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Stat4,一种在早期髓系分化中表达的新型γ干扰素激活位点结合蛋白。

Stat4, a novel gamma interferon activation site-binding protein expressed in early myeloid differentiation.

作者信息

Yamamoto K, Quelle F W, Thierfelder W E, Kreider B L, Gilbert D J, Jenkins N A, Copeland N G, Silvennoinen O, Ihle J N

机构信息

Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, Tennessee 38105.

出版信息

Mol Cell Biol. 1994 Jul;14(7):4342-9. doi: 10.1128/mcb.14.7.4342-4349.1994.

Abstract

Interferon regulation of gene expression is dependent on the tyrosine phosphorylation and activation of the DNA-binding activity of two related proteins of 91 kDa (STAT1) and/or 113 kDa (STAT2). Recent studies have suggested that these proteins are substrates of Janus kinases and that proteins related in STAT1 are involved in a number of signalling pathways, including those activated in myeloid cells by erythropoietin and interleukin-3 (IL-3). To clone STAT-related proteins from myeloid cells, degenerate oligonucleotides were used in PCRs to identify novel family members expressed in myeloid cells. This approach allowed the identification and cloning of the Stat4 gene, which is 52% identical to STAT1. Unlike STAT1, Stat4 expression is restricted but includes myeloid cells and spermatogonia. In the erythroid lineage, Stat4 expression is differentially regulated during differentiation. Functionally, Stat4 has the properties of other STAT family genes. In particular, cotransfection of expression constructs for Stat4 and Jak1 and Jak2 results in the tyrosine phosphorylation of Stat4 and the acquisition of the ability to bind to the gamma interferon (IFN-gamma)-activated sequence of the interferon regulatory factor 1 (IRF-1) gene. Stat4 is located on mouse chromosome 1 and is tightly linked to the Stat1 gene, suggesting that the genes arose by gene duplication. Unlike Stat1, neither IFN-alpha nor IFN-gamma activates Stat4. Nor is Stat4 activated in myeloid cells by a number of cytokines, including erythropoietin, IL-3, granulocyte colony-stimulating factor, stem cell factor, colon-stimulating factor 1, hepatocyte growth factor, IL-2, IL-4, and IL-6.

摘要

干扰素对基因表达的调控依赖于91 kDa(STAT1)和/或113 kDa(STAT2)这两种相关蛋白的酪氨酸磷酸化及其DNA结合活性的激活。最近的研究表明,这些蛋白是Janus激酶的底物,且与STAT1相关的蛋白参与了许多信号通路,包括在髓样细胞中由促红细胞生成素和白细胞介素-3(IL-3)激活的信号通路。为了从髓样细胞中克隆与STAT相关的蛋白,在聚合酶链反应(PCR)中使用简并寡核苷酸来鉴定在髓样细胞中表达的新家族成员。这种方法使得Stat4基因得以鉴定和克隆,它与STAT1有52%的同源性。与STAT1不同,Stat4的表达受到限制,但包括髓样细胞和精原细胞。在红系谱系中,Stat4的表达在分化过程中受到差异调控。在功能上,Stat4具有其他STAT家族基因的特性。特别是,将Stat4、Jak1和Jak2的表达构建体共转染会导致Stat4的酪氨酸磷酸化,并获得与干扰素调节因子1(IRF-1)基因的γ干扰素(IFN-γ)激活序列结合的能力。Stat4位于小鼠1号染色体上,与Stat1基因紧密连锁,这表明这些基因是通过基因复制产生的。与Stat1不同,干扰素-α和干扰素-γ均不能激活Stat4。在髓样细胞中,促红细胞生成素、IL-3、粒细胞集落刺激因子、干细胞因子、结肠刺激因子1、肝细胞生长因子、IL-2、IL-4和IL-6等多种细胞因子也不能激活Stat4。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f073/358805/c48f256d58b6/molcellb00007-0021-a.jpg

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