Identification of microRNAs Derived from Transposable Elements in the Macaca mulatta (Rhesus Monkey) Genome

Author:

Park Eun Gyung12ORCID,Lee Yun Ju12,Huh Jae-Won34,Park Sang-Je3,Imai Hiroo5ORCID,Kim Woo Ryung12,Lee Du Hyeong12,Kim Jung-min12,Shin Hae Jin12,Kim Heui-Soo26

Affiliation:

1. Department of Integrated Biological Sciences, Pusan National University, Busan 46241, Republic of Korea

2. Institute of Systems Biology, Pusan National University, Busan 46241, Republic of Korea

3. National Primate Research Center, Korea Research Institute of Bioscience and Biotechnology, Cheongju 28116, Republic of Korea

4. Department of Functional Genomics, KRIBB School of Bioscience, Korea University of Science and Technology (UST), Daejeon 34113, Republic of Korea

5. Molecular Biology Section, Center for the Evolutionary Origins of Human Behavior, Kyoto University, Inuyama, Aichi 484-8506, Japan

6. Department of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 46241, Republic of Korea

Abstract

Transposable elements (TEs) are mobile DNA entities that can move within the host genome. Over long periods of evolutionary time, TEs are typically silenced via the accumulation of mutations in the genome, ultimately resulting in their immobilization. However, they still play an important role in the host genome by acting as regulatory elements. They influence host transcription in various ways, one of which as the origin of the generation of microRNAs (miRNAs), which are so-called miRNAs derived from TEs (MDTEs). miRNAs are small non-coding RNAs that are involved in many biological processes by regulating gene expression at the post-transcriptional level. Here, we identified MDTEs in the Macaca mulatta (rhesus monkey) genome, which is phylogenetically close species to humans, based on the genome coordinates of miRNAs and TEs. The expression of 5 out of 17 MDTEs that were exclusively registered in M. mulatta from the miRBase database (v22) was examined via quantitative polymerase chain reaction (qPCR). Moreover, Gene Ontology analysis was performed to examine the functional implications of the putative target genes of the five MDTEs.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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