Human RNase MRP is a ribonucleoprotein (RNP) enzyme that processes precursor rRNA (pre-rRNA) at ITS1 site 2 and may have additional activities. It is an endonuclease related to RNase P, which processes pre-tRNAs and pre-tRNA-like substrates. In Saccharomyces cerevisiae, these two RNPs utilize distinct catalytic RNAs with eight shared and one or two specific protein subunits. However, the human RNase MRP-specific protein subunits remain unidentified. Our genome-wide forward genetic screening identifies two poorly characterized human genes, which we name ribonuclease MRP subunit P24 (RMP24) and RMP64. We show that Rmp24 and Rmp64 are required for pre-rRNA ITS1 site 2 processing and associate with MRP RNA but are not required for RNase P activity and do not associate with RNase P-specific H1 RNA. Despite limited sequence homology, Rmp24 and Rmp64 exhibit predicted structural similarities to two RNase MRP-specific components in S. cerevisiae. Collectively, our functional screening and validation reveal two protein components unique to human nuclear RNase MRP.
Identification of RMP24 and RMP64, human ribonuclease MRP-specific protein components.
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作者:Che Rui, Mirani Bhoomi, Panah Monireh, Chen Xiaotong, Luo Hong, Alexandrov Andrei
| 期刊: | Cell Reports | 影响因子: | 6.900 |
| 时间: | 2025 | 起止号: | 2025 Jun 24; 44(6):115752 |
| doi: | 10.1016/j.celrep.2025.115752 | ||
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