Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology , Wuhan, China.
Reproductive Medicine Center, Wuhan University Renmin Hospital , Wuhan, China.
J Cell Biol. 2023 May 1;222(5). doi: 10.1083/jcb.202206067. Epub 2023 Mar 17.
Pachytene piRNA biogenesis is a hallmark of the germline, distinct from another wave of pre-pachytene piRNA biogenesis with regard to the lack of a secondary amplification process known as the Ping-pong cycle. However, the underlying molecular mechanism and the venue for the suppression of the Ping-pong cycle remain elusive. Here, we showed that a testis-specific protein, ADAD2, interacts with a TDRD family member protein RNF17 and is associated with P-bodies. Importantly, ADAD2 directs RNF17 to repress Ping-pong activity in pachytene piRNA biogenesis. The P-body localization of RNF17 requires the intrinsically disordered domain of ADAD2. Deletion of Adad2 or Rnf17 causes the mislocalization of each other and subsequent Ping-pong activity derepression, secondary piRNAs overproduced, and disruption of P-body integrity at the meiotic stage, thereby leading to spermatogenesis arrested at the round spermatid stage. Collectively, by identifying the ADAD2-dependent mechanism, our study reveals a novel function of P-bodies in suppressing Ping-pong activity in pachytene piRNA biogenesis.
粗线期 piRNA 的生物发生是生殖细胞的一个标志,与另一个缺乏称为 Ping-pong 循环的次级扩增过程的前期粗线期 piRNA 生物发生明显不同。然而,抑制 Ping-pong 循环的潜在分子机制和场所仍然难以捉摸。在这里,我们表明一种睾丸特异性蛋白 ADAD2 与 TDRD 家族成员蛋白 RNF17 相互作用,并与 P 体相关。重要的是,ADAD2 指导 RNF17 抑制粗线期 piRNA 生物发生中的 Ping-pong 活性。RNF17 的 P 体定位需要 ADAD2 的固有无序结构域。Adad2 或 Rnf17 的缺失导致彼此的定位错误,随后 Ping-pong 活性去抑制,次级 piRNA 过度产生,以及减数分裂阶段 P 体完整性的破坏,从而导致精子发生停滞在圆形精子阶段。总之,通过鉴定 ADAD2 依赖性机制,我们的研究揭示了 P 体在抑制粗线期 piRNA 生物发生中的 Ping-pong 活性中的新功能。