2017
DOI: 10.3390/genes8110335
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Differential Expression Patterns of Pleurotus ostreatus Catalase Genes during Developmental Stages and under Heat Stress

Abstract: Catalases are ubiquitous hydrogen peroxide-detoxifying enzymes. They participate in fungal growth and development, such as mycelial growth and cellular differentiation, and in protecting fungi from oxidative damage under stressful conditions. To investigate the potential functions of catalases in Pleurotus ostreatus, we obtained two catalase genes from a draft genome sequence of P. ostreatus, and cloned and characterized them (Po-cat1 and Po-cat2). Po-cat1 (group II) and Po-cat2 (group III) encoded putative pe… Show more

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Cited by 42 publications
(47 citation statements)
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References 49 publications
(55 reference statements)
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“…Although, the heat shock response has been studied in considerable detail in yeast and plant (McAlister and Finkelstein 1980;Richter et al 2010;Song et al 2012), the mechanism of heat shock response in basidiomycetes remains elusive. Mushrooms evolved various strategies to response and alleviate heat shock stress, including HSPs synthesis, trehalose accumulation, and reactive oxygen species scavenging (Chen et al 2017;Liu et al 2016Liu et al , 2018Liu et al , 2019Wang et al 2017). In this study, we focused on a HSPs gene involved in heat shock response in H. marmoreus.…”
Section: Discussionmentioning
confidence: 99%
“…Although, the heat shock response has been studied in considerable detail in yeast and plant (McAlister and Finkelstein 1980;Richter et al 2010;Song et al 2012), the mechanism of heat shock response in basidiomycetes remains elusive. Mushrooms evolved various strategies to response and alleviate heat shock stress, including HSPs synthesis, trehalose accumulation, and reactive oxygen species scavenging (Chen et al 2017;Liu et al 2016Liu et al , 2018Liu et al , 2019Wang et al 2017). In this study, we focused on a HSPs gene involved in heat shock response in H. marmoreus.…”
Section: Discussionmentioning
confidence: 99%
“…The ChamQ SYBR qPCR master mix kit (Vazyme, Nanjing, China) and the ABI 7500 real-time PCR amplifier (Applied Biosystems, Foster City, CA, USA) were used for qPCR. The qPCR amplification procedure was as follows: 95°C for 3 min, 40 cycles at 95°C for 3 s and at 60°C for 32 s, and a final extension at 72°C for 30 s. Relative gene expression was analyzed according to the 2 ϪooCT method (55).…”
Section: Methodsmentioning
confidence: 99%
“…High temperature is one of the abiotic stresses that impact the cultivation of P. ostreatus. To simulate heat stress in growth, the strains were cultured and treated according to our previous methods (55). The mycelia were cultured at 28°C for 5 days, treated at 40°C, and then returned to growth at 28°C.…”
Section: Methodsmentioning
confidence: 99%
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“…According to our previous study [68], qPCR was performed to analyze the mRNA expression levels of the aox gene and key antioxidant enzyme genes in the CCMSSC00389 strain and aox-transformed strains subjected to the different treatments. The β-actin and β-tubulin genes were used as internal reference genes, and the relative gene expression was determined according to the 2 −△△CT method.…”
Section: Rna Extraction Reverse Transcription and Qpcrmentioning
confidence: 99%