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1.
利用人粒细胞集落刺激因子(hG-CSF)cDNA3′端非翻译区(3′-UTR)中存在的DraⅠ酶切位点,通过部分酶切与完全酶切,删除3′-UTR不同长度,构建了四种hG-CSFcDNA瞬时重组表达质粒。转染COS-7细胞后,生物活性测定结果提示,hG-CSFcDNA3′-UTR对其表达起负调控作用,其关键性序列位于紧接终止密码子TGA下游的65bp范围内,3′-UTR对hG-CSFcDNA表达的影响与转录水平的差别有一定关系。  相似文献   

2.
用富集文库克隆人胰岛素基因组基因   总被引:1,自引:0,他引:1  
通过构建可富集人胰岛素基因的λ噬菌体文库,克隆了人胰岛素基因组基因.首先从中国人血液白细胞中提取到人基因组DNA,用EcoRⅠ和BglⅡ对基因组DNA进行全酶切,经0.4%琼脂糖凝胶电泳,特异回收9.5kb左右的DNA片段.将该片段与λEMBL3/BamHⅠ臂连接,构建成一个特殊的人基因组λ噬菌体文库(富集文库),效价为2×104.同时采用PCR方法及用引物Ⅰ:5′GGACAGGCTACATCAGGAAGAGG3′,引物Ⅱ:5′CTGCGTCTAATTGCAGTAGTTC3′,从人基因组DNA中扩增出一段含胰岛素基因的1.36kbDNA片段,做为放射性标记探针,对文库进行了噬菌斑原位杂交筛选,从1×104个噬菌斑中筛选到一个含人胰岛素基因组基因的阳性克隆,并进一步完成了亚克隆和该基因1732bpDNA序列的测定.结果该基因的1732bpDNA序列包括部分5′端和3′端与国外发表的人胰岛素α型等位基因的序列相同  相似文献   

3.
利用COS7细胞暂时表达系统,研究转译起始序列对EPO-cDNA表达的影响。通过DNA重组技术,构建了原EPO-cDNA表达载体pCSV-EPO(1),其转译起始序列为5'AATTCATGG3'。同时通过定点突变技术,将起始序列改变成5'CCACCATGG3',而构建了另一表达载体PCSV-EPO(2)。后经序列分析证明无误后和前均通过DEAE-dextran法转染COS7细胞上清,测定结果为  相似文献   

4.
利用人粒细胞集落刺激因子(hG-CSF()cDNA3'端非翻译区(3'UTR)中存在的DraI酶切位点,通过部分酶切与完全酶切,删除3'-UTR不同长度构建了四种hG-CSF cDNA瞬时重组表达质粒,转染COS-7细胞手,生物活性测定结果提示,hG-CSFcDNA3'-UTR对其表达起负调控作用,其关键性序列位于紧接终止密码子TGA下游的65bp范围内,3'-UTR对hG-CSF cDNA表达的  相似文献   

5.
补调连蛋白     
1986年,德国BernbardNocht热带医学研究所的Kristine等在克隆补体调节蛋白H因子的cDNA时,首次从人肝cDNA里分离了克隆CHH17/pFH1.8,其5′端序列1408bp与H因子5′端序列完全相同,并且其编码的蛋白质一级结构含...  相似文献   

6.
番茄抗病基因Cf9的3′UTR区含有内含子序列   总被引:2,自引:0,他引:2  
从番茄(LycopersiconesculentumMil.)抗病品种“中杂9号”基因组DNA中扩增并克隆了番茄抗叶霉病基因Cf9。序列分析结果表明,该基因全长2751bp,含有一个编码863个氨基酸的开放阅读框架。在该基因的3′UTR区发现了一段未曾报道的内含子序列,长115bp,它所处的位置与番茄另一个抗叶霉病基因Cf2内含子的位置相似,其5′和3′边界序列为一重复序列,TCCAGG(T)ATTC,并与Cf2基因内含子边界序列高度同源。与已报道的Cf9的cDNA序列相比,它的第371位的核苷酸T突变成了C,从而使其编码蛋白的LRR区第121位的亮氨酸突变为脯氨酸。  相似文献   

7.
用从基因文库中所克隆的促红细胞生成素(EPO)基因组基因,构建了3种由不同启动子调控的表达载体——pOP13/EPO,pRSV/EPO,pCMV/EPO,在这3个表达载体的构建过程中对基因的转录起始效率、内含子的剪接、5′非翻译区和3′非翻译区对基因表达的影响等因素都加以考虑.用脂质体转染法分别将上述3个载体导入CHO细胞,经瞬时表达,用ELISA方法检测,表达量分别为190mIU/ml、160mIU/ml、447mIU/ml.用表达载体pOP13/EPO转染CHO-K12细胞,在400μg/ml的G418浓度下筛选稳定表达细胞克隆,获得了表达量约为160IU/106细胞(48h)的C10细胞株.表达产物经Westernblot检测发现了EPO阳性条带.用TF-1细胞对EPO进行了生物活性检测,初步证实所表达的EPO有生物活性.  相似文献   

8.
为研究胰岛素样生长因子-1(IGF1)及其突变体与IGF结合蛋白-3(IGFBP3)的相互作用,针对IGF1的第3、4、15、16位氨基酸残基,采用定点突变的方法构建了「Y15L16」IGF1和「Q3A4Y15L16」IGF1。然后分别将IGF1/IGF1突变体和IGFBP3 cDNA克隆至酵母表达载体pGBT9和pACT2中,利用用酵母双杂交技术检测IGF1/IGF1突变体和IGFBP3之间的相  相似文献   

9.
通过对猪生长激素(pGH)基因的cDNA进行测序,得到pGHcDNA的全序列,并与Seeburg等报道的序列进行了比较和讨论。然后利用具人工合成启动子和多角体蛋白XIV启动子的转移载体质粒pSXIVVI^+X3/4构建出含pGH基因的重组质粒pX3/4-pGH。将pX3/4-pGH与致死缺失型线性化AcMNPV-OCC^-DNA共转染Sf9细胞,构建出既能形成多角体又能表达pGH基因的苜蓿丫纹夜蛾  相似文献   

10.
分别利用5’RACE和3’RACE确定了CMV-SDRNA2的5’和3’未端序列,在此基础上,利用RT-PCR得到了RNA2的5’端一半的cDNADQ BTG Pc25和3’端一半的cDNA克隆PC23,并通过拼接构建了RNA2全长cDNA克隆PC2F。  相似文献   

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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases  相似文献   

14.
Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

18.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

19.
The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.  相似文献   

20.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

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