Meiotic recombination generates genetic diversity and promotes proper chromosomal segregation of parental chromosomes. This process requires a set of recombinases polymerized on single-stranded (ss)DNAs called the nucleoprotein filament to undergo homology search and strand exchange between homologous DNAs. In Saccharomyces cerevisiae meiosis, programmed DNA double-strand breaks (DSBs) are formed by Spo11 to generate 3’-ssDNA tails. Once formed, ssDNA overhangs are rapidly bound by the abundant high-affinity ssDNA-binding protein, Replication protein A (RPA), to protect these ssDNAs from nucleolytic degradations or formation of the higher-order DNA structures. RPA-coated ssDNA substrates are distinct from bare ssDNA substrates due to RPA’s high affinity for ssDNA; therefore, recombination mediator Mei5-Sae3 protein complex is required for the binding of recombinases onto RPA-coated ssDNA. However, the mechanistic role of Mei5-Sae3 in mediating Dmc1 activity remains unclear.
To investigate how Mei5-Sae3 stimulates Dmc1 to displace RPA and form nucleoprotein filaments, the research team consists of NTU chemistry, NTU IBS, and Osaka University utilizes Biochemical protein purification techniques, and single-molecule FRET and Colocalization Single-Molecule Spectroscopy (CoSMoS) techniques to real-time capture the binding of Dmc1 and dissociation of RPA on individual DNA with exceptional time resolution. Unlike traditional biological approaches, which mostly look at the final equilibrium products of the ensemble reactions, single-molecule methods could elucidate the contributions of individual biochemical steps from individual molecules, uncovering transient intermediate states that could give insights into how the reaction progresses.
The result showed that Mei5-Sae3 stabilized Dmc1 nucleating clusters with 2-3 molecules on naked DNA by preferentially reducing Dmc1 dissociation rates. Mei5-Sae3 also stimulated Dmc1 assembly on RPA-coated DNA. Using GFP-labelled RPA, the co-existence of an intermediate with Dmc1 and RPA on ssDNA was observed before RPA dissociation. Moreover, the displacement efficiency of RPA depended on Dmc1 concentration, and its dependence was positively correlated to the stability of Dmc1 clusters on short ssDNA. These findings suggest a molecular model that Mei5-Sae3 mediates Dmc1 binding on RPA-coated ssDNA by stabilizing Dmc1 nucleating clusters, thereby influencing RPA dynamics on DNA to promote RPA dissociation. This research contributes to the first ever reported detailed molecular model for this unique mediator protein Mei5-Sae3, elucidating how a mediator-recombinase interaction can stimulate recombinase assembly on RPA-coated ssDNA.
p at NTU Chemistry. The other co-first author, Dr. Hao-Yen Chang, is a joint postdoctoral fellow from Prof. Peter Chi’s (NTU IBS) and Prof. Li’s group. Other contributing authors are Chia-Hua Lu, Chih-Chun Chang, and the Japanese team Asako Furukohri and Stephen Mwaniki from Professor Akira Shinohara lab at Osaka University. This research is supported by NSTC, NTU, and Osaka University.
Full article: https://doi.org/10.1093/nar/gkae780 (Nucleic Acids Research 2024)
Hung-Wen Li (NTU Chemistry): https://www.ch.ntu.edu.tw/hwli.html
Peter Chi (NTU IBS): https://ibs.ntu.edu.tw/home.jsp
Akira Shinohara (Osaka Univ., IPR): https://www.protein.osaka-u.ac.jp
Figure 1-Model of Mei5-Sae3 accessory complex stimulating Dmc1 assembly on RPA-coated DNA
Figure 2-Team photo. Front row (from left) Hung-Wen Li, Miki Shinohara, Akira Shinohara, and Peter Chi. Back row (from left) Qiao-Hong Zhang, Chin-Dian Wei, and Hao-Yen Chang.