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BMC Genomics. 2018 Aug 6;19(1):590. doi: 10.1186/s12864-018-4954-9.

Small RNA-seq analysis of single porcine blastocysts revealed that maternal estradiol-17beta exposure does not affect miRNA isoform (isomiR) expression.

Author information

1
ETH Zurich, Animal Physiology, Institute of Agricultural Sciences, Zurich, Switzerland.
2
Physiology Weihenstephan, Technische Universität München, Freising, Germany.
3
Institute of Molecular Life Sciences and SIB Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.
4
University of Zurich, Genetics and Functional Genomics, Clinic for Animal Reproduction Medicine, Zurich, Switzerland.
5
ETH Zurich, Animal Physiology, Institute of Agricultural Sciences, Zurich, Switzerland. susanne.ulbrich@usys.ethz.ch.

Abstract

BACKGROUND:

The expression of microRNAs (miRNAs) is essential for the proper development of the mammalian embryo. A maternal exposure to endocrine disrupting chemicals during preimplantation bears the potential for transgenerational inheritance of disease through the epigenetic perturbation of the developing embryo. A comprehensive assembly of embryo-specific miRNAs and respective isoforms (isomiR) is lacking to date. We aimed at revealing the sex-specific miRNA expression profile of single porcine blastocysts developing in gilts orally exposed to exogenous estradiol-17 (E2). Therefore we analyzed the miRNA profile specifically focusing on isomiRs and potentially embryo-specific miRNAs.

RESULTS:

Deep sequencing of small RNA (small RNA-seq) result in the detection of miRNA sequences mapping to known and predicted porcine miRNAs as well as novel miRNAs highly conserved in human and cattle. A set of highly abundant miRNAs and a large number of rarely expressed miRNAs were identified by using a small RNA analysis pipeline, which was integrated into a novel Galaxy workflow specifically benefits incompletely annotated species. In particular, orthologue species information increased the total number of annotated miRNAs, while mapping to other non-coding RNAs avoided falsely annotated miRNAs. Neither the low nor the high dose of E2 treatment (10 and 1000 µ E2/kg body weight daily, respectively) affected the miRNA profile in blastocysts despite the distinct differential mRNA expression and DNA methylation found in previous studies. The high number of generated sequence reads enabled a comprehensive analysis of the isomiR repertoire showing various templated and non-templated modifications. Furthermore, potentially blastocyst-specific miRNAs were identified.

CONCLUSIONS:

In pre-implantation embryos, numerous distinct isomiRs were discovered indicating a high complexity of miRNA expression. Neither the sex of the embryo nor a maternal E2 exposure affected the miRNA expression profile of developing porcine blastocysts. The adaptation to the continuous duration of the E2 treatment might explain the lack of an effect.

KEYWORDS:

Estradiol treatment; Pig embryos; Small RNA-seq; isomiRs; miRNAs

PMID:
30081835
PMCID:
PMC6090871
DOI:
10.1186/s12864-018-4954-9
[Indexed for MEDLINE]
Free PMC Article

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