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利用探针通过单分子荧光杂交对mRNA与增强型绿色荧光蛋白融合蛋白进行相关定位分析。

Correlative Localization Analysis Between mRNA and Enhanced Green Fluorescence Protein-Fused Protein by a Single-Molecule Fluorescence Hybridization Using an Probe in .

作者信息

Morita Yuki, Katakura Yoshinori, Takegawa Kaoru, Higuchi Yujiro

机构信息

Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka, Japan.

出版信息

Front Fungal Biol. 2021 Oct 13;2:721398. doi: 10.3389/ffunb.2021.721398. eCollection 2021.

DOI:10.3389/ffunb.2021.721398
PMID:37744096
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10512357/
Abstract

Although subcellular localization analysis of proteins fused with enhanced green fluorescence protein (EGFP) has been widely conducted in filamentous fungi, little is known about the localization of messenger RNAs (mRNAs) encoding the EGFP-fused proteins. In this study, we performed single-molecule fluorescence hybridization (smFISH) using an probe to simultaneously visualize EGFP-fused proteins and their mRNAs in the hyphal cells of the filamentous fungus . We investigated the subcellular localization of mRNAs encoding cytoplasmic EGFP, an actin marker protein Lifeact tagged with EGFP, and several EGFP-fused proteins AoSec22, AoSnc1, AoVam3, and AoUapC that localize to the endoplasmic reticulum (ER), the apical vesicle cluster Spitzenkörper, vacuolar membrane, and plasma membrane, respectively. Visualization of these mRNAs by smFISH demonstrated that each mRNA exhibited distinct localization patterns likely depending on the mRNA sequence. In particular, we revealed that mRNAs encoding Lifeact-EGFP, EGFP-AoSec22, EGFP-AoVam3, and AoUapC-EGFP, but not cytoplasmic EGFP and EGFP-AoSnc1, were preferentially localized at the apical cell, suggesting certain mechanisms to regulate the existence of these transcripts among hyphal regions. Our findings provide the distinct localization information of each mRNA in the hyphal cells of .

摘要

尽管在丝状真菌中,对与增强型绿色荧光蛋白(EGFP)融合的蛋白质进行亚细胞定位分析已广泛开展,但对于编码EGFP融合蛋白的信使核糖核酸(mRNA)的定位却知之甚少。在本研究中,我们使用一种探针进行单分子荧光杂交(smFISH),以同时在丝状真菌的菌丝细胞中可视化EGFP融合蛋白及其mRNA。我们研究了编码细胞质EGFP、标记有EGFP的肌动蛋白标记蛋白Lifeact以及几种分别定位于内质网(ER)、顶端囊泡簇Spitzenkörper、液泡膜和质膜的EGFP融合蛋白AoSec22、AoSnc1、AoVam3和AoUapC的mRNA的亚细胞定位。通过smFISH对这些mRNA的可视化显示,每个mRNA都表现出可能取决于mRNA序列的独特定位模式。特别是,我们发现编码Lifeact-EGFP、EGFP-AoSec22、EGFP-AoVam3和AoUapC-EGFP的mRNA,但不包括细胞质EGFP和EGFP-AoSnc1,优先定位于顶端细胞,这表明在菌丝区域之间存在调节这些转录本存在的某些机制。我们的研究结果提供了每种mRNA在该丝状真菌菌丝细胞中的独特定位信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/d031a6c2814a/ffunb-02-721398-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/f0bea68ac4f6/ffunb-02-721398-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/3c35c2fcf1c7/ffunb-02-721398-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/dba832628323/ffunb-02-721398-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/1e191b2390a9/ffunb-02-721398-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/b7d67ce52d22/ffunb-02-721398-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/44c98429e997/ffunb-02-721398-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/639ec4fc67a0/ffunb-02-721398-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/d031a6c2814a/ffunb-02-721398-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/f0bea68ac4f6/ffunb-02-721398-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/3c35c2fcf1c7/ffunb-02-721398-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/dba832628323/ffunb-02-721398-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/1e191b2390a9/ffunb-02-721398-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/b7d67ce52d22/ffunb-02-721398-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/44c98429e997/ffunb-02-721398-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/639ec4fc67a0/ffunb-02-721398-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a328/10512357/d031a6c2814a/ffunb-02-721398-g0008.jpg

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