确定两个转录因子,它们协调工作,调控恩塔米巴虫的早期发育。

IF 5.1 1区 生物学 Q1 MICROBIOLOGY
mBio Pub Date : 2024-11-14 DOI:10.1128/mbio.02250-24
Daniela Lozano-Amado, Upinder Singh
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引用次数: 0

摘要

原生寄生虫恩塔米巴虫的生命周期在感染性包囊和侵袭性滋养体之间转换。囊变是寄生虫生物学中的一个关键过程,由包括转录控制在内的不同机制控制。我们在侵袭性恩塔莫巴虫中发现了两种核蛋白--EIN_066100和EIN_085620,它们通过与阶段转换最初8小时内上调的基因启动子区域的DNA基序(TCACTTTC)结合来调控寄生虫的发育。过表达MAK16蛋白的同源物EIN_066100会导致阿米巴增殖减少,但不影响包囊效率。EIN_085620是一种具有RNA识别基序(RRM)的蛋白质,它的过量表达可提高包囊的效率。谷胱甘肽 S-转移酶(GST)牵引试验显示,EIN_066100与EIN_085620在体内和体外都有相互作用,这种相互作用是由EIN_085620的RRM结构域介导的。通过评估在EIN_066100的N端或C端缺失的截短蛋白,我们阐明了其N端区域在适当的蛋白定位、增殖、细胞分裂以及与EIN_085620相互作用中的重要性。综上所述,这些结果表明EIN_066100和EIN_085620在调控恩塔米巴虫的发育过程中起着协调作用。重要意义在恩塔莫阿虫的生物学中,一个重要的生物学过程是阶段转换,它在疾病传播中起着至关重要的作用,有利于寄生虫在宿主外存活并传播到新的宿主。阿米巴阶段特异性基因的表达受多种机制控制,如表观遗传和转录控制。鉴定早期转录控制调节因子对于了解阿米巴酵母化级联的启动至关重要。我们发现了两种核蛋白,EIN_066100 和 EIN_085620,它们参与了侵袭伊蚊的增殖和发育调控。这两个蛋白通过直接相互结合发挥作用,并介导了细胞分裂效率。对参与恩塔米巴虫发育的新调节因子的研究是寄生虫生物学一个重要方面的重要进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of two transcription factors that work coordinately to regulate early development in Entamoeba.

The protozoan parasite Entamoeba has a life cycle that switches between infective cysts and invasive trophozoites. Encystation, a crucial process in parasite biology, is controlled by different mechanisms including transcriptional control. We identified two nuclear proteins in Entamoeba invadens, EIN_066100 and EIN_085620, that regulate parasite development by binding to a DNA motif (TCACTTTC) in the promoter regions of genes upregulated in the first 8 h of stage conversion. Overexpression of EIN_066100, a homolog of MAK16 protein, resulted in reduced amoebic proliferation without affecting encystation efficiency. Overexpression of EIN_085620, a protein with an RNA-recognition motif (RRM), led to increased encystation efficiency. Glutathione S-transferase (GST) pull down assays revealed that EIN_066100 interacts with EIN_085620 both in vivo and in vitro, and this interaction is mediated by the EIN_085620 RRM domain. By evaluating truncated proteins with deletions at either the N-terminal or C-terminal regions of EIN_066100, we elucidated the importance of its N-terminal region in proper protein localization, proliferation, encystation, and interaction with EIN_085620. Taken together, these results indicate a coordinated role of EIN_066100 and EIN_085620 in regulating Entamoeba development. This work sheds light on the molecular mechanisms in the earliest stages of Entamoeba encystation.IMPORTANCEAn important biological process in the biology of Entamoeba is stage conversion, which plays a crucial role in disease propagation, facilitating parasite survival outside the host and spreading to new hosts. Multiple mechanisms contribute to controlling the expression of amebic stage-specific genes such as epigenetic and transcriptional control. Identification of early transcriptional control regulators is crucial to understanding the initiation of the encystation cascade. We identified two nuclear proteins, EIN_066100 and EIN_085620, involved in the proliferation and developmental regulation of E. invadens. These proteins work by direct binding to each other and mediating encystation efficiency. Study of new regulators involved in Entamoeba development represents an important advance in a critical aspect of parasite biology.

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来源期刊
mBio
mBio MICROBIOLOGY-
CiteScore
10.50
自引率
3.10%
发文量
762
审稿时长
1 months
期刊介绍: mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.
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