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新型CIS家族基因的克隆与特性分析

Cloning and characterization of novel CIS family genes.

作者信息

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

机构信息

Institute of Life Science, Kurume University, Japan.

出版信息

Biochem Biophys Res Commun. 1997 Oct 20;239(2):439-46. doi: 10.1006/bbrc.1997.7484.

Abstract

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.

摘要

我们已经报道了两种结构相关的JAK信号调节剂,即细胞因子诱导的SH2蛋白(CIS)和JAK2结合蛋白(JAB)。在此,我们基于表达序列标签(EST)数据库搜索克隆了另外三个CIS家族基因(CIS2、CIS3和CIS4)。我们还在数据库中发现了该基因家族的至少另外两个候选基因。这些基因在某些造血细胞系中由促红细胞生成素和粒细胞巨噬细胞集落刺激因子诱导表达。SH2结构域和一个C端40个氨基酸的区域(称为CIS同源结构域,CH结构域)在该家族中高度保守,而这些蛋白质的N端区域相似度很低。酵母双杂交实验以及体外和体内结合实验表明,除JAB外,CIS3也与JAK2酪氨酸激酶结构域(JH1)结合,尽管CIS3与JAK2-JH1结构域的相互作用比JAB弱得多。JAB和CIS3(而非其他CIS)的瞬时表达强烈抑制了白血病抑制因子(LIF)诱导的293细胞中STAT3报告基因的激活。此外,JAB和CIS3在M1白血病细胞中的组成型过表达阻止了LIF诱导的分化和生长停滞。尽管其生理功能仍有待研究,但CIS家族基因可能通过与特定靶点相互作用在细胞因子信号的负调控中发挥作用。

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