文献类型: 外文期刊
作者: Jia, Jun-Qiang;Xin, Xiang-Dong;Weng, Yu-Jie;Li, Shao-Hui;Gui, Zhong-Zheng;Jia, Jun-Qiang;Yin, Juan;Gui, Zhong-Zheng
作者机构:
关键词: Analysis; Cordyceps militaris; Degenerative; Genotypic
期刊名称: ENTOMOLOGICAL RESEARCH
ISSN: 1738-2297
年卷期: 2018 年 48 卷 3 期
页码:
摘要: The chemical composition and pharmacological effects of Cordyceps militaris are similar to those of Cordyceps sinensis, with the former undergoing greater development and utilization. Strain degeneration is a common phenomenon that occurs with high frequency during the subculturing of C. militaris, however, and the mechanism underlying strain degeneration remains unclear. In this study, we used touch-down PCR to compare the ITS1+5.8S+ITS2, 18S, 28S and mating-type (MAT) regions sequence of wild-type and degenerated strains of C. militaris. We also used quantitative real-time PCR to analyze expression levels of the CmMAT gene. Sequence analysis showed that the ITS1+5.8S+ITS2 and 28S regions of degenerated and wild-type strains were completely identical, the 18S region of the degenerated strain contained seven single-base mutations, including six base substitutions and one single-base insertion. Compared with the wild-type strain, the degenerated strain contained a deletion of the MAT1-2-1 region, three base substitutions in the MAT1-1-1 region, and a base substitution in the MAT1-1-2 region that causes a glycine-to-valine amino acid substitution. Quantitative real-time PCR analysis detected no CmMAT1-2-1 gene expression in the degenerated strain, confirming the deletion of the CmMAT1-2-1 gene. Expression levels of the CmMAT1-1-1 and CmMAT1-1-2 genes were significantly down-regulated to only 7.5% and 4.4%, respectively, that of the wild-type strain. These results indicate that 18S and MAT region mutations, as well as down-regulated of CmMAT gene expression levels, may play important roles in C. militaris degeneration. This study provides a theoretical basis for further elucidation of the molecular mechanisms of C. militaris degeneration.
分类号:
- 相关文献
作者其他论文 更多>>
-
Genome-Wide Analysis Of Dna Methylation I.n Subcultured Cordyceps Militaris
作者:Li, Zhiyong;Xin, Xiangdong;Gui, Zhongzheng;Gui, Zhongzheng;Zhao, Shan;Zhang, Bei;Yin, Juan
关键词:Cordyceps militaris; Bisulfite sequencing; DNA methylation; Degenerative; Analysis
-
Antioxidant And Hemolysis Protective Effects O.f Polyphenol-Rich Extract From M ulberry Fruits
作者:Gui, Zhong-Zheng;Wang, Chu-Yan;Jia, Jun-Qiang;Sivakumar, Thasma Raman;Li, Shao-Hui;Yin, Juan;Gui, Zhong-Zheng;Jia, Jun-Qiang;Jin, Chao;Krishna, Palanigounder Ganeshan Ajay;Weng, Yu-Jie
关键词:Antioxidant activity; hemolysis protective; mulberry fruit; polyphenols; purification
-
Effects Of Different Modification Techniques O.n Molecular Structure And B ioactivity Of Bombyx Mori Pupa Protein
作者:Ren, Zi-Xu;Yu, Hai-Yan;Zhou, Zhi-Feng;Jia, Jun-Qiang;Gui, Zhong-Zheng;Gui, Zhong-Zheng;Jia, Jun-Qiang
关键词:Biological activity; Bombyx mori pupa protein; Modification techniques; Physicochemical properties
-
Transcriptome-Wide Analysis Reveals The Progress O.f Cordyceps Militaris Subculture D egeneration
作者:Gui, Zhongzheng;Gui, Zhongzheng;Yin, Juan;Weng, Yujie;Xin, Xiangdong
关键词:
-
Cloning, expression and functional analysis of a delta 6-desaturase gene from the silkworm, Bombyx mori L.
作者:Yu, Hai-Yan;Zhou, Zhi-Feng;Jia, Jun-Qiang;Gui, Zhong-Zheng;Jia, Jun-Qiang;Gui, Zhong-Zheng
关键词:Bombyx mori;BmD6DES;Cloning;Expression;Functional analysis
-
Cordyceps militaris polysaccharide triggers apoptosis and G(0)/G(1) cell arrest in cancer cells
作者:Chen, Cheng;Wang, Mei-Lin;Jin, Chao;Chen, Hui-Juan;Li, Shao-Hui;Jia, Jun-Qiang;Gui, Zhong-Zheng;Li, Shu-Ying;Dou, Xing-Fan;Jia, Jun-Qiang;Gui, Zhong-Zheng
关键词:Cordyceps militaris;Polysaccharides;Cancer cells;G(0)/G(1) phase;S phase;Apoptosis
-
Identification and characterization of a novel endoglucanase (CMCase) isolated from the larval gut of Bombyx mori
作者:Ma, Ru-Jian;Wang, Chun-Yan;Liu, Yan-Wei;Sivakumar, Thasma Raman;Ren, Zi-Xu;Fang, Ying;Jia, Jun-Qiang;Gui, Zhong-Zheng;Jia, Jun-Qiang;Gui, Zhong-Zheng
关键词:Bombyx mori;Cellulase;Identification;Enzymatic characteristics