microRNA Expression during Trophectoderm Specification

被引:74
作者
Viswanathan, Srinivas R.
Mermel, Craig H.
Lu, Jun
Lu, Chi-Wei
Golub, Todd R.
Daley, George Q.
机构
[1] Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Harvard Stem Cell Institute, Boston, MA
[2] Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA
[3] Department of Obstetrics, Gynecology and Reproductive Science, UMDNJ-Robert Wood Johnson Med School Piscataway, Piscataway, NJ
[4] Howard Hughes Medical Institute, Boston, MA
[5] Stem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Danaa Farber Cancer Institute, Boston, MA
[6] Division of Hematology, Brigham and Women's Hospital, Boston, MA
[7] Manton Center for Orphan Disease Research, Boston, MA
来源
PLOS ONE | 2009年 / 4卷 / 07期
关键词
D O I
10.1371/journal.pone.0006143
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Segregation of the trophectoderm from the inner cell mass of the embryo represents the first cell-fate decision of mammalian development. Transcription factors essential for specifying trophectoderm have been identified, but the role of microRNAs (miRNAs) in modulating this fate-choice has been largely unexplored. We have compared miRNA expression in embryonic stem cell (ESC)-derived trophectoderm and in staged murine embryos to identify a set of candidate miRNAs likely to be involved in trophectoderm specification. Results: We profiled embryonic stem cells (ESCs) as they were induced to differentiate into trophectodermal cells by ectopic expression of HRas/Q61L. We also profiled murine embryos at progressive stages of preimplantation development (zygote, 2-cell, 4-cell, 8-cell, morula, and blastocyst), which includes the time window in which the trophectoderm is specified in vivo. Q61L/H Conclusions: We describe miRNA expression changes that occur during trophectoderm specification and validate that our in vitro system faithfully recapitulates trophectoderm specification in vivo. By comparing our in vitro and in vivo datasets, we have identified a minimal set of candidate miRNAs likely to play a role in trophectoderm specification. These miRNAs are predicted to regulate a host of development-associated target genes, and many of these miRNAs have previously reported roles in development and differentiation. Additionally, we highlight a number of miRNAs whose tight developmental regulation may reflect a functional role in other stages of embryogenesis. Our embryo profiling data may be useful to investigators studying trophectoderm specification and other stages of preimplantation development.
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页数:10
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