Developmental expression of Pim kinases suggests functions also outside of the hematopoietic system

被引:94
作者
Eichmann, A
Yuan, L
Bréant, C
Alitalo, K
Koskinen, PJ
机构
[1] CNRS, Inst Embryol Cellulaire & Mol, F-94736 Nogent Sur Marne, France
[2] Coll France, F-94736 Nogent Sur Marne, France
[3] Univ Helsinki, Haartman Inst, FIN-00014 Helsinki, Finland
[4] Univ Turku, Abo Akad Univ, Turku Ctr Biotechnol, FIN-20520 Turku, Finland
基金
芬兰科学院;
关键词
pim kinases; quail; expression; embryonic development;
D O I
10.1038/sj.onc.1203355
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
We have cloned a novel quail cDNA with strong homology to the pint family of proto-oncogenes. The deduced amino acid (aa) sequence of the cDNA, named qpim, is more closely related to Xenopus Pim and to the recently identified rat Pim-3 than to human or rodent Pim-1 or Pim-2. The protein encoded by the qpim cDNA can autophosphorylate itself and share substrates with murine Pim-l, suggesting functional redundancy to other Pim family serine/threonine kinases. We have compared the expression of qpim in avian embryos to mouse pim-1, -2 and -3 by in situ hybridization. qpim shows a highly dynamic expression pattern, particularly at early developmental stages. Surprisingly, its expression pattern is not identical to any of the murine pint genes, which show complementary and/or partially overlapping expression sites both in- and outside of the hematopoietic system. Altogether, our results suggest novel functions for Pim family kinases during embryonic development, in particular in epithelia and in the central nervous system.
引用
收藏
页码:1215 / 1224
页数:10
相关论文
共 37 条
[1]  
Acton D, 1992, Curr Top Microbiol Immunol, V182, P293
[2]   Pim-2 transgene induces lymphoid tumors, exhibiting potent synergy with c-myc [J].
Allen, JD ;
Verhoeven, E ;
Domen, J ;
vanderValk, M ;
Berns, A .
ONCOGENE, 1997, 15 (10) :1133-1141
[3]   THE HUMAN PROTOONCOGENE PRODUCT P33PIM IS EXPRESSED DURING FETAL HEMATOPOIESIS AND IN DIVERSE LEUKEMIAS [J].
AMSON, R ;
SIGAUX, F ;
PRZEDBORSKI, S ;
FLANDRIN, G ;
GIVOL, D ;
TELERMAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8857-8861
[4]   VERY HIGH-FREQUENCY OF LYMPHOMA INDUCTION BY A CHEMICAL CARCINOGEN IN PIM-1 TRANSGENIC MICE [J].
BREUER, M ;
SLEBOS, R ;
VERBEEK, S ;
VANLOHUIZEN, M ;
WIENTJENS, E ;
BERNS, A .
NATURE, 1989, 340 (6228) :61-63
[5]  
CUYPERS HT, 1984, CELL, V37, P141
[6]  
DAUTRY F, 1988, J BIOL CHEM, V263, P17615
[7]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[8]  
DOMEN J, 1993, BLOOD, V82, P1445
[9]   PIM-1 LEVELS DETERMINE THE SIZE OF EARLY B-LYMPHOID COMPARTMENTS IN BONE-MARROW [J].
DOMEN, J ;
VANDERLUGT, NMT ;
ACTON, D ;
LAIRD, PW ;
LINDERS, K ;
BERNS, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1665-1673
[10]   KID-1, a protein kinase induced by depolarization in brain [J].
Feldman, JD ;
Vician, L ;
Crispino, M ;
Tocco, G ;
Marcheselli, VL ;
Bazan, NG ;
Baudry, M ;
Herschman, HR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (26) :16535-16543