Editorial on “PNLDC1 is essential for piRNA 3' end trimming and transposon silencing during spermatogenesis in mice”
Editorial

Editorial on “PNLDC1 is essential for piRNA 3' end trimming and transposon silencing during spermatogenesis in mice”

Zachary T. Dye, Paul W. Dyce

Department of Animal Sciences, College of Agriculture, Auburn University, Auburn, AL, USA

Correspondence to: Paul W. Dyce. Auburn University, CASIC Building, 559 Devall Drive, Auburn, AL 36849, USA. Email: pwd0003@auburn.edu.

Provenance: This is an invited Editorial commissioned by the Section Editor Dr. Weijun Jiang (Nanjing Normal University, Department of Reproductive and Genetics, Institute of Laboratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China).

Comment on: Ding D, Liu J, Dong K, et al. PNLDC1 is essential for piRNA 3' end trimming and transposon silencing during spermatogenesis in mice. Nat Commun 2017;8:819.


Submitted Jul 06, 2018. Accepted for publication Jul 31, 2018.

doi: 10.21037/tcr.2018.07.26


Piwi-interacting RNA (piRNA) are a class of small non-coding RNAs expressed in the germline. These piRNAs are processed to a mature piRNA by endonucleases and exonucleases that are bound to PIWI family proteins (1-3). In mouse, three Piwi proteins have been shown to be critical for spermatogenesis, namely Miwi, Mili and Miwi2 (4-6). Mili and Miwi show different temporal expression during testes development. Mili is expressed earlier until the pachytene stage of meiosis, and Miwi is expressed from pachytene until the haploid round spermatid stage. Disruption of the genes encoding Mili and Miwi results in sterile males due to spermatogenesis arresting at the pachytene stage, resulting from a failure of piRNA retrotransposon silencing (5-11). Transposon silencing within the germline requires the correct processing of piRNA. Immature piRNA requires 3'-5' trimming to generate mature piRNAs (12-14). A protein related to the poly(A)-specific ribonuclease (PARN) family, poly(A)-specific ribonuclease-like domain containing 1 (PNLDC1), has been recognized as an enzyme “trimmer” for pre-piRNA 3' end trimming and maturation processing in silkworms (14). PNLDC1 has also been found to be expressed in mammalian species including mouse and human (15). The potential role of PNLDC1 in mammals was unclear until recent reports have implicated it in piRNA processing in mice during spermatogenesis (16-18).

The expression pattern of Pnldc1 has been specifically found in the testis tissue of mice (18). Furthermore, the expression is higher in spermatogonial stem cells compared to that in pachytene spermatocytes and round spermatids (18). Ding et al. utilized CRISPR-Cas9 genome editing to generate Pnldc1-deficient mice in order to investigate the potential role of PNLDC1 in piRNA processing and subsequent spermatogenesis (16). Five male Pnldc1Mut mice were examined that all had distinct mutations on Pnldc1 alleles. All were viable and grew normally but had 30% smaller testes compared to the control mice by weight. Pnldc1Mut mice also lacked normal spermatozoa and germ cell numbers were drastically reduced (16). Male mice that were Pnldc knockout mice also displayed similar spermiogenic arrest as was observed in the Pnldc1Mut males. Independently also using CRISPR-Cas9 Nishimura et al. produced Pnldc1 mutant mice. Adult Pnldc1Mut males had testis that were approximately half the size of age matched wildtype mice (17). Similarly they found Pnldc1Mut mice were not able to produce mature sperm. Finally, a third study also found Pnldc1 knockout mice were unable to produce mature sperm and had significantly smaller testes (18). In all case defects were seen in both meiosis and spermiogenesis, supporting that Pnldc1 plays an important role in these processes.

Long interspersed nuclear element 1 (LINE1) is the dominant transposable element in the DNA of placental mammals including mice. Ding et al. utilized LINE1 messenger RNA (mRNA) expression to determine the ability of the piRNA pathway to silence transposons. LINE1 was measured in adult Pnldc1Mut testes to examine possible roles of Pnldc1 in transposon silencing. Significant elevation in LINE1 mRNA expression was observed in Pnldc1Mut spermatocytes. Western blot results also revealed increased LINE1 protein levels in Pnldc1Mut testes. This is consistent with the findings of that LINE1 protein was increased at postnatal day 14 in PnldcMut mouse testes (17). Similarly, Zhang et al. found a significant increase in LINE1 mRNA and protein in Pnldc knockout mice testes from postnatal day 18 increasing to day 60 (18). These results indicate, in mammals, that PNLDC1 is required to correctly repress transposons in male germ cells.

