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1.
2.
The protozoan parasite Trypanosoma brucei is lysed by apolipoprotein L-I, a component of human high-density lipoprotein (HDL) particles that are also characterized by the presence of haptoglobin-related protein. We report that this process is mediated by a parasite glycoprotein receptor, which binds the haptoglobin-hemoglobin complex with high affinity for the uptake and incorporation of heme into intracellular hemoproteins. In mice, this receptor was required for optimal parasite growth and the resistance of parasites to the oxidative burst by host macrophages. In humans, the trypanosome receptor also recognized the complex between hemoglobin and haptoglobin-related protein, which explains its ability to capture trypanolytic HDLs. Thus, in humans the presence of haptoglobin-related protein has diverted the function of the trypanosome haptoglobin-hemoglobin receptor to elicit innate host immunity against the parasite.  相似文献   

3.
Vitamin D3 receptors are intracellular proteins that mediate the nuclear action of the active metabolite 1,25-dihydroxyvitamin D3 [1,25(OH)2D3]. Two receptor-specific monoclonal antibodies were used to recover the complementary DNA (cDNA) of this regulatory protein from a chicken intestinal lambda gt11 cDNA expression library. The amino acid sequences that were deduced from this cDNA revealed a highly conserved cysteine-rich region that displayed homology with a domain characteristic of other steroid receptors and with the gag-erbA oncogene product of avian erythroblastosis virus. RNA selected via hybridization with this DNA sequence directed the cell-free synthesis of immunoprecipitable vitamin D3 receptor. Northern blot analysis of polyadenylated RNA with these cDNA probes revealed two vitamin D receptor messenger RNAs (mRNAs) of 2.6 and 3.2 kilobases in receptor-containing chicken tissues and a major cross-hybridizing receptor mRNA species of 4.2 kilobases in mouse 3T6 fibroblasts. The 4.2-kilobase species was substantially increased by prior exposure of 3T6 cells to 1,25(OH)2D3. This cDNA represents perhaps the rarest mRNA cloned to date in eukaryotes, as well as the first receptor sequence described for an authentic vitamin.  相似文献   

4.
Radioreceptor assay for 1 alpha,25-dihydroxyvitamin D3   总被引:14,自引:0,他引:14  
A competitive protein binding assay with a sensitivity of 80 picograms has been developed for 1alpha,25-dihydroxyvitamin D(3), the hormonal form of vitamin D(3). lalpha,25-Dihydroxyvitamin D(3) displaced tritiated hormone from a cytosol-chromatin receptor preparation isolated from chick small intestine, providing a simple assay for the hormone. The concentration of lalpha, 25-dihydroxyvitamin D(3) in human plasma, as determined by this assay, is approximately 6 nanograms per 100 milliliters; in patients with renal disease the concentration of this kidney-produced hormone is significantly lower.  相似文献   

5.
从骨形态发生蛋白15(BMP15)基因、生长分化因子9(GDF9)基因、视黄醇结合蛋白4(RBP4)基因、视黄酸受体γ(RARG)基因、催乳素(PRL)基因、催乳素受体(PRLR)基因、褪黑激素受体基因、促性腺激素释放激素(GnRH)及其受体(GnRHR)基因方面综述了羊多胎性状候选基因的研究进展.  相似文献   

6.
A chemoattractant receptor controls development in Dictyostelium discoideum   总被引:39,自引:0,他引:39  
During the early stages of its developmental program, Dictyostelium discoideum expresses cell surface cyclic adenosine monophosphate (cyclic AMP) receptors. It has been suggested that these receptors coordinate the aggregation of individual cells into a multicellular organism and regulate the expression of a large number of developmentally regulated genes. The complementary DNA (cDNA) for the cyclic AMP receptor has now been cloned from lambda gt-11 libraries by screening with specific antiserum. The 2-kilobase messenger RNA (mRNA) that encodes the receptor is undetectable in growing cells, rises to a maximum at 3 to 4 hours of development, and then declines. In vitro transcribed complementary RNA, when hybridized to cellular mRNA, specifically arrests in vitro translation of the receptor polypeptide. When the cDNA is expressed in Dictyostelium cells, the undifferentiated cells specifically bind cyclic AMP. Cell lines transformed with a vector that expresses complementary mRNA (antisense) do not express the cyclic AMP receptor protein. These cells fail to enter the aggregation stage of development during starvation, whereas control and wild-type cells aggregate and complete the developmental program within 24 hours. The phenotype of the antisense transformants suggests that the cyclic AMP receptor is essential for development. The deduced amino acid sequence of the receptor reveals a high percentage of hydrophobic residues grouped in seven domains, similar to the rhodopsins and other receptors believed to interact with G proteins. It shares amino acid sequence identity and is immunologically cross-reactive with bovine rhodopsin. A model is proposed in which the cyclic AMP receptor crosses the bilayer seven times with a serine-rich cytoplasmic carboxyl terminus, the proposed site of ligand-induced receptor phosphorylation.  相似文献   

