Targeted disruption of the β adducin gene (Add2) causes red blood cell spherocytosis in mice

被引:100
作者
Gilligan, DM
Lozovatsky, L
Gwynn, B
Brugnara, C
Mohandas, N
Peters, LL
机构
[1] Yale Univ, Sch Med, Dept Internal Med Hematol, New Haven, CT 06510 USA
[2] Jackson Lab, Bar Harbor, ME 04609 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[4] Childrens Hosp, Dept Lab Med, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.96.19.10717
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adducins are a family of cytoskeleton proteins encoded by three genes (alpha, beta, gamma), In a comprehensive assay of gene expression, we show the ubiquitous expression of alpha- and gamma-adducins in contrast to the restricted expression of beta-adducin, beta-adducin is expressed at high levels in brain and hematopoietic tissues (bone marrow in humans, spleen in mice). To elucidate adducin's role in vivo, we created beta-adducin null mice by gene targeting, deleting exons 9-13, A 55-kDa chimeric polypeptide is produced from the first eight exons of beta-adducin and part of the neo cassette in spleen but is not detected in peripheral RBCs or brain. beta-adducin null RBCs are osmotically fragile, spherocytic, and dehydrated compared with the wild type, resembling RBCs from patients with hereditary spherocytosis, The lack of beta-adducin in RBCs leads to decreased membrane incorporation of alpha-adducin (30% of normal) and unexpectedly promotes a 5-fold increase in gamma-adducin incorporation into the RBC membrane skeleton. This study demonstrates adducin's importance to RBC membrane stability in vivo.
引用
收藏
页码:10717 / 10722
页数:6
相关论文
共 23 条
[11]   Regulation of the association of adducin with actin filaments by Rho-associated kinase (Rho-kinase) and myosin phosphatase [J].
Kimura, K ;
Fukata, Y ;
Matsuoka, Y ;
Bennett, V ;
Matsuura, Y ;
Okawa, K ;
Iwamatsu, A ;
Kaibuchi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5542-5548
[12]   A new function for adducin - Calicium calmodulin-regulated capping of the barbed ends of actin filaments [J].
Kuhlman, PA ;
Hughes, CA ;
Bennett, V ;
Fowler, VM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (14) :7986-7991
[13]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[14]   GENOMIC ORGANIZATION OF THE HUMAN ALPHA-ADDUCIN GENE AND ITS ALTERNATELY SPLICED ISOFORMS [J].
LIN, BY ;
NASIR, J ;
MCDONALD, H ;
GRAHAM, R ;
ROMMENS, JM ;
GOLDBERG, YP ;
HAYDEN, MR .
GENOMICS, 1995, 25 (01) :93-99
[15]   Adducin regulation - Definition of the calmodulin-binding domain and sites of phosphorylation by protein kinase A and C [J].
Matsuoka, Y ;
Hughes, CA ;
Bennett, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (41) :25157-25166
[16]   ERYTHROCYTE ADDUCIN - A CALMODULIN-REGULATED ACTIN-BUNDLING PROTEIN THAT STIMULATES SPECTRIN ACTIN BINDING [J].
MISCHE, SM ;
MOOSEKER, MS ;
MORROW, JS .
JOURNAL OF CELL BIOLOGY, 1987, 105 (06) :2837-2845
[17]  
PALFREY HC, 1985, J BIOL CHEM, V260, P6021
[18]  
PETERS LL, 1992, BLOOD, V80, P2122
[19]  
PETERS LL, 1999, IN PRESS HEMATOPOIES
[20]  
Robertson E. J., 1987, TERATOCARCINOMAS EMB