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Three Genes Related to Trehalose Metabolism Affect Sclerotial Development of Rhizoctonia solani AG-1 IA,Causal Agent of Rice Sheath Blight
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作者 WANG Chenjiaozi ZHAO Mei +1 位作者 SHU Canwei ZHOU Erxun 《Rice science》 SCIE CSCD 2022年第3期268-276,共9页
Trehalose metabolism is related to the sclerotial development of Rhizoctonia solani AG-1 IA,the causal agent of rice sheath blight(RSB).Here,we further elucidated the functions of three genes Rstre,Rstps1 and Rstpp th... Trehalose metabolism is related to the sclerotial development of Rhizoctonia solani AG-1 IA,the causal agent of rice sheath blight(RSB).Here,we further elucidated the functions of three genes Rstre,Rstps1 and Rstpp that encode three key enzymes trehalase(TRE),alpha,alpha-trehalosephosphate synthase(TPS1)and trehalose 6-phosphate phosphatase(TPP)in the sclerotial development of R.solani AG-1 IA.Due to the lack of a stable genetic transformation system for R.solani,the heterologous expression of these three genes in Pichia pastoris GS115 was performed.The results showed that reactive oxygen species(ROS)contents and enzyme activities in R.solani decreased significantly in the treatments of the fermentation broths of Rstps1 and Rstpp transformants,and that in the treatment of the fermentation broth of Rstre transformant visibly increased.Furthermore,the fermentation broths of the transformants of all the three genes were added to potato dextrose agar(PDA)medium for the cultivation of R.solani,as a result,the dry weight of sclerotia in each PDA plate containing the fermentation broths of Rstps1 and Rstpp transformants significantly increased compared with the control,and that of Rstre transformant obviously decreased.Finally,178 proteins were found to interact with RSTPS1,and 16 of them were associated with ROS.Taken together,the findings suggest that all these three genes related to trehalose metabolism play important roles in the sclerotial development of R.solani AG-1 IA,and can be used as new targets for the development of novel high-efficiency fungicides for the controlling of RSB. 展开更多
关键词 Rhizoctonia solani AG-1 ia rice sheath blight reactive oxygen species trehalose metabolism gene functional analysis sclerotial development
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乙醛脱氢酶ALDH7A1基因多态性与2型糖尿病的相关性研究 被引量:1
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作者 刘国政 刘方方 +4 位作者 晏文强 刘双 谢明水 许诚楷 蒋从清 《检验医学》 CAS 2013年第10期897-900,903,共5页
目的探讨ALDH7A1基因多态性位点rs2306619、rs2306618、rs12514417、rs2306617、rs4379190与中国湖北随州汉族居民2型糖尿病(T2DM)的相关性。方法收集220名健康对照者和240例T2DM患者,所有研究对象均来自湖北随州汉族城镇居民。从外周... 目的探讨ALDH7A1基因多态性位点rs2306619、rs2306618、rs12514417、rs2306617、rs4379190与中国湖北随州汉族居民2型糖尿病(T2DM)的相关性。方法收集220名健康对照者和240例T2DM患者,所有研究对象均来自湖北随州汉族城镇居民。从外周血的白细胞中应用标准法提取DNA。通过设计测序引物对相邻的5个所选位点(rs2306619、rs2306618、rs12514417、rs2306617、rs4379190)进行基因扩增,然后直接送样测序,采用SHEsis软件进行统计分析ALDH7A1基因5个位点的单核甘酸多态性及连锁不平衡,分析糖尿病组与对照组5个位点等位基因频率和基因型频率的差异及构建单体型。结果 5个位点的最低等位基因频率分别是0.492、0.084、0.124、0.277、0.259,连锁不平衡检验发现5个位点呈现强的连锁不平衡,ALDH7A1基因的5个位点基因的等位基因频率和基因型频率在2组中差异均无统计学意义,单体型分析发现C-A-A-A-T、T-A-A-A-T、T-A-AG-C、T-A-C-A-T、T-G-A-G-C 5种单体型,并且这5种单体型在糖尿病组和对照组差异无统计学意义。结论 ALDH7A1基因的5个多态性位点可能不是湖北随州汉族2型糖尿病患者的易感基因;本研究结果尚需在更大规模人群中进一步验证。 展开更多
