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Selenocysteine methyltransferase SMT catalyzed the synthesis of Se-methylselenocysteine to regulate the accumulation of glucosinolates and sulforaphane in broccoli
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作者 Qi Wu Junwei Wang +4 位作者 Yuxiao Tian Chunyan Zhou Shuxiang Mao Qiuyun Wu Ke Huang 《Horticultural Plant Journal》 SCIE CAS CSCD 2024年第5期1151-1164,共14页
Selenocysteine methyltransferase(SMT)is a key enzyme involved in the Se metabolism pathway,and it is responsible for the catalysis of Se-methylselenocysteine(SeMSC)compound formation.Previous studies showed that selen... Selenocysteine methyltransferase(SMT)is a key enzyme involved in the Se metabolism pathway,and it is responsible for the catalysis of Se-methylselenocysteine(SeMSC)compound formation.Previous studies showed that selenium treatment activated SMT expression and promoted the accumulation of glucosinolates(GSLs)and sulforaphane,but the roles and functional mechanisms of SMT in mediating GSLs and sulforaphane synthesis remain unclear.In this study,we identified the BoSMT gene in broccoli and uncovered its roles in mediating GSLs biosynthesis.Transgenic assays revealed that BoSMT is involved in SeMSC biosynthesis in broccoli.More importantly,the contents of GSLs and sulforaphane were significantly increased in the BoSMT-overexpressing broccoli lines but decreased in the knockdown lines,suggesting that BoSMT played a positive role in regulating GSLs and sulforaphane synthesis.Further evidence indicated that BoSMT-mediated overaccumulation of GSLs and sulforaphane might be due to the increase in the endogenous SeMSC content.Compared with the mock(water)treatment,selenite-induced significantly increases of the SeMSC content in the BoSMT-knockdown plants partially compensated the phenotype of GSLs and sulforaphane loss.Compared with the mock treatment,exogenous SeMSC treatment significantly increased the contents of GSL and sulforaphane and activated GSL synthesis-related gene expression,suggesting that SeMSC acted as a positive regulator for GSL and sulforaphane production.Our findings provided novel insights into selenium-mediated GSLs and sulforaphane accumulation.The genetic manipulation of BoSMT might be a useful strategy for improving the dietary nutritional values of broccoli. 展开更多
关键词 selenocysteine methyltransferase Transgenic broccoli Se-methylselenocysteine Glucosinolate sulforaphane Selenium
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Selenocysteine antagonizes oxygen glucose deprivation-induced damage to hippocampal neurons 被引量:3
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作者 Xian-Jun Wang Mei-Hong Wang +5 位作者 Xiao-Ting Fu Ya-Jun Hou Wang Chen Da-Chen Tian Su-Yun Bai Xiao-Yan Fu 《Neural Regeneration Research》 SCIE CAS CSCD 2018年第8期1433-1439,共7页
