A novel missense mutation in the factor XII gene in a litter of cats with factor XII deficiency

被引:4
|
作者
Maruyama, Haruhiko [1 ]
Hosoe, Haruki [1 ]
Nagamatsu, Kota [2 ]
Kano, Rui [1 ]
Kamata, Hiroshi [1 ]
机构
[1] Nihon Univ, Dept Vet Med, Lab Vet Clin Pathol, 1866 Kameino, Fujisawa, Kanagawa 2520880, Japan
[2] Nagamatsu Anim Hosp, 2-3-10 Nishiku Sakaisunayama, Niigata 9502044, Japan
来源
JOURNAL OF VETERINARY MEDICAL SCIENCE | 2017年 / 79卷 / 05期
关键词
cat; factor XII; mutation; COAGULATION-FACTOR-XII; THROMBUS FORMATION; IN-VIVO;
D O I
10.1292/jvms.16-0602
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The feline F12 gene was examined to identify a mutation associated with coagulation factor XII (FXII) deficiency in a litter of 6 cats, including 2 cats with severely reduced FXII activity (7.1 and 9.3%, respectively) and 4 cats with moderately reduced FXII activity (range 36.0 to 46.3%). Cats with severely reduced FXII activity were homozygous for a G to C missense mutation in exon 13 of the F12 gene, resulting in an amino acid change (p.G544A). Cats with moderately reduced FXII activity were heterozygous for this mutation. Expression studies revealed reduced secretion of p.G544A mutant FXII protein from transfected HEK293 cells compared with wild type FXII. These results reveal a novel F12 mutation in FXII deficient cats and define the underlying mechanism for low FXII activity in homozygotes.
引用
收藏
页码:822 / 826
页数:5
相关论文
共 50 条
  • [41] Factor XII deficiency in women with recurrent miscarriage
    Yamada, H
    Kato, EH
    Ebina, Y
    Kishida, T
    Hoshi, N
    Kobashi, G
    Sakuragi, N
    Fujimoto, S
    GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 2000, 49 (02) : 80 - 83
  • [42] The discrimination of factor XII deficiency and lupus anticoagulant
    Halbmayer, WM
    Haushofer, A
    Angerer, V
    Fischer, M
    THROMBOSIS AND HAEMOSTASIS, 1996, 75 (04) : 698 - 699
  • [43] Idiopathic Angioedema and Coagulation Factor XII Mutation
    Dewald, G.
    Aygoeren-Puersuen, E.
    Saguer, I. Martinez
    Rusicke, E.
    Kreuz, W.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 127 (02) : AB99 - AB99
  • [44] Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation
    Sheng-Chieh Chou
    Ching-Yeh Lin
    Hsuan-Yu Lin
    Chen-Hsueh Pai
    Cheng-Ye Yu
    Su-Feng Kuo
    Jen-Shiou Lin
    Po-Te Lin
    Mei-Hua Hung
    Han-Ni Hsieh
    Hsiang-Chun Liu
    Ming-Ching Shen
    International Journal of Hematology, 2022, 116 : 528 - 533
  • [45] Characterization of congenital factor XII deficiency in Taiwanese patients: identification of one novel and one common mutation
    Chou, Sheng-Chieh
    Lin, Ching-Yeh
    Lin, Hsuan-Yu
    Pai, Chen-Hsueh
    Yu, Cheng-Ye
    Kuo, Su-Feng
    Lin, Jen-Shiou
    Lin, Po-Te
    Hung, Mei-Hua
    Hsieh, Han-Ni
    Liu, Hsiang-Chun
    Shen, Ming-Ching
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2022, 116 (04) : 528 - 533
  • [46] NEW FAMILIES WITH FACTOR-XII DEFICIENCY
    EGEBERG, O
    THROMBOSIS ET DIATHESIS HAEMORRHAGICA, 1970, 23 (03): : 441 - &
  • [47] A novel urticarial and Factor XII mutation-related autoinflammatory syndrome
    Mahnke, N. A.
    Scheffel, J.
    Wu, J.
    de Maat, S.
    Maas, C.
    Hofman, Z. L.
    Ennis, S.
    Holloway, J. W.
    Pengelly, R. J.
    Maurer, M.
    Krause, K.
    EXPERIMENTAL DERMATOLOGY, 2018, 27 (03) : E32 - E32
  • [48] COMPARATIVE HEMATOLOGY - STUDIES ON CATS INCLUDING ONE WITH FACTOR-XII (HAGEMAN) DEFICIENCY
    LEWIS, JH
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 1981, 68 (03): : 355 - 360
  • [49] A family with a new factor XII deficiency in Japan:: Mutation of factor XII Ichinomiya-Daiyukai identified in exon 13, codon 532 (TGC→TAC).
    Daimaru, O
    Satoh, A
    Itou, S
    Nitta, M
    Ueda, R
    BLOOD, 2000, 96 (11) : 81B - 81B
  • [50] Factor XII gene missense mutation Thr328Lys in an Arab family with hereditary angioedema type III
    Baeza, M. L.
    Rodriguez-Marco, A.
    Prieto, A.
    Rodriguez-Sainz, C.
    Zubeldia, J. M.
    Rubio, M.
    ALLERGY, 2011, 66 (07) : 981 - 982