The size and quantity of the small RNA populations in adult wild-type and Pnldc1Mut testes were compared to explore the role of PNLDC1 in piRNA maturation. In wild-type mice the piRNA population found to be ~30 nt in length. Interestingly, in Pnldc1Mut testes a longer small RNA population of 30–40 nt was observed. Further support is provided by Nishimura et al. who utilized deep sequencing to analyze the size distribution of small RNAs (17). They found the majority of small RNAs were 24–31 nt in control mice whereas they were distributed from 24–50 nt in the mutant embryonic testes (17). Furthermore, these findings were independently verified in a study by Zhang et al. who found a reduction in the population of 24–32 nt small RNAs and an increase in the small RNAs >30 nt, in the Pnldc1 knockout mice (18). This indicated a role for PNLDC1 in the production of mature piRNAs and the facilitation of pre-piRNA processing.

Genome mapping of the small RNA libraries for wild-type and Pnldc1Mut mice was done to examine the extended piRNA species. The first nucleotide composition was measured specifically in the Pnldc1Mut pre-piRNAs, and piRNAs from both 24–32 and 33–40 nt reads had a U bias. This suggested the 3' end was incorrectly processed in the Pnldc1Mut species. To test this, 5' end match analysis was performed on piRNA from wild-type testes and Pnldc1Mut testes. It was found that while the 5' ends had similar nucleotides in the wild-type and Pnldc1Mut piRNAs, the 3' end was variable. This strongly supports a role for PNLDC1 in pre-piRNA 3' end trimming. It is important to note that two other studies arrived at the same conclusion, namely that PNLDC1 is required for the correct 3' processing of piRNAs (17,18).

To explore the pachytene piRNA precursor cleavage mechanism, untrimmed pachytene pre-piRNAs in Pnldc1Mut mice were analyzed by genomic mapping (16). Wild-type and Pnldc1Mut small RNA libraries were mapped using 24–48 nt reads. They were also analyzed at the 5' and 3' end sequences from mapped piRNAs. It was found that U residues are enriched in the first position downstream of the 3' end in the Pnldc1Mut piRNA. This is a signature of phased piRNA processing and is known to be linked to the production of phased pre-pachytene piRNAs. This phased pachytene piRNA biogenesis was confirmed by further coupling analysis. The piRNA 5' ends in wild-type mice were distributed randomly around the upstream piRNA 3' ends, however, in untrimmed Pnldc1Mut pre-piRNAs, the 5' ends were enriched immediately downstream of the piRNA 3' ends. These results suggest a single cleavage event generates the 3' end of one piRNA and the 5' end of the next downstream piRNA. This supports phased biogenesis of piRNA contributing to mammalian pachytene piRNA production.

Neonatal Pnldc1 heterozygous and Pnldc1 homozygous knockout mutant mice were analyzed to investigate PNLDC1’s role in pre-pachytene piRNA production. Both MIWI and MILI mislocalization was observed in knockout mice with expression in large perinuclear granules consisting of clustered mitochondria (16). However, while the expression level of Mili was similar in the control and mutant testes, the expression of Miwi was significantly decreased in the mutant testes (16). As expected Mili bound Pnldc1 knockout piRNAs had an extended nucleotide length compared to the control, indicating a piRNA trimming defect. Mapping of piRNAs from Pnldc1 knockout testes found 3' end extensions supporting a deficiency in 3' end trimming. LINE1 immunostaining was performed on Pnldc1 knockout germ cells, and no upregulation was observed. These results suggest that PNLDC1-deficient neonatal male germ cells have functional LINE1 silencing but defective piRNA trimming along with incomplete MIWI2 localization. In all three studies it appears that Miwi is more sensitive to PNLDC1 loss when compared to Mili (16-18). Due to Mili being expressed prior to Miwi it is possible that it facilitates piRNA processing for interaction with Miwi and the loss of PNLDC1 destabilizes this process.

The intercellular activities of PNLDC1 remain largely undefined. It has been proposed to play a role in the maintenance of multipotency, genome surveillance, and re-programming in early development (15). Recently, PNLDC1 was reported to provide the elusive 3' pre-piRNA trimming activities in B. mori, C. elegans, and silkworm (14,15). In recent reports using PNLDC1 mutant mice, three independent studies have confirmed a role in piRNA processing for PNLDC1 (16-18). It has shown to be critical for the correct meiosis and spermiogenesis in mice. It was demonstrated that PNLDC1 is required for the 3' end maturation of piRNAs. This results in a failure to silence the LINE1 transposon and male sterility. It is important to note that female Pnldc1 mutants display apparent normal fertility. These recent results provide new insights into the critical functions of piRNA in both meiosis and spermatogenesis.


Acknowledgements

Lab funding is provided from the Alabama Cattlemen’s Association and the Alabama Agricultural Experiment Station and Hatch program of the National Institute of Food and Agriculture, U.S. Department of Agriculture.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


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Cite this article as: Dye ZT, Dyce PW. Editorial on “PNLDC1 is essential for piRNA 3' end trimming and transposon silencing during spermatogenesis in mice”. Transl Cancer Res 2018;7(Suppl 7):S755-S757. doi: 10.21037/tcr.2018.07.26