7.
采用PCR-RFLP方法检测了NCOA1基因,OPN基因和RBP4基因的多态性,并且分析了不同基因型对仔猪出生重和30日龄体重效应的大小。结果表明:NCOA1基因可显著影响仔猪的30日龄体重,AA型个体比BB型个体增重显著(P0.05)。而OPN和RBP4基因的不同基因型对这2个性状的效应差异均不显著。在试验群体内,NCOA1基因可作为一个有效的候选基因进行研究应用,而OPN和RBP4基因还需进一步扩大样本量进行相关性分析。  相似文献   

8.
八个猪种PRLR和RBP4基因PCR-RFLP检测及群体遗传特性研究   总被引:2,自引:0,他引:2  
本研究采用PCR-RFLP方法,对莱芜黑猪、鲁莱黑猪、里岔黑猪、鲁烟白猪、新沂蒙黑猪5个山东本地猪种和大约克夏、长白、杜洛克3个引进猪种共八个猪种323头繁殖母猪进行PRLR和RBP4基因的多态性检测,并对其遗传多样性进行分析。结果表明:两个基因位点在八个猪种的测定群体中均存在多态性,在三种基因型中AB基因型出现频率最高,山东本地猪种与引进猪种间基因型频率存在显著差异(P<0.05)。八个猪种PRLR和RBP4基因位点的期望杂合度分别在0.3265~0.5062和0.2655~0.5019之间,多态信息含量分别在0.2688~0.4268和0.2264~0.3736之间。研究结果提示:杜洛克猪在这两个基因位点的杂合度最低,其遗传一致性最好,其余猪种均表现为中度多态,表明这些猪种具有较为丰富的遗传多态性。  相似文献   

9.
Estrogen-receptor interaction   总被引:27,自引:0,他引:27  
The interaction of estradiol with uterine cells involves the association of the hormone with an extranuclear receptor protein, followed by temperature dependent translocation of the resulting complex to the nucleus. During this process, the steroid binding unit of the protein undergoes an alteration, called "receptor transformation," that can be recognized by an increase in its sedimentation rate from 3.8S to 5.2S, and by its acquisition of the ability to bind to isolated uterine nuclei and to alleviate a tissue specific deficiency in the RNA synthesizing capacity of such nuclei. Receptor transformation can be effected in the absence of nuclei by warming uterine cytosol with estradiol. This preparation of transformed complex resembles that extracted from nuclei both in its sedimentation rate (5.3S) and in its ability to bind to uterine nuclei and augment RNA synthesis, properties that are not shown by the native complex. It is proposed that receptor transformation is an important step in estrogen action and that a principal role of the hormone is to induce conversion of the receptor protein to a biochemically functional form.  相似文献   

