5-methylcytosine modification by<i>Plasmodium</i>NSUN2 stabilizes mRNA and mediates the development of gametocytes
Abstract 5-methylcytosine (m5C) is an important epitranscriptomic modification involved in mRNA stability and translation efficiency in various biological processes. However, it remains unclear if m5C modification contributes to the dynamic regulation of the transcriptome during the developmental cycles ofPlasmodiumparasites. Here, we characterize the landscape of m5C mRNA modifications at single nucleotide resolution in the asexual replication stages and gametocyte sexual stages of rodent (P. yoelii) and human (P. falciparum) malaria parasites. While different representations of m5C-modified mRNAs are associated with the different stages, the abundance of the m5C marker is strikingly enhanced in the transcriptomes of gametocytes. Our results show that m5C modifications confer stability to thePlasmodiumtranscripts and that aPlasmodiumortholog of NSUN2 is a major mRNA m5C methyltransferase in malaria parasites. Upon knock-out ofP. yoelii nsun2(pynsun2), marked reductions of m5C modification were observed in a panel of gametocytogenesis-associated transcripts. These reductions correlated with impaired gametocyte production in rodent and human malaria parasites. Restoration of thensun2gene in the knock-out parasites rescued the gametocyte production phenotype as well as m5C modification of the gametocytogenesis-associated transcripts. Together with the mRNA m5C profiles for two species ofPlasmodium, our findings demonstrate a major role for NSUN2-mediated m5C modifications in mRNA transcript stability and sexual differentiation in malaria parasites.Significance Modifications of RNA including methylations of cytosine (m5C) and adenosine (m6A) have important roles in RNA metabolism, cellular responses to stress, and biological processes of differentiation and development. Here, we report on the profiles of m5C mRNA modifications in malaria parasites that infect rodents (Plasmodium yoelii) and humans (Plasmodium falciparum). These parasites have genes that encode homologs of human and plant NSUN2 methyltransferases (m5C “writers”). We show that one of these homologs, termed PyNSUN2, stabilizes mRNA transcripts inP. yoeliiand mediates m5C-associated development of the parasite sexual stages (gametocytes). Further research on m5C and other epitranscriptomic modifications may yield new insights into molecular pathways of gametocyte development and mosquito infectivity that can be exploited to interrupt malaria transmission..
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Preprint| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
bioRxiv.org - (2023) vom: 04. Nov. Zur Gesamtaufnahme - year:2023 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Liu, Meng [VerfasserIn] |
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| doi: |
10.1101/2021.06.06.447275 |
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| PPN (Katalog-ID): |
XBI031949568 |
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| 100 | 1 | |a Liu, Meng |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a 5-methylcytosine modification by<i>Plasmodium</i>NSUN2 stabilizes mRNA and mediates the development of gametocytes |
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| 520 | |a Abstract 5-methylcytosine (m5C) is an important epitranscriptomic modification involved in mRNA stability and translation efficiency in various biological processes. However, it remains unclear if m5C modification contributes to the dynamic regulation of the transcriptome during the developmental cycles ofPlasmodiumparasites. Here, we characterize the landscape of m5C mRNA modifications at single nucleotide resolution in the asexual replication stages and gametocyte sexual stages of rodent (P. yoelii) and human (P. falciparum) malaria parasites. While different representations of m5C-modified mRNAs are associated with the different stages, the abundance of the m5C marker is strikingly enhanced in the transcriptomes of gametocytes. Our results show that m5C modifications confer stability to thePlasmodiumtranscripts and that aPlasmodiumortholog of NSUN2 is a major mRNA m5C methyltransferase in malaria parasites. Upon knock-out ofP. yoelii nsun2(pynsun2), marked reductions of m5C modification were observed in a panel of gametocytogenesis-associated transcripts. These reductions correlated with impaired gametocyte production in rodent and human malaria parasites. Restoration of thensun2gene in the knock-out parasites rescued the gametocyte production phenotype as well as m5C modification of the gametocytogenesis-associated transcripts. Together with the mRNA m5C profiles for two species ofPlasmodium, our findings demonstrate a major role for NSUN2-mediated m5C modifications in mRNA transcript stability and sexual differentiation in malaria parasites.Significance Modifications of RNA including methylations of cytosine (m5C) and adenosine (m6A) have important roles in RNA metabolism, cellular responses to stress, and biological processes of differentiation and development. Here, we report on the profiles of m5C mRNA modifications in malaria parasites that infect rodents (Plasmodium yoelii) and humans (Plasmodium falciparum). These parasites have genes that encode homologs of human and plant NSUN2 methyltransferases (m5C “writers”). We show that one of these homologs, termed PyNSUN2, stabilizes mRNA transcripts inP. yoeliiand mediates m5C-associated development of the parasite sexual stages (gametocytes). Further research on m5C and other epitranscriptomic modifications may yield new insights into molecular pathways of gametocyte development and mosquito infectivity that can be exploited to interrupt malaria transmission. | ||
| 650 | 4 | |a Biology |7 (dpeaa)DE-84 | |
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| 700 | 1 | |a Guo, Gangqiang |4 aut | |
| 700 | 1 | |a Qian, Pengge |4 aut | |
| 700 | 1 | |a Mu, Jianbing |0 (orcid)0000-0001-6012-8389 |4 aut | |
| 700 | 1 | |a Lu, Binbin |4 aut | |
| 700 | 1 | |a He, Xiaoqin |4 aut | |
| 700 | 1 | |a Shang, Xiaomin |4 aut | |
| 700 | 1 | |a Yang, Guang |4 aut | |
| 700 | 1 | |a Shen, Shijun |4 aut | |
| 700 | 1 | |a Liu, Wenju |4 aut | |
| 700 | 1 | |a Wang, Liping |4 aut | |
| 700 | 1 | |a Gu, Liang |4 aut | |
| 700 | 1 | |a Mu, Quankai |4 aut | |
| 700 | 1 | |a Yu, Xinyu |4 aut | |
| 700 | 1 | |a Zhao, Yuemeng |4 aut | |
| 700 | 1 | |a Culleton, Richard |4 aut | |
| 700 | 1 | |a Cao, Jun |4 aut | |
| 700 | 1 | |a Jiang, Lubin |4 aut | |
| 700 | 1 | |a Wellems, Thomas E. |0 (orcid)0000-0003-3899-8454 |4 aut | |
| 700 | 1 | |a Yuan, Jing |4 aut | |
| 700 | 1 | |a Jiang, Cizhong |4 aut | |
| 700 | 1 | |a Zhang, Qingfeng |0 (orcid)0000-0002-8759-9102 |4 aut | |
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