Designing and/or searching for novel antioxidants against oxygen glucose effective strategy for the treatment of human isdlemic stroke. Selenium is deprivation (OGD)-induced oxidative damage represents an an essenti... Designing and/or searching for novel antioxidants against oxygen glucose effective strategy for the treatment of human isdlemic stroke. Selenium is deprivation (OGD)-induced oxidative damage represents an an essential trace dement, which is beneficial in the chemo- prevention and chemotherapy of cerebral ischemic stroke. The underlying mechanisms for its therapeutic effects, however, are not well documented. Selenocysteine (SeC) is a selenium-containing amino acid with neuroprotective potential. Studies have shown that SeC can reduce irradiation-induced DNA apoptosis by reducing DNA damage. In this study, the in vitro protective potential and mechanism of action of SeC against OGD-induced apoptosis and neurotoxicity were evaluated in HT22 mouse hippocampal neurons. We cultured HT22 cells in a glucose-free medium containing 2 mM Na2S402, which formed an OGD environment, for 90 minutes. Findings from MTT, flow cytometry and TUNEL staining showed obvious cytotoxicity and apoptosis in HT22 cells in the OGD condition. The activation of Caspa se-7 and Caspase-9 further revealed that OGD-induced apoptosis of HT22 cells was mainly achieved by triggering a mitochondrial-medi- ated pathway. Moreover, the OGD condition also induced serious DNA damage through the accumulation of reactive oxygen species and superoxide anions. However, SeC pre-treatment for 6 hours effectively inhibited OGD-induced cytotoxicity and apoptosis in HT22 cells by inhibiting reactive oxygen species-mediated oxidative damage. Our findings provide evidence that SeC has the potential to suppress OGD-induced oxidative damage and apoptosis in hippocampal neurons. 展开更多
关键词 SELENIUM selenocysteine ischemic stroke oxygen glucose deprivation hippocampal neuron MITOCHONDRIA reaction oxygen species superoxide anion oxidative damage APOPTOSIS
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Quantitative Analysis of ATP Sulfurylase and Selenocysteine Methyltransferase Gene Expression in Different Organs of Tea Plant (<i>Camellia sinensis</i>) 被引量:3
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作者 Shaoqiang Tao Juan Li +4 位作者 Xungang Gu Yanan Wang Qiang Xia Bing Qin Lin Zhu 《American Journal of Plant Sciences》 2012年第1期51-59,共9页
