regulating the human and mouse pluripotency. Nevertheless, to our knowledge, miRNAs in the pluripotent stem cells of one of the most commonly used model organisms - the Rattus norvegicus have not been studied. In the present study, we performed deep sequencing of small RNA molecules in the embryonic fibroblasts, embryonic stem cells, and induced pluripotent stem cells of laboratory rats. Bioinformatics analysis revealed 674 known miRNAs and 394 novel miRNA candidates in all of the samples. Expression of known pluripotency-associated miRNAs, such as the miR-290-295 and miR-183-96-182 clusters as well as members of the miR-200 family, was detected in rat pluripotent stem cells. Analysis of the targets of differentially expressed known and novel miRNAs showed their involvement in the regulation of pluripotency and the reprogramming process in rats. Bioinformatics and systems biology approaches identified potential pathways that are regulated by these miRNAs. This study contributes to our understanding of miRNAs in the regulation of pluripotency and cell reprogramming in the laboratory rat.
KW - Animals
KW - Cell Line
KW - Computational Biology/methods
KW - Gene Expression Profiling
KW - Gene Expression Regulation, Developmental
KW - Genome-Wide Association Study
KW - MicroRNAs/genetics
KW - Molecular Sequence Annotation
KW - Pluripotent Stem Cells/cytology
KW - Rats
KW - Transcriptome
KW - MOUSE EMBRYOS
KW - SELF-RENEWAL
KW - MIR-200 FAMILY
KW - REPRESSORS ZEB1
KW - MURINE
KW - EPITHELIAL-MESENCHYMAL TRANSITION
KW - PATHWAY
KW - TARGETS
KW - BLASTOCYSTS
KW - HUMAN SOMATIC-CELLS
UR - http://www.scopus.com/inward/record.url?scp=85020419666&partnerID=8YFLogxK
U2 - 10.1038/s41598-017-02632-0
DO - 10.1038/s41598-017-02632-0
M3 - Article
C2 - 28584262
AN - SCOPUS:85020419666
VL - 7
SP - 2787
JO - Scientific Reports
JF - Scientific Reports
SN - 2045-2322
IS - 1
M1 - 2787
ER -
ID: 8798041