10.
富硒米糠蛋白的优化制备及其蛋白营养复配研究   总被引:3,自引:0,他引:3  
胡秋辉    陈曦  方勇    陈悦  杨文建  马宁  赵立艳 《中国农业科学》2014,47(2):374-382
【目的】优化碱法提取富硒米糠蛋白的条件,根据蛋白质互补作用原理,研究并评价富硒米糠蛋白(RBP)的营养复配。【方法】碱法提取富硒米糠蛋白,按正交试验L9(34)优化富硒米糠蛋白的提取条件。将富硒米糠蛋白与大豆分离蛋白(SP)按比例60%、70%、80%、90%和100%进行复配,用凯氏定氮法、氢化物原子荧光光谱法和便携式色差仪分别测定富硒米糠蛋白和复配蛋白中的蛋白质含量、硒含量和色差值。利用高速氨基酸分析仪测定各蛋白产品的氨基酸含量,并根据必需氨基酸参考模式(WHO/ FAO)和氨基酸比值系数法,对各蛋白产品进行营养价值评价,得出营养价值最高的复配蛋白。【结果】通过正交试验考察富硒米糠蛋白的提取率、硒含量和富硒米糠蛋白的色差值,获得富硒米糠蛋白最佳提取条件为:料液比1﹕20、NaOH 浓度0.08 mol•L-1、温度30℃和时间3 h,富硒米糠蛋白纯度为(80.2±1.1)%,硒含量为(0.269±0.132)mg•kg-1,蛋白色差值为69.7±1.2,将此最优条件下提取出的富硒米糠与普通米糠蛋白产品的蛋白质和硒含量分别进行比较,结果表明,富硒米糠与普通米糠的蛋白质含量、富硒米糠蛋白与普通米糠蛋白的蛋白质含量都无显著性差异(P<0.01),而富硒米糠的硒含量为(0.401±0.021)mg•kg-1,显著高于普通米糠硒含量(0.023±0.010)mg•kg-1(P<0.01),同时富硒米糠蛋白的硒含量为(0.269±0.132)mg•kg-1,也显著高于普通米糠蛋白硒含量(0.052±0.011)mg•kg-1(P<0.01)。将富硒米糠蛋白与大豆分离蛋白(SP)按照不同比例进行营养复配,比较不同复配蛋白产品的蛋白纯度和硒含量,得出富硒米糠蛋白和各复配蛋白的硒含量均显著高于大豆分离蛋白硒含量(0.013±0.005)mg•kg-1,不同配比的复配蛋白硒含量随富硒米糠蛋白含量增加从(0.141±0.014)mg•kg-1增加至(0.269±0.032)mg•kg-1。根据必需氨基酸参考模式,采用氨基酸比值系数法评价各蛋白产品营养价值,根据比值系数分(SRC)富硒米糠蛋白和各复配蛋白的营养价值按高低顺序排列如下:60% RBP > 70% RBP > 50% RBP > 80% RBP > 90% RBP > RBP,结果表明,各复配蛋白SRC值均高于RPB的SRC值64.1,由此证明各复配蛋白营养价值均高于RBP,其中含60%富硒米糠蛋白的复配蛋白具有最高的营养价值,且其硒含量为(0.167±0.024)mg•kg-1,蛋白纯度为(84.1±0.8)%。【结论】将大豆蛋白与富硒米糠蛋白进行复配可提高蛋白的营养价值,获得一种含丰富微量元素硒的高品质蛋白。  相似文献   

11.
E2F-6 contributes to gene silencing in a manner independent of retinoblastoma protein family members. To better elucidate the molecular mechanism of repression by E2F-6, we have purified the factor from cultured cells. E2F-6 is found in a multimeric protein complex that contains Mga and Max, and thus the complex can bind not only to the E2F-binding site but also to Myc- and Brachyury-binding sites. Moreover, the complex contains chromatin modifiers such as a novel histone methyltransferase that modifies lysine 9 of histone H3, HP1gamma, and Polycomb group (PcG) proteins. The E2F-6 complex preferentially occupies target promoters in G0 cells rather than in G1 cells. These data suggest that these chromatin modifiers contribute to silencing of E2F- and Myc-responsive genes in quiescent cells.  相似文献   

12.
Sequence and expression of human estrogen receptor complementary DNA   总被引:95,自引:0,他引:95  
The mechanism by which the estrogen receptor and other steroid hormone receptors regulate gene expression in eukaryotic cells is not well understood. In this study, a complementary DNA clone containing the entire translated portion of the messenger RNA for the estrogen receptor from MCF-7 human breast cancer cells was sequenced and then expressed in Chinese hamster ovary (CHO-K1) cells to give a functional protein. An open reading frame of 1785 nucleotides in the complementary DNA corresponded to a polypeptide of 595 amino acids and a molecular weight of 66,200, which is in good agreement with published molecular weight values of 65,000 to 70,000 for the estrogen receptor. Homogenates of transformed Chinese hamster ovary cells containing a protein that bound [3H]estradiol and sedimented as a 4S complex in salt-containing sucrose gradients and as an 8 to 9S complex in the absence of salt. Interaction of this receptor-[3H]estradiol complex with a monoclonal antibody that is specific for primate ER confirms the identity of the expressed complementary DNA as human estrogen receptor. Amino acid sequence comparisons revealed significant regional homology among the human estrogen receptor, the human glucocorticoid receptor, and the putative v-erbA oncogene product. This suggests that steroid receptor genes and the avian erythroblastosis viral oncogene are derived from a common primordial gene. The homologous region, which is rich in cysteine, lysine, and arginine, may represent the DNA-binding domain of these proteins.  相似文献   

13.
Herpes simplex virus type 1 (HSV-1) is a ubiquitous pathogen responsible for considerable morbidity in the general population. The results presented herein establish the basic fibroblast growth factor (FGF) receptor as a means of entry of HSV-1 into vertebrate cells. Inhibitors of basic FGF binding to its receptor and competitive polypeptide antagonists of basic FGF prevented HSV-1 uptake. Chinese hamster ovary (CHO) cells that do not express FGF receptors are resistant to HSV-1 entry; however, HSV-1 uptake is dramatically increased in CHO cells transfected with a complementary DNA encoding a basic FGF receptor. The distribution of this integral membrane protein in vivo may explain the tissue and cell tropism of HSV-1.  相似文献   

