RNase H1 facilitates recombinase recruitment by degrading DNA–RNA hybrids during meiosis
Chao Liu, Liying Wang, Yanan Li, Mengmeng Guo, Jun Hu, Teng Wang, Mengjing Li, Zhuo Yang, Ruoyao Lin, Wei Xu, Yinghong Chen, Mengcheng Luo, Fei Gao, Jiayu Chen, Qianwen Sun, Hongbin Liu, Bo Sun, Wei Li
Abstract
DNA-RNA hybrids play various roles in many physiological progresses, but how this chromatin structure is dynamically regulated during spermatogenesis remains largely unknown. Here, we show that germ cell-specific knockout of Rnaseh1, a specialized enzyme that degrades the RNA within DNA-RNA hybrids, impairs spermatogenesis and causes male infertility. Notably, Rnaseh1 knockout results in incomplete DNA repair and meiotic prophase I arrest. These defects arise from the altered RAD51 and DMC1 recruitment in zygotene spermatocytes. Furthermore, single-molecule experiments show that RNase H1 promotes recombinase recruitment to DNA by degrading RNA within DNA-RNA hybrids and allows nucleoprotein filaments formation. Overall, we uncover a function of RNase H1 in meiotic recombination, during which it processes DNA-RNA hybrids and facilitates recombinase recruitment.