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一种新型多蛋白桥联因子1样蛋白诱导囊肿壁蛋白基因表达及囊肿分化。

A Novel Multiprotein Bridging Factor 1-Like Protein Induces Cyst Wall Protein Gene Expression and Cyst Differentiation in .

作者信息

Huang Shao-Wei, Lin Zi-Qi, Tung Szu-Yu, Su Li-Hsin, Ho Chun-Che, Lee Gilbert Aaron, Sun Chin-Hung

机构信息

Department of Tropical Medicine and Parasitology, College of Medicine, National Taiwan University, Taipei 100, Taiwan.

Department of Medical Research, Taipei Medical University Hospital, Taipei 110, Taiwan.

出版信息

Int J Mol Sci. 2021 Jan 29;22(3):1370. doi: 10.3390/ijms22031370.

DOI:10.3390/ijms22031370
PMID:33573049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7866390/
Abstract

The capacity to synthesize a protective cyst wall is critical for infectivity of . It is of interest to know the mechanism of coordinated synthesis of three cyst wall proteins (CWPs) during encystation, a differentiation process. Multiprotein bridging factor 1 (MBF1) gene family is a group of transcription coactivators that bridge various transcription factors. They are involved in cell growth and differentiation in yeast and animals, or in stress response in fungi and plants. We asked whether has MBF1-like genes and whether their products influence gene expression. BLAST searches of the genome database identified one gene encoding a putative MBF1 protein with a helix-turn-helix domain. We found that it can specifically bind to the AT-rich initiator promoters of the encystation-induced cwp1-3 and myb2 genes. MBF1 localized to cell nuclei and cytoplasm with higher expression during encystation. In addition, overexpression of MBF1 induced cwp1-3 and myb2 gene expression and cyst generation. Mutation of the helixes in the helix-turn-helix domain reduced cwp1-3 and myb2 gene expression and cyst generation. Chromatin immunoprecipitation assays confirmed the binding of MBF1 to the promoters with its binding sites in vivo. We also found that MBF1 can interact with E2F1, Pax2, WRKY, and Myb2 transcription factors that coordinately up-regulate the cwp genes during encystation. Using a CRISPR/Cas9 system for targeted disruption of mbf1 gene, we found a downregulation of cwp1-3 and myb2 genes and decrease of cyst generation. Our results suggest that MBF1 is functionally conserved and positively regulates cyst differentiation.

摘要

合成保护性包囊壁的能力对于[某种生物]的感染性至关重要。了解在包囊形成(一种分化过程)期间三种包囊壁蛋白(CWPs)的协同合成机制很有意义。多蛋白桥联因子1(MBF1)基因家族是一组转录共激活因子,可桥接各种转录因子。它们参与酵母和动物的细胞生长与分化,或真菌和植物的应激反应。我们询问[某种生物]是否具有MBF1样基因及其产物是否影响基因表达。对[某种生物]基因组数据库进行BLAST搜索,鉴定出一个编码具有螺旋-转角-螺旋结构域的推定MBF1蛋白的基因。我们发现它可以特异性结合包囊形成诱导的cwp1 - 3和myb2基因富含AT的起始启动子。MBF1定位于细胞核和细胞质,在包囊形成期间表达较高。此外,MBF1的过表达诱导cwp1 - 3和myb2基因表达以及包囊产生。螺旋-转角-螺旋结构域中螺旋的突变降低了cwp1 - 3和myb2基因表达以及包囊产生。染色质免疫沉淀分析证实MBF1在体内与其结合位点结合到启动子上。我们还发现MBF1可以与E2F1、Pax2、WRKY和Myb2转录因子相互作用,这些转录因子在包囊形成期间协同上调cwp基因。使用CRISPR/Cas9系统靶向破坏mbf1基因,我们发现cwp1 - 3和myb2基因下调以及包囊产生减少。我们的结果表明MBF1在功能上是保守的,并正向调节[某种生物]的包囊分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1fb/7866390/f79c290c70fe/ijms-22-01370-g010.jpg
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