Tea plant (Camellia sinensis) has unique biological features for the study of cellular and molecular mechanisms, an evergreen broad-leaved woody plant which can accumulate selenium in soil abundant of Selenium. Expres... Tea plant (Camellia sinensis) has unique biological features for the study of cellular and molecular mechanisms, an evergreen broad-leaved woody plant which can accumulate selenium in soil abundant of Selenium. Expression of the genes related to Selenium (Se) metabolism is an adaptation to the soil environment for a long period. The purpose of the present study was to explore if there exist differences of expression about these genes in tea plant between growing in Selenium-abundant and normal soil. A quantitative real-time reverse transcription polymerase chain reaction (Q-RT-PCR) assay was done for quantification of ATP sulfurylase (APS) and selenocysteine methyltransferase (SMT) mRNA normalized to Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene in tea plant. Young leaves, mature leaves and tender roots from tea plants growing in soil abundant of Selenium were respectively obtained from Shitai County, Anhui Province, and also the relevant materials of the selenium un-enriched tea plant planted at agricultural garden of Ahui Agriculture University were taken as control for real-time PCR analysis. The results showed that APS1, APS2 and SMT expression levels for either young or mature leaves in selenium-enriched tea plant were lower than that in ordinary (selenium un-enriched) tea plant. In contrast, the APS1, APS2 and SMT expression level of roots in selenium-enriched tea plant were all higher than that in ordinary tea plant. APS1 gene expression level of roots in selenium-enriched tea plant was about 1.6 times higher than that in the ordinary tea plant, APS2 gene expression level was about 4.8-fold higher than that in the ordinary tea plant, SMT gene expression level was about 3.3 times higher than that in the ordinary tea plant. Among various tissues of selenium-enriched tea plant, APS1 gene relative expression level of young leaves was similar to or slightly higher than mature leaves, and the one of roots was the lowest among them;APS2 gene relative expression level of young leaves was similar to or slightly higher than the roots, and the one of mature leaves was the lowest among them;SMT gene relative expression level of young leaves was similar to or slightly higher than mature leaves, and the one of roots was the highest among them. Our results suggest that there existed correlation between selenium and expression levels of these genes. 展开更多
关键词 Quantitative Real-Time Polymerase Chain Reaction ATP Sulfurylase selenocysteine METHYLTRANSFERASE Tea Plant (Camellia sinensis)
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Selenocysteine tRNAs as Central Components of Selenoprotein Biosynthesis in Eukaryotes 被引量:2
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作者 SANG ICK PARK JIN Mo PARK +4 位作者 HAROLD S. CHITTUM EUN SUNG YANG BRADLEY A. CARLSON BYEONG JAE LEE AND DOLPH L. HATFIELD(Laboratory of Experimental Chrcinogenesis, National Cancer Insti tute, National Institutes of Health, Bethesda, MD 20892USA Laboratory o 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 1997年第2期116-124,共9页
