Spindlin1, a novel nuclear protein with a role in the transformation of NIH3T3 cells

spindlin1, a novel human gene recently isolated by our laboratory, is highly homologous to mouse spindlin gene. In this study, we cloned cDNA full-length of this novel gene and send it to GenBank database as spindlin1 (Homo sapiens spindlin1) with Accession No. AF317228. In order to investigate the function of spindlin1, we studied further the subcellular localization of Spindlin1 protein and the effects of spindlin1 overexpression in NIH3T3 cells. The results showed that the fusion protein pEGFP-N1-spindlin1 was located in the nucleus and the C-terminal is correlated with nuclear localization of Spindlin1 protein. NIH3T3 cells which could stably express spindlin1 as a result of RT-PCR analysis compared with the control cells displayed a complete morphological change; made cell growth faster; and increased the percentage of cells in G2/M and S phase. Furthermore, overexpressed spindlin1 cells formed colonies in soft agar in vitro and formed tumors in nude mice. Our findings provide direct evidence that spindlin1 gene may contribute to tumorigenesis.     

植酸酶及其热稳定性研究进展

植酸酶能降解植物性饲料中的植酸盐类,释放出无机磷酸,对于提高饲料中磷的利用率,减轻畜禽高磷排泄物对环境的污染以及促进单胃动物对饲料中矿质营养的吸收利用有重要作用,因此植酸酶的研究有重要的科学和实用价值。获得高活性高热稳定性的植酸酶是近年来植酸酶工业的研究热点和难点,综述了植酸酶及其热稳定性研究的现状和提高植酸酶热稳定性方法的最新进展 。     

A strategy for fusion expression and preparation of functional glucagon-like peptide-1 (GLP-1) analogue by introducing an enterokinase cleavage site

KGLP-1, a 31-amino acid glucagon-like peptide-1 (GLP-1) analogue, has a great therapeutic potential for anti-diabetes. In this work, a strategy for expression and purification of functional KGLP-1 peptide has been established. KGLP-1 cDNA was fused with glutathione S-transferase (GST), with an enterokinase cleavage site in the fusion junction. The recombinant fusion protein GST–KGLP-1 was affinity purified via the GST-tag, and then digested with enterokinase. The resulting GST part as well as the enzymes were eliminated by ultra-filtration followed by size exclusion chromatograph. The yield of purified KGLP-1 was approximately 12.1 mg/L, with purity of 96.18 %. The recombinant KGLP-1 was shown to have similar bioactivity as native GLP-1 when evaluated in a Chinese hamster ovary cell line expressing a GLP-1 receptor-egfp reporter gene.     

流行性乙型脑炎病毒E基因的克隆、表达及初步应用

参照GenBank中的日本乙型脑炎病毒(Japanese encephalitis virus,JEV)SA14-14株序列设计了一对特异性引物,用PCR方法从SA14-14扩增E基因全长,然后克隆到pMD18-T载体中,转化宿主菌DH5a,提取阳性克隆质粒进行双酶切鉴定,将目的片段定向克隆到pET32a( )中,转化入BL21(DE3),经IPTG诱导可表达分子量约73ka的蛋白,Western blotting试验呈阳性,表明E基因得到表达。以纯化的表达产物为核心抗原,猪抗JEV血清为一抗,HRP标记羊抗猪IgG抗体为二抗建立间接ELISA方法,并初步检测了一些血清样品,结果提示表达的蛋白具有很好的应用开发价值。     

基于土地利用变化情景的生态系统服务价值评估: 以钱江源国家公园体制试点区为例

土地利用变化是生物多样性与生态系统服务变化的主要原因之一。评估土地利用变化对生物多样与生态系统服务影响对于政府决策具有重要作用。钱江源国家公园体制试点区是钱塘江的源头, 也是国家的重点生态功能区。本研究以钱江源国家公园体制试点区为研究区, 首先设计自然发展情景、规划情景、生态保护情景和开发利用情景等4种2025年不同土地利用变化情景, 随后采用InVEST模型和CLUE-S模型分析不同情景下钱江源国家公园水资源供给、涵养水源、固碳释氧、土壤保持、环境净化和生境质量等生态系统服务及其价值变化。结果表明: (1)核心保护区和生态保育区的生态系统服务价值占钱江源国家公园总价值的88.30%。(2)生态保护情景下钱江源国家公园生态系统服务价值最高, 有129.17亿元; 规划情景下生态系统服务价值次之, 有126.92亿元。(3)规划情景下钱江源国家公园水资源供给服务优于生态保护情景, 其他生态系统服务则次于生态保护情景。考虑到钱江源国家公园为下游提供重要的水资源这一功能, 将规划情景作为试点区2025年最优的土地利用变化情景。     

苏云金芽孢杆菌S1478-1分离株的特性鉴定及cry1Ac同源基因克隆

本研究对从海南岛尖峰岭热带雨林自然保护区的土壤样品中分离出的Bt菌株S1478-1进行了特性鉴定,研究表明S1478-1分离株菌落形态和生长特征和Bt参照菌株HD73极其相似.16S rDNA序列分析表明,S1478-1分离株与其它B.thuringiensis、B.cereus和B.anthracis的16S rDNA序列相似性达到99%.分离株能产菱形伴胞晶体,SDS-PAGE蛋白电泳分析表明,菌株在生长后期,形成芽孢同时分泌130 kD大小的晶体蛋白.生物测定表明S1478-1分离株对小菜蛾具有很高的毒杀活性,LC50卯值高达5.159 ×108cfu/mL.初步显示S1478-1分离株可作为防治鳞翅目害虫的生物农药菌株.利用PCR-RFLP方法鉴定S1478-1分离株含有cry1Ac同源基因,以PCR粘性端克隆方法扩增全长基因,序列测定表明该基因ORF为3 537bp,编码1178个氨基酸,推定的编码蛋白分子量为133.3 kD,与其它cry1Ac基因序列最高达到99%同源,因此,该基因可作为杀虫工程菌及培育转基因抗虫作物的候选基因.     

p16蛋白在子宫内膜癌中表达的研究

为探讨P16基因在子宫内膜癌发生及发展过程中所起的作用,采用免疫组化SP法对38例子宫内膜癌(腺癌33例,腺棘皮癌4例,浆液性乳头状腺癌1例)及19例正常组织进行了p16蛋白的免疫组化检测,结果p16蛋白在正常组织中表达率为56.8%,在腺癌中的表达率为21.7%,在腺棘皮和浆液性乳头腺癌中的表达率为25.1%,与正常组差异显著,同时,p16蛋白在Ⅰ-Ⅱ期子宫内膜中的表达率为26.4%。而在Ⅲ-Ⅳ期子宫内膜癌中的表达率为11.7% ,二者差异显著,说明p16蛋白在子宫内膜癌的发生及进展过程中起重要作用。 Abstract:To understand the role of P16 gene in the progression of carcinoma of endometrium,the expression of P16 gene was detected in 38 carcinoma of endometrium specimens and 19 controls by immunhistochemical SP method.The p16 protein positive rates of carcinoma of endometrium and control had significant difference (P<0.05),and the expression of p16 protein was also significant different between I～II grades and III～IV grades of adenocarcinoma of endometrium.So the p16 protein was closely associated with the generation and development of the carcinoma of endometrium.     

The molecular basis of spinocerebellar ataxia type 48 caused by a de novo mutation in the ubiquitin ligase CHIP

The spinocerebellar ataxias (SCAs) are a class of incurable diseases characterized by degeneration of the cerebellum that results in movement disorder. Recently, a new heritable form of SCA, spinocerebellar ataxia type 48 (SCA48), was attributed to dominant mutations in STIP1 homology and U box-containing 1 (STUB1); however, little is known about how these mutations cause SCA48. STUB1 encodes for the protein C terminus of Hsc70 interacting protein (CHIP), an E3 ubiquitin ligase. CHIP is known to regulate proteostasis by recruiting chaperones via a N-terminal tetratricopeptide repeat domain and recruiting E2 ubiquitin-conjugating enzymes via a C-terminal U-box domain. These interactions allow CHIP to mediate the ubiquitination of chaperone-bound, misfolded proteins to promote their degradation via the proteasome. Here we have identified a novel, de novo mutation in STUB1 in a patient with SCA48 encoding for an A52G point mutation in the tetratricopeptide repeat domain of CHIP. Utilizing an array of biophysical, biochemical, and cellular assays, we demonstrate that the CHIP^A52G point mutant retains E3-ligase activity but has decreased affinity for chaperones. We further show that this mutant decreases cellular fitness in response to certain cellular stressors and induces neurodegeneration in a transgenic Caenorhabditis elegans model of SCA48. Together, our data identify the A52G mutant as a cause of SCA48 and provide molecular insight into how mutations in STUB1 cause SCA48.     

Targeting UPR branches,a potential strategy for enhancing efficacy of cancer chemotherapy

Cancer cells are often exposed to cell intrinsic stresses and environmental perturbations that may lead to accumulation of unfolded and/or misfolded proteins in...