期刊
MICROORGANISMS
卷 10, 期 7, 页码 -出版社
MDPI
DOI: 10.3390/microorganisms10071419
关键词
Plasmodium falciparum; malaria; histone methylation; polyamine biosynthesis; SAMS; SAM; interactome; transcriptional regulation; proteasome; drug target
类别
资金
- Deutsche Forschungsgemeinschaft [PR905/19-1, TE599/9-1]
- DFG [SPP 2225, PR905/20-1, NG170/1-1]
- German Academic Exchange Service (DAAD)
S-adenosylmethionine synthetase (SAMS) is a crucial enzyme involved in the synthesis of S-adenosyl methionine (SAM), which plays important roles in cellular processes and may serve as a drug target in the malaria parasite.
S-adenosylmethionine synthetase (SAMS) is a key enzyme for the synthesis of the lone methyl donor S-adenosyl methionine (SAM), which is involved in transmethylation reactions and hence required for cellular processes such as DNA, RNA, and histone methylation, but also polyamine biosynthesis and proteostasis. In the human malaria parasite Plasmodium falciparum, PfSAMS is encoded by a single gene and has been suggested to be crucial for malaria pathogenesis and transmission; however, to date, PfSAMS has not been fully characterized. To gain deeper insight into the function of PfSAMS, we generated a conditional gene knockdown (KD) using the glmS ribozyme system. We show that PfSAMS localizes to the cytoplasm and the nucleus of blood-stage parasites. PfSAMS-KD results in reduced histone methylation and leads to impaired intraerythrocytic growth and gametocyte development. To further determine the interaction network of PfSAMS, we performed a proximity-dependent biotin identification analysis. We identified a complex network of 1114 proteins involved in biological processes such as cell cycle control and DNA replication, or transcription, but also in phosphatidylcholine and polyamine biosynthesis and proteasome regulation. Our findings highlight the diverse roles of PfSAMS during intraerythrocytic growth and sexual stage development and emphasize that PfSAMS is a potential drug target.
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