Selenocysteine (Sec) tRNAs serve as carrier molecules for the biosynthesis of Sec from serine and to donate Sec to protein in response to specific UGA codons. In this study, we describe the current status of Sec tRNAs... Selenocysteine (Sec) tRNAs serve as carrier molecules for the biosynthesis of Sec from serine and to donate Sec to protein in response to specific UGA codons. In this study, we describe the current status of Sec tRNAs in higher animals and further we exarnine: (i) the Sec tRNA population in Drosophila; (ii) transcription of the Sec tRNA in vivo (in Xenopus oocytes) and in vitro (in Xenopus oocyte extracts); (iii) the effect of selenium on the Sec tRNA population in various rat tissues following replenishment of extremely selenium deficient rats with this element; and (iv) the biosynthesis of the modified bases on Sec tRNA in Xenopus oocytes 展开更多
关键词 tRNA gene selenocysteine tRNAs as Central Components of Selenoprotein Biosynthesis in Eukaryotes
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Preliminary Study of Selenium (Se) Toxicity in Human Prostate Carcinoma (PC3) Cells with the Overexpression of Selenocysteine Synthase (SecS) Gene
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作者 Tomilowo Abijo Jiahua Xie 《Open Journal of Genetics》 2016年第4期79-86,共9页
Selenium (Se) is a trace element required for normal body function. Its supplementation of human diet at standard optimum amount prevents oxidative damages in cells and could be a viable method in the prevention of di... Selenium (Se) is a trace element required for normal body function. Its supplementation of human diet at standard optimum amount prevents oxidative damages in cells and could be a viable method in the prevention of diseases related to DNA damage, including cancer, neurodegenerative diseases and aging. While Se anticancer properties have been linked to its ability to remove excess Reactive Oxygen Species (ROS) in cells, the underlying molecular mechanism remains unknown. Recent studies have shown that the removal of ROS alone cannot account for Se anticancer properties. To really comprehend the molecular basis of Se anticancer properties, current researches now focus on the metabolism of Se in the cell, especially Se-containing amino acids. Selenocysteine (Sec) is a novel amino acid and one of the selenium-containing compounds in the cell. It is essential in the maintenance of the integrity of its parent proteins, some of which include enzymes such as Glutathione Peroxidases (GPXs) and Thioredoxin Reductases (TrXs). We propose in this study that the overproduction of Sec via the overexpression of Selenocysteine synthase (SecS) gene and Se supplementation induced cell death in Prostate Carcinoma (PC-3) cells. Although the mechanism underlying the cell death induction is unknown, we propose it could be due to the random incorporation of Sec into proteins at high concentration, causing premature protein degradation and cell death. The outcome of this study showed that increasing the concentration of intracellular Se-containing amino acids may provide important clinical implications for the treatment of cancer. 展开更多
