The abundance of a transfer RNA-derived RNA fragment small RNA subpopulation is enriched in cauda spermatozoa

ExRNA

Matthew D. Dun¹  Kate Hutcheon²  Andrew L. Eamens³  Ilana R. Bernstein³  Brett Nixon³  Amanda L. Anderson³  Simone J. Stanger³ 

[1] Cancer Signalling Research Group, Medical Biochemistry, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, The University of Newcastle, 2308, Callaghan, New South Wales, Australia;Priority Research Centre for Cancer Research, Innovation and Translation, Faculty of Health and Medicine, Hunter Medical Research Institute, 2305, New Lambton, New South Wales, Australia;Perth Children’s Hospital, 6009, Nedlands, Western Australia, Australia;Priority Research Centre for Reproduction Science, School of Environmental and Life Sciences, The University of Newcastle, 2308, Callaghan, New South Wales, Australia;

关键词: Mouse epididymis;    Caput;    Corpus and cauda epididymis;    Spermatozoa;    sRNA abundance;    tRF subpopulation enrichment;    sRNA sequencing;    RT-qPCR;    ANGIOGENIN;    Immunoblotting;   

DOI  :  10.1186/s41544-020-00058-x

来源: Springer

【 摘 要 】

The small RNA (sRNA) landscape of mammalian spermatozoa is considerably altered as these gametic cells migrate through the segment specific microenvironments of the epididymis. More specifically, the microRNA (miRNA) species of sRNA dominates the sRNA landscape of spermatozoa of the proximal caput segment of the epididymis. However, in sperm cells sourced from the distal cauda epididymal segment, the transfer RNA (tRNA)-derived RNA fragment (tRF) sRNA species is the most abundant. Here we show that the 5′ halves of fifteen mature tRNAs were used as processing substrates for the production of a specific subpopulation of tRF sRNAs, 30 to 33 nucleotides (30–33-nt) in length. A quantitative reverse transcriptase polymerase chain reaction (RT-qPCR) approach was used to experimentally validate the sRNA sequencing identified trend of enriched abundance of this specific 30–33-nt tRF subpopulation in cauda spermatozoa. The length, and exclusive alignment of the cauda spermatozoa enriched tRF subpopulation to the 5′ half of each processed tRNA precursor, identified ANGIOGENIN (ANG) as the endonuclease likely responsible for tRF production in the mouse epididymis: a prediction confirmed via immunoblotting assessment of ANG abundance in spermatozoa sourced from the caput, corpus and cauda epididymal segments. When taken together with our previous profiling of miRNA and Piwi-interacting RNA (piRNA) sRNA abundance in spermatozoa sourced from the three segments of physiologically normal mouse epididymides, the tRF profile reported here adds greater depth of coverage to the global sRNA landscape of the mouse epididymis; a roadmap constructed to assist with the future molecular characterization of sRNA-directed responses to a wide range of imposed environmental stressors.

【 授权许可】

CC BY