Life Science Research Laboratories, Wako Pure Chemical Industries Ltd., Hyogo, Japan.
Biosci Trends. 2012 Oct;6(5):248-61. doi: 10.5582/bst.2012.v6.5.248.
MIWI is one of the PIWI subfamily of proteins mainly expressed in mouse germ cells, and associates with pachytene piRNAs. MIWI has been thought to play an essential role in spermatogenesis and spermiogenesis via biogenesis and/or stability of pachytene piRNAs, retrotransposon silencing, and post-transcriptional regulation of target mRNAs. However, MIWI's detailed role and function are not well understood. In this study, we produced an anti-MIWI mouse monoclonal antibody and identified MIWI-associated poly(A) RNAs by immunoprecipitation from adult mouse testes lysates. Approximately 70% of the MIWI-associated poly(A) RNAs were known mRNAs and 30% of them were unknown non-coding RNAs. These poly(A) RNAs contained piRNA-encoding RNAs transcribed from piRNA cluster regions and piRNA-encoding mRNA, such as Aym1 mRNA. Mature piRNAs specifically encoded in these piRNA-encoding RNAs were generated in pachytene spermatocytes and not detected in Miwi-deficient (Miwi-/-) testes. Moreover, MIWI associated with a large number of known mRNAs whose expression levels were increased in pachytene spermatocytes, and the expression of these mRNAs was decreased in Miwi-/- testes at 20 days postpartum when pachytene spermatocytes were most abundant. These results strongly suggest that MIWI is involved in pachytene piRNA biogenesis and the positive regulation of target mRNA metabolism in pachytene spermatocytes via association with pachytene piRNA precursors and target mRNAs.
MIWI 是 PIWI 蛋白家族的一个亚家族,主要在小鼠生殖细胞中表达,与粗线期 piRNA 相关。MIWI 被认为通过调控粗线期 piRNA 的生物发生和/或稳定性、反转录转座子沉默以及靶 mRNA 的转录后调控,在精子发生和精子形成中发挥重要作用。然而,MIWI 的详细作用和功能尚不清楚。在本研究中,我们制备了抗 MIWI 的小鼠单克隆抗体,并通过从成年小鼠睾丸裂解物中进行免疫沉淀,鉴定出与 MIWI 相关的 poly(A) RNA。大约 70%的 MIWI 相关 poly(A) RNA 是已知的 mRNAs,30%是未知的非编码 RNA。这些 poly(A) RNA 包含从 piRNA 簇区域转录而来的 piRNA 编码 RNA 和 piRNA 编码 mRNA,如 Aym1 mRNA。这些 piRNA 编码 RNA 特异性编码的成熟 piRNA 仅在粗线期精母细胞中产生,而在 Miwi 缺失(Miwi-/-)的睾丸中未检测到。此外,MIWI 与大量已知的 mRNAs 相关,这些 mRNAs 在粗线期精母细胞中的表达水平增加,而在产后 20 天(此时粗线期精母细胞最为丰富)的 Miwi-/-睾丸中,这些 mRNAs 的表达水平降低。这些结果强烈表明,MIWI 通过与粗线期 piRNA 前体和靶 mRNA 结合,参与粗线期 piRNA 的生物发生以及靶 mRNA 代谢的正向调控。