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两个启动子控制小鼠Nmp4/CIZ转录因子基因。

Two promoters control the mouse Nmp4/CIZ transcription factor gene.

作者信息

Alvarez Marta, Shah Rita, Rhodes Simon J, Bidwell Joseph P

机构信息

Department of Anatomy and Cell Biology, Indiana University School of Medicine, Medical Science Bldg 5035, 635 Barnhill Drive, Indianapolis, IN 46202, USA.

出版信息

Gene. 2005 Feb 28;347(1):43-54. doi: 10.1016/j.gene.2004.10.025. Epub 2005 Jan 21.

Abstract

Nmp4/CIZ proteins (nuclear matrix protein 4/cas interacting zinc finger protein) contribute to gene regulation in bone, blood, and testis. In osteoblasts, they govern the magnitude of gene response to osteotropic factors like parathyroid hormone (PTH). Nmp4/CIZ is recurrently involved in acute leukemia and it has been implicated in spermatogenesis. However, these conserved proteins, derived from a single gene, are expressed in numerous tissues indicative of a more generalized housekeeping function in addition to their tissue-specific roles. To address how Nmp4/CIZ expression is governed, we characterized the 5' regulatory region of the mouse Nmp4 gene, located on chromosome 6. Two adjacent promoters P(1) [-2521 nucleotide (nt)/-597 nt] and P(2) (-2521 nt/+1 nt) initiate transcription of alternative first exons (U(1) and U(2)). Both promoters lack TATA and CCAAT boxes but contain initiator sites and CpG islands. Northern analysis revealed expression of both U(1) and U(2) in numerous adult tissues consistent with the constitutive and ubiquitous activity of a housekeeping gene. Sequence analysis identified numerous potential transcription factor-binding sites significant to osteogenesis, hematopoeisis, and gonadal development. The promoters are active in both osteoblast-like cells and in the M12 B-lymphocyte cell line. Low doses of PTH attenuated P(1)/P(2) activity in osteoblast-like cells. The Nmp4/CIZ promoters are autoregulated and deletion analysis identified regions that drive P(1) and P(2) basal activities as well as regions that contain positive and negative regulatory elements affecting transcription. The Nmp4/CIZ promoters comprise a genomic regulatory architecture that supports constitutive expression as well as cell- and tissue-specific regulation.

摘要

Nmp4/CIZ蛋白(核基质蛋白4/与钙调蛋白相互作用的锌指蛋白)在骨骼、血液和睾丸的基因调控中发挥作用。在成骨细胞中,它们控制着对甲状旁腺激素(PTH)等促骨因子的基因反应强度。Nmp4/CIZ经常参与急性白血病,并且与精子发生有关。然而,这些源自单一基因的保守蛋白,除了其组织特异性作用外,还在许多组织中表达,这表明它们具有更广泛的管家功能。为了研究Nmp4/CIZ的表达是如何调控的,我们对位于6号染色体上的小鼠Nmp基因的5'调控区进行了特征分析。两个相邻的启动子P(1) [-2521核苷酸(nt)/-597 nt]和P(2) (-2521 nt/+1 nt)启动了不同的第一个外显子(U(1)和U(2))的转录。两个启动子都缺乏TATA盒和CCAAT盒,但含有起始位点和CpG岛。Northern分析显示,U(1)和U(2)在许多成年组织中均有表达,这与管家基因的组成性和普遍活性一致。序列分析确定了许多对成骨、造血和性腺发育具有重要意义的潜在转录因子结合位点。这些启动子在成骨样细胞和M12 B淋巴细胞系中均具有活性。低剂量的PTH可减弱成骨样细胞中P(1)/P(2)的活性。Nmp4/CIZ启动子存在自我调控,缺失分析确定了驱动P(1)和P(2)基础活性的区域,以及包含影响转录的正调控和负调控元件的区域。Nmp4/CIZ启动子构成了一种基因组调控结构,支持组成性表达以及细胞和组织特异性调控。

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