The full-length leptin receptor has signaling capabilities of interleukin 6-type cytokine receptors

被引:709
作者
Baumann, H
Morella, KK
White, DW
Dembski, M
Bailon, PS
Kim, HK
Lai, CF
Tartaglia, LA
机构
[1] MILLENNIUM PHARMACEUT INC,CAMBRIDGE,MA 02139
[2] HOFFMANN LA ROCHE INC,NUTLEY,NJ 07110
关键词
obesity; transcription induction; signal transducer and activator of transcription activation;
D O I
10.1073/pnas.93.16.8374
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
The leptin receptor (OB-R) is a single membrane-spanning protein that mediates the weight regulatory effects of leptin (OB protein). The mutant allele (db) of the OB-R gene encodes a protein with a truncated cytoplasmic domain that is predicted to be functionally inactive. Several mRNA splice variants encoding OB-Rs with different length cytoplasmic domains have been detected in various tissues. Here we demonstrate that the full-length OB-R (predominantly expressed in the hypothalamus), but not a major naturally occurring truncated form or a mutant form found in db/db mice, can mediate activation of signal transducer and activator of transcription (STAT) proteins and stimulate transcription through interleukin 6 responsive gene elements. Reconstitution experiments suggest that, although OB-R mediates intracellular signals with a specificity similar to interleukin 6-type cytokine receptors, signaling appears to be independent of the gp130 signal transducing component of the interleukin 6-type cytokine receptors.
引用
收藏
页码:8374 / 8378
页数:5
相关论文
共 30 条
[1]   MULTIPLE REGIONS WITHIN THE CYTOPLASMIC DOMAINS OF THE LEUKEMIA INHIBITORY FACTOR-RECEPTOR AND GP130 COOPERATE IN SIGNAL-TRANSDUCTION IN HEPATIC AND NEURONAL CELLS [J].
BAUMANN, H ;
SYMES, AJ ;
COMEAU, MR ;
MORELLA, KK ;
WANG, YP ;
FRIEND, D ;
ZIEGLER, SF ;
FINK, JS ;
GEARING, DP .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (01) :138-146
[2]  
BAUMANN H, 1989, ANN NY ACAD SCI, V557, P280
[3]   Evidence that the diabetes gene encodes the leptin receptor: Identification of a mutation in the leptin receptor gene in db/db mice [J].
Chen, H ;
Charlat, O ;
Tartaglia, LA ;
Woolf, EA ;
Weng, X ;
Ellis, SJ ;
Lakey, ND ;
Culpepper, J ;
Moore, KJ ;
Breitbart, RE ;
Duyk, GM ;
Tepper, RI ;
Morgenstern, JP .
CELL, 1996, 84 (03) :491-495
[4]   IDENTIFICATION AND CLONING OF ELF-1, A DEVELOPMENTALLY EXPRESSED LIGAND FOR THE MEK4 AND SEK RECEPTOR TYROSINE KINASES [J].
CHENG, HJ ;
FLANAGAN, JG .
CELL, 1994, 79 (01) :157-168
[5]  
Chevalier S, 1995, ANN NY ACAD SCI, V762, P482
[6]   Phenotypes of mouse diabetes and rat fatty due to mutations in the OB (leptin) receptor [J].
Chua, SC ;
Chung, WK ;
WuPeng, XS ;
Zhang, YY ;
Liu, SM ;
Tartaglia, L ;
Leibel, RL .
SCIENCE, 1996, 271 (5251) :994-996
[7]   EFFECTS OF PARABIOSIS OF OBESE WITH DIABETES AND NORMAL MICE [J].
COLEMAN, DL .
DIABETOLOGIA, 1973, 9 (04) :294-298
[8]   OBESE AND DIABETES - 2 MUTANT-GENES CAUSING DIABETES-OBESITY SYNDROMES IN MICE [J].
COLEMAN, DL .
DIABETOLOGIA, 1978, 14 (03) :141-148
[9]   NEW TECHNIQUE FOR ASSAY OF INFECTIVITY OF HUMAN ADENOVIRUS 5 DNA [J].
GRAHAM, FL ;
VANDEREB, AJ .
VIROLOGY, 1973, 52 (02) :456-467
[10]   A GENERAL-METHOD OF INVITRO PREPARATION AND SPECIFIC MUTAGENESIS OF DNA FRAGMENTS - STUDY OF PROTEIN AND DNA INTERACTIONS [J].
HIGUCHI, R ;
KRUMMEL, B ;
SAIKI, RK .
NUCLEIC ACIDS RESEARCH, 1988, 16 (15) :7351-7367