关键词 SELENIUM Reactive Oxygen Species selenocysteine Prostate Carcinoma selenocysteine Synthase Gene
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Solution Structure of SECIS, the mRNA Element Required for Eukaryotic Selenocysteine Insertion──Interaction Studies Withthe SECIS-Binding Protein SBP
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作者 ROBERT WALCZAK NADIA HUBERT PHILIPPE CARBON, AND ALAIN KROL(UPR 9002 du CANS"Structure des MAcromolecules Biologiques et Mecanismes de Reconnaissance", IBMC, 15, Rue Rene Descartes, 67084 Strasbourg Cedex, France) 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 1997年第2期177-181,共5页
Selenocysteine, a selenium-containing analog of cysteine, is found in the prokaryotic and eukaryotic kingdoms in active sites of enzymes involved in oxidation-reduction reactions. This aminoacid is cotranslationally i... Selenocysteine, a selenium-containing analog of cysteine, is found in the prokaryotic and eukaryotic kingdoms in active sites of enzymes involved in oxidation-reduction reactions. This aminoacid is cotranslationally incorporated at UGA codons which usually act as translation stop codons. In eukaryotes, decoding of selenocysteine necessitates the participation of the selenocysteine insertion sequence (SECIS), an element lying in the 3' -untranslated region of selenoprotein mRNAs. A detailed experimental study of the secondary structures of the SECIS elements of rat and human type 1 iodothyronine deiodinases and rat glutathione peroxidase was performed. Enzymatic and chemical structure probing led us to propose a secondary structure model, supported by sequence comparison of 23 SECIS mRNAs. The secondary structure model revealed the existence of a novel type of RNA motif composed of four consecutive non-Watson-Crick base-pairs. Using gel shift experiments, we identified in several mammalian cell type extracts the protein SBP,for SECIS-binding protein, that specifically recognizes the iodothyronine deiodinases and glutathione peroxidase SECIS elements. The structural model that we derived for the SECIS RNAs discloses RNA features possibly implicated in the binding of SBP and/or SECIS function 展开更多
关键词 MRNA the mRNA Element Required for Eukaryotic selenocysteine Insertion UGA Solution Structure of SECIS Interaction Studies Withthe SECIS-Binding Protein SBP
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关于蛋白质教学中几个问题的探讨
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作者 骆启林 邓湘 《生物学教学》 北大核心 2024年第5期85-86,共2页
