4.5 Article

Meiosis-specific cohesin complexes display essential and distinct roles in mitotic embryonic stem cell chromosomes

期刊

GENOME BIOLOGY
卷 23, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-022-02632-y

关键词

Meiosis; Mitosis; Embryonic stem cell; Cohesin; Chromosome

资金

  1. National Research Foundation of Korea - Ministry of Science, ICT & Future Planning [2020R1A2C2011887, 2018R1A5A1025077]
  2. BioGreen 21 Program, Rural Development Administration, Republic of Korea [PJ015708]
  3. National Research Foundation of Korea [2020R1A2C2011887] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The study reveals the functional roles of meiosis-specific cohesin complexes in mitotic chromosomes and their impact on chromosomal organization and the mitotic program in embryonic stem cells. The delicate balance between mitotic and meiotic cohesins is crucial for maintaining proper chromosome structure and function in ESCs.
Background Cohesin is a chromosome-associated SMC-kleisin complex that mediates sister chromatid cohesion, recombination, and most chromosomal processes during mitosis and meiosis. However, it remains unclear whether meiosis-specific cohesin complexes are functionally active in mitotic chromosomes. Results Through high-resolution 3D-structured illumination microscopy (3D-SIM) and functional analyses, we report multiple biological processes associated with the meiosis-specific cohesin components, alpha-kleisin REC8 and STAG3, and the distinct loss of function of meiotic cohesin during the cell cycle of embryonic stem cells (ESCs). First, we show that STAG3 is required for the efficient localization of REC8 to the nucleus by interacting with REC8. REC8-STAG3-containing cohesin regulates topological properties of chromosomes and maintains sister chromatid cohesion. Second, REC8-cohesin has additional sister chromatid cohesion roles in concert with mitotic RAD21-cohesin on ESC chromosomes. SIM imaging of REC8 and RAD21 co-staining revealed that the two types of alpha-kleisin subunits exhibited distinct loading patterns along ESC chromosomes. Third, knockdown of REC8 or RAD21-cohesin not only leads to higher rates of premature sister chromatid separation and delayed replication fork progression, which can cause proliferation and developmental defects, but also enhances chromosome compaction by hyperloading of retinoblastoma protein-condensin complexes from the prophase onward. Conclusions Our findings indicate that the delicate balance between mitotic and meiotic cohesins may regulate ESC-specific chromosomal organization and the mitotic program.

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