Mizuno K, Hasegawa K, Katagiri T, Ogimoto M, Ichikawa T, Yakura H
Tokyo Metropolitan Institute for Neuroscience, Japan.
Mol Cell Biol. 1993 Sep;13(9):5513-23. doi: 10.1128/mcb.13.9.5513-5523.1993.
Protein tyrosine phosphatases (PTPs), together with protein tyrosine kinases (PTKs), are involved in the regulation of cell activation, growth, and differentiation. To further elucidate the fine tuning of cell growth and differentiation through tyrosine phosphorylation, we tried to isolate mouse receptor-type PTP (RPTP) cDNA clones by screening mouse brain cDNA libraries with mouse CD45 PTP domain probes under reduced-stringency conditions. Characterization of isolated cDNA clones for RPTP showed that the cytoplasmic region contains two tandem repeats of PTP domain of about 230 amino acids with intrinsic phosphatase activity. The extracellular region was composed of immunoglobulin (Ig)-like domains and fibronectin type III (FN-III)-like domains. The gene was highly homologous to human PTP delta (HPTP delta) and thus was named MPTP delta (murine counterpart of HPTP delta). The MPTP delta gene appeared to generate at least three species of mRNA, which differ in the composition of the extracellular domain: type A, one Ig-like and four FN-III-like domains; type B, one Ig-like and eight FN-III-like domains; and type C, three Ig-like and eight FN-III-like domains. Interestingly, the 5' untranslated region and the leader peptide of types A and B were completely different from those of type C. Northern (RNA) blot analysis demonstrated that brain, kidney, and heart cells express three mRNA species of about 7 kb. Antibody directed against part of the extracellular domain of type A MPTP delta recognized a 210-kDa protein in brain and kidney lysates. In situ hybridization of brain samples revealed that MPTP delta mRNA is present in the hippocampus, thalamic reticular nucleus, and piriform cortex, where some Src family PTKs have been also demonstrated to exist. Although MPTP delta mRNA was not detected in lymphoid tissues, all of the pre-B-cell lines tested and one of three B-cell lines tested expressed MPTP delta mRNA, whereas antibody-producing B-cell hybridomas and T-cell and macrophage lines did not. Finally, the MPTP delta locus was tightly linked to the brown (b) locus on mouse chromosome 4.
蛋白酪氨酸磷酸酶(PTP)与蛋白酪氨酸激酶(PTK)共同参与细胞活化、生长和分化的调控。为了进一步阐明通过酪氨酸磷酸化对细胞生长和分化的精细调节,我们尝试在低严谨条件下,用小鼠CD45 PTP结构域探针筛选小鼠脑cDNA文库,以分离小鼠受体型PTP(RPTP)cDNA克隆。对分离出的RPTP cDNA克隆的表征显示,其胞质区域包含两个约230个氨基酸的PTP结构域串联重复序列,具有内在磷酸酶活性。细胞外区域由免疫球蛋白(Ig)样结构域和纤连蛋白III型(FN-III)样结构域组成。该基因与人PTPδ(HPTPδ)高度同源,因此被命名为MPTPδ(HPTPδ的小鼠对应物)。MPTPδ基因似乎产生至少三种mRNA,它们在细胞外结构域的组成上有所不同:A型,一个Ig样和四个FN-III样结构域;B型,一个Ig样和八个FN-III样结构域;C型,三个Ig样和八个FN-III样结构域。有趣的是,A型和B型的5'非翻译区和前导肽与C型完全不同。Northern(RNA)印迹分析表明,脑、肾和心脏细胞表达三种约7 kb的mRNA。针对A型MPTPδ细胞外结构域部分的抗体在脑和肾裂解物中识别出一种210 kDa的蛋白质。脑样本的原位杂交显示,MPTPδ mRNA存在于海马体、丘脑网状核和梨状皮质中,在这些部位也已证明存在一些Src家族PTK。尽管在淋巴组织中未检测到MPTPδ mRNA,但所有测试的前B细胞系和三个测试的B细胞系中的一个表达MPTPδ mRNA,而产生抗体的B细胞杂交瘤以及T细胞和巨噬细胞系则不表达。最后,MPTPδ基因座与小鼠4号染色体上的棕色(b)基因座紧密连锁。