The novel CALM interactor CATS influences the subcellular localization of the leukemogenic fusion protein CALM/AF10

被引:46
作者
Archangelo, L. Froehlich
Glaeser, J.
Krause, A.
Bohlander, S. K.
机构
[1] Univ Munich, Dept Med 3, Grosshadern Hosp, D-81377 Munich, Germany
[2] GSF Munich, Clin Cooperat Grp Leukemia, Munich, Germany
[3] Univ Gottingen, Inst Human Genet, D-3400 Gottingen, Germany
关键词
CALM/AF10; PICALM; leukemia; nucleolus;
D O I
10.1038/sj.onc.1209438
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Clathrin Assembly Lymphoid Myeloid leukemia gene (CALM or PICALM) was first identified as the fusion partner of AF10 in the t(10;11)(p13;q14) translocation, which is observed in acute myeloid leukemia (AML), acute lymphoblastic leukemia (ALL) and malignant lymphoma. The CALM/AF10 fusion protein plays a crucial role in t(10;11)(p13;q14) associated leukemogenesis. Using the N-terminal half of CALM as a bait in a yeast two-hybrid screen, a novel protein named CATS (CALM interacting protein expressed in thymus and spleen) was identified. Multiple tissue Northern blot analysis showed predominant expression of CATS in thymus, spleen and colon. CATS codes for two protein isoforms of 238 and 248 amino acids (aa). The interaction between CALM and CATS could be confirmed using pull down assays, co-immunoprecipitation and colocalization experiments. The CATS interaction domain of CALM was mapped to aa 221-335 of CALM. This domain is contained in the CALM/AF10 fusion protein. CATS localizes to the nucleus and shows a preference for nucleoli. Expression of CATS was able to markedly increase the nuclear localization of CALM and of the leukemogenic fusion protein CALM/AF10. The possible implications of these findings for CALM/AF10-mediated leukemogenesis are discussed.
引用
收藏
页码:4099 / 4109
页数:11
相关论文
共 41 条
[1]   Incidence of MLL rearrangement in acute myeloid leukemia, and a CALM-AF10 fusion in M4 type acute myeloblastic leukemia [J].
Abdou, SMH ;
Jadayel, DM ;
Min, T ;
Swansbury, GJ ;
Dainton, MG ;
Jafer, O ;
Powles, RL ;
Catovsky, D .
LEUKEMIA & LYMPHOMA, 2002, 43 (01) :89-95
[2]   CALM-AF10 is a common fusion transcript in T-ALL and is specific to the TCR-γδ lineage [J].
Asnafi, V ;
Radford-Weiss, I ;
Dastugue, N ;
Bayle, C ;
Leboeuf, D ;
Charrin, C ;
Garand, R ;
Lafage-Pochitaloff, M ;
Delabesse, E ;
Buzyn, A ;
Troussard, X ;
Macintyre, E .
BLOOD, 2003, 102 (03) :1000-1006
[3]   Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins [J].
Ayton, PM ;
Cleary, ML .
ONCOGENE, 2001, 20 (40) :5695-5707
[4]   Molecular analysis of the CALM/AF10 fusion: identical rearrangements in acute myeloid leukemia, acute lymphoblastic leukemia and malignant lymphoma patients [J].
Bohlander, SK ;
Muschinsky, V ;
Schrader, K ;
Siebert, R ;
Schlegelberger, B ;
Harder, L ;
Schemmel, V ;
Fonatsch, C ;
Ludwig, WD ;
Hiddemann, W ;
Dreyling, MH .
LEUKEMIA, 2000, 14 (01) :93-99
[5]   Identification and molecular characterization of CALM/AF10 fusion products in T cell acute lymphoblastic leukemia and acute myeloid leukemia [J].
Carlson, KM ;
Vignon, C ;
Bohlander, S ;
Martinez-Climent, JA ;
Le Beau, MM ;
Rowley, JD .
LEUKEMIA, 2000, 14 (01) :100-104
[6]   Perturbed endocytosis by CALM-containing fusion proteins: A leukemogenic mechanism in AML. [J].
Chao, MM ;
Walker, AC ;
Pendergast, MB ;
Bohlander, SK ;
Wechsler, DS .
BLOOD, 2004, 104 (11) :922A-923A
[7]   A NOVEL CLASS OF ZINC-FINGER LEUCINE-ZIPPER GENES IDENTIFIED FROM THE MOLECULAR-CLONING OF THE T(10-11) TRANSLOCATION IN ACUTE-LEUKEMIA [J].
CHAPLIN, T ;
AYTON, P ;
BERNARD, OA ;
SAHA, V ;
DELLAVALLE, V ;
HILLION, J ;
GREGORINI, A ;
LILLINGTON, D ;
BERGER, R ;
YOUNG, BD .
BLOOD, 1995, 85 (06) :1435-1441
[8]   The ENTH domain [J].
De Camilli, P ;
Chen, H ;
Hyman, J ;
Panepucci, E ;
Bateman, A ;
Brunger, AT .
FEBS LETTERS, 2002, 513 (01) :11-18
[9]  
Delabesse E, 2004, BLOOD, V104, p315A
[10]  
Deshpande A, 2003, BLOOD, V102, p216A