基因敲除鼠疾病模型的研究进展

基因敲除是研究生物体基因功能的有效手段。通过基因敲除建立的鼠疾病模型,在研究基因功能及人类疑难病症致病机制等方面发挥着前所未有的作用。本文对目前已获得的基因敲除鼠疾病模型进行了分类和总结,为相关研究的展开奠定了基础。 Abstract:The knock-out technology is an effective means in studying the gene function of organism.The disease model of gene knock-out mouse is of significance in understanding the gene function and pathogenesis of human disease.The available models of gene knock-out mouse are classified and summarized to promote the development of related research.     

黑素皮质激素受体1（MC1R）基因与猪的毛色

猪的真黑色素与褐黑色素的合成量与分布主要受控于黑素皮质激素受体1基因。本文综述了该基因的定位、突变与多态检测,黑素皮质激素受体的作用机制,提出了对黑素皮质激素受体1基因进一步研究的看法。 Abstract：The amount and distribution of eumelanin and phaeomelanin are mainly controlled by Melanocortin Receptor 1 gene.The location、mutation and polymorphism testing of Melanocortin Receptor 1 gene and mechanism of Melanocortin Receptor 1 in pigs are discussed in the paper.The further research about the gene is also suggested.     

猪显性白毛调控基因（KIT）的研究

猪的白毛色性状由显性基因KIT决定。本文从KIT基因的定位、突变分析、分子基础和作用机制等方面综述了对该基因的研究现状,叙述了KIT基因的研究意义。 Abstract：The dominant coat color in pigs is controlled by KIT gene.The current status of KIT gene is expressed in location、mutation、molecular basis and mechanism.Significance of KIT gene is also discussed in this paper.     

Inhibition of the growth of human hepatoma cell line both in vitro and in vivo by transducing CKI gene p21~(WAF-1) with GE7 targeting gene delivery system

The EGF receptor-mediated targeting gene delivery system GE7 was used to transduce exogenous gene pCEP-p21WAF-1 into human hepatocellular carcinoma cell both in vitro and in vivo. After in vitro transduction of the exogenous gene, the growth of the cell lines SMMC-7721 and BEL-7402 was significantly inhibited compared with the control. On day 8 the inhibition rates of the above cell lines reached 56.0% and 66.7%, respectively. The in vivo experiment showed that the growth of human hepatoma transplanted in nude mice injected with GE7 gene delivery system subcutaneously once a week for 3 weeks was remarkably inhibited compared with that of untrans-fected control. The average tumor weight of the experiment group was (0.083 ?0.043) g, while that of the control group was (0.28110.173) g. The difference is significant (P<0.05). It was indicated that GE7 gene delivery system could efficiently transduce exogenous gene pCEP-p21WAF-1 into hepatoma cell with high EGF receptor expression, and inhibit the cell growt     

黑素皮质素受体1——哺乳动物黑色素形成中的关键基因MC1R——the Key Gene in Mammalian Melanin Synthesis

黑色素的形成与产生在动物的生长发育过程中受到许多基因的调控。本文综述了近年来被广泛研究的哺乳动物黑色素形成调控中的一个关键基因——黑素皮质素受体1（melanocortin-1-receptor, MC1R）基因的作用机制、DNA序列变异与黑色素性状之间的关系,并且对另一重要的脊椎动物类群——鸟类中MC1R基因的确定与突变情况作以概述,此外对乌骨鸡富含黑色素的原因和鸟类的黑色素形成机制也进行了探讨。Abstract: The study of the molecular regulation mechanism of melanin synthesis during animal development has become a new focus recently .The synthesis and production of melanin during animal development are regulated by many genes. This paper summarized the molecular function mechanism of melanocortin-1-receptor (MC1R) gene and the relationship between the consequences of polymorphic variation of the gene and melanin traits, in addition to summarized the identification and mutation of MC1R gene in birds. Furthermore, the reason of abundant melanin in silkies and melanin synthesis mechanism in birds are all also discussed here.     

猪激素敏感脂肪酶(HSL)基因的研究概况

激素敏感脂肪酶(HSL)基因影响着脂肪的沉积,它在表达或活性上的轻微变异均有可能影响猪的背膘厚和瘦肉率。从激素敏感脂肪酶的功能及作用机制出发,通过候选基因策略克隆出HSL基因,将其精确定位于猪6号染色体6p1.1-1.2上;进而分析了HSL及其基因的分子结构,比较HSL基因在不同物种间的同源性。不同产肉型猪种间存在HSL基因的多态性,籍此可为了解猪脂肪沉积的基因效应、寻找与背膘厚及瘦肉率相连锁的分子标记提供通途,最终实现利用MAS、MAI等技术手段提高猪的瘦肉率。 Abstract:The gene affects the accumulation of lipid and its small variation on the activity or gene expression can influence the lean percentage and backfat traits.Based on the function and acting mechanism,this gene was cloned by candidate approach and located on the porcine chromosome 6P1.1～1.2.The molecular structure of HSL and HSL gene were analyzed.The homologies was attained by comparison between different mammal animals.The polymorphism of the gene in different pig breeds was detected.This will help the understanding of the genic effect on porcine fat deposition.The HSL gene should be regarded as a candidate gene for fatness in pis.It may have a potential use in MAS or MAI to increase the lean percentage of pig.     

Reversion of malignancy in human gastric cancer MKN—45 cells through the transfection of transforming growth factor—β type Ⅱ receptor gene

Human gastric cancer MKN-45 cells which are resistant to TGF-β growth inhibition and possess TGF-β type I and type Ⅲ receptors,but not type Ⅱ receptors,have been used as a model system to reconstitute these cancer cells with TGF-β RII cDNA.The results of these experiments indicated that the reexpression of TGF-β RII gene in MKN-45 cells can restore their sensitivity to TGF-β growth inhibition,decrease their growth rate,reduce their cloning efficiency in soft agar and tumorigenicity in nude mice in stable transfectants,in comparison with their control MKN-45 cells.Among different RII transfectants,their difference in the changes of these parameters,as a result of the regain of autocrine negative growth control by TGF-β,is roughly proportional to their level of expression of transfected RII mRNA.From these data,it is concluded that the inactivation of TGF-β RII gene is related to the escape of growth control by TGF-β in MKN-45 cells.The importance of the study of the interplay of TGF-β and its receptor system in the negative growth control of gastric cancer,and possibly also of other cancers,is discussed.     

内蒙古三个民族舌运动类型的遗传学研究

调查了内蒙古汉、蒙古、回族舌运动类型(卷舌、翻舌、叠舌、三叶舌与尖舌),共716例。研究结果显示:各种舌运动类型出现率性别间均无显著性差异;卷舌基因分别与叠、翻、尖、三叶舌基因间存在着互相作用关系,卷舌基因对叠舌基因是隐性上位基因,对翻舌、尖舌、三叶舌基因是修饰基因;内蒙古3个民族间卷、叠、尖舌出现率接近。本文首次调查并研究了尖舌性状。尖舌在过去国内外文献中未见报道。 Abstract:The tongue moving types(including tongue rolling,tongue twisting,tongue folding,clover-leaf tongue and pointed tongue)of 716 cases of Han,Mongol and Hui nationalities in Inner Mongolia were investigated.The results showed that no difference in the frequencies of various tongue moving types between male and female and that the frequencies of rolling,folding and pointed tongue were close to each other among the three nationalities of Inner Mongolia.However,some interactions between genes were revealed,that the rolling gene is a recessive epistatic gene to folding gene and a modifier gene to twisting,pointed and clover-leaf gene respectively.The research on pointed tongue in this paper has never been reported in China and abroad.     

Cloning and restriction fragment length polymorphism analysis of a cDNA for swine PIT-1, a gene controlling growth hormone expression*

A partial swine cDNA which encodes the functional domain of PIT-1 was isolated by the polymerse chain reaction (PCR). The swine PIT-1 cDNA clone is 95% identical at the protein level to the rat Pit-1 gene. Thus, Pit-l's known function in control of rat growth hormone and prolactin expression is likely to be conserved in swine. This swine cDNA clone was used to investigate genetic variability at PIT-1 in several American and Chinese breeds. Polymorphic BamIII fragments were found in pure-bred Meishan animals (n= 13), but only monomorphic fragments in five American breeds (n= 36).     

Expression pattern, genomic cloning and RFLP analyses of the swine PIT-1 gene

The swine PIT-1 POU domain cDNA was used to study PIT-1 expression and to clone the PIT-1 genomic region to identify additional PIT-1 polymorphisms. PIT-1 was expressed only in the pituitary, confirming the swine cDNA identity. To study the PIT-1 genomic region, a clone containing 13.7 kb DNA was isolated. EcoRI fragments hybridizing to PIT-1 were sequenced, and the 3′ portion of PIT-1 gene identified. Primers for polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) analysis were then designed. Restriction analysis of PCR products identified a RsaI RFLP. In contrast to other PIT-1 RFLPs, the RsaI PCR-RFLP was widely distributed in American breeds. Thus, the RsaI RFLP and the previously reported PIT-1 RFLPs allow detection of PIT-1 alleles in most, if not all, breeds currently used in the US and European reference/resource pig mapping families.     

PROP1与联合垂体激素缺乏症

垂体特异性转录因子祖先蛋白(PROP l),是成对同源转录因子,在垂体腺中呈特异性表达,参与早期胚胎垂体的发育,因此,PROP1基因对于垂体前叶的发育是必需的。PROP1启动胚胎期垂体特异性转录因子(PIT-1)的起始表达并维持个体出生后的持续表达,且可直接促使PIT-1细胞系的前体分化为促性腺细胞系。其基因突变可使人、鼠患有联合垂体激素缺乏症(CPHD),表现为生长激素(GH)、促乳素(PRL)、促甲状腺素(TSH)以及促黄体激素(LH)、促卵泡激素(FSH)或促肾上腺皮质激素(ACTH)缺乏,垂体核磁共振成像显示垂体萎缩。在其它哺乳动物中PROP1突变也会引起垂体和性腺激素异常。就PROP1基因的结构与功能,以及与CPHD间的关系作一综述。     

Dose-Dependent Dual Role of PIT-1 (POU1F1) in Somatolactotroph Cell Proliferation and Apoptosis

To test the role of wtPIT-1 (PITWT) or PIT-1 (R271W) (PIT271) in somatolactotroph cells, we established, using inducible lentiviral vectors, sublines of GH4C1 somatotroph cells that allow the blockade of the expression of endogenous PIT-1 and/or the expression of PITWT or PIT271, a dominant negative mutant of PIT-1 responsible for Combined Pituitary Hormone Deficiency in patients. Blocking expression of endogenous PIT-1 induced a marked decrease of cell proliferation. Overexpressing PITWT twofold led also to a dose-dependent decrease of cell proliferation that was accompanied by cell death. Expression of PIT271 induced a strong dose-dependent decrease of cell proliferation accompanied by a very pronounced cell death. These actions of PIT271 are independent of its interaction/competition with endogenous PIT-1, as they were unchanged when expression of endogenous PIT-1 was blocked. All these actions are specific for somatolactotroph cells, and could not be observed in heterologous cells. Cell death induced by PITWT or by PIT271 was accompanied by DNA fragmentation, but was not inhibited by inhibitors of caspases, autophagy or necrosis, suggesting that this cell death is a caspase-independent apoptosis. Altogether, our results indicate that under normal conditions PIT-1 is important for the maintenance of cell proliferation, while when expressed at supra-normal levels it induces cell death. Through this dual action, PIT-1 may play a role in the expansion/regression cycles of pituitary lactotroph population during and after lactation. Our results also demonstrate that the so-called “dominant-negative” action of PIT271 is independent of its competition with PIT-1 or a blockade of the actions of the latter, and are actions specific to this mutant variant of PIT-1.     

Modulation of phosphate uptake and amphotropic murine leukemia virus entry by posttranslational modifications of PIT-2

PIT-2 is a type III sodium phosphate cotransporter and the receptor for amphotropic murine leukemia viruses. We have investigated the expression and the functions of a tagged version of PIT-2 in CHO cells. PIT-2 remained equally abundant at the cell surface within 6 h following variation of the phosphate supply. In contrast, the efficiency of phosphate uptake and retrovirus entry was inversely related to the extracellular phosphate concentration, indicating that PIT-2 activities are modulated by posttranslational modifications of cell surface molecules induced by phosphate. Conformational changes of PIT-2 contribute to both activities, as shown by the inhibitory effect of sulfhydryl reagents known as inhibitors of type II cotransporters. A physical association of PIT-2 with actin was demonstrated. Modifications of the actin network were induced by variations of the concentrations of extracellular phosphate, cytochalasin D, or lysophosphatidic acid. They revealed that the formation of actin stress fibers determines the cell surface distribution of PIT-2, the internalization of the receptor in response to virus binding, and the capacity to process retrovirus entry. Thus, the presence of PIT-2 at the cell surface is not sufficient to ensure phosphate transport and susceptibility to amphotropic retrovirus infection. Further activation of cell surface PIT-2 molecules is required for these functions.