关键词 2型糖尿病 aldh7A1基因 单核苷酸多态性 单倍体
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1型糖尿病患者维生素D受体基因多态性及自身抗体的研究
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作者 刘喆隆 肖新华 +2 位作者 王姮 孙琦 杨国华 《国际内科双语杂志(中英文)》 2006年第1期63-72,共10页
目的探讨中国汉族人群中维生素D受体(VDR)基因多态性对1型糖尿病易感性的影响,及其与谷氨酸脱羧酶抗体(GADA)和酪氨酸磷酸酶抗体(IA-2A)的关联性。方法采用PCR—RFLP技术,检测93名1型糖尿病患者和122名没有亲缘关系的正常对照的... 目的探讨中国汉族人群中维生素D受体(VDR)基因多态性对1型糖尿病易感性的影响,及其与谷氨酸脱羧酶抗体(GADA)和酪氨酸磷酸酶抗体(IA-2A)的关联性。方法采用PCR—RFLP技术,检测93名1型糖尿病患者和122名没有亲缘关系的正常对照的VDR基因型,鉴定VDR基因上的3个限制性位点的多态性:ApaI,BsmI和TaqI,并用放射配体免疫沉淀法检测1型糖尿病患者中50人的自身抗体(GAD65,IA-2)。结果1型糖尿病患者VDR基因BsmI位点等位基因B的频率显著高于正常对照(P=0.004),基因型BB和Bb的频率也相应高于对照组(P=0.038),而ApaI和TaqI位点的多态性分布在两组间未见明显差异。1型糖尿病患者VDR基因ApaI位点不同基因型自身抗体IA-2的阳性率有一定的差异(P=0.052),即在排除病程和发病年龄等因素的影响后,aa基因型组的阳性率比AA/Aa组要高。此研究的汉族人群中的1型糖尿病患者,各基因型分布和我国台湾地区汉族患者无显著性差异,但是与克罗地亚患者存在显著性差异,A、B、t等位基因频数分布均明显低于克罗地亚人。结论汉族1型糖尿病患者中,VDR基因BsmI位点多态性可能与1型糖尿病的易感性有关。而1型糖尿病患者VDR基因多态性可能与其自身抗体I—A-2A存在一定的关联,未见与自身抗体GADA的关联。 展开更多
关键词 1型糖尿病 维生素D受体基因多态性 谷氨酸 脱羧酶抗体 酪氨酸磷酸酶抗体
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Frequent 3p21 Allelic Loss and Methylation-Associated RASSF1A Inactivation in Non-Small Cell Lung Cancer and Its Clinical Implication
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作者 ZHU Hong WONG Maria P 《Wuhan University Journal of Natural Sciences》 CAS 2009年第5期457-464,共8页
A total of 110 primary NSCLCs (non-small cell lung cancers) were recruited in this study to characterize the pattern of 3p21 LOH together with the RASSF1A methylation status and their clinical implication. 3p21 LOH ... A total of 110 primary NSCLCs (non-small cell lung cancers) were recruited in this study to characterize the pattern of 3p21 LOH together with the RASSF1A methylation status and their clinical implication. 3p21 LOH by 8 microsatellite markers, RASSF1A methylation status by methylation-specific PCR (MSPCR) as well as bisulfite genomic sequencing (BGS), and RASSF1A expression level by real-time quantitative PCR was performed. 3p21 LOH is frequent in NSCLC with a mean frequency of (41.2±3.7)%. Significant associations between 3p21 LOH and gender, smoking history, histological type, and tumor size were observed. Cases with LOH have a slightly lower RASSF1A expression than cases without LOH but not statistically significant. Comparison of RASSF1A methylation that resulted from the three analyses shows significant correlations from one another. Higher frequency of methylation was observed in larger tumors and in smokers compared with smaller tumors and non-smokers, respectively. A significant correlation was also observed in extent between methylation and RASSF1A expression, illustrating that epigenetic mechanism could affect gene expression. The significant clinicopathological relations of 3p21 LOH may be of great use for both early detection and therapeutic interventions. 展开更多
关键词 non-small cell lung cancer loss of heterozygosity RAS association domain family ia gene (RASSF1A) METHYLATION real-time quantitative PCR
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