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揭示生物发光应激依赖性调控的生物发光基因的克隆与表达分析。

Cloning and Expression Analysis of Bioluminescence Genes in Reveal Stress-Dependent Regulation of Bioluminescence.

作者信息

Park Mi-Jeong, Kim Eunjin, Kim Min-Jun, Jang Yeongseon, Ryoo Rhim, Ka Kang-Hyeon

机构信息

Forest Microbiology Division, Department of Forest Bio-Resources, National Institute of Forest Science, Suwon, Republic of Korea.

出版信息

Mycobiology. 2024 Jan 23;52(1):42-50. doi: 10.1080/12298093.2024.2302661. eCollection 2024.

DOI:10.1080/12298093.2024.2302661
PMID:38415178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10896133/
Abstract

Bioluminescence is a type of chemiluminescence that arises from a luciferase-catalyzed oxidation reaction of luciferin. Molecular biology and comparative genomics have recently elucidated the genes involved in fungal bioluminescence and the evolutionary history of their clusters. However, most studies on fungal bioluminescence have been limited to observing the changes in light intensity under various conditions. To understand the molecular basis of bioluminescent responses in under different environmental conditions, we cloned and sequenced the genes of hispidin synthase, hispidin-3-hydroxylase, and luciferase enzymes, which are pivotal in the fungal bioluminescence pathway. Each gene showed high sequence similarity to that of other luminous fungal species. Furthermore, we investigated their transcriptional changes in response to abiotic stresses. Wound stress enhanced the bioluminescence intensity by increasing the expression of bioluminescence pathway genes, while temperature stress suppressed the bioluminescence intensity the non-transcriptional pathway. Our data suggested that regulates bioluminescence to respond differentially to specific environmental stresses. To our knowledge, this is the first study on fungal bioluminescence at the gene expression level. Further studies are required to address the biological and ecological meaning of different bioluminescence responses in changing environments, and could be a potential model species.

摘要

生物发光是一种化学发光,它源于荧光素酶催化的荧光素氧化反应。分子生物学和比较基因组学最近阐明了参与真菌生物发光的基因及其基因簇的进化历史。然而,大多数关于真菌生物发光的研究仅限于观察各种条件下光强度的变化。为了了解不同环境条件下真菌生物发光反应的分子基础,我们克隆并测序了在真菌生物发光途径中起关键作用的漆斑菌素合酶、漆斑菌素-3-羟化酶和荧光素酶的基因。每个基因与其他发光真菌物种的基因显示出高度的序列相似性。此外,我们研究了它们对非生物胁迫的转录变化。伤口胁迫通过增加生物发光途径基因的表达来增强生物发光强度,而温度胁迫则通过非转录途径抑制生物发光强度。我们的数据表明,真菌通过调节生物发光来对特定的环境胁迫做出不同的反应。据我们所知,这是首次在基因表达水平上对真菌生物发光进行研究。需要进一步研究来探讨在不断变化的环境中不同生物发光反应的生物学和生态学意义,并且该真菌可能是一个潜在的模式物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/eda7e21adbff/TMYB_A_2302661_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/169da2a44ff4/TMYB_A_2302661_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/cd70c1141594/TMYB_A_2302661_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/b89a99175891/TMYB_A_2302661_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/083f5419a014/TMYB_A_2302661_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/eda7e21adbff/TMYB_A_2302661_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/169da2a44ff4/TMYB_A_2302661_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/cd70c1141594/TMYB_A_2302661_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/b89a99175891/TMYB_A_2302661_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/083f5419a014/TMYB_A_2302661_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21f7/10896133/eda7e21adbff/TMYB_A_2302661_F0005_C.jpg

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Genome-wide identification and expression analyses of C2H2 zinc finger transcription factors in .
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The transcription factor FvHmg1 negatively regulates fruiting body development in Winter Mushroom Flammulina velutipes.转录因子FvHmg1对金针菇子实体发育起负调控作用。
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