Mouse Ror2 receptor tyrosine kinase is required for the heart development and limb formation

被引:189
作者
Takeuchi, S
Takeda, K
Oishi, I
Nomi, M
Ikeya, M
Itoh, K
Tamura, S
Ueda, T
Hatta, T
Otani, H
Terashima, T
Takada, S
Yamamura, H
Akira, S
Minami, Y
机构
[1] Kobe Univ, Sch Med, Dept Biochem, Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Hyogo Coll Med, Dept Biochem, Nishinomiya, Hyogo 6638131, Japan
[3] JST, CREST, Chiyoda Ku, Tokyo 1020081, Japan
[4] Kyoto Univ, Grad Sch Sci, Ctr Mol & Dev Biol, Sakyo Ku, Kyoto 6068502, Japan
[5] Kobe Univ, Sch Med, Dept Pathol, Chuo Ku, Kobe, Hyogo 6500017, Japan
[6] Shimane Med Univ, Dept Anat, Izumo, Shimane 6938501, Japan
[7] JST, ERATO, Kondoh Differentiat Signalling Project, Sakyo Ku, Kobe, Hyogo 6500017, Japan
关键词
D O I
10.1046/j.1365-2443.2000.00300.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Backgrounds: A mouse receptor tyrosine kinase (RTK), mRor2, which belongs to the Ror-family of RTKs consisting of at least two structurally related members, is primarily expressed in the heart and nervous system during mouse development. To elucidate the function of mRor2, we generated mice with a mutated mRor2 locus. Results: Mice with a homozygous mutation in mRor2 died just after birth, exhibiting dwarfism, severe cyanosis, and short limbs and tails. Whole-mount in situ hybridization analysis showed that mRor2 was expressed in the branchial arches, heart and limb/tailbuds, in addition to the developing nervous system. The mutants had cardiac septal defects, mainly a ventricular septal defect. In addition, an examination of the skeletal systems revealed that the mutants had shorter limbs, vertebrae and facial structure, with a particular defect in their distal portions, and that almost no calcification was observed in their distal limbs. Histological examination showed abnormalities in the chondrocytes. Conclusions: Our findings suggest that mRor2 plays essential roles in the development of the heart and in limb/tail formation, in particular cardiac septal formation and ossification of distal portions of limbs and tails.
引用
收藏
页码:71 / 78
页数:8
相关论文
共 38 条
[1]   Tracking down mutations that can stop the heart [J].
Barinaga, M .
SCIENCE, 1998, 281 (5373) :32-34
[2]   Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations [J].
Basson, CT ;
Huang, TS ;
Lin, RC ;
Bachinsky, DR ;
Weremowicz, S ;
Vaglio, A ;
Bruzzone, R ;
Quadrelli, R ;
Lerone, M ;
Romeo, G ;
Silengo, M ;
Pereira, A ;
Krieger, J ;
Mesquita, SF ;
Kamisago, M ;
Morton, CC ;
Pierpont, MEM ;
Müller, CW ;
Seidman, JG ;
Seidman, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2919-2924
[3]   Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome [J].
Basson, CT ;
Bachinsky, DR ;
Lin, RC ;
Levi, T ;
Elkins, JA ;
Soults, J ;
Grayzel, D ;
Kroumpouzou, E ;
Traill, TA ;
LeblancStraceski, J ;
Renault, B ;
Kucherlapati, R ;
Seidman, JG ;
Seidman, CE .
NATURE GENETICS, 1997, 15 (01) :30-35
[4]   Developmental genetics of the heart [J].
Burn, J ;
Goodship, J .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (03) :322-325
[5]  
Chapman DL, 1996, DEV DYNAM, V206, P379, DOI 10.1002/(SICI)1097-0177(199608)206:4<379::AID-AJA4>3.0.CO
[6]  
2-F
[7]   Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum [J].
de la Pompa, JL ;
Timmerman, LA ;
Takimoto, H ;
Yoshida, H ;
Elia, AJ ;
Samper, E ;
Potter, J ;
Wakeham, A ;
Marengere, L ;
Langille, BL ;
Crabtree, GR ;
Mak, TW .
NATURE, 1998, 392 (6672) :182-186
[8]   A C-elegans Ror receptor tyrosine kinase regulates cell motility and asymmetric cell division [J].
Forrester, WC ;
Dell, M ;
Perens, E ;
Garriga, G .
NATURE, 1999, 400 (6747) :881-885
[9]   MUSCLE-SPECIFIC TRK-RELATED RECEPTOR WITH A KRINGLE DOMAIN DEFINES A DISTINCT CLASS OF RECEPTOR TYROSINE KINASES [J].
JENNINGS, CGB ;
DYER, SM ;
BURDEN, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2895-2899
[10]   Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts [J].
Komori, T ;
Yagi, H ;
Nomura, S ;
Yamaguchi, A ;
Sasaki, K ;
Deguchi, K ;
Shimizu, Y ;
Bronson, RT ;
Gao, YH ;
Inada, M ;
Sato, M ;
Okamoto, R ;
Kitamura, Y ;
Yoshiki, S ;
Kishimoto, T .
CELL, 1997, 89 (05) :755-764