14.
The insulin receptor contains a calmodulin-binding domain   总被引:3,自引:0,他引:3  
Substantial evidence suggests that calcium has a pivotal role in regulating the initial events through which insulin alters plasma membrane metabolism. Because binding of insulin to its receptor represents the initial site of insulin action in the plasma membrane, studies were undertaken to determine whether the insulin receptor is a calmodulin-binding protein. Preparations enriched in the insulin receptor and calmodulin-binding proteins were isolated from detergent-solubilized rat adipocyte membranes by chromatography with wheat germ agglutinin agarose and calmodulin-conjugated Sepharose, respectively. Substantial purification of a manganese-dependent, insulin-sensitive phosphoprotein of 95K identified as the beta subunit of the insulin receptor was accomplished. Binding and photocovalent cross-linking of iodine-125-labeled calmodulin to these affinity-purified preparations and to isolated plasma membranes, followed by immunoadsorption with insulin receptor antibodies bound to protein A Sepharose, resulted in significant purification of a binding complex of 110K to 140K. These results indicate that the adipocyte insulin receptor or a polypeptide closely associated with the receptor is a calmodulin-binding protein.  相似文献   

15.
Transport and storage of vitamin A   总被引:34,自引:0,他引:34  
  相似文献   

16.
Embryonic chick intestine maintained in organ culture responded to vitamin D(3) and its metabolites 25-hydroxycholecalciferol and 1,25-dihydroxycholecalciferol by synthesis of calcium-binding protein and enchanced calcium-45 uptake. The dihydroxy metabolite was by far the most potent inducer of the protein and also acted more rapidly than vitamin D(3) to stimulate isotope uptake. Despite its lower potency, vitamin D(3) itself was effective.  相似文献   

17.
Homology of beta-lactoglobulin, serum retinol-binding protein, and protein HC   总被引:13,自引:0,他引:13  
The milk protein beta-lactoglobulin has been extensively studied but its function has not been identified. A clue regarding the function of a protein can be obtained by discovering a genetic relationship with a protein of known function through comparisons of amino acid sequence. Such comparisons revealed that beta-lactoglobulin is similar to human serum retinol-binding protein and to another human protein of unknown function known as complex-forming glycoprotein heterogeneous in charge (protein HC). beta-Lactoglobulins from several species have been found to bind retinol, while the absorption and fluorescence properties reported for the unidentified heterogeneous prosthetic group of protein HC are retinoid-like. The role of serum retinol-binding protein in vitamin A transport in the circulation suggests that the other two homologous proteins may function in the binding and transport of retinoids; beta-lactoglobulin may facilitate the absorption of vitamin A from milk and protein HC may mediate the excretion of retinol-derived metabolites.  相似文献   

18.
19.
Netrins stimulate and orient axon growth through a mechanism requiring receptors of the DCC family. It has been unclear, however, whether DCC proteins are involved directly in signaling or are mere accessory proteins in a receptor complex. Further, although netrins bind cells expressing DCC, direct binding to DCC has not been demonstrated. Here we show that netrin-1 binds DCC and that the DCC cytoplasmic domain fused to a heterologous receptor ectodomain can mediate guidance through a mechanism involving derepression of cytoplasmic domain multimerization. Activation of the adenosine A2B receptor, proposed to contribute to netrin effects on axons, is not required for rat commissural axon outgrowth or Xenopus spinal axon attraction to netrin-1. Thus, DCC plays a central role in netrin signaling of axon growth and guidance independent of A2B receptor activation.  相似文献   

20.
Mononuclear blood cells were obtained from a patient with type A insulin resistance. The cells showed a normal ability to bind iodine 125-labeled insulin. Analysis of solubilized insulin receptors from the patient's cells revealed a defect in insulin-stimulated tyrosine kinase activity, which is closely associated with the receptor itself. The enzyme failed to phosphorylate the insulin receptor and showed a markedly reduced ability to phosphorylate exogenously added substrates. It appears that receptors from this insulin-resistant patient have a defect distal to the insulin-binding site (the alpha subunit of the receptor). The defect could be located in the beta subunit, which has an adenosine triphosphate-binding site, or in another receptor component that transfers a signal of insulin binding into kinase activity. This dissociation between the normal binding and the defective protein kinase component of the insulin receptor represents the first biochemical defect of the receptor distal to ligand binding.  相似文献   

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