Suppr超能文献

人类肉豆蔻酰化富含丙氨酸的C激酶底物(MARCKS)基因(MACS)。对其基因产物、启动子及染色体定位的分析。

The human myristoylated alanine-rich C kinase substrate (MARCKS) gene (MACS). Analysis of its gene product, promoter, and chromosomal localization.

作者信息

Harlan D M, Graff J M, Stumpo D J, Eddy R L, Shows T B, Boyle J M, Blackshear P J

机构信息

Howard Hughes Medical Institute Laboratories, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

J Biol Chem. 1991 Aug 5;266(22):14399-405.

PMID:1860846
Abstract

The expression of a major cellular substrate for protein kinase C, the MARCKS protein, is regulated in a cell-, tissue-, and developmental stage-specific fashion; in addition, this expression can be stimulated acutely by various cytokines in certain cell types. We have begun to characterize the human gene in order to elucidate the genetic elements responsible for this highly regulated expression. We first cloned a human MARCKS cDNA, which encoded a predicted protein of 332 amino acids (Mr 31,600) that was approximately 89, 74, and 59% identical to the bovine, mouse, and chicken proteins, respectively. Regions conserved at the amino acid level included the amino-terminal myristoylation consensus sequence, the site of intron splicing, and the phosphorylation site domain. The human cDNA was used to demonstrate that tumor necrosis factor-alpha could rapidly stimulate MARCKS gene transcription in the human promyelocytic leukemia cell line HL60. Genomic clones were then isolated; sequence analysis identified a putative promoter region that had no TATA box and contained multiple transcription initiation sites in a region spanning 57 base pairs (bp). This was followed by a 5'-untranslated region of approximately 400 bp, which displayed a complex predicted secondary structure with a delta G of -73.4 kcal/mol. Plasmid constructions containing between 52 and 1453 bp of the human MARCKS promoter linked to the human growth hormone gene were then used in transient expression experiments. Constructions containing 52 and 110 bp of the MARCKS promoter did not exhibit promoter function while the larger constructions all exhibited promotor function; the 248-bp fragment of the MARCKS promoter was 80% as effective as the human ferritin promoter in stimulating expression of human growth hormone in intact cells. Using an insert from the human genomic clone as a probe, we identified human chromosome 6, q21-qter, as the location of the MARCKS gene; this has been assigned the gene symbol MACS.

摘要

蛋白激酶C的一种主要细胞底物即MARCKS蛋白的表达,在细胞、组织和发育阶段具有特异性调控方式;此外,在某些细胞类型中,这种表达可被多种细胞因子急性刺激。为了阐明负责这种高度调控表达的遗传元件,我们已开始对人类基因进行特征分析。我们首先克隆了一个人类MARCKS cDNA,它编码一个预测的332个氨基酸的蛋白质(分子量31,600),分别与牛、小鼠和鸡的蛋白质具有约89%、74%和59%的同源性。在氨基酸水平保守的区域包括氨基末端肉豆蔻酰化共有序列、内含子剪接位点和磷酸化位点结构域。利用人类cDNA证明肿瘤坏死因子-α可快速刺激人类早幼粒细胞白血病细胞系HL60中的MARCKS基因转录。随后分离出基因组克隆;序列分析确定了一个推定的启动子区域,该区域没有TATA框,在跨越57个碱基对(bp)的区域包含多个转录起始位点。接着是一个约400 bp的5'非翻译区,其预测的二级结构复杂,ΔG为-73.4 kcal/mol。然后将含有52至1453 bp人类MARCKS启动子并与人类生长激素基因相连的质粒构建体用于瞬时表达实验。含有52和110 bp MARCKS启动子的构建体不表现出启动子功能,而较大的构建体均表现出启动子功能;MARCKS启动子的248 bp片段在完整细胞中刺激人类生长激素表达的效率是人类铁蛋白启动子的80%。使用来自人类基因组克隆的插入片段作为探针,我们确定人类6号染色体q21-qter为MARCKS基因的位置;该基因已被赋予基因符号MACS。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验