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通过Pax6、Nrl-Maf和脑抑制位点对ζ-晶体蛋白进行晶状体特异性基因招募。

Lens-specific gene recruitment of zeta-crystallin through Pax6, Nrl-Maf, and brain suppressor sites.

作者信息

Sharon-Friling R, Richardson J, Sperbeck S, Lee D, Rauchman M, Maas R, Swaroop A, Wistow G

机构信息

Section on Molecular Structure and Function, National Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Mol Cell Biol. 1998 Apr;18(4):2067-76. doi: 10.1128/MCB.18.4.2067.

Abstract

Zeta-Crystallin is a taxon-specific crystallin, an enzyme which has undergone direct gene recruitment as a structural component of the guinea pig lens through a Pax6-dependent mechanism. Tissue specificity arises through a combination of effects involving three sites in the lens promoter. The Pax6 site (ZPE) itself shows specificity for an isoform of Pax6 preferentially expressed in lens cells. High-level expression of the promoter requires a second site, identical to an alphaCE2 site or half Maf response element (MARE), adjacent to the Pax6 site. A promoter fragment containing Pax6 and MARE sites gives lens-preferred induction of a heterologous promoter. Complexes binding the MARE in lens nuclear extracts are antigenically related to Nrl, and cotransfection with Nrl elevates zeta-crystallin promoter activity in lens cells. A truncated zeta promoter containing Nrl-MARE and Pax6 sites has a high level of expression in lens cells in transgenic mice but is also active in the brain. Suppression of the promoter in the brain requires sequences between -498 and -385, and a site in this region forms specific complexes in brain extract. A three-level model for lens-specific Pax6-dependent expression and gene recruitment is suggested: (i) binding of a specific isoform of Pax6; (ii) augmentation of expression through binding of Nrl or a related factor; and (iii) suppression of promoter activity in the central nervous system by an upstream negative element in the brain but not in the lens.

摘要

ζ-晶体蛋白是一种特定分类群的晶体蛋白,它是一种通过Pax6依赖机制直接被招募作为豚鼠晶状体结构成分的酶。组织特异性是由晶状体启动子中三个位点的综合作用产生的。Pax6位点(ZPE)本身对优先在晶状体细胞中表达的Pax6同工型具有特异性。启动子的高水平表达需要第二个位点,该位点与αCE2位点或半Maf反应元件(MARE)相同,与Pax6位点相邻。包含Pax6和MARE位点的启动子片段可诱导异源启动子优先在晶状体中表达。晶状体核提取物中与MARE结合的复合物与Nrl存在抗原相关性,并且与Nrl共转染可提高晶状体细胞中ζ-晶体蛋白启动子的活性。包含Nrl-MARE和Pax6位点的截短ζ启动子在转基因小鼠的晶状体细胞中具有高水平表达,但在脑中也具有活性。脑中启动子的抑制需要-498至-385之间的序列,并且该区域中的一个位点在脑提取物中形成特异性复合物。本文提出了一个关于晶状体特异性Pax6依赖表达和基因招募的三级模型:(i)特定Pax6同工型的结合;(ii)通过Nrl或相关因子的结合增强表达;(iii)脑中上游负调控元件抑制中枢神经系统中的启动子活性,但在晶状体中不抑制。

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