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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Differential expression of microRNAs in porcine placentas on Days 30 and 90 of gestation

Lijie Su A , Shuhong Zhao A , Mengjin Zhu A and Mei Yu A B
+ Author Affiliations
- Author Affiliations

A Key Lab of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education, Huazhong (Central China) Agricultural University, Wuhan, 430070, Hubei, PR China.

B Corresponding author. Email: yumei@mail.hzau.edu.cn

Reproduction, Fertility and Development 22(8) 1175-1182 https://doi.org/10.1071/RD10046
Submitted: 9 March 2010  Accepted: 7 April 2010   Published: 1 October 2010

Abstract

The porcine placenta is classified as a non-invasive epitheliochorial type. To meet the increasing demands for nutrients by the rapidly growing conceptus and/or fetus, the placental microscopic folds undergo significant morphological and biochemical changes during two periods critical for conceptus and/or fetus, namely Days 30–40 and after Day 90 of gestation. MicroRNAs (miRNAs) are a class of small non-coding RNAs that can modulate gene activity by inhibiting the translation or regulation of mRNA degradation. In the present study, we identified 17 differentially expressed miRNAs in porcine placenta on Days 30 and 90 of gestation using a locked nucleic acid (LNA) microRNA array. Stem–loop real-time reverse transcription–polymerase chain reaction confirmed the differential expression of eight selected miRNAs (miR-24, miR-125b, miR-92b, miR-106a, miR-17, let-7i, miR-27a and miR-20). Analysis of targets and the pathways in which these miRNAs are involved revealed that the differentially expressed miRNAs target many genes that are important in various processes, including cell growth, trophoblast differentiation, angiogenesis and formation and maintenance of adherens junctions. The results of the present study suggest potential roles for these differentially expressed miRNAs in porcine placental growth and function.

Additional keywords: epitheliochorial placenta, microarray, miRNAs, pig, target gene.


Acknowledgements

This research was supported by the National High Science and Technology Foundation of China ‘863’ (2007AA10Z148), National Natural Science Foundation of China (30771537), the Program for New Century Excellent Talents in University (NCET-08–0784) and Excellent Youth Foundation of Hubei Scientific Committee (2008CDB106). The authors thank Dr Quanyong Zhou, Yi Li and Xue Bai for sample collection and preparation.


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