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Sc1-70是否调节系统性硬化症中的胶原蛋白生成?

Does Sc1-70 modulate collagen production in systemic sclerosis?

作者信息

Douvas A

机构信息

Clinical Immunology and Rheumatic Disease Section, University of Southern California, Los Angeles 90033.

出版信息

Lancet. 1988 Aug 27;2(8609):475-7. doi: 10.1016/s0140-6736(88)90122-5.

Abstract

Sc1-70, an autoantigen in systemic sclerosis, may accelerate collagen gene transcription by virtue of its activity as a topoisomerase I (topo I), a DNA template-modifying enzyme. A survey of sequences corresponding to all or part of the known topo I binding sequence AGAACTTAGAGAAAATTTAAA in four fibrillar collagen genes (three of them dermal) and sixteen non-collagen genes showed a striking preponderance of the tetramer 5'-CTTA-3', comprising the core of this binding sequence, at the exon-intron junctions of the fibrillar collagen genes (59% compared with 16% in the control group). In addition, a non-random clustering of three potential topo I binding sites was seen within 350 base-pairs of 5' flanking DNA in the dermal collagen gene alpha 2(I), and a fourth site occurred in the promoter region of the alpha 1(III) gene. The findings suggest that a selective vulnerability to the action of Sc1-70/topo I is built into the structure of the dermal collagen genes.

摘要

硬皮病中的自身抗原Sc1-70,可能因其作为拓扑异构酶I(拓扑酶I)(一种DNA模板修饰酶)的活性而加速胶原蛋白基因转录。对四个纤维状胶原蛋白基因(其中三个为真皮基因)和十六个非胶原蛋白基因中全部或部分已知拓扑酶I结合序列AGAACTTAGAGAAAATTTAAA的对应序列进行调查,结果显示,在纤维状胶原蛋白基因的外显子-内含子连接处,包含该结合序列核心的四聚体5'-CTTA-3'显著占优势(59%,而对照组为16%)。此外,在真皮胶原蛋白基因α2(I)的5'侧翼DNA的350个碱基对内,发现了三个潜在拓扑酶I结合位点的非随机聚集,并且在α1(III)基因的启动子区域出现了第四个位点。这些发现表明,真皮胶原蛋白基因的结构中存在对Sc1-70/拓扑酶I作用的选择性易感性。

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