通过对高中生物学蛋白质教学过程中常出现的一些问题进行分析和阐释,准确理解相关概念,以期提高教学效率,培养学生的科学思维。
关键词 氨基酸 硒代半胱氨酸 吡咯赖氨酸 蛋白质
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HPLC-ESI-MS法检测香菇中甲基硒代半胱氨酸 硒代蛋氨酸 硒代半胱氨酸含量 被引量:2
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作者 胡超 李琎杰 +2 位作者 毛自欣 袁波 刘塞纳 《农产品加工》 2023年第24期59-62,共4页
建立一种提取和测定香菇中甲基硒代半胱氨酸(methyl selenocysteine,MeSeCys)、硒代蛋氨酸(selenom-ethionine,SeMet)、硒代半胱氨酸(selenocysteine,Sec)含量的超高效液相色谱串联质谱方法。对比3种不同前处理方法对香菇样品中硒代氨... 建立一种提取和测定香菇中甲基硒代半胱氨酸(methyl selenocysteine,MeSeCys)、硒代蛋氨酸(selenom-ethionine,SeMet)、硒代半胱氨酸(selenocysteine,Sec)含量的超高效液相色谱串联质谱方法。对比3种不同前处理方法对香菇样品中硒代氨基酸的提取效果,选Agilent ZORBAX SB-AQ型亲水色谱柱(柱长100 mm,内径3.0 mm,粒径1.8μm),1%甲酸水和甲醇流动相梯度洗脱,柱温35℃,流量0.2 mL/min。结果表明,3种提取方法中,酶解提取法提取效率最高,能较好地提取香菇中甲基硒代半胱氨酸、硒代蛋氨酸、硒代半胱氨酸,采用HPLC-MS检测3种氨基酸在质量浓度0.2~20.0 ng/mL呈现较好的线性关系,平均回收率分别为92.3%,93.0%,92.4%,相对标准偏差分别为2.71%,2.14%,1.83%。该方法简单、快速、准确,适用于香菇中甲基硒代半胱氨酸、硒代蛋氨酸、硒代半胱氨酸含量的测定。 展开更多
关键词 甲基硒代半胱氨酸 硒代蛋氨酸 硒代半胱氨酸 酶解提取法
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Physiological Function of Selenium in Plants
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作者 Meiping CHEN Qiqi HONG +1 位作者 Sitong LI Chengxiang XU 《Agricultural Biotechnology》 2023年第6期45-47,共3页
The global understanding of selenium(Se)in plant biology mainly comes from the fields of medicine and animal science,while the research on Se in plant biology in the field of plant science lags behind.This paper summa... The global understanding of selenium(Se)in plant biology mainly comes from the fields of medicine and animal science,while the research on Se in plant biology in the field of plant science lags behind.This paper summarized the physiological functions of Se in plants.These studies indicate that Se can promote plant seed development and growth and plant photosynthesis,increase plant economic yield and quality,and enhance plant antioxidant capacity and resistance to stress.However,its effects have a"dual"character,and its concentration or dosage range is very narrow.At appropriate concentrations,Se has an important impact on the physiological processes of plants and is a beneficial element for many plants to maintain health and good growth and development. 展开更多
关键词 PLANT SELENIUM selenocysteine SELENOPROTEIN Selenium biofortification
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荧光探针用于细胞内硒代半胱氨酸检测的研究进展
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作者 张姻 赵美 +1 位作者 胡婉迪 卢丹青 《化学世界》 CAS 2023年第2期73-81,共9页
硒代半胱氨酸(Sec)在人体调控免疫反应、抑制癌症的发生,以及维持生理氧化还原平衡等方面发挥着十分重要的作用。采用荧光探针直接在分子水平上对硒代半胱氨酸进行体内实时无损检测是探索生理活动机制的最有效的方法。总结了不同类型的... 硒代半胱氨酸(Sec)在人体调控免疫反应、抑制癌症的发生,以及维持生理氧化还原平衡等方面发挥着十分重要的作用。采用荧光探针直接在分子水平上对硒代半胱氨酸进行体内实时无损检测是探索生理活动机制的最有效的方法。总结了不同类型的荧光探针分子的设计原理及其对应的传感检测机制和成像应用。对比了不同的分析检测方式以及效果,介绍了用于生物硒代半胱氨酸检测的特异性荧光探针的最新进展。 展开更多
关键词 荧光探针 硒代半胱氨酸 荧光检测 细胞成像
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硒蛋白的抗氧化性研究与第21个氨基酸的发现 被引量:21
