Molecular cloning of a cDNA encoding canine factor IX.

Abstract:

:Factor IX (F.IX) is a vitamin K-dependent plasma protein, a deficiency of which results in hemophilia B. A canine model of hemophilia B exists; attempts to use this model for gene transfer experiments or characterization of the hemophilic defect require elucidation of normal canine F.IX structure. We report the isolation and characterization of the coding region for canine F.IX cDNA. Canine F.IX possesses 86% identity at the amino-acid level with human F.IX. The leader peptide, Gla domain, EGF domains, and the carboxy-terminal portion of the heavy chains show extensive sequence conservation between the canine and human. All Glu residues undergoing gamma-carboxylation in humans are conserved in canines. The complete coding sequence for canine F.IX has been determined, and the derived translation product has been analyzed. A similar approach should allow identification of the causative mutation in canine hemophilia B. Furthermore, this clone may prove a valuable resource in gene transfer experiments for this disease.

journal_name

Blood

journal_title

Blood

authors

Evans JP,Watzke HH,Ware JL,Stafford DW,High KA

subject

Has Abstract

pub_date

1989-07-01 00:00:00

pages

207-12

issue

1

eissn

0006-4971

issn

1528-0020

journal_volume

74

pub_type

杂志文章

相关文献

BLOOD文献大全
  • Caspase activation is required for nitric oxide-mediated, CD95(APO-1/Fas)-dependent and independent apoptosis in human neoplastic lymphoid cells.

    abstract::Nitric oxide (NO), an important effector molecule involved in immune regulation and host defense, was shown to induce apoptosis in lymphoma cells. In the present report the NO donor glycerol trinitrate was found to induce apoptosis in Jurkat cells that are sensitive to CD95-mediated kill. In contrast, a CD95-resistant...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Chlichlia K,Peter ME,Rocha M,Scaffidi C,Bucur M,Krammer PH,Schirrmacher V,Umansky V

    更新日期:1998-06-01 00:00:00

  • Transforming genes in human leukemia cells.

    abstract::High-molecular weight DNAs of fresh bone marrow cells from 32 patients with fresh leukemia were assayed for the presence of transmissible activated transforming genes by a DNA-mediated gene transfer technique using NIH/3T3 cells. DNAs of bone marrow cells from four of the 32 patients induced transformation of NIH/3T3 ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Hirai H,Tanaka S,Azuma M,Anraku Y,Kobayashi Y,Fujisawa M,Okabe T,Urabe A,Takaku F

    更新日期:1985-12-01 00:00:00

  • Persistent macrocytosis assessed by erythrocyte subpopulation analysis following erythrocyte regeneration in cats.

    abstract::Serial erythrocyte volume distribution curves were used to characterize changes in erythrocyte subpopulations following the induction of Heinz body hemolytic anemia in cats. Macrocytes produced in response to hemolysis were observed after loss of reticulum. After recovery from hemolysis, a gradual reduction in mean ce...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Weiser MG,Kociba GJ

    更新日期:1982-08-01 00:00:00

  • Molecular mechanisms of thrombus formation in ischemic stroke: novel insights and targets for treatment.

    abstract::In ischemic stroke, treatment options are limited. Therapeutic thrombolysis is restricted to the first few hours after stroke, and the utility of current platelet aggregation inhibitors, including GPIIb/IIIa receptor antagonists, and anticoagulants is counterbalanced by the risk of intracerebral bleeding complications...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2008-04-144758

    authors: Stoll G,Kleinschnitz C,Nieswandt B

    更新日期:2008-11-01 00:00:00

  • Exploiting the kinetic interplay between GPIbα-VWF binding interfaces to regulate hemostasis and thrombosis.

    abstract::Platelet-von Willebrand factor (VWF) interactions must be tightly regulated in order to promote effective hemostasis and prevent occlusive thrombus formation. However, it is unclear what role the inherent properties of the bond formed between the platelet receptor glycoprotein Ibα and the A1 domain of VWF play in thes...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-04-569392

    authors: Chen J,Zhou H,Diacovo A,Zheng XL,Emsley J,Diacovo TG

    更新日期:2014-12-11 00:00:00

  • The cytoplasmic NPM mutant induces myeloproliferation in a transgenic mouse model.

    abstract::Although NPM1 gene mutations leading to aberrant cytoplasmic expression of nucleophosmin (NPMc(+)) are the most frequent genetic lesions in acute myeloid leukemia, there is yet no experimental model demonstrating their oncogenicity in vivo. We report the generation and characterization of a transgenic mouse model expr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-03-208587

    authors: Cheng K,Sportoletti P,Ito K,Clohessy JG,Teruya-Feldstein J,Kutok JL,Pandolfi PP

    更新日期:2010-04-22 00:00:00

  • A deletion mutation causes hemophilia B in Lhasa Apso dogs.

    abstract::Hemophilia B is a bleeding disorder caused by a deficiency of clotting factor IX (FIX). A colony of FIX deficient Lhasa Apso dogs has been established and the molecular basis of hemophilia B has been determined. The plasma factor IX levels were < 1% of normal canine levels in affected dogs. A complex deletion mutation...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Mauser AE,Whitlark J,Whitney KM,Lothrop CD Jr

    更新日期:1996-11-01 00:00:00

  • B-cell development in the thymus is limited by inhibitory signals from the thymic microenvironment.

    abstract::B-cell precursors are present in the thymus, and the thymic microenvironment is the source of lymphopoietic factors that include interleukin-7 (IL-7). Despite the fact that intrathymic B-cell progenitors are bone marrow-derived cells, the data in this report demonstrate that these progenitors accumulate at an early pr...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-03-0733

    authors: Hashimoto Y,Montecino-Rodriguez E,Leathers H,Stephan RP,Dorshkind K

    更新日期:2002-11-15 00:00:00

  • Targeting Sirt-1 controls GVHD by inhibiting T-cell allo-response and promoting Treg stability in mice.

    abstract::Graft-versus-host disease (GVHD) remains one of the major complications after allogeneic bone marrow transplantation (allo-BMT). Sirtuin-1 (Sirt-1) plays a crucial role in various biological processes including cellular senescence, metabolism, and inflammatory responses. Sirt-1 deacetylation regulates different transc...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2018-07-863233

    authors: Daenthanasanmak A,Iamsawat S,Chakraborty P,Nguyen HD,Bastian D,Liu C,Mehrotra S,Yu XZ

    更新日期:2019-01-17 00:00:00

  • Myocardial fibrosis in mice with overexpression of human blood coagulation factor IX.

    abstract::Elevated circulatory levels of many blood coagulation factors are known to be a risk factor for deep vein thrombosis in humans. Here we report the first direct demonstration of a close association between elevated circulatory factor IX levels in mice with thrombosis as well as myocardial fibrosis. Transgenic mice over...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-05-1581

    authors: Ameri A,Kurachi S,Sueishi K,Kuwahara M,Kurachi K

    更新日期:2003-03-01 00:00:00

  • Retinoic acid inhibits CD40 + interleukin-4-mediated IgE production in vitro.

    abstract::To elucidate the role of retinoic acid (RA) in anti-CD40 + interleukin-4 (IL-4)-mediated B-cell activation, the effect of 10(-12) to 10(-6) mol/L RA was studied in anti-CD40 (1 microgram/mL) + IL-4 (5 ng/mL)-mediated proliferation and Ig synthesis by human peripheral blood mononuclear cells (PBMC) and B cells in healt...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Worm M,Krah JM,Manz RA,Henz BM

    更新日期:1998-09-01 00:00:00

  • Notch1 as a potential therapeutic target in cutaneous T-cell lymphoma.

    abstract::Deregulation of Notch signaling has been linked to the development of T-cell leukemias and several solid malignancies. Yet, it is unknown whether Notch signaling is involved in the pathogenesis of mycosis fungoides and Sézary syndrome, the most common subtypes of cutaneous T-cell lymphoma. By immunohistochemistry of 4...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-12-260216

    authors: Kamstrup MR,Gjerdrum LM,Biskup E,Lauenborg BT,Ralfkiaer E,Woetmann A,Ødum N,Gniadecki R

    更新日期:2010-10-07 00:00:00

  • Toward a stem cell gene therapy for breast cancer.

    abstract::Current approaches for treatment of late-stage breast cancer rarely result in a long-term cure. In part this is due to tumor stroma that prevents access of systemically or intratumorally applied therapeutics. We propose a stem cell gene therapy approach for controlled tumor stroma degradation that uses the pathophysio...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2008-10-187237

    authors: Li Z,Liu Y,Tuve S,Xun Y,Fan X,Min L,Feng Q,Kiviat N,Kiem HP,Disis ML,Lieber A

    更新日期:2009-05-28 00:00:00

  • Changing the differentiation program of hematopoietic cells: retinoic acid-induced shift of eosinophil-committed cells to neutrophils.

    abstract::The mechanisms by which hematopoietic progenitor cells become lineage-committed remain poorly understood. A cloned subline of the AML14 cell line (AML14.3D10) that spontaneously differentiates to eosinophilic myelocytes in the absence of cytokine stimulation was obtained by limiting dilution. This subline exhibits aug...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Paul CC,Mahrer S,Tolbert M,Elbert BL,Wong I,Ackerman SJ,Baumann MA

    更新日期:1995-11-15 00:00:00

  • VH gene rearrangement events can modify the immunoglobulin heavy chain during progression of B-lineage acute lymphoblastic leukemia.

    abstract::The presence of multiple VHDJH joinings in upwards of 30% of acute lymphoblastic leukemias (ALL) suggests a relative instability of the rearranged immunoglobulin heavy chain (IgH) gene, but the mechanisms involved are not completely understood. An investigation of the structure of the VHDJH joinings using complementar...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Wasserman R,Yamada M,Ito Y,Finger LR,Reichard BA,Shane S,Lange B,Rovera G

    更新日期:1992-01-01 00:00:00

  • Acute graft-versus-host disease: a bench-to-bedside update.

    abstract::Over the past 5 years, many novel approaches to early diagnosis, prevention, and treatment of acute graft-versus-host disease (aGVHD) have been translated from the bench to the bedside. In this review, we highlight recent discoveries in the context of current aGVHD care. The most significant innovations that have alre...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2014-01-514786

    authors: Holtan SG,Pasquini M,Weisdorf DJ

    更新日期:2014-07-17 00:00:00

  • Antithrombin Milano: a new variant with monomeric and dimeric inactive antithrombin III.

    abstract::A qualitative defect of antithrombin III (AT III) has been demonstrated over three generations in eight members of an Italian family by the discrepancy between a normal amount of antigen and decreased antithrombin and anti-Xa activity in the presence or in the absence of heparin. By two-dimensional immunoelectrophores...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Wolf M,Boyer C,Tripodi A,Meyer D,Larrieu MJ,Mannucci PM

    更新日期:1985-02-01 00:00:00

  • Expression of the thymosin beta 4 gene during differentiation of hematopoietic cells.

    abstract::Thymosin beta 4 (T beta 4) was originally isolated as a thymic hormone. Its functional properties remain obscure; however, the N-terminal peptidic sequence could have a regulatory function on hematopoietic stem cell proliferation. To investigate the mechanism of T beta 4 expression, we studied T beta 4 gene expression...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Shimamura R,Kudo J,Kondo H,Dohmen K,Gondo H,Okamura S,Ishibashi H,Niho Y

    更新日期:1990-09-01 00:00:00

  • An autonomous CEBPA enhancer specific for myeloid-lineage priming and neutrophilic differentiation.

    abstract::Neutrophilic differentiation is dependent on CCAAT enhancer-binding protein α (C/EBPα), a transcription factor expressed in multiple organs including the bone marrow. Using functional genomic technologies in combination with clustered regularly-interspaced short palindromic repeat (CRISPR)/CRISPR-associated protein 9 ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2016-01-695759

    authors: Avellino R,Havermans M,Erpelinck C,Sanders MA,Hoogenboezem R,van de Werken HJ,Rombouts E,van Lom K,van Strien PM,Gebhard C,Rehli M,Pimanda J,Beck D,Erkeland S,Kuiken T,de Looper H,Gröschel S,Touw I,Bindels E,Delwel

    更新日期:2016-06-16 00:00:00

  • Murine malaria decreases hemopoietic stem cells.

    abstract::The causes of anemia and immunosuppression, major outcomes of malaria, are not well established. This study was undertaken to investigate whether erythropoietin (EP) production is adequate and whether the hemopoietic stem cells (CFU-S) were affected during the course of infection. Groups of female Balb/c mice infected...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Silverman PH,Schooley JC,Mahlmann LJ

    更新日期:1987-02-01 00:00:00

  • X-linked chronic granulomatous disease: correction of NADPH oxidase defect by retrovirus-mediated expression of gp91-phox.

    abstract::Chronic granulomatous disease (CGD) is an inherited immunodeficiency resulting from the inability of an individual's phagocytes to produce superoxide anions because of defective NADPH oxidase. The disease may be treated by bone marrow transplantation and as such is a candidate for somatic gene therapy. Two thirds of p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Porter CD,Parkar MH,Levinsky RJ,Collins MK,Kinnon C

    更新日期:1993-10-01 00:00:00

  • Kinetics and mechanism of the bactericidal action of human neutrophils against Escherichia coli.

    abstract::A mutant strain of Escherichia coli (E. coli ML-35) was used to follow the kinetics of phagocytosis, perforation of the bacterial cell envelope, and inactivation of bacterial proteins by human neutrophils. This particular E. coli mutant strain has no lactose permease, but constitutively forms the cytoplasmic enzyme be...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Hamers MN,Bot AA,Weening RS,Sips HJ,Roos D

    更新日期:1984-09-01 00:00:00

  • Clonal chromosomal abnormalities appearing in Philadelphia chromosome-negative metaphases during CML treatment.

    abstract::Clonal chromosomal abnormalities in Philadelphia chromosome-negative (CCA/Ph-) metaphases emerge as patients with chronic phase chronic myeloid leukemia (CP-CML) are treated with tyrosine kinase inhibitors (TKIs). We assessed the characteristics and prognostic impact of 598 patients with CP-CML treated on clinical tri...

    journal_title:Blood

    pub_type: 临床试验,杂志文章

    doi:10.1182/blood-2017-07-792143

    authors: Issa GC,Kantarjian HM,Gonzalez GN,Borthakur G,Tang G,Wierda W,Sasaki K,Short NJ,Ravandi F,Kadia T,Patel K,Luthra R,Ferrajoli A,Garcia-Manero G,Rios MB,Dellasala S,Jabbour E,Cortes JE

    更新日期:2017-11-09 00:00:00

  • How I treat lymphoma in pregnancy.

    abstract::Lymphomas afflict all age groups of people, with certain types demonstrating a female predilection in adolescents and young adults. A proportion of lymphomas that are diagnosed in this population demographic occur in the setting of pregnancy. Most of these behave aggressively at presentation and require immediate or u...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2019000961

    authors: Dunleavy K,McLintock C

    更新日期:2020-11-05 00:00:00

  • Serotonin induces the expression of tissue factor and plasminogen activator inhibitor-1 in cultured rat aortic endothelial cells.

    abstract::Serotonin (5-hydroxytryptamine, or 5-HT), released from activated platelets, not only accelerates aggregation of platelets but also is known to promote mitosis, migration, and contraction of vascular smooth muscle cells (VSMCs). These effects are considered to contribute to thrombus formation and atherosclerosis. The ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v97.6.1697

    authors: Kawano H,Tsuji H,Nishimura H,Kimura S,Yano S,Ukimura N,Kunieda Y,Yoshizumi M,Sugano T,Nakagawa K,Masuda H,Sawada S,Nakagawa M

    更新日期:2001-03-15 00:00:00

  • Myeloablative radiochemotherapy followed by autologous stem cell transplantation in first remission prolongs progression-free survival in follicular lymphoma: results of a prospective, randomized trial of the German Low-Grade Lymphoma Study Group.

    abstract::Conventional chemotherapy has failed to substantially prolong survival for patients with advanced follicular lymphoma. To improve outcomes, the German Low-Grade Lymphoma Study Group (GLSG) initiated a randomized trial to compare the effect of potentially curative myeloablative radiochemotherapy followed by autologous ...

    journal_title:Blood

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1182/blood-2004-03-0982

    authors: Lenz G,Dreyling M,Schiegnitz E,Forstpointner R,Wandt H,Freund M,Hess G,Truemper L,Diehl V,Kropff M,Kneba M,Schmitz N,Metzner B,Pfirrmann M,Unterhalt M,Hiddemann W,German Low-Grade Lymphoma Study Group.

    更新日期:2004-11-01 00:00:00

  • Clinical relevance of BCL-2 overexpression in childhood acute lymphoblastic leukemia.

    abstract::Enforced BCL-2 gene expression in leukemic cell lines suppresses apoptosis and confers resistance to anticancer drugs, but the clinical significance of increased BCL-2 protein levels in acute lymphoblastic leukemia (ALL) is unknown. Among 52 children with newly diagnosed ALL, BCL-2 expression in leukemic lymphoblasts ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Coustan-Smith E,Kitanaka A,Pui CH,McNinch L,Evans WE,Raimondi SC,Behm FG,Aricò M,Campana D

    更新日期:1996-02-01 00:00:00

  • Proteins encoded by genes involved in chromosomal alterations in lymphoma and leukemia: clinical value of their detection by immunocytochemistry.

    abstract::Acquired chromosomal anomalies (most commonly translocations) in lymphoma and leukemia usually result in either activation of a quiescent gene (by means of immunoglobulin or T-cell-receptor promotors) and expression of an intact protein product, or creation of a fusion gene encoding a chimeric protein. This review sum...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood.v99.2.409

    authors: Falini B,Mason DY

    更新日期:2002-01-15 00:00:00

  • HLA class II-restricted antigen presentation of endogenous bcr-abl fusion protein by chronic myelogenous leukemia-derived dendritic cells to CD4(+) T lymphocytes.

    abstract::Bcr-abl fusion peptide-specific CD4+ T-lymphocyte clones have recently been shown to augment colony formation by chronic myelogenous leukemia (CML) cells in a bcr-abl type-specific and HLA class II-restricted manner without addition of exogenous antigen. These findings suggest that CML cells can naturally process and ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.v98.5.1498

    authors: Yasukawa M,Ohminami H,Kojima K,Hato T,Hasegawa A,Takahashi T,Hirai H,Fujita S

    更新日期:2001-09-01 00:00:00

  • MALT1 and the API2-MALT1 fusion act between CD40 and IKK and confer NF-kappa B-dependent proliferative advantage and resistance against FAS-induced cell death in B cells.

    abstract::The most frequently recurring translocations in mucosa-associated lymphoid tissue (MALT) B-cell non-Hodgkin lymphoma, t(11;18)(q21;q21) and t(14;18)(q32; q21), lead to formation of an API2-MALT1 fusion or IgH-mediated MALT1 overexpression. Various approaches have implicated these proteins in nuclear factor kappaB (NF-...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2004-06-2297

    authors: Ho L,Davis RE,Conne B,Chappuis R,Berczy M,Mhawech P,Staudt LM,Schwaller J

    更新日期:2005-04-01 00:00:00