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鉴定合子中新型 AP2 转录因子,该因子在疟原虫配子体发育中起关键作用。

Identification of a novel AP2 transcription factor in zygotes with an essential role in Plasmodium ookinete development.

机构信息

Laboratory of Medical Zoology, Department of Medicine, Mie University.

Department of Molecular Protozoology, Research Institute for Microbial Diseases, Osaka University.

出版信息

PLoS Pathog. 2022 Aug 10;18(8):e1010510. doi: 10.1371/journal.ppat.1010510. eCollection 2022 Aug.

DOI:10.1371/journal.ppat.1010510
PMID:35947628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9394825/
Abstract

The sexual phase of Plasmodium represents a crucial step in malaria transmission, during which these parasites fertilize and form ookinetes to infect mosquitoes. Plasmodium development after fertilization is thought to proceed with female-stored mRNAs until the formation of a retort-form ookinete; thus, transcriptional activity in zygotes has previously been considered quiescent. In this study, we reveal the essential role of transcriptional activity in zygotes by investigating the function of a newly identified AP2 transcription factor, AP2-Z, in P. berghei. ap2-z was previously reported as a female transcriptional regulator gene whose disruption resulted in developmental arrest at the retort stage of ookinetes. In this study, although ap2-z was transcribed in females, we show that it was translationally repressed by the DOZI complex and translated after fertilization with peak expression at the zygote stage. ChIP-seq analysis of AP2-Z shows that it binds on specific DNA motifs, targeting the majority of genes known as an essential component of ookinetes, which largely overlap with the AP2-O targets, as well as genes that are unique among the targets of other sexual transcription factors. The results of this study also indicate the existence of a cascade of transcription factors, beginning with AP2-G, that proceeds from gametocytogenesis to ookinete formation.

摘要

疟原虫的有性阶段代表了疟疾传播的关键步骤,在此期间,这些寄生虫受精并形成卵囊以感染蚊子。受精后疟原虫的发育被认为是利用雌性储存的 mRNA 进行的,直到形成扭曲状卵囊;因此,以前认为合子中的转录活性是静止的。在这项研究中,我们通过研究新鉴定的 AP2 转录因子 AP2-Z 在 P. berghei 中的功能,揭示了合子中转录活性的重要作用。ap2-z 先前被报道为一个雌性转录调控基因,其缺失导致卵囊的扭曲阶段发育停滞。在这项研究中,尽管 ap2-z 在雌性中被转录,但我们表明它被 DOZI 复合物翻译抑制,并在受精后翻译,在合子阶段表达达到峰值。AP2-Z 的 ChIP-seq 分析表明,它与特定的 DNA 基序结合,靶向大多数已知的卵囊的必需成分的基因,这些基因与 AP2-O 的靶基因大部分重叠,也与其他性转录因子靶基因中的独特基因重叠。这项研究的结果还表明存在一个转录因子级联,从配子体发生开始,一直到卵囊形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/d48ad210ed84/ppat.1010510.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/517a3e8a18f6/ppat.1010510.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/fc07c7a139c2/ppat.1010510.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/e163a24411d3/ppat.1010510.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/a5774f68bec3/ppat.1010510.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/6c735ddf5b2c/ppat.1010510.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/1558d0712bc0/ppat.1010510.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/539e0389055c/ppat.1010510.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/23d6460c955a/ppat.1010510.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/601c64933e48/ppat.1010510.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/d48ad210ed84/ppat.1010510.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/517a3e8a18f6/ppat.1010510.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/fc07c7a139c2/ppat.1010510.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/e163a24411d3/ppat.1010510.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/a5774f68bec3/ppat.1010510.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/6c735ddf5b2c/ppat.1010510.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/1558d0712bc0/ppat.1010510.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/539e0389055c/ppat.1010510.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/23d6460c955a/ppat.1010510.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/601c64933e48/ppat.1010510.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e505/9394825/d48ad210ed84/ppat.1010510.g010.jpg

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