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鉴定恶性疟原虫红内期的一种新型和独特的转录因子。

Identification of a novel and unique transcription factor in the intraerythrocytic stage of Plasmodium falciparum.

机构信息

Research Institute, National Center for Global Health and Medicine, Shinjuku-ku, Tokyo, Japan.

出版信息

PLoS One. 2013 Sep 5;8(9):e74701. doi: 10.1371/journal.pone.0074701. eCollection 2013.

DOI:10.1371/journal.pone.0074701
PMID:24040327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3764013/
Abstract

The mechanisms of stage-specific gene regulation in the malaria parasite Plasmodium falciparum are largely unclear, with only a small number of specific regulatory transcription factors (AP2 family) having been identified. In particular, the transcription factors that function in the intraerythrocytic stage remain to be elucidated. Previously, as a model case for stage-specific transcription in the P. falciparum intraerythrocytic stage, we analyzed the transcriptional regulation of pf1-cys-prx, a trophozoite/schizont-specific gene, and suggested that some nuclear factors bind specifically to the cis-element of pf1-cys-prx and enhance transcription. In the present study, we purified nuclear factors from parasite nuclear extract by 5 steps of chromatography, and identified a factor termed PREBP. PREBP is not included in the AP2 family, and is a novel protein with four K-homology (KH) domains. The KH domain is known to be found in RNA-binding or single-stranded DNA-binding proteins. PREBP is well conserved in Plasmodium species and partially conserved in phylum Apicomplexa. To evaluate the effects of PREBP overexpression, we used a transient overexpression and luciferase assay combined approach. Overexpression of PREBP markedly enhanced luciferase expression under the control of the pf1-cys-prx cis-element. These results provide the first evidence of a novel transcription factor that activates the gene expression in the malaria parasite intraerythrocytic stage. These findings enhance our understanding of the evolution of specific transcription machinery in Plasmodium and other eukaryotes.

摘要

疟原虫(Plasmodium falciparum)阶段特异性基因调控的机制在很大程度上尚不清楚,仅鉴定出少数特定的调节转录因子(AP2 家族)。特别是,在红内期起作用的转录因子仍有待阐明。以前,作为疟原虫红内期阶段特异性转录的模型案例,我们分析了 pf1-cys-prx 的转录调控,pf1-cys-prx 是一个滋养体/裂殖体特异性基因,表明一些核因子特异性结合 pf1-cys-prx 的顺式元件并增强转录。在本研究中,我们通过 5 步色谱法从寄生虫核提取物中纯化核因子,并鉴定出一种称为 PREBP 的因子。PREBP 不属于 AP2 家族,是一种具有四个 K 同源(KH)结构域的新型蛋白。KH 结构域已知存在于 RNA 结合或单链 DNA 结合蛋白中。PREBP 在疟原虫物种中高度保守,在门顶复动物中部分保守。为了评估 PREBP 过表达的影响,我们采用了瞬时过表达和荧光素酶测定相结合的方法。PREBP 的过表达显着增强了 pf1-cys-prx 顺式元件控制下的荧光素酶表达。这些结果提供了第一个证据,证明了一种新型转录因子可激活疟原虫红内期的基因表达。这些发现增强了我们对疟原虫和其他真核生物中特定转录机制进化的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/c5d82ad26bfa/pone.0074701.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/d2ec3728ece2/pone.0074701.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/c31b686d0384/pone.0074701.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/06ac8efca4ea/pone.0074701.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/91f040be5ef5/pone.0074701.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/42011c595438/pone.0074701.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/c5d82ad26bfa/pone.0074701.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/d2ec3728ece2/pone.0074701.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/c31b686d0384/pone.0074701.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/06ac8efca4ea/pone.0074701.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/91f040be5ef5/pone.0074701.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/42011c595438/pone.0074701.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7491/3764013/c5d82ad26bfa/pone.0074701.g006.jpg

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