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编码S-腺苷甲硫氨酸脱羧酶的两个大鼠基因的结构与染色体定位

Structures and chromosomal localizations of two rat genes encoding S-adenosylmethionine decarboxylase.

作者信息

Pulkka A, Ihalainen R, Suorsa A, Riviere M, Szpirer J, Pajunen A

机构信息

Biocenter University of Oulu, Finland.

出版信息

Genomics. 1993 May;16(2):342-9. doi: 10.1006/geno.1993.1195.

DOI:10.1006/geno.1993.1195
PMID:8314573
Abstract

S-Adenosylmethionine decarboxylase (AdoMetDC) is a ubiquitous enzyme in eukaryotic cells and responds to a wide variety of stimuli affecting growth. To provide a framework for understanding the molecular basis of the mechanisms responsible for regulating the expression of this enzyme activity, we recently cloned and sequenced the rat gene for AdoMetDC. Now we have isolated another, slightly different AdoMetDC gene from a rat genomic library. Comparison of the two genes shows a high degree of conservation of sequence and structural organization. The two genes share the following characteristics: (1) both are approximately 16 kb in size, have identical exon/intron boundaries, and exhibit similar intron/exon structural organization; and (2) the nucleotide sequences are highly conserved in the coding regions and in many introns. Analysis of mouse-rat somatic cell hybrids has localized both rat genes to chromosome 20. The most interesting feature of these genes is that their 5' flanking regions are totally different. The promoter activities of the 5' regulatory regions were assessed by transient gene expression assays in Rat-2 cells after fusion to the chloramphenicol acetyltransferase gene. Transient transfections with the chimeric DNAs demonstrated that these fragments were able to function as efficient promoters, indicating that the diverging 5' regions of two AdoMetDC genes contain functional, but different, regulatory transcription elements.

摘要

S-腺苷甲硫氨酸脱羧酶(AdoMetDC)是真核细胞中一种普遍存在的酶,对影响生长的多种刺激作出反应。为了提供一个框架来理解调节这种酶活性表达机制的分子基础,我们最近克隆并测序了大鼠AdoMetDC基因。现在我们从大鼠基因组文库中分离出了另一个略有不同的AdoMetDC基因。对这两个基因的比较显示出高度的序列和结构组织保守性。这两个基因具有以下共同特征:(1)两者大小均约为16 kb,具有相同的外显子/内含子边界,并呈现相似的内含子/外显子结构组织;(2)核苷酸序列在编码区和许多内含子中高度保守。对小鼠-大鼠体细胞杂种的分析已将两个大鼠基因都定位到第20号染色体上。这些基因最有趣的特征是它们的5'侧翼区域完全不同。在与氯霉素乙酰转移酶基因融合后,通过在Rat-2细胞中的瞬时基因表达测定来评估5'调控区的启动子活性。用嵌合DNA进行的瞬时转染表明,这些片段能够作为有效的启动子发挥作用,这表明两个AdoMetDC基因不同的5'区域含有功能性但不同的调控转录元件。

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