Novel Drosophila tumor necrosis factor class molecule (
    1.
    发明申请
    Novel Drosophila tumor necrosis factor class molecule ("DmTNF") and variants thereof 审中-公开
    新型果蝇肿瘤坏死因子分子(“DmTNF”)及其变体

    公开(公告)号:US20060147974A1

    公开(公告)日:2006-07-06

    申请号:US11345126

    申请日:2006-02-01

    CPC分类号: C07K14/525 A01K2217/05

    摘要: The present invention provides novel polynucleotides encoding Drosophila DmTNF polypeptides, fragments and homologs thereof. The present invention also is directed to novel polynucleotides encoding two Drosophila DmTNF variants, DmTNFv1 and DmTNFv2 polypeptides, fragments and homologs thereof. Also provided are vectors, host cells, antibodies, and recombinant and synthetic methods for producing said polypeptides. The invention further relates to screening methods for identifying agonists and antagonists of the polynucleotides and polypeptides of the present invention, in addition to methods of genetically modifying Drosophila or cultured cells to express or mis-express DmTNF, DmTNFv1, or DmTNFv2. The invention also relates to the use of such modified insects or cells to characterize DmTNF activity, identify TNF-like genes and/or genes implicated in modulating TNF, characterize TNF signaling pathways, and/or to identify modulators of DmTNF activity.

    摘要翻译: 本发明提供了编码果蝇DmTNF多肽的新型多核苷酸,其片段和同系物。 本发明还涉及编码两种果蝇DmTNF变体,DmTNFv1和DmTNFv2多肽的新型多核苷酸,其片段和同系物。 还提供了载体,宿主细胞,抗体以及用于产生所述多肽的重组和合成方法。 除了遗传修饰果蝇或培养细胞以表达或错误表达DmTNF,DmTNFv1或DmTNFv2的方法之外,本发明还涉及用于鉴定本发明的多核苷酸和多肽的激动剂和拮抗剂的筛选方法。 本发明还涉及这种修饰的昆虫或细胞用于表征DmTNF活性,鉴定涉及调节TNF,表征TNF信号传导途径和/或鉴定DmTNF活性调节剂的TNF-样基因和/或基因的用途。

    Dropsophila tumor necrosis factor class molecule (“DmTNFv2”)
    2.
    发明授权
    Dropsophila tumor necrosis factor class molecule (“DmTNFv2”) 有权
    谷类肿瘤坏死因子分子(“DmTNFv2”)

    公开(公告)号:US07288632B2

    公开(公告)日:2007-10-30

    申请号:US11142736

    申请日:2005-06-01

    IPC分类号: C07K14/00

    CPC分类号: C07K14/525 A01K2217/05

    摘要: The present invention provides novel polynucleotides encoding Drosophila DmTNF polypeptides, fragments and homologs thereof. The present invention also is directed to novel polynucleotides encoding two Drosophila DmTNF variants, DmTNFv1 and DmTNFv2 polypeptides, fragments and homologs thereof. Also provided are vectors, host cells, antibodies, and recombinant and synthetic methods for producing said polypeptides. The invention further relates to screening methods for identifying agonists and antagonists of the polynucleotides and polypeptides of the present invention, in addition to methods of genetically modifying Drosophila or cultured cells to express or mis-express DmTNF, DmTNFv1, or DmTNFv2. The invention also relates to the use of such modified insects or cells to characterize DmTNF activity, identify TNF-like genes and/or genes implicated in modulating TNF, characterize TNF signaling pathways, and/or to identify modulators of DmTNF activity.

    摘要翻译: 本发明提供了编码果蝇DmTNF多肽的新型多核苷酸,其片段和同系物。 本发明还涉及编码两种果蝇DmTNF变体,DmTNFv1和DmTNFv2多肽的新型多核苷酸,其片段和同系物。 还提供了载体,宿主细胞,抗体以及用于产生所述多肽的重组和合成方法。 除了遗传修饰果蝇或培养细胞以表达或错误表达DmTNF,DmTNFv1或DmTNFv2的方法之外,本发明还涉及用于鉴定本发明的多核苷酸和多肽的激动剂和拮抗剂的筛选方法。 本发明还涉及这种修饰的昆虫或细胞用于表征DmTNF活性,鉴定涉及调节TNF,表征TNF信号传导途径和/或鉴定DmTNF活性调节剂的TNF-样基因和/或基因的用途。

    Recombinant gene which enhances the ability of fish to tolerate low dissolved oxygen stress and the use thereof
    3.
    发明授权
    Recombinant gene which enhances the ability of fish to tolerate low dissolved oxygen stress and the use thereof 失效
    提高鱼容忍低溶解氧应激能力的重组基因及其应用

    公开(公告)号:US08546644B2

    公开(公告)日:2013-10-01

    申请号:US12879931

    申请日:2010-09-10

    摘要: The invention discloses a recombinant gene which enhances the ability of fish to tolerate low dissolved oxygen (DO) stress and the use thereof. Carp β-actin gene promoter is used as a promoter and Vitreoscilla hemoglobin gene is used as a target gene, so as to construct the recombinant Vitreoscilla hemoglobin gene driven by carp β-actin promoter. The modeling organism zebrafish is used as the research object, and the recombinant gene is microinjected into zygotes of zebrafish. After PCR screening and 156 h low DO stress test, transgenic fish are obtained with a survival rate of 92%, which is significantly different from the survival rate of 65% of the control fish group. The vhb transgenic zebrafish obtain hypoxia tolerance. When the recombinant gene is applied to the economically farmed species, i.e., blunt snout bream (Megalobrama amblycephala) and common carp (Cyprinus carpio L.), it enhances their hypoxia tolerance as well. Such genetically improved breeding technique may be widely used for breeding new excellent farmed species with the hypoxia tolerance.

    摘要翻译: 本发明公开了一种提高鱼耐受低溶解氧(DO)应力的能力及其用途的重组基因。 将鲤鱼β-肌动蛋白基因启动子用作启动子,并使用透明颤菌血红蛋白基因作为靶基因,构建由鲤鱼β-肌动蛋白启动子驱动的重组透明颤菌血红蛋白基因。 将造型生物斑马鱼作为研究对象,将重组基因显微注射到斑马鱼的合子中。 PCR筛选和156小时DO胁迫试验后,获得转基因鱼的成活率为92%,与对照鱼组65%的存活率显着不同。 vhb转基因斑马鱼获得缺氧耐受。 当将重组基因应用于经济养殖的物种,即钝鼻鲷(Megalobrama amblycephala)和鲤鱼(Cyprinus carpio L.)时,也增强了它们的缺氧耐受性。 这种遗传改良育种技术可广泛用于育种具有缺氧耐受性的新优良种植品种。

    RECOMBINANT GENE WHICH ENHANCES THE ABILITY OF FISH TO TOLERATE LOW DISSOLVED OXYGEN STRESS AND THE USE THEREOF
    4.
    发明申请
    RECOMBINANT GENE WHICH ENHANCES THE ABILITY OF FISH TO TOLERATE LOW DISSOLVED OXYGEN STRESS AND THE USE THEREOF 失效
    提高鱼的耐受能力,以减少低溶解氧的应力及其使用的重组基因

    公开(公告)号:US20110099648A1

    公开(公告)日:2011-04-28

    申请号:US12879931

    申请日:2010-09-10

    摘要: The invention discloses a recombinant gene which enhances the ability of fish to tolerate low dissolved oxygen (DO) stress and the use thereof. Carp β-actin gene promoter is used as a promoter and Vitreoscilla hemoglobin gene is used as a target gene, so as to construct the recombinant Vitreoscilla hemoglobin gene driven by carp β-actin promoter. The modeling organism zebrafish is used as the research object, and the recombinant gene is microinjected into zygotes of zebrafish. After PCR screening and 156 h low DO stress test, transgenic fish are obtained with a survival rate of 92%, which is significantly different from the survival rate of 65% of the control fish group. The vhb transgenic zebrafish obtain hypoxia tolerance. When the recombinant gene is applied to the economically farmed species, i.e., blunt snout bream (Megalobrama amblycephala) and common carp (Cyprinus carpio L.), it enhances their hypoxia tolerance as well. Such genetically improved breeding technique may be widely used for breeding new excellent farmed species with the hypoxia tolerance.

    摘要翻译: 本发明公开了一种提高鱼耐受低溶解氧(DO)应力的能力及其用途的重组基因。 使用鲤鱼β-肌动蛋白基因启动子作为启动子,将透明颤菌血红蛋白基因作为靶基因,构建由鲤鱼和肌动蛋白启动子驱动的重组透明颤菌血红蛋白基因。 将造型生物斑马鱼作为研究对象,将重组基因显微注射到斑马鱼的合子中。 PCR筛选和156小时DO胁迫试验后,获得转基因鱼的成活率为92%,与对照鱼组65%的存活率显着不同。 vhb转基因斑马鱼获得缺氧耐受。 当将重组基因应用于经济养殖的物种,即钝鼻鲷(Megalobrama amblycephala)和鲤鱼(Cyprinus carpio L.)时,也增强了它们的缺氧耐受性。 这种遗传改良育种技术可广泛用于育种具有缺氧耐受性的新优良种植品种。

    Drosophila tumor necrosis factor class molecule (
    5.
    发明申请
    Drosophila tumor necrosis factor class molecule ("DmTNFv2") 有权
    果蝇肿瘤坏死因子分子(“DmTNFv2”)

    公开(公告)号:US20050227283A1

    公开(公告)日:2005-10-13

    申请号:US11142736

    申请日:2005-06-01

    CPC分类号: C07K14/525 A01K2217/05

    摘要: The present invention provides novel polynucleotides encoding Drosophila DmTNF polypeptides, fragments and homologs thereof. The present invention also is directed to novel polynucleotides encoding two Drosophila DmTNF variants, DmTNFv1 and DmTNFv2 polypeptides, fragments and homologs thereof. Also provided are vectors, host cells, antibodies, and recombinant and synthetic methods for producing said polypeptides. The invention further relates to screening methods for identifying agonists and antagonists of the polynucleotides and polypeptides of the present invention, in addition to methods of genetically modifying Drosophila or cultured cells to express or mis-express DmTNF, DmTNFv1, or DmTNFv2. The invention also relates to the use of such modified insects or cells to characterize DmTNF activity, identify TNF-like genes and/or genes implicated in modulating TNF, characterize TNF signaling pathways, and/or to identify modulators of DmTNF activity.

    摘要翻译: 本发明提供了编码果蝇DmTNF多肽的新型多核苷酸,其片段和同系物。 本发明还涉及编码两种果蝇DmTNF变体,DmTNFv1和DmTNFv2多肽的新型多核苷酸,其片段和同系物。 还提供了载体,宿主细胞,抗体以及用于产生所述多肽的重组和合成方法。 除了遗传修饰果蝇或培养细胞以表达或错误表达DmTNF,DmTNFv1或DmTNFv2的方法之外,本发明还涉及用于鉴定本发明的多核苷酸和多肽的激动剂和拮抗剂的筛选方法。 本发明还涉及这种修饰的昆虫或细胞用于表征DmTNF活性,鉴定涉及调节TNF,表征TNF信号传导途径和/或鉴定DmTNF活性调节剂的TNF-样基因和/或基因的用途。