Polarity-dependent expression and localization of secretory glucoamylase mRNA in filamentous fungal cells

被引:2
作者
Morita, Yuki [1 ]
Takegawa, Kaoru [1 ]
Collins, Brett M. [2 ]
Higuchi, Yujiro [1 ]
机构
[1] Kyushu Univ, Fac Agr, Dept Biosci & Biotechnol, 744 Motooka, Fukuoka 8190395, Japan
[2] Univ Queensland, Inst Mol Biosci, Ctr Cell Biol Chron Dis, St Lucia, Qld 4072, Australia
关键词
Endoplasmic reticulum; Filamentous fungi; Glucoamylase; Kinesin; Stress granule; mRNA; ENDOPLASMIC-RETICULUM; ASPERGILLUS-ORYZAE; BINDING PROTEIN; STRESS GRANULE; ENDOSOME MOTILITY; MYOSIN MOTOR; P-BODIES; TRANSLATION; DYNEIN; YEAST;
D O I
10.1016/j.micres.2024.127653
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In multinuclear and multicellular filamentous fungi little is known about how mRNAs encoding secreted enzymes are transcribed and localized spatiotemporally. To better understand this process we analyzed mRNA encoding GlaA, a glucoamylase secreted in large amounts by the industrial filamentous fungus Aspergillus oryzae, by the MS2 system, in which mRNA can be visualized in living cells. We found that glaA mRNA was significantly transcribed and localized near the hyphal tip and septum, which are the sites of protein secretion, in polaritydependent expression and localization manners. We also revealed that glaA mRNA exhibits long-range dynamics in the vicinity of the endoplasmic reticulum (ER) in a manner that is dependent on the microtubule motor proteins kinesin-1 and kinesin-3, but independent of early endosomes. Moreover, we elucidated that although glaA mRNA localized to stress granules (SGs) and processing bodies (PBs) under high temperature, glaA mRNA was not seen under ER stress, suggesting that there are different regulatory mechanisms of glaA mRNA by SG and PB under high temperature and ER stress. Collectively, this study uncovers a dynamic regulatory mechanism of mRNA encoding a secretory enzyme in filamentous fungi.
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页数:21
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