Arginine methyltransferases PRMT2 and PRMT3 are essential for biosynthesis of plant-polysaccharide-degrading enzymes in Penicillium oxalicum.

IF 4.5 2区 生物学 Q1 Agricultural and Biological Sciences
Shuai Zhao, Li-Xiang Mo, Wen-Tong Li, Lian-Li Jiang, Yi-Yuan Meng, Jian-Feng Ou, Lu-Sheng Liao, Yu-Si Yan, Xue-Mei Luo, Jia-Xun Feng
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Abstract

Many filamentous fungi produce plant-polysaccharide-degrading enzymes (PPDE); however, the regulatory mechanism of this process is poorly understood. A Gal4-like transcription factor, CxrA, is essential for mycelial growth and PPDE production in Penicillium oxalicum. Its N-terminal region, CxrAΔ207-733 is required for the regulatory functions of whole CxrA, and contains a DNA-binding domain (CxrAΔ1-16&Δ59-733) and a methylated arginine (R) 94. Methylation of R94 is mediated by an arginine N-methyltransferase, PRMT2 and appears to induce dimerization of CxrAΔ1-60. Overexpression of prmt2 in P. oxalicum increases PPDE production by 41.4-95.1% during growth on Avicel, compared with the background strain Δku70;hphR+. Another arginine N-methyltransferase, PRMT3, appears to assist entry of CxrA into the nucleus, and interacts with CxrAΔ1-60 in vitro under Avicel induction. Deletion of prmt3 resulted in 67.0-149.7% enhanced PPDE production by P. oxalicum. These findings provide novel insights into the regulatory mechanism of fungal PPDE production.

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精氨酸甲基转移酶PRMT2和PRMT3是草青霉合成植物多糖降解酶所必需的酶。
许多丝状真菌产生植物多糖降解酶(PPDE);然而,这一过程的调控机制尚不清楚。一种gal4样转录因子CxrA对草青霉菌丝生长和PPDE的产生至关重要。它的n端区域CxrAΔ207-733是整个CxrA调控功能所必需的,包含一个dna结合域(CxrAΔ1-16&Δ59-733)和一个甲基化精氨酸(R) 94。R94的甲基化由精氨酸n -甲基转移酶PRMT2介导,并诱导CxrAΔ1-60的二聚化。与背景菌株Δku70;hphR+相比,草藻在Avicel上的生长过程中,prmt2的过表达使PPDE产量增加了41.4-95.1%。另一种精氨酸n -甲基转移酶PRMT3似乎有助于CxrA进入细胞核,并在体外Avicel诱导下与CxrAΔ1-60相互作用。prmt3的缺失导致草藻PPDE产量增加67.0 ~ 149.7%。这些发现为真菌PPDE产生的调控机制提供了新的见解。
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来源期刊
PLoS Genetics
PLoS Genetics 生物-遗传学
CiteScore
8.10
自引率
2.20%
发文量
438
审稿时长
1 months
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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