Cloning and characterization of novel CIS family genes

被引:231
作者
Masuhara, M
Sakamoto, H
Matsumoto, A
Suzuki, R
Yasukawa, H
Mitsui, K
Wakioka, T
Tanimura, S
Sasaki, A
Misawa, H
Yokouchi, M
Ohtsubo, M
Yoshimura, A
机构
[1] KURUME UNIV,INST LIFE SCI,KURUME,FUKUOKA 839,JAPAN
[2] KURUME UNIV,FAC MED,DEPT SURG,KURUME,FUKUOKA 830,JAPAN
[3] KURUME UNIV,FAC MED,DEPT ORTHOPAED SURG,KURUME,FUKUOKA 830,JAPAN
关键词
D O I
10.1006/bbrc.1997.7484
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 reported two JAK-signaling modulators, CIS (cytokine-inducible SH2 protein) and JAB (JAK2 binding protein), which are structurally related. Here we cloned three additional CIS family genes (CIS2, CIS3, and CIS4) on the basis of an expression sequence tag (EST) database search. We also found at least two additional candidates of this gene family in the database. These genes were induced by erythropoietin and granulocyte-macrophage colony stimulating factor in certain hematopoietic cell lines. The SH2 domain and a C-terminal 40 amino acid region, designated the CIS homology domain (CH domain), are highly conserved in this family, while the N-terminal regions of these proteins share little similarity. A yeast two hybrid assay and in vitro and in vivo binding assays revealed that in addition to JAB, CIS3 bound to the JAK2 tyrosine kinase domain (JH1), although the interaction of CIS3 with the JAK2-JH1 domain was much weaker than that of JAB. Transient expression of JAB and CIS3, but not other CISs, strongly inhibited leukemia inhibitory factor (LIF)-induced STAT3-reporter gene activation in 293 cells. Furthermore, constitutive overexpression of JAB and CIS3 in M1 leukemia cells prevented LIF-induced differentiation and growth arrest. Although the physiological function remains to be investigated, CIS family genes could play a role in the negative regulation of cytokine signaling by interacting with specific targets. (C) 1997 Academic Press.
引用
收藏
页码:439 / 446
页数:8
相关论文
共 26 条
  • [1] [Anonymous], P NATL ACAD SCI US
  • [2] CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES
    ARAI, K
    LEE, F
    MIYAJIMA, A
    MIYATAKE, S
    ARAI, N
    YOKOTA, T
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 : 783 - 836
  • [3] CHIBA S, 1991, BLOOD, V78, P2261
  • [4] JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS
    DARNELL, JE
    KERR, IM
    STARK, GR
    [J]. SCIENCE, 1994, 264 (5164) : 1415 - 1421
  • [5] ENDO AT, 1997, NATURE, V387, P921
  • [6] CYTOKINE RECEPTOR SIGNALING
    IHLE, JN
    [J]. NATURE, 1995, 377 (6550) : 591 - 594
  • [7] STATs: Signal transducers and activators of transcription
    Ihle, JN
    [J]. CELL, 1996, 84 (03) : 331 - 334
  • [8] Regulation of interferon-gamma-activated STAT1 by the ubiquitin-proteasome pathway
    Kim, TK
    Maniatis, T
    [J]. SCIENCE, 1996, 273 (5282) : 1717 - 1719
  • [9] CONSTITUTIVELY ACTIVATING MUTATIONS OF C-KIT RECEPTOR TYROSINE KINASE CONFER FACTOR-INDEPENDENT GROWTH AND TUMORIGENICITY OF FACTOR-DEPENDENT HEMATOPOIETIC-CELL LINES
    KITAYAMA, H
    KANAKURA, Y
    FURITSU, T
    TSUJIMURA, T
    ORITANI, K
    IKEDA, H
    SUGAHARA, H
    MITSUI, H
    KANAYAMA, Y
    KITAMURA, Y
    MATSUZAWA, Y
    [J]. BLOOD, 1995, 85 (03) : 790 - 798
  • [10] SPECIFIC RECRUITMENT OF SH-PTP1 TO THE ERYTHROPOIETIN RECEPTOR CAUSES INACTIVATION OF JAK2 AND TERMINATION OF PROLIFERATIVE SIGNALS
    KLINGMULLER, U
    LORENZ, U
    CANTLEY, LC
    NEEL, BG
    LODISH, HF
    [J]. CELL, 1995, 80 (05) : 729 - 738