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作者 黄开勋 刘琼 徐辉碧 《无机化学学报》 SCIE CAS CSCD 北大核心 2008年第8期1213-1218,共6页
硒是人体必需的微量元素,以硒代半胱氨酸(Sec)的形式存在于蛋白质中作为硒酶的活性中心发挥作用,其生物功能主要是抗氧化。由于硒与人体健康具有十分密切的关系,所以硒蛋白的研究有着重要的理论和实际意义。本文以第一个硒蛋白细胞谷胱... 硒是人体必需的微量元素,以硒代半胱氨酸(Sec)的形式存在于蛋白质中作为硒酶的活性中心发挥作用,其生物功能主要是抗氧化。由于硒与人体健康具有十分密切的关系,所以硒蛋白的研究有着重要的理论和实际意义。本文以第一个硒蛋白细胞谷胱甘肽过氧化物酶为例,结合作者自己的工作,重点对该硒酶的结构、催化机制和模拟进行了综述,并就TGA编码Sec致第21个氨基酸的发现以及基于硒代半胱氨酸插入元件(SECIS)的特征寻找新硒蛋白的研究进展进行了介绍。 展开更多
关键词 硒蛋白 硒代半胱氨酸 抗氧化 谷胱甘肽过氧化物酶的模拟 第21个氨基酸
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硒蛋白的分子生物学研究进展 被引量:27
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作者 黄峙 向军俭 郭宝江 《生物化学与生物物理进展》 SCIE CAS CSCD 北大核心 2001年第5期642-645,共4页
已有 35种硒蛋白被分离和表征 ,但许多硒蛋白及其功能仍未完全阐明 .硒半胱氨酸 (Sec)作为参入蛋白质的第 2 1种氨基酸 ,由硒蛋白mRNA上的UGA编码 .在原核生物 ,Sec参入硒蛋白的复杂机制已经较为明确 ,需要四种基因产物 (SELA、SELB、S... 已有 35种硒蛋白被分离和表征 ,但许多硒蛋白及其功能仍未完全阐明 .硒半胱氨酸 (Sec)作为参入蛋白质的第 2 1种氨基酸 ,由硒蛋白mRNA上的UGA编码 .在原核生物 ,Sec参入硒蛋白的复杂机制已经较为明确 ,需要四种基因产物 (SELA、SELB、SELC和SELD)和一个存在于硒蛋白mRNA上的被称为Sec插入序列(SECIS)的茎环 (stemloop)样二级结构 .在真核生物 ,硒蛋白生物合成途径可能在SECIS的结构和位置、特异的延伸因子及其他RNA RNA或RNA 蛋白质因子之间的相互作用等方面与原核生物不同 .另外 ,哺乳动物硒蛋白mRNA上的UGA翻译为Sec的过程低效 ,特定位点的UGA密码子不同功能 (终止密码和Sec密码 ) 展开更多
关键词 硒蛋白 硒半胱氨酸 生物合成 分子生物学
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植物硒代谢积累及相关酶的研究进展 被引量:25
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作者 杜玉潇 李亚男 陈大清 《热带亚热带植物学报》 CAS CSCD 北大核心 2007年第3期269-276,共8页
阐述了植物硒代谢的基本途径及其积累的分子机制,详细介绍了几种参与硒代谢的关键性酶的分子生物学特性。并展望了有关植物硒代谢的发展趋势。
关键词 植物 代谢 ATP硫酸化酶 谷光甘肽过氧化物酶 硒代半胱氨酸甲基转移酶 综述
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硒在前列环素生物合成中作用机制的研究 被引量:8
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作者 黄开勋 瞿祥虎 +3 位作者 邓利群 刘红梅 田涛 徐辉碧 《营养学报》 CAS CSCD 北大核心 2000年第1期1-4,共4页
目的 评价硒在前列环素生物合成中的作用机制。方法 用低硒饲料、补硒饲料和常规饲料饲养雄性大鼠 1 4周后 ,测定血液和某些组织中硒、前列环素 ( PGI2 )、血栓素 ( TXA2 )和脂质过氧化物 ( LPO)的含量 ,谷胱甘肽过氧化物酶 ( GSH- Px... 目的 评价硒在前列环素生物合成中的作用机制。方法 用低硒饲料、补硒饲料和常规饲料饲养雄性大鼠 1 4周后 ,测定血液和某些组织中硒、前列环素 ( PGI2 )、血栓素 ( TXA2 )和脂质过氧化物 ( LPO)的含量 ,谷胱甘肽过氧化物酶 ( GSH- Px)活性及前列腺素内过氧化物合成酶( PGHS)的过氧化物酶活性 ,并采用 RNA折叠程序对 3个前列环素合成酶 ( PGIS)基因 3 非翻译区 ( UTR)的二级结构进行计算机预测 ,与已知的 39个真核生物硒蛋白基因的硒代半胱氨酸插入序列 ( SECIS)进行比较。结果 低硒大鼠血浆 PGI2 浓度、血和组织中硒含量及 GSH- Px活性显著下降 ,LPO水平升高 ,但三组之间血浆 TXA2 水平和组织中 PGHS-过氧化物酶活性均无显著差异 ,在 PGIS基因中未见到硒蛋白所特有的 SECIS。结论 PGIS可能不是硒酶 ,硒可能是通过 GSH-Px或其他硒蛋白抑制过氧化物的产生而影响 PGI2 展开更多
关键词 硒缺乏 前列环素合成酶 硒蛋白 SECIS
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谷胱甘肽过氧化物酶的硒代半胱氨酸插入元件 被引量:13
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作者 瞿祥虎 黄开勋 +1 位作者 高中洪 徐辉碧 《中国生物化学与分子生物学报》 CAS CSCD 1999年第2期274-278,共5页
真核生物将硒代半胱氨酸插入蛋白质必需硒代半胱氨酸插入元件(SECIS)的参与,后者位于硒蛋白mRNA的3′非翻译区.采用RNA折叠程序对15个谷胱甘肽过氧化物酶基因进行计算机处理发现,其可能的SECIS中都具有3段保... 真核生物将硒代半胱氨酸插入蛋白质必需硒代半胱氨酸插入元件(SECIS)的参与,后者位于硒蛋白mRNA的3′非翻译区.采用RNA折叠程序对15个谷胱甘肽过氧化物酶基因进行计算机处理发现,其可能的SECIS中都具有3段保守碱基AUGA-A(G)AA-GA.根据A(G)AA位于顶环或者顶环上游5′臂的突环上。 展开更多
关键词 谷胱甘肽 过氧化物酶 硒代半胱氨酸 插入元件
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硒代半胱氨酸的生物合成及参入 被引量:6
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作者 向天勇 杨三东 吴永尧 《湖北民族学院学报(自然科学版)》 CAS 2005年第2期114-117,共4页
硒代半胱氨酸是蛋白硒的主要存在形式,其合成和参入有不同于其它氨基酸的生物学特点系统.阐述了原核生物和真核生物的硒代半胱氨酸的合成途径和参入机制,并比较了原核生物和真核生物硒蛋白基因中硒代半胱氨酸插入序列元件的结构特点.
关键词 硒代半胱氨酸 硒代半胱氨酸插入序列(SECIS) 硒蛋白
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硒蛋白的基因表达与调控 被引量:4
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作者 胥保华 许梓荣 《动物营养学报》 CAS CSCD 2003年第3期12-17,共6页
硒蛋白是微量元素硒以硒代半胱氯酸(SeC)形式进入多肽链的蛋白质。SeC的遗传密码是UGA。在原核细胞中,4种基因产物SELA、SELB、SELC和SELD参与了硒蛋白的合成过程。真核生物硒蛋白mRNA3’-UTR的硒代半胱氨酸插入序列(SECIS)是真核细胞UG... 硒蛋白是微量元素硒以硒代半胱氯酸(SeC)形式进入多肽链的蛋白质。SeC的遗传密码是UGA。在原核细胞中,4种基因产物SELA、SELB、SELC和SELD参与了硒蛋白的合成过程。真核生物硒蛋白mRNA3’-UTR的硒代半胱氨酸插入序列(SECIS)是真核细胞UGA密码编码SeC的顺式作用元件。动物的硒营养状态不影响硒蛋白基因的转录,但影响硒蛋白mRNA的稳定性。饲料硒水平与含硒酶活性呈正相关。 展开更多
关键词 硒蛋白 基因表达 基因调控 硒代半胱氨酸 多肽链 蛋白质 遗传密码 原核细胞 真核细胞
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气相色谱-三重四极杆质谱测定中老年奶粉中甲基硒代半胱氨酸 被引量:8
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作者 廖且根 李伟红 罗林广 《分析测试学报》 CAS CSCD 北大核心 2012年第4期491-494,共4页
采用气相色谱-三重四极杆质谱联用仪对中老年奶粉中的甲基硒代半胱氨酸进行定性确证和定量分析。样品经三氯乙酸和乙腈提取后,用氯甲酸乙酯在乙醇吡啶介质中衍生,衍生物经HP-5MS色谱柱分离并使用多反应监测模式进行定性和定量分析。甲... 采用气相色谱-三重四极杆质谱联用仪对中老年奶粉中的甲基硒代半胱氨酸进行定性确证和定量分析。样品经三氯乙酸和乙腈提取后,用氯甲酸乙酯在乙醇吡啶介质中衍生,衍生物经HP-5MS色谱柱分离并使用多反应监测模式进行定性和定量分析。甲基硒代半胱氨酸的线性范围为0.005~1.0 mg/L,方法检出限和定量下限分别为0.01、0.05 mg/kg。奶粉样品在0.05、0.2、0.4 mg/kg 3个加标水平下的平均回收率为79%~86%,相对标准偏差为2.8%~4.0%。该方法能满足中老年奶粉中甲基硒代半胱氨酸的质量控制需要。 展开更多
关键词 甲基硒代半胱氨酸 气相色谱-三重四极杆质谱仪 中老年奶粉 氯甲酸乙酯
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茶树ATP硫化酶和硒半胱氨酸甲基转移酶基因植物表达载体的构建 被引量:1
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作者 朱林 江昌俊 +4 位作者 叶爱华 李叶云 余梅 邓威威 房婉萍 《南京农业大学学报》 CAS CSCD 北大核心 2008年第2期121-125,共5页
采用能有效转化双子叶植物的表达载体pBI121构建植物硒营养代谢关键酶基因的表达载体,将原载体中GUS基因用茶树ATP硫化酶基因(APS1和APS2)替换,将硒半胱氨酸甲基转移酶基因(CsSMT)连接到pBI121载体上直接与GUS基因相连,分别构建了目的... 采用能有效转化双子叶植物的表达载体pBI121构建植物硒营养代谢关键酶基因的表达载体,将原载体中GUS基因用茶树ATP硫化酶基因(APS1和APS2)替换,将硒半胱氨酸甲基转移酶基因(CsSMT)连接到pBI121载体上直接与GUS基因相连,分别构建了目的基因植物表达载体pBI-APS1、pBI-APS2和pBI-CsSMT。通过三亲杂交法将重组质粒导入根癌农杆菌LBA4404中,获得转化工程菌,为通过植物基因工程获得富硒农产品打下基础。 展开更多
关键词 茶树 ATP硫化酶 硒半胱氨酸甲基转移酶 基因 植物表达载体
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茶树硒营养代谢关键酶硒半胱氨酸甲基转移酶基因克隆及启动子结构分析 被引量:1
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作者 王雅楠 陈晶晶 朱林 《中国农学通报》 CSCD 2013年第28期138-143,共6页
为探明茶树硒营养代谢关键酶基因硒半胱氨酸甲基转移酶(SMT,GenBank登录号:DQ480337)的表达调控规律,通过PCR和基因步移技术获得SMT的DNA全长和部分启动子序列,用PLACE、PlantCARE分析SMT内含子和启动子的序列,预测其顺式作用元件及功... 为探明茶树硒营养代谢关键酶基因硒半胱氨酸甲基转移酶(SMT,GenBank登录号:DQ480337)的表达调控规律,通过PCR和基因步移技术获得SMT的DNA全长和部分启动子序列,用PLACE、PlantCARE分析SMT内含子和启动子的序列,预测其顺式作用元件及功能。结果表明,SMT基因全长5473 bp,有7个外显子和6个内含子,内含子富含光响应元件、激素响应元件和抗逆性相关元件。通过基因步移法克隆得到的SMT启动子长375 bp,除了含核心启动子保守元件TATA-box和CAAT-box外,还有其他重要顺式作用元件,如光响应元件、低温响应元件和胚乳表达特异性元件等。植物硒营养代谢关键酶SMT启动子的克隆及结构分析为进一步揭示SMT基因的生物学功能和表达调控机制奠定了理论基础。 展开更多
关键词 富硒茶(嫩叶) 硒半胱氨酸甲基转移酶 启动子 基因组步移
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