Pre-rRNAs control mitosis by maintaining chromosomal segregation through protecting SMC2 from AURKA-mediated phosphorylation
In interphase, 47S pre-rRNA is transcribed by RNA polymerase I (Pol I) and processed to form intermediate pre-rRNAs and finally produce mature rRNAs in the nucleolus. During mitosis, nucleolus disassembles and pre-rRNAs including 45S, 30S and 32S pre-rRNAs relocate in the peri-chromosomal region (PR). Inhibition of pre-rRNA transcription impairs chromosome dispersion in prometaphase. However, how pre-rRNAs regulate mitosis remains elusive. Here, we unravel a novel mechanism for pre-rRNAs to control mitosis. Inhibition of Pol I prolongs the mitotic process and induces defective chromosomal segregation, resulting in mitotic catastrophe. We isolated chromosome and determined the chromosome-binding proteins by mass-spectrometry. Using quantitative proteomics analysis, immunoprecipitation and immunofluorescent staining, we found that AURKA approaches chromosome when Pol I is inhibited. The AURKA-binding proteins on the chromosome were determined by immunoprecipitation and mass-spectrometry after cells were treated with Act D, BMH-21 or CX5461, respectively, and the chromosomal segregation controlling proteins were selected. When Pol I was inhibited, the binding of AURKA with SMC2, the crucial component of Condensin, is significantly enhanced. Importantly, SMC2 is phosphorylated by AURKA only when Pol I was inhibited. Alignment of SMC2 amino acid sequence with substrates of AURKA shows that SMC2 possesses the consensus R/K/N-R-X-S/T-B, and T574 is the only potential AURKA-catalyzed phosphorylation site. Indeed, SMC2 T574 is phosphorylated by AURKA in cell and in vitro. Thereafter, we generated SMC2 T574-P specific antibody, and confirmed that endogenous SMC2 T574 is phosphorylated by AURKA in mitosis in the absence of pre-rRNAs. Consequently, phosphorylation of SMC2 T574 disrupts the SMC2/SMC4 binding and the binding of SMC2 and SMC4 to chromosomal DNA, leading to chromosomal segregation defect. The phosphorylation deficient Flag-SMC2 T574A reverses the mitotic catastrophe caused by Pol I inhibition. Collectively, we demonstrate that pre-rRNAs protect SMC2 from the AURKA-mediated phosphorylation to maintain normal mitosis.
Authors
- Zhuochen Zhao (ORCID: https://orcid.org/0000-0001-9187-0199)
- Baocai Xing (ORCID: https://orcid.org/0000-0002-7527-4650)
- Xiaojuan Du (ORCID: https://orcid.org/0000-0002-0108-511X)
- Shiqi Sun (ORCID: https://orcid.org/0009-0009-7257-7996)
- Yang Jiang (ORCID: https://orcid.org/0000-0001-9066-9418)
- Kunqi Su (ORCID: https://orcid.org/0000-0003-3086-4312)
- Yang Hu (ORCID: https://orcid.org/0000-0002-7980-1649)
- Changjiang Wang (ORCID: https://orcid.org/0000-0002-0425-7976)
- Chunfeng Zhang (ORCID: https://orcid.org/0000-0002-0402-2683)
- Yuying Wang (ORCID: https://orcid.org/0009-0003-3740-8472)
Institutions
- Peking University (CN)
- Ministry of Education (ET)
Publication Details
- Journal
- Cell Death and Disease
- Published
- 2025-11-07
- DOI
- https://doi.org/10.1038/s41419-025-08169-9
- Primary Topic
- Genomics and Chromatin Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China