SH2-B is required for both male and female reproduction

被引:55
作者
Ohtsuka, S
Takaki, S
Iseki, M
Miyoshi, K
Nakagata, N
Kataoka, Y
Yoshida, N
Takatsu, K
Yoshimura, A
机构
[1] Kyushu Univ, Med Inst Bioregulat, Div Mol & Cellular Immunol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kurume Univ, Inst Life Sci, Div Mol Genet, Kurume, Fukuoka 8390861, Japan
[3] Kumamoto Univ, Ctr Anim Res & Dev, Div Reprod Engn, Kumamoto 8600811, Japan
[4] Univ Tokyo, Inst Med Sci, Div Immunol, Dept Microbiol & Immunol,Minato Ku, Tokyo 1088639, Japan
[5] Univ Tokyo, Inst Med Sci, Lab Gene Express & Regulat, Ctr Med Expt,Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.1128/MCB.22.9.3066-3077.2002
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
Many growth factors and hormones modulate the reproductive status in mammals. Among these, insulin and insulin-like growth factor I (IGF-I) regulate the development of gonadal tissues. SH2-B has been shown to interact with insulin and IGF-I receptors, although the role of SH2-B in these signals has not been clarified. To investigate the role of SH2-B, we generated mice with a targeted disruption of the SH2-B gene. Both male and female SH2-B-/- mice showed slight retardation in growth and impaired fertility. Female knockout mice possess small, anovulatory ovaries with reduced numbers of follicles and male SH2-B-/- mice have small testes with a reduced number of sperm. SH2-B-/- cumulus cells do not respond to either follicle-stimulating hormone or IGF-I. These data suggest that SH2-B plays a critical role in the IGF-1-mediated reproductive pathway in mice.
引用
收藏
页码:3066 / 3077
页数:12
相关论文
共 48 条
[31]   Jak2 is essential for signaling through a variety of cytokine receptors [J].
Parganas, E ;
Wang, D ;
Stravopodis, D ;
Topham, DJ ;
Marine, JC ;
Teglund, S ;
Vanin, EF ;
Bodner, S ;
Colamonici, OR ;
van Deursen, JM ;
Grosveld, G ;
Ihle, JN .
CELL, 1998, 93 (03) :385-395
[32]   Identification and characterization of novel substrates of TrK receptors in developing neurons [J].
Qian, XZ ;
Riccio, A ;
Zhang, Y ;
Ginty, DD .
NEURON, 1998, 21 (05) :1017-1029
[33]  
Riedel H, 1997, J BIOCHEM-TOKYO, V122, P1105
[34]   Differential binding to and regulation of JAK2 by the SH2 domain and N-terminal region of SH2-Bβ [J].
Rui, LY ;
Gunter, DR ;
Herrington, J ;
Carter-Su, C .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (09) :3168-3177
[35]   SH2-B, a membrane-associated adapter, is phosphorylated on multiple serines/threonines in response to nerve growth factor by kinases within the MEK/ERK cascade [J].
Rui, LY ;
Herrington, J ;
Carter-Su, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26485-26492
[36]   Platelet-derived growth factor (PDGF) stimulates the association of SH2-Bβ with PDGF receptor and phosphorylation of SH2-Bβ [J].
Rui, LY ;
Carter-Su, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (33) :21239-21245
[37]   Identification of SH2-Bβ as a potent cytoplasmic activator of the tyrosine kinase Janus kinase 2 [J].
Rui, LY ;
Carter-Su, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7172-7177
[38]   Identification of SH2-B beta as a substrate of the tyrosine kinase JAK2 involved in growth hormone signaling [J].
Rui, LY ;
Mathews, LS ;
Hotta, K ;
Gustafson, TA ;
CarterSu, C .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (11) :6633-6644
[39]   Characterization of Lnk - An adaptor protein expressed in lymphocytes [J].
Takaki, S ;
Watts, JD ;
Forbush, KA ;
Nguyen, NT ;
Hayashi, J ;
AlberolaIla, J ;
Aebersold, R ;
Perlmutter, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) :14562-14570
[40]   Enhanced Hematopoiesis by hematopoietic progenitor cells lacking intracellular adaptor protein, Lnk [J].
Takaki, S ;
Morita, H ;
Tezuka, Y ;
Takatsu, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (02) :151-160