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成肌细胞分化过程中α1(VI)胶原蛋白基因的转录激活由多个GA盒介导。

Transcriptional activation of the alpha 1(VI) collagen gene during myoblast differentiation is mediated by multiple GA boxes.

作者信息

Piccolo S, Bonaldo P, Vitale P, Volpin D, Bressan G M

机构信息

Institute of Histology and Embryology, University of Padova, Italy.

出版信息

J Biol Chem. 1995 Aug 18;270(33):19583-90. doi: 10.1074/jbc.270.33.19583.

Abstract

During differentiation of ClC12 myoblasts in vitro, expression of alpha 1(VI) collagen mRNA was transiently stimulated severalfold. Promoter assays on cells transfected with chloramphenicol acetyltransferase (CAT) chimeric constructs have identified a region of the alpha 1(VI) a collagen promoter that increases CAT activity about 8-fold during differentiation. The region, which overlaps with transcription initiation sites, was shown to contain three protected segments (A, B, and C) in DNase I footprinting assays. The contact points between nuclear factors and the protected segments were determined by methylation interference assay and included the sequence GGGAGGG (GA box) in all segments. Experiments in which CAT constructs were cotransfected with double-stranded oligonucleotides containing the GA box suggested that this motif was necessary for induction. Transfections with deletion constructs of the natural promoter and with minipromoters made of three copies of A, B, or C showed that the elements have inducing activity and that elements C and, to a lower extent, B are stimulatory for basal transcription, whereas the contribution of A in this process is limited. Electrophoretic mobility shift assays with nuclear extracts from C2C12 cells indicated that the three GA box-containing elements bound several transcription factors, including Sp1. Comparison of the properties of the bands shifted under different experimental conditions (presence of 10 mM EDTA, heating of the nuclear extracts, addition of different concentrations of competitor oligonucleotides) established that A, B, and C probes form nine, eight and five main retarded complexes, respectively, and indicated that nuclear factors binding to C and B are subsets of proteins binding to A. UV cross-linking assays identified several peptides (seven with probe A, six with B, And five with C) in the range of 150-32 kDa. Comparison of the gel retardation pattern obtained with nuclear extracts from proliferating and differentiating cells revealed a particular increased intensity of two retarded bands. The data establish that multiple GA boxes mediate induction of the alpha 1(VI) collagen promoter during myoblast differentiation and suggest the attractive hypothesis that the effect may be related to variations of expression of transcription factors binding to these motifs.

摘要

在体外培养的ClC12成肌细胞分化过程中,α1(VI)胶原蛋白mRNA的表达会短暂地被刺激增加数倍。对用氯霉素乙酰转移酶(CAT)嵌合构建体转染的细胞进行启动子分析,已确定α1(VI) a胶原蛋白启动子的一个区域,该区域在分化过程中可使CAT活性增加约8倍。该区域与转录起始位点重叠,在DNase I足迹分析中显示包含三个受保护片段(A、B和C)。通过甲基化干扰分析确定了核因子与受保护片段之间的接触点,所有片段中均包含序列GGGAGGG(GA框)。将CAT构建体与含有GA框的双链寡核苷酸共转染的实验表明,该基序是诱导所必需的。用天然启动子的缺失构建体和由A、B或C的三个拷贝组成的微型启动子进行转染表明,这些元件具有诱导活性,元件C以及程度较低的元件B对基础转录有刺激作用,而A在此过程中的作用有限。用C2C12细胞的核提取物进行的电泳迁移率变动分析表明,三个含GA框的元件结合了几种转录因子,包括Sp1。比较在不同实验条件下(存在10 mM EDTA、加热核提取物、添加不同浓度的竞争寡核苷酸)迁移的条带的性质,确定A、B和C探针分别形成九个、八个和五个主要的滞后复合物,并表明与C和B结合的核因子是与A结合的蛋白质的子集。紫外线交联分析在150 - 32 kDa范围内鉴定出几种肽(探针A有七个,B有六个,C有五个)。比较增殖细胞和分化细胞的核提取物获得的凝胶阻滞模式,发现两个滞后条带的强度特别增加。数据表明多个GA框在成肌细胞分化过程中介导α1(VI)胶原蛋白启动子的诱导,并提出了一个有吸引力的假设,即这种效应可能与结合这些基序的转录因子表达的变化有关。

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