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人心房钠尿肽基因中心脏特异性表达的顺式作用决定因素。

Cis-active determinants of cardiac-specific expression in the human atrial natriuretic peptide gene.

作者信息

Wu J P, Kovacic-Milivojević B, Lapointe M C, Nakamura K, Gardner D G

机构信息

Department of Medicine, University of California, San Francisco 94143-0516.

出版信息

Mol Endocrinol. 1991 Sep;5(9):1311-22. doi: 10.1210/mend-5-9-1311.

Abstract

Expression of the human atrial natriuretic peptide (hANP)gene is controlled by a series of positive and negative cis-acting regulatory elements present in the 5' flanking sequences (5'FS) of the gene. Positive elements located between -1150 and -222, relative to the transcription start site, appear to be responsible for the major portion of ANP gene expression in neonatal rat cardiac atrial cells. While neonatal ventricular cardiocytes, at a qualitative level, seem to employ regulatory signals similar to their atrial counterparts, they do so with reduced efficiency. Expression of the hANP gene in nonmyocardial cells is limited by the presence of silencer elements in the distal (-2593 to -1150) and proximal (-222 to the CAP site) 5'FS. Further characterization of a 64-base pair cardiac-specific element (-410 to -332), described previously, revealed that a core sequence of 40 base pairs is required for functional activity. This core sequence includes a previously defined DNAse-I footprint region flanked by two GC-rich segments arranged in an inverted repeat-like array. These findings suggest that the disparity in atrial vs. ventricular cardiocyte expression of the ANP gene reflects differences that are largely quantitative in nature, while differences in myocardial vs. nonmyocardial cells result from fundamental qualitative differences in the way these cells recognize and use the regulatory elements present within the 5'FS.

摘要

人心房钠尿肽(hANP)基因的表达受该基因5'侧翼序列(5'FS)中一系列正负顺式作用调节元件的控制。相对于转录起始位点,位于-1150至-222之间的正向元件似乎负责新生大鼠心脏心房细胞中ANP基因表达的主要部分。虽然新生心室心肌细胞在定性水平上似乎采用与其心房对应细胞相似的调节信号,但效率较低。hANP基因在非心肌细胞中的表达受到远端(-2593至-1150)和近端(-222至CAP位点)5'FS中沉默元件的限制。先前描述的一个64个碱基对的心脏特异性元件(-410至-332)的进一步表征表明,功能活性需要一个40个碱基对的核心序列。该核心序列包括一个先前定义的DNA酶I足迹区域,两侧是两个富含GC的片段,以反向重复样阵列排列。这些发现表明,ANP基因在心房与心室心肌细胞中的表达差异在很大程度上反映了数量上的差异,而心肌细胞与非心肌细胞之间的差异则源于这些细胞识别和利用5'FS中存在的调节元件方